Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Sophora flavescens, known in traditional Chinese medicine as Ku Shen, is chiefly used as a decoction of its dried root to treat inflammatory and infectious conditions. Among the Han Chinese, the root is boiled with water for 30–60 minutes and the resulting tea is drunk to relieve fever, sore throat, and skin eruptions (Li et al., 2015). In Korean folk medicine, a similar decoction of the root is employed to reduce swelling and pain in rheumatic joints, and the plant is also macerated in alcohol to produce a tincture for topical application on bruises (Kim et al., 2018). Vietnamese practitioners prepare a poultice by crushing the root, mixing it with a small amount of water, and applying the paste to ulcers and abscesses to promote healing (Nguyen et al., 2019). These preparations are all based on infusions or decoctions of the root, the principal medicinal part of the plant.

A simple decoction recipe that can be made at home is as follows: take 10 g of dried Sophora flavescens root, add 200 ml of boiling water, and simmer for 30 minutes. Strain the liquid, discard the solids, and drink 1–2 cups of the tea per day. This dose is considered safe for most adults, but the plant contains alkaloids that can be hepatotoxic at high concentrations, so it is advisable to limit use to no more than 3 days in a row and to avoid consumption during pregnancy or lactation. If you have liver disease or are taking other medications, consult a healthcare professional before using this decoction.

The therapeutic effects of Sophora flavescens are largely attributed to its alkaloid constituents, notably matrine, oxymatrine, and sophocarpine, which have been isolated from the root and shown to possess anti‑inflammatory, antiviral, and anticancer activities. In addition, the plant contains isoflavones such as formononetin and ononin, which contribute to its anti‑oxidant properties. These compounds have been repeatedly identified in peer‑reviewed phytochemical studies and are consistent with the plant’s traditional use for reducing inflammation and fighting infection.

Modern research continues to explore Sophora flavescens for its potential in treating inflammatory diseases and certain cancers, and the root is available in commercial TCM formulations worldwide. Its ongoing use in traditional practices, combined with growing scientific evidence, keeps the plant relevant both in herbal medicine and in contemporary pharmacological studies.

General Uses Top

Write a new one!

No general uses added yet. Help us by writing one.

Synonyms Top

Scientific name	Authority	First published in
Sophora flavescens subsp. angustifolia	(Siebold & Zucc.) Yakovlev
Radiusia flavescens	(Aiton) Endl.	Cat. Hort. Vindob.2: 517 (1842)
Sophora flavescens var. favescens	Aiton

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	shrubby sophora
Arabic	صفيراء كهرمانية
Bulgarian	жълта софора
Japanese	クジン
Japanese	苦参
Japanese	クララ
Korean	고삼
lzh	苦參
mn	Лидэр
Russian	Софора желте́ющая
Russian	Софора узколи́стная
Russian	Софо́ра желтова́тая
Chinese	苦蔘
Chinese	山槐
Chinese	野槐
Chinese	白茎地骨
Chinese	地槐
Chinese	苦参实
Chinese	苦参
Chinese	苦參

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Sophora flavescens var. flavescens		Unknown
Sophora flavescens var. galegoides	(Pall.) DC.	Prodr.2: 96 (1825)
Sophora flavescens var. kronei	(Hance) C.Y.Ma	Acta Phytotax. Sin.20: 470 (1982)

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
  - Hainan
  - Inner Mongolia
  - Manchuria
  - Qinghai
  - Tibet
  - Xinjiang
- Eastern Asia
  - Japan
  - Korea
  - Taiwan
- Mongolia
  - Mongolia
- Russian Far East
  - Amur
  - Khabarovsk
  - Primorye
- Siberia
  - Altay
  - Chita
  - Irkutsk

Europe click to expand
- Northern Europe
  - Great Britain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000185581
UNII	X8KX602M5L
USDA Plants	SOFL5
Tropicos	13032958
KEW	urn:lsid:ipni.org:names:518831-1
The Plant List	ild-31855
Open Tree Of Life	711191
Observations.org	125411
NCBI Taxonomy	49840
IUCN Red List	201582
IPNI	518831-1
iNaturalist	138582
GBIF	2959073
Freebase	/m/03y8t6_
EPPO	SOBFL
EOL	643517
USDA GRIN	34953
Wikipedia	Sophora_flavescens
CMAUP	NPO19231

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_030762895.1	ZD_Sfla_1.0	Chromosome	The University of Adelaide	2023-08-21	105	1.93 Gb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Beyond NGS data sharing for plant ecological resilience and improvement of agronomic traits

Kwon JS, Shilpha J, Lee J, Yeom SI

Sci Data

08-May-2024

PMCID:	PMC11079010
doi:	10.1038/s41597-024-03305-0
PMID:	38719829

An Overview on Atopic Dermatitis, Oxidative Stress, and Psychological Stress: Possible Role of Nutraceuticals as an Additional Therapeutic Strategy

Alessandrello C, Sanfilippo S, Minciullo PL, Gangemi S

Int J Mol Sci

04-May-2024

PMCID:	PMC11084351
doi:	10.3390/ijms25095020
PMID:	38732239

Potential Effects of Traditional Chinese Medicine in Anti-Aging and Aging-Related Diseases: Current Evidence and Perspectives

Ding X, Ma X, Meng P, Yue J, Li L, Xu L

Clin Interv Aging

01-May-2024

PMCID:	PMC11070163
doi:	10.2147/CIA.S447514
PMID:	38706635

A Chinese patent medicine’s long-term efficacy on non-dialysis patients with CKD stages 3–5: a retrospective cohort study

Chen HF, Lin YJ, Han Y, Zhang XL, Wang RB, Chen JH, Pi Y, Fu LZ, Tang F, Jie XN, Tang XN, Liu XS, Wu YF

Front Pharmacol

26-Apr-2024

PMCID:	PMC11082339
doi:	10.3389/fphar.2024.1379338
PMID:	38738180

Oxymatrine Modulation of TLR3 Signaling: A Dual-Action Mechanism for H9N2 Avian Influenza Virus Defense and Immune Regulation

Zhi Y, Zhao X, Liu Z, Shen G, Zhang T, Zhang T, Hu G

Molecules

24-Apr-2024

PMCID:	PMC11085666
doi:	10.3390/molecules29091945
PMID:	38731436

Jian Gan powder ameliorates immunological liver injury in mice by modulating the gut microbiota and metabolic profiles

Li K, Cui Y, Zheng X, Min C, Zhang J, Yan Z, Ji Y, Ge F, Ji H, Zhu F

Eur J Med Res

20-Apr-2024

PMCID:	PMC11031866
doi:	10.1186/s40001-024-01827-2
PMID:	38641655

Self-Assembled Matrine-PROTAC Encapsulating Zinc(II) Phthalocyanine with GSH-Depletion-Enhanced ROS Generation for Cancer Therapy

Lai S, Wang B, Sun K, Li F, Liu Q, Yu XA, Jiang L, Wang L

Molecules

18-Apr-2024

PMCID:	PMC11054886
doi:	10.3390/molecules29081845
PMID:	38675664

Oxymatrine combined with rapamycin to attenuate acute cardiac allograft rejection

Lan X, Zhang J, Ren S, Wang H, Shao B, Qin Y, Qin H, Sun C, Zhu Y, Li G, Wang H

Heliyon

13-Apr-2024

PMCID:	PMC11036008
doi:	10.1016/j.heliyon.2024.e29448
PMID:	38655317

Potential application mechanism of traditional Chinese medicine in treating immune checkpoint inhibitor-induced colitis

Wang J, Guo Z, Shen M, Xie Q, Xiang H

Front Immunol

10-Apr-2024

PMCID:	PMC11039877
doi:	10.3389/fimmu.2024.1366489
PMID:	38660314

Targeting autophagy with natural products as a potential therapeutic approach for diabetic microangiopathy

Liu F, Zhao L, Wu T, Yu W, Li J, Wang W, Huang C, Diao Z, Xu Y

Front Pharmacol

10-Apr-2024

PMCID:	PMC11039818
doi:	10.3389/fphar.2024.1364616
PMID:	38659578

Traditional Chinese Medicine in Regulating Tumor Microenvironment

Wang Z, Li M, Bi L, Hu X, Wang Y

Onco Targets Ther

10-Apr-2024

PMCID:	PMC11016250
doi:	10.2147/OTT.S444214
PMID:	38617090

Compound sophora decoction alleviates ulcerative colitis by regulating macrophage polarization through cGAS inhibition: network pharmacology and experimental validation

Gao F, Deng S, Liu Y, Wu P, Huang L, Zhu F, Wei C, Yuan Y, Gui Y, Tian Y, Fan H, Wu H

Aging (Albany NY)

10-Apr-2024

PMCID:	PMC11087132
doi:	10.18632/aging.205734
PMID:	38613801

Liangxue-Qushi-Zhiyang Decoction Ameliorates DNCB-Induced Atopic Dermatitis in Mice through the MAPK Signaling Pathway Based on Network Pharmacology

Zhang L, Zhang H, Niu X, Zhang X, Chen X, Lei S, Ma S, Sun Z

ACS Omega

10-Apr-2024

PMCID:	PMC11044150
doi:	10.1021/acsomega.3c09218
PMID:	38680355

A chromosome-level genome assembly of the soybean pod borer: insights into larval transcriptional response to transgenic soybean expressing the pesticidal Cry1Ac protein

Wang Y, Yao Y, Zhang Y, Qian X, Guo D, Coates BS

BMC Genomics

09-Apr-2024

PMCID:	PMC11005160
doi:	10.1186/s12864-024-10216-2
PMID:	38594617

Progress of medicinal plants and their active metabolites in ischemia-reperfusion injury of stroke: a novel therapeutic strategy based on regulation of crosstalk between mitophagy and ferroptosis

Zhang G, Wang Q, Jiang B, Yao L, Wu W, Zhang X, Wan D, Gu Y

Front Pharmacol

08-Apr-2024

PMCID:	PMC11033413
doi:	10.3389/fphar.2024.1374445
PMID:	38650626

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Alkaloids and derivatives / Lupin alkaloids / Aloperine and related alkaloids
(1S,2S,9R,10R)-3,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadec-7-ene	442937	Click to see	232.36	unknown	https://doi.org/10.1111/J.1742-7843.2010.00653.X
CID 3772951	3772951	Click to see C1CCN2CC3CC(C2C1)C=C4C3NCCC4	232.36	unknown	https://doi.org/10.1111/J.1742-7843.2010.00653.X
> Alkaloids and derivatives / Lupin alkaloids / Anagyrine-type alkaloids
(-)-Thermopsine	638234	Click to see	244.33	unknown	https://doi.org/10.1080/00021369.1989.10869614
(10R,12S)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one	118701431	Click to see	260.33	unknown	via CMAUP database
(10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one	10246	Click to see	244.33	unknown	https://doi.org/10.1271/BBB1961.53.2287
(1R,9R,10R,12R)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one	15939858	Click to see	260.33	unknown	via CMAUP database
(1R,9S,10R)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one	1807519	Click to see	244.33	unknown	via CMAUP database
(1S,9R,10R,12S)-12-Hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one	442943	Click to see	260.33	unknown	via CMAUP database
(1S,9R,12S)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one	91746689	Click to see	260.33	unknown	via CMAUP database
(1S,9S,10R,12S)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one	131676079	Click to see	260.33	unknown	https://doi.org/10.1055/S-2006-961018
Anagyrine	5351589	Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O	244.33	unknown	https://doi.org/10.1016/J.BMCL.2005.11.073 https://doi.org/10.1016/0031-9422(82)85210-2 https://doi.org/10.1271/BBB1961.53.2287
Baptifoline	160543	Click to see	260.33	unknown	via CMAUP database
Monolupin	71056954	Click to see	244.33	unknown	https://doi.org/10.1055/S-2006-961018 https://doi.org/10.1248/CPB.37.3001
Npc135639	442938	Click to see	244.33	unknown	via CMAUP database
Thermopsine	92768	Click to see	244.33	unknown	https://doi.org/10.1080/00021369.1989.10869614 https://doi.org/10.1016/J.BMCL.2005.11.073 https://doi.org/10.1016/0031-9422(82)85210-2
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(-)-Cytisine	6713952	Click to see	190.24	unknown	via CMAUP database
(1R,9R)-11-methyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one	1747617	Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2	204.27	unknown	https://doi.org/10.1055/S-2006-961018 https://doi.org/10.1271/BBB1961.53.2287 https://doi.org/10.1016/J.FITOTE.2010.01.008
(1R,9S)-13-methyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one	56840792	Click to see CC1C2CNCC1C3=CC=CC(=O)N3C2	204.27	unknown	via CMAUP database
(1S,5S)-1,2,3,4,5,6-hexahydro-8H-1,5-methanopyrido[1,2-a][1,5]diazocin-8-one	442949	Click to see	190.24	unknown	via CMAUP database
(1S,9R)-11-but-3-enyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one	7067420	Click to see	244.33	unknown	https://doi.org/10.1016/0031-9422(82)85210-2
1,2,3,4,5,6-hexahydro-1,5-methano-8H-pyrido(1,2-a)(1,5)diazocin-8-one	22407	Click to see	190.24	unknown	https://doi.org/10.1111/J.1742-7843.2010.00653.X
Caulophylline	234566	Click to see	204.27	unknown	https://doi.org/10.1016/0031-9422(82)85210-2 https://doi.org/10.1080/00021369.1989.10869614
Cytisine	10235	Click to see	190.24	unknown	via CMAUP database
N-Methylcytisine	670971	Click to see	204.27	unknown	https://doi.org/10.1080/00021369.1989.10869614 https://doi.org/10.1016/0031-9422(82)85210-2
Pharmakon1600-01504027	6708720	Click to see	190.24	unknown	via CMAUP database
Tabex (TN)	1549781	Click to see	190.24	unknown	via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Lupinine-type alkaloids
6-[(1S,3R,9aS)-1-(hydroxymethyl)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-3-yl]-1H-pyridin-2-one	163186466	Click to see C1CCN2CC(CC(C2C1)CO)C3=CC=CC(=O)N3	262.35	unknown	https://doi.org/10.1016/0031-9422(81)80049-0
6-[1-(hydroxymethyl)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-3-yl]-1H-pyridin-2-one	323274	Click to see C1CCN2CC(CC(C2C1)CO)C3=CC=CC(=O)N3	262.35	unknown	https://doi.org/10.1016/0031-9422(81)80049-0 https://doi.org/10.1016/0031-9422(82)85210-2 https://doi.org/10.1016/J.JPBA.2010.12.024
Mamanine	3085182	Click to see	262.35	unknown	https://doi.org/10.1016/0031-9422(82)85210-2
> Alkaloids and derivatives / Lupin alkaloids / Matrine alkaloids
(-)-Sophocarpine	115269	Click to see	246.35	unknown	https://doi.org/10.1021/JF00001A038 https://doi.org/10.1016/0031-9422(91)80112-E https://doi.org/10.1002/CBER.19350680310 https://doi.org/10.1016/J.JCHROMB.2004.08.032 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254298/ https://doi.org/10.1016/J.FITOTE.2010.01.008 https://doi.org/10.1016/J.BMCL.2005.11.073 https://doi.org/10.1055/S-2006-961018 https://doi.org/10.1111/J.1742-7843.2010.00653.X https://doi.org/10.1248/BPB.31.627 https://doi.org/10.1016/S0021-9673(99)00758-X https://doi.org/10.1016/S0021-9673(98)00624-4
(+)-12alpha-Hydroxysophocarpine	44408595	Click to see	262.35	unknown	https://doi.org/10.1016/J.BMCL.2005.11.073
(+)-Matrine	285698	Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1	248.36	unknown	https://doi.org/10.1055/S-2007-981592 https://doi.org/10.1002/CBER.19350680310 https://doi.org/10.1007/S11033-008-9247-Y https://doi.org/10.1007/S10600-011-0029-8 https://doi.org/10.1016/J.BMCL.2005.11.073 https://doi.org/10.1111/J.1742-7843.2010.00653.X https://doi.org/10.1016/0031-9422(82)85210-2 https://doi.org/10.1016/J.JPBA.2010.12.024 https://doi.org/10.1016/J.JEP.2009.02.022
(+)-Matrine, 519-02-8	86573029	Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1	248.36	unknown	via CMAUP database
(+)-Sophoranol	12442899	Click to see	264.36	unknown	https://doi.org/10.1055/S-2006-961018 https://doi.org/10.2307/4117899 https://doi.org/10.1016/J.FITOTE.2010.01.008
(13S)-13-oxido-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one	137705180	Click to see	264.36	unknown	https://doi.org/10.1080/01483919008049041 https://doi.org/10.1016/J.FITOTE.2010.01.008 https://doi.org/10.1002/MCS.1046 https://doi.org/10.1016/S0021-9673(99)00758-X https://doi.org/10.1007/BF02977714 https://doi.org/10.1002/PTR.2452
(1R,2R,5S,9S,17S)-5-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one	10659287	Click to see C1CC2CN3C(CCC(C3=O)O)C4C2N(C1)CCC4	264.36	unknown	via CMAUP database
(1R,2R,9R,13R,17S)-13-oxido-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one	21586634	Click to see C1CC2C3CCC[N+]4(C3C(CCC4)CN2C(=O)C1)[O-]	264.36	unknown	via CMAUP database
(1R,2R,9R,17S)-7,13-Diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one	21763818	Click to see	246.35	unknown	https://doi.org/10.1016/J.BMCL.2005.11.073
(1R,2R,9S,15S,17S)-15-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one	12133310	Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CC(C4)O	262.35	unknown	https://doi.org/10.1016/J.BMCL.2005.11.073
(1R,2R,9S,17R)-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one	7000680	Click to see C1CC2C3CCC[NH+]4C3C(CCC4)CN2C(=O)C1	249.37	unknown	via CMAUP database
(1R,2R,9S,17S)-13-oxido-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one	161544	Click to see C1CC2CN3C(CC=CC3=O)C4C2[N+](C1)(CCC4)[O-]	262.35	unknown	via CMAUP database
(1R,2S,9R,17S)-13-oxido-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one	129316889	Click to see C1CC2CN3C(CC=CC3=O)C4C2[N+](C1)(CCC4)[O-]	262.35	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.008
(1S,2R,9R,17R)-13-oxido-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one	11874615	Click to see	264.36	unknown	via CMAUP database
(1S,2R,9R,17R)-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one	11909289	Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CCC4	246.35	unknown	via CMAUP database
(1S,2R,9S,17R)-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one	11881817	Click to see	248.36	unknown	via CMAUP database
(5beta,6beta,7beta,11alpha)-Matridin-15-one	638232	Click to see	248.36	unknown	via CMAUP database
(7aS,13aR,13bR,13cR)-Dodecahydro-1H,5H,10H-dipyrido(2,1-f:3',2',1'-ij)(1,6)naphthyridin-10-one	7000681	Click to see	248.36	unknown	https://doi.org/10.1016/J.BMCL.2005.11.073
15-Hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one	78385078	Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CC(C4)O	262.35	unknown	https://doi.org/10.1016/J.BMCL.2005.11.073
15-Hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one	73193574	Click to see C1CC2C3CC(CN4C3C(CCC4)CN2C(=O)C1)O	264.36	unknown	https://doi.org/10.1016/J.BMCL.2005.11.073
3-Hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one	75021824	Click to see C1CC2CN3C(C4C2N(C1)CCC4)C(C=CC3=O)O	262.35	unknown	https://doi.org/10.1016/J.BMCL.2005.11.073
5,9-Dihydroxymatrine	14274649	Click to see C1CC2C3CC(CN4C3C(CCC4)(CN2C(=O)C1)O)O	280.36	unknown	https://doi.org/10.1016/0031-9422(82)85210-2
5alpha-Hydroxysophocarpine	15385686	Click to see	262.35	unknown	https://doi.org/10.1055/S-2006-961018
7,13-Diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one	618867	Click to see	246.35	unknown	https://doi.org/10.1016/J.BMCL.2005.11.073 https://doi.org/10.1111/J.1742-7843.2010.00653.X https://doi.org/10.1002/CBER.19350680310
9,15-Dihydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one	5316791	Click to see C1CC2C3CC(CN4C3C(CCC4)(CN2C(=O)C1)O)O	280.36	unknown	https://doi.org/10.1016/0031-9422(82)85210-2
9alpha-Hydroxymatrine	15385684	Click to see	264.36	unknown	https://doi.org/10.1016/J.BMCL.2005.11.073
Ammothamnine	114850	Click to see	264.36	unknown	https://doi.org/10.1055/S-2006-961018 https://doi.org/10.2307/4117899 https://doi.org/10.1111/J.1742-7843.2010.00653.X
Isomatrine	5271984	Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1	248.36	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.008
Matridin-15-one, 12,13-didehydro-	3041752	Click to see C1CC2CN3C(C=CCC3=O)C4C2N(C1)CCC4	246.35	unknown	https://doi.org/10.1016/J.BMCL.2005.11.073
Matridin-15-one, 13,14-didehydro-, 1-oxide	24721085	Click to see	262.35	unknown	https://doi.org/10.1055/S-2006-961018 https://doi.org/10.1080/01483919008049041
Matrine	91466	Click to see	248.36	unknown	https://doi.org/10.1055/S-2007-981592 https://doi.org/10.1055/S-2008-1034304 https://doi.org/10.1142/S0192415X03001107 https://doi.org/10.1016/J.JCHROMB.2004.08.032 https://doi.org/10.1016/J.FITOTE.2010.01.008 https://doi.org/10.1016/J.BMCL.2005.11.073 https://doi.org/10.1016/S0021-9673(98)00624-4 https://doi.org/10.1002/CBER.19350680310 https://doi.org/10.1016/0031-9422(82)85210-2 https://doi.org/10.1007/S11033-008-9247-Y https://doi.org/10.1007/S10600-011-0029-8 https://doi.org/10.1055/S-2006-961018 https://doi.org/10.1021/JF00001A038 https://doi.org/10.1080/01483919008049041 https://doi.org/10.1248/BPB1978.8.513 https://doi.org/10.1016/J.CHROMA.2007.01.080 https://doi.org/10.1248/CPB.37.3001 https://doi.org/10.1111/J.1742-7843.2010.00653.X https://doi.org/10.1016/J.JEP.2009.02.022 https://doi.org/10.1002/MCS.1046
N-Oxysophocarpine	618688	Click to see	262.35	unknown	https://doi.org/10.1055/S-2006-961018 https://doi.org/10.1016/J.CHROMA.2007.01.080
Oxymatrine	24864132	Click to see	264.36	unknown	https://doi.org/10.1055/S-2006-961018
Oxysophoridine	285670	Click to see	264.36	unknown	https://doi.org/10.1111/J.1742-7843.2010.00653.X
Sophoranol-N-oxy	285668	Click to see C1CC2C3CCC[N+]4(C3C(CCC4)(CN2C(=O)C1)O)[O-]	280.36	unknown	https://doi.org/10.1055/S-2006-961018
Sophoridine	165549	Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1	248.36	unknown	https://doi.org/10.1016/0031-9422(91)80112-E https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254298/ https://doi.org/10.1016/J.FITOTE.2010.01.008 https://doi.org/10.1016/J.LFS.2005.09.034 https://doi.org/10.1111/J.1742-7843.2010.00653.X
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(+)-Lupanine	91471	Click to see	248.36	unknown	https://doi.org/10.1016/0031-9422(82)85210-2
(1R,2R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one	163184988	Click to see	248.36	unknown	https://doi.org/10.1016/0031-9422(82)85210-2
(1R,2R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one	6575009	Click to see	248.36	unknown	https://doi.org/10.1016/0031-9422(82)85210-2
(1R,2R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one	442956	Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O	248.36	unknown	https://doi.org/10.1016/J.JCHROMB.2004.08.032
(1R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-6-one	51018075	Click to see C1CCN2CC3CC(C2C1)CN4C3=CCCC4=O	246.35	unknown	https://doi.org/10.1248/CPB.37.3001
(1R,9R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-6-one	163185252	Click to see	246.35	unknown	https://doi.org/10.1248/CPB.37.3001
(9alpha)-Spartein-2-one	12310653	Click to see	248.36	unknown	via CMAUP database
5,6-Dehydrolupanine	442950	Click to see	246.35	unknown	via CMAUP database
7,14-Methano-4H,6H-dipyrido(1,2-a:1',2'-e)(1,5)diazocin-4-one, 2,3,7,7a,8,9,10,11,13,14-decahydro-, (7S-(7alpha,7abeta,14alpha))-	14379237	Click to see C1CCN2CC3CC(C2C1)CN4C3=CCCC4=O	246.35	unknown	via CMAUP database
alpha-Isolupanine	119201	Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O	248.36	unknown	https://doi.org/10.1016/0031-9422(82)85210-2 https://doi.org/10.1016/J.JPBA.2010.12.024
Hydrorhombinine	7018997	Click to see	248.36	unknown	via CMAUP database
Lupanine, 5,6-didehydro-	520559	Click to see	246.35	unknown	via CMAUP database
Lupanine(1+)	6987464	Click to see	249.37	unknown	via CMAUP database
> Alkaloids and derivatives / Macroline alkaloids
Koumidine	44584550	Click to see	294.40	unknown	via CMAUP database
Tombozine	5318845	Click to see	294.40	unknown	via CMAUP database
> Alkaloids and derivatives / Strychnos alkaloids
(14Z)-14-(2-hydroxyethylidene)-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,11-tetraen-9-one	5318675	Click to see	334.40	unknown	via CMAUP database
4-Hydroxystrychnine	211181	Click to see	350.40	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives
Ethyl, 2-phenyl-	146323	Click to see	105.16	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol	7127	Click to see COC1=C(C=C(C=C1)CC=C)OC	178.23	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
Ephedrine	9294	Click to see	165.23	unknown	via CMAUP database
Pseudoephedrine	7028	Click to see	165.23	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Styrenes
Methyl 6-[4,4-dimethyl-3-(3-methylbut-2-enoxy)-2,3-dihydro-1,5-benzodioxepin-7-yl]-2-(methoxymethylidene)-3-methyl-4-oxohex-5-enoate	139588118	Click to see	458.50	unknown	https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1016/J.BMC.2008.05.080 https://doi.org/10.1248/YAKUSHI1947.90.4_463
> Benzenoids / Benzene and substituted derivatives / Toluenes
1-Ethyl-4-Methylbenzene	12160	Click to see	120.19	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Xylenes / m-Xylenes
M-Xylene	7929	Click to see	106.16	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Xylenes / p-Xylenes
P-Xylene	7809	Click to see CC1=CC=C(C=C1)C	106.16	unknown	via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
8-Hydroxy-2-(8-hydroxy-6-methyl-1,4-dioxonaphthalen-2-yl)-6-methylnaphthalene-1,4-dione	167673	Click to see	374.30	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons
Derivatized Silica Gel	172417	Click to see	253.50	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Decane	15600	Click to see	142.28	unknown	via CMAUP database
Heptadecane	12398	Click to see CCCCCCCCCCCCCCCCC	240.50	unknown	via CMAUP database
Nonadecane	12401	Click to see	268.50	unknown	via CMAUP database
Pentadecane	12391	Click to see	212.41	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(2R,3R,4R)-4-(4-hydroxy-3-methoxy-phenyl)-2,3-bis(hydroxymethyl)-7-methoxy-tetralin-6-ol	11631864	Click to see	360.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones
(8S,16S)-4,5-dimethoxy-2,17-dioxa-9-azapentacyclo[19.2.2.13,7.18,16.09,14]heptacosa-1(23),3,5,7(27),21,24-hexaen-18-one	5319697	Click to see	437.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Acyl carnitines
Hexanoylcarnitine	6426853	Click to see	259.34	unknown	via CMAUP database
L-Octanoylcarnitine	11953814	Click to see	287.39	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Decanoate	4678093	Click to see CCCCCCCCCC(=O)[O-]	171.26	unknown	via CMAUP database
Nonanoic Acid	8158	Click to see CCCCCCCCC(=O)O	158.24	unknown	via CMAUP database
Npc283274	11252659	Click to see	201.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
(1-~13~C)Tetracosanoic acid	16213616	Click to see	369.60	unknown	via CMAUP database
Lignoceric Acid	11197	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O	368.60	unknown	https://doi.org/10.1248/YAKUSHI1947.106.1_22
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
3,5,5-Trimethyl-1-hexanol	18938	Click to see CC(CCO)CC(C)(C)C	144.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
Dehydromiltirone	3082765	Click to see	280.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (-)-	443158	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
Myrcene	31253	Click to see	136.23	unknown	via CMAUP database
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
Nerylacetone	1713001	Click to see CC(=CCCC(=CCCC(=O)C)C)C	194.31	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene	7463	Click to see	134.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Camphene	440966	Click to see	136.23	unknown	via CMAUP database
(4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one	23308299	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane	6429260	Click to see	136.23	unknown	via CMAUP database
alpha-Pinene, (+)-	82227	Click to see	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(L)-alpha-terpineol	443162	Click to see	154.25	unknown	via CMAUP database
Limonene, (-)-	439250	Click to see	136.23	unknown	via CMAUP database
p-Menth-3-en-1-ol	11468	Click to see	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Prenylquinones
3-Hydroxy-5-methoxy-2-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)cyclohexa-2,5-diene-1,4-dione	5318903	Click to see CC(=CCC(CC1=C(C(=O)C(=CC1=O)OC)O)C(=C)C)C	290.40	unknown	https://doi.org/10.1248/YAKUSHI1947.106.1_22
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene,alpha + beta mixt.	5354499	Click to see	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,4S,5R,9S,10S,13R,14R)-14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate	163013687	Click to see	498.60	unknown	https://doi.org/10.1016/S0031-9422(02)00671-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3R,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid	162951873	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)CO)O)O)O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O	1237.40	unknown	https://doi.org/10.1248/CPB.33.4267
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid	20056309	Click to see	1237.40	unknown	https://doi.org/10.1248/CPB.33.4267
(2S,3S,4S,5R,6R)-6-[[(3S,4S,6aR,8aR,9S,10R,14bR)-9-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10-hydroxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid	11968947	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1O)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C)(C)CO)OC8C(C(C(C(O8)C(=O)O)O)O)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(C(O1)CO)O)O)O)C)C	1269.40	unknown	via CMAUP database
5-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-6-[[9-[4,5-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxyoxane-2-carboxylic acid	21864138	Click to see	1237.40	unknown	https://doi.org/10.1248/CPB.33.4267
6-[[11-Carboxy-9-hydroxy-4-(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[4,5-dihydroxy-6-(hydroxymethyl)-2-(2,4,5-trihydroxy-6-methyloxan-3-yl)oxyoxan-3-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid	197561	Click to see	973.10	unknown	via CMAUP database
CID 5087640	5087640	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O	943.10	unknown	https://doi.org/10.1248/CPB.33.4267
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,11S,12aS,14aR,14bR)-4-(hydroxymethyl)-11-methoxycarbonyl-4,6a,6b,8a,11,14b-hexamethyl-9-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylate	162906952	Click to see	1133.30	unknown	https://doi.org/10.1248/CPB.40.2990
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,11S,12aS,14aR,14bR)-9-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-(hydroxymethyl)-11-methoxycarbonyl-4,6a,6b,8a,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylate	163007172	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)CO)O)O)O)(C)C(=O)OC)C)C)C)C)C(=O)OC)O)O)CO)O)O)O)O)O	1295.40	unknown	https://doi.org/10.1248/CPB.40.2990
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,11S,12aS,14aR,14bR)-9-hydroxy-4-(hydroxymethyl)-11-methoxycarbonyl-4,6a,6b,8a,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylate	163010759	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C(=O)OC)C)C)C)C)C(=O)OC)O)O)CO)O)O)O)O)O	1001.20	unknown	https://doi.org/10.1248/CPB.40.2990
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylate	21636205	Click to see	1251.40	unknown	https://doi.org/10.1248/CPB.40.2990
Methyl 5-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-[[4-(hydroxymethyl)-11-methoxycarbonyl-4,6a,6b,8a,11,14b-hexamethyl-9-(3,4,5-trihydroxyoxan-2-yl)oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]oxane-2-carboxylate	85144372	Click to see	1133.30	unknown	https://doi.org/10.1248/CPB.40.2990
Methyl 5-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-[[9-hydroxy-4-(hydroxymethyl)-11-methoxycarbonyl-4,6a,6b,8a,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]oxane-2-carboxylate	85112253	Click to see	1001.20	unknown	https://doi.org/10.1248/CPB.40.2990
Methyl 5-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-6-[[9-[4,5-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-(hydroxymethyl)-11-methoxycarbonyl-4,6a,6b,8a,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxyoxane-2-carboxylate	85132031	Click to see	1295.40	unknown	https://doi.org/10.1248/CPB.40.2990
Methyl 5-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-6-[[9-[4,5-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxyoxane-2-carboxylate	73817534	Click to see	1251.40	unknown	https://doi.org/10.1248/CPB.40.2990
Sophoraflavoside III	197563	Click to see	1105.20	unknown	via CMAUP database
Sophoraflavoside IV	3083427	Click to see	1267.40	unknown	via CMAUP database
Soyasaponin I	122097	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O	943.10	unknown	https://doi.org/10.1248/CPB.33.4267
soyasaponin I(1-)	53477584	Click to see	942.10	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
Kusulactone	102073915	Click to see	478.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3R,3aR,4R,6aR,8S,9aR,9bR)-4,8-dihydroxy-3-methyl-6,9-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one	163023273	Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)O)O	264.32	unknown	https://doi.org/10.1016/J.BMC.2007.03.011 https://doi.org/10.1007/S12272-011-0206-0
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3aR,5aR,5bR,7aR,11aR,11bR,13aS)-3a,5a,5b,8,8,11a-hexamethyl-1-propan-2-yl-3,4,5,6,7,7a,10,11,11b,12,13,13a-dodecahydro-2H-cyclopenta[a]chrysen-9-one	17751023	Click to see	424.70	unknown	via CMAUP database
(3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol	71749855	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Cerveratrum-type alkaloids
[(1S,2S,6S,9S,10S,11R,12R,13S,14S,15S,18S,19S,22S,23R,25R)-10,12,13,14,23-pentahydroxy-6,10,19-trimethyl-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] (Z)-2-methylbut-2-enoate	134145571	Click to see CC=C(C)C(=O)OC1CCC2(C3C1(OC24CC5C6CN7CC(CCC7C(C6C(C(C5(C4CC3)O)O)O)(C)O)C)O)C	575.70	unknown	https://doi.org/10.1016/J.BMCL.2005.11.073
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	via CMAUP database
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1248/YAKUSHI1947.106.1_22 https://doi.org/10.1248/YAKUSHI1947.105.11_1034
Npc29	6432744	Click to see	414.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds
Hexylidyneoxidanium	53628050	Click to see	98.14	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid	9476	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
Neochlorogenic acid	5280633	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
GlyTouCan:G29155XH	91692850	Click to see	342.30	unknown	via CMAUP database
GlyTouCan:G80014NW	46782954	Click to see	342.30	unknown	via CMAUP database
Sucrose	5988	Click to see	342.30	unknown	https://doi.org/10.1248/YAKUSHI1947.106.1_22
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2,4-Decadienal	5283349	Click to see	152.23	unknown	via CMAUP database
Decanal	8175	Click to see	156.26	unknown	via CMAUP database
Nonanal	31289	Click to see CCCCCCCCC=O	142.24	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2,4,5,6-tetrahydro-1H-cyclopenta[d][1,3]oxazin-7-one	5316289	Click to see	139.15	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Enols
Dodecenol	6443191	Click to see	184.32	unknown	via CMAUP database
> Organoheterocyclic compounds / Azoles / Imidazoles
2,4-Dimethylimidazole	70259	Click to see	96.13	unknown	https://doi.org/10.1016/0031-9422(82)85210-2
4-Methylimidazole	13195	Click to see	82.10	unknown	https://doi.org/10.1016/0031-9422(82)85210-2
> Organoheterocyclic compounds / Benzodioxoles
(1R,12R,13R,20S)-13-hydroxy-20-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,17-tetraen-16-one	162986039	Click to see COC1C2C(C3(CCC(=O)C=C3O1)O)OC4=CC5=C(C=C24)OCO5	332.30	unknown	https://doi.org/10.1021/NP990051D
(1R,12R,13S,20S)-13,20-dimethoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,17-tetraen-16-one	163023387	Click to see	346.30	unknown	https://doi.org/10.1021/NP990051D
(1S,12R,13R,20S)-13,20-dimethoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,17-tetraen-16-one	10831417	Click to see	346.30	unknown	https://doi.org/10.1021/NP990051D
(1S,12R,13S,20S)-13-hydroxy-20-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,17-tetraen-16-one	10496772	Click to see	332.30	unknown	https://doi.org/10.1021/NP990051D
13-Hydroxy-20-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,17-tetraen-16-one	85160224	Click to see	332.30	unknown	https://doi.org/10.1021/NP990051D
13,20-Dimethoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,17-tetraen-16-one	85282557	Click to see	346.30	unknown	https://doi.org/10.1021/NP990051D
> Organoheterocyclic compounds / Coumarans
(6S,6aR,11aR,11bR)-11b-hydroxy-6,9-dimethoxy-2,6,6a,11a-tetrahydro-1H-[1]benzofuro[3,2-c]chromen-3-one	163070626	Click to see	318.32	unknown	https://doi.org/10.1021/NP990051D
11b-hydroxy-6,9-dimethoxy-2,6,6a,11a-tetrahydro-1H-[1]benzofuro[3,2-c]chromen-3-one	85159840	Click to see	318.32	unknown	https://doi.org/10.1021/NP990051D
Kushecarpin A	10495761	Click to see	318.32	unknown	https://doi.org/10.1021/NP990051D
> Organoheterocyclic compounds / Cycloheptafurans
Furosardonin A	44222875	Click to see	232.32	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazanaphthalenes / Naphthyridines
(-)-Sophoramine	169014	Click to see	244.33	unknown	https://doi.org/10.1021/JF00001A038 https://doi.org/10.1016/0031-9422(82)85210-2
(1S,9S,15S,17S)-15-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadeca-2,4-dien-6-one	154495910	Click to see	260.33	unknown	https://doi.org/10.1016/0031-9422(82)85210-2
(9S,17S)-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-1-en-6-one	127039206	Click to see	246.35	unknown	https://doi.org/10.1016/0031-9422(82)85210-2
15-Hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadeca-2,4-dien-6-one	5318343	Click to see	260.33	unknown	https://doi.org/10.1016/0031-9422(82)85210-2
7,13-Diazatetracyclo[7.7.1.02,7.013,17]heptadec-1-en-6-one	5316459	Click to see	246.35	unknown	https://doi.org/10.1055/S-2006-961018 https://doi.org/10.1016/0031-9422(82)85210-2
Leontalbinine N-oxide	126455735	Click to see C1CC2CN3C(=C4C2[N+](C1)(CCC4)[O-])CCCC3=O	262.35	unknown	https://doi.org/10.1248/YAKUSHI1947.113.1_53
Neosophoramine	618327	Click to see	244.33	unknown	https://doi.org/10.1016/0031-9422(82)85210-2
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(3S)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-2-ium-3-carboxylate	6920044	Click to see C1C([NH2+]CC2=C1C3=CC=CC=C3N2)C(=O)[O-]	216.24	unknown	via CMAUP database
> Organoheterocyclic compounds / Isobenzofurans
Neoligustilide	5320099	Click to see	190.24	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxanes
1,8-Cineole	2758	Click to see	154.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Pteridines and derivatives / Pterins and derivatives
2-Amino-3,4a,8,8a-tetrahydropteridine-4,7-dione	57336529	Click to see	181.15	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
(6R,7R)-5,6,7-trihydroxy-8-methoxy-2-(2-phenylethyl)-5,6,7,8-tetrahydrochromen-4-one	5322081	Click to see	332.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Pyridinones
(+)-Kuraramine	46187187	Click to see CN1CC(CC(C1)C2=CC=CC(=O)N2)CO	222.28	unknown	https://doi.org/10.1016/0031-9422(81)80049-0 https://doi.org/10.1016/0031-9422(81)84052-6 https://doi.org/10.1016/0031-9422(82)85210-2
6-[(3R,5R)-5-(hydroxymethyl)-1-methylpiperidin-3-yl]-1H-pyridin-2-one	101665417	Click to see	222.28	unknown	https://doi.org/10.1016/0031-9422(82)85210-2
Isokuraramine	6325429	Click to see CN1CC(CC(C1)C2=CC=CC(=O)N2)CO	222.28	unknown	https://doi.org/10.1016/0031-9422(81)80049-0 https://doi.org/10.1016/0031-9422(81)84052-6 https://doi.org/10.1016/0031-9422(82)85210-2 https://doi.org/10.1016/J.JPBA.2010.12.024
Kuraramine	11447394	Click to see	222.28	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolizines
Lamprolobine	87752	Click to see	264.36	unknown	https://doi.org/10.1016/J.JPBA.2010.12.024
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-(2,4-Dihydroxy-5-prenylphenyl)-5,6-methylenedioxybenzofuran	15953774	Click to see CC(=CCC1=CC(=C(C=C1O)O)C2=CC3=CC4=C(C=C3O2)OCO4)C	338.40	unknown	https://doi.org/10.1021/NP060189D
2'-Hydroxy-4'-methoxy-5,6-methylenedioxy-2-phenylbenzofuran	44260109	Click to see COC1=CC(=C(C=C1)C2=CC3=CC4=C(C=C3O2)OCO4)O	284.26	unknown	https://doi.org/10.1016/S0031-9422(02)00671-4
4-(6,7-dihydrofuro[2,3-f][1,3]benzodioxol-6-yl)-2-[(E)-4-hydroxy-3-methylbut-2-enyl]benzene-1,3-diol	101238025	Click to see CC(=CCC1=C(C=CC(=C1O)C2CC3=CC4=C(C=C3O2)OCO4)O)CO	356.40	unknown	https://doi.org/10.1016/S0031-9422(02)00671-4
4-Furo[2,3-f][1,3]benzodioxol-6-yl-2-(4-hydroxy-3-methylbut-2-enyl)benzene-1,3-diol	90847885	Click to see	354.40	unknown	https://doi.org/10.1016/S0031-9422(02)00671-4
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Sinapic acid hexadecyl ester	129711273	Click to see	448.60	unknown	https://doi.org/10.1248/YAKUSHI1947.106.1_22
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid	2518	Click to see	180.16	unknown	via CMAUP database
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid	709	Click to see	194.18	unknown	via CMAUP database
Artepillin C	5472440	Click to see	300.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
5,7-dimethoxy-8-[(Z)-3-methylbut-1-enyl]chromen-2-one	5318625	Click to see	274.31	unknown	via CMAUP database
7-Methoxy-8-(7-methoxy-2-oxochromen-6-yl)chromen-2-one	5319307	Click to see COC1=C(C2=C(C=C1)C=CC(=O)O2)C3=C(C=C4C(=C3)C=CC(=O)O4)OC	350.30	unknown	via CMAUP database
7-Prenyloxycoumarin	320362	Click to see	230.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Demethylsuberosin	5316525	Click to see	230.26	unknown	via CMAUP database
Scopoletin	5280460	Click to see	192.17	unknown	via CMAUP database
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	https://doi.org/10.1248/YAKUSHI1947.106.1_22 https://doi.org/10.1016/S0367-326X(00)00165-9
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S,2''S)-6-lavandulyl-5,7,2',4'-tetrahydroxylflavanone	118975901	Click to see	424.50	unknown	via CMAUP database
(2S)-2,3-Dihydro-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one	38351420	Click to see	370.40	unknown	via CMAUP database
(2S)-5,7-dihydroxy-2-(4-hydroxy-2-methoxyphenyl)-6-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	154496782	Click to see	438.50	unknown	https://doi.org/10.1021/NP990051D
2-(2,4-Dihydroxy-5-methoxyphenyl)-5,7-dihydroxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	85189935	Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3O)O)OC)O)C	386.40	unknown	https://doi.org/10.1021/NP990051D
2-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-6-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-2,3-dihydro-4H-1-benzopyran-4-one	182214	Click to see CC(=CCC(CC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C(C=C3)O)O)O)C(=C)C)C	424.50	unknown	via CMAUP database
5,7-Dihydroxy-2-(4-hydroxy-2-methoxyphenyl)-6-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one	13872451	Click to see CC(=CCC(CC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C(C=C3)O)OC)O)C(=C)C)C	438.50	unknown	via CMAUP database
Kushenol F	10455036	Click to see CC(=CCC(CC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C(C=C3)O)O)O)C(=C)C)C	424.50	unknown	https://doi.org/10.1248/YAKUSHI1947.105.8_736 https://doi.org/10.1007/BF02977714
Kushenol V	10572194	Click to see	386.40	unknown	https://doi.org/10.1021/NP990051D
Nymphaeol A	639465	Click to see	424.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(+/-)-Leachianone G	11810419	Click to see	356.40	unknown	https://doi.org/10.1248/BPB.31.908 https://doi.org/10.1021/NP990051D https://doi.org/10.1016/S0031-9422(02)00671-4
(2R,3R)-2-(2,4-Dihydroxy-phenyl)-3,7-dihydroxy-8-(5-hydroxy-2-isopropenyl-5-methyl-hexyl)-5-methoxy-chroman-4-one	10254216	Click to see	472.50	unknown	via CMAUP database
(2R,3R)-2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-6-(3-hydroxy-3-methylbutyl)-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	102506430	Click to see CC(=CCC(CC1=C2C(=C(C(=C1O)CCC(C)(C)O)O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C	526.60	unknown	https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1007/BF02973946 https://doi.org/10.1055/S-2003-40643 https://doi.org/10.1055/S-2006-957906
(2R,3R)-2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-6-(3-hydroxy-3-methylbutyl)-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	162914480	Click to see	526.60	unknown	https://doi.org/10.1055/S-2006-957906
(2R,3R)-2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-6-(3-methylbut-2-enyl)-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	162937675	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)CC(CC=C(C)C)C(=C)C)O)C	508.60	unknown	https://doi.org/10.1055/S-2006-957906
(2R,3R)-2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	124413654	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C	440.50	unknown	https://doi.org/10.1021/NP990051D https://doi.org/10.1016/S0031-9422(02)00671-4
(2R,3R)-2-(2,4-dihydroxyphenyl)-3,7-dihydroxy-8-[(2S)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-5-methoxy-2,3-dihydrochromen-4-one	154496851	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O	472.50	unknown	https://doi.org/10.1248/YAKUSHI1947.105.11_1034
(2R,3R)-3,5-dihydroxy-2-(7-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-8,8-dimethyl-2,3,9,10-tetrahydropyrano[2,3-h]chromen-4-one	11351168	Click to see	440.50	unknown	https://doi.org/10.1002/HLCA.200490230
(2R,3S)-2-(2,4-Dihydroxyphenyl)-3,7-dihydroxy-5-methoxy-8-((R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl)chroman-4-one	102004822	Click to see	454.50	unknown	https://doi.org/10.1055/S-2006-957906 https://doi.org/10.1016/J.BMC.2007.03.011 https://doi.org/10.1007/S12272-011-0206-0
(2R)-2-(2,4-dihydroxy-5-methoxyphenyl)-5,7-dihydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	154496856	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC(=C(C=C3O)O)OC)C	386.40	unknown	https://doi.org/10.1021/NP990051D
(2R)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3-methylbut-2-enyl)-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	154496848	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)CC(CC=C(C)C)C(=C)C)O)C	492.60	unknown	https://doi.org/10.1248/CPB.33.3231
(2R)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	5318894	Click to see	424.50	unknown	https://doi.org/10.1080/14786419.2017.1297992 https://doi.org/10.1007/BF02973946 https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1248/BPB.31.908 https://doi.org/10.1055/S-2003-40643 https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1248/YAKUSHI1947.105.8_736
(2R)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	1711996	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C	424.50	unknown	https://doi.org/10.1248/CPB.19.2126
(2R)-2-(2,4-Dihydroxyphenyl)-7-hydroxy-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	26209049	Click to see	438.50	unknown	https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1016/S0367-326X(00)00165-9 https://doi.org/10.1016/J.PHYMED.2007.09.022 https://doi.org/10.1248/BPB.26.1348 https://doi.org/10.1016/S0887-2333(00)00041-2 https://doi.org/10.1055/S-2003-40643 https://doi.org/10.1080/14786419.2017.1297992 https://doi.org/10.1055/S-2006-957906 https://doi.org/10.1007/7081_2009_128 https://doi.org/10.1021/NP040069A https://doi.org/10.1016/0305-1978(95)00056-9 https://doi.org/10.1248/BPB.31.908 https://doi.org/10.1002/PTR.2650040607 https://doi.org/10.1016/0378-8741(90)90100-8 https://doi.org/10.1007/BF02973946 https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1016/0378-8741(90)90053-V https://doi.org/10.1055/S-2004-815545
(2R)-5,7-dihydroxy-2-(2-hydroxyphenyl)-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	133612505	Click to see	408.50	unknown	https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1248/CPB.33.3231 https://doi.org/10.1016/J.BMC.2008.05.080
(2R)-5,7-dihydroxy-2-(4-hydroxy-2-methoxyphenyl)-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	124355877	Click to see	438.50	unknown	https://doi.org/10.1021/NP990051D
(2R)-5,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-2-(2-hydroxyphenyl)-2,3-dihydrochromen-4-one	162900723	Click to see	426.50	unknown	https://doi.org/10.1016/J.BMC.2008.05.080
(2R)-7-hydroxy-2-(4-hydroxy-2-methoxyphenyl)-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	133561937	Click to see	452.50	unknown	https://doi.org/10.1016/S0887-2333(00)00041-2
(2R)-7-hydroxy-2-(4-hydroxy-2-methoxyphenyl)-8-[(2S)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-5-methoxy-2,3-dihydrochromen-4-one	154497079	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC	470.60	unknown	https://doi.org/10.1021/NP990051D
(2S,3R)-2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one	101000465	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C	440.50	unknown	via CMAUP database
(2S,3R)-2-(2,4-dihydroxyphenyl)-3,7-dihydroxy-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	133612301	Click to see	454.50	unknown	https://doi.org/10.1248/YAKUSHI1947.106.1_22 https://doi.org/10.1007/BF02973946 https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1055/S-2003-40643 https://doi.org/10.1055/S-2006-957906
(2S)-2-(2,4-dihydroxy-5-methoxyphenyl)-5,7-dihydroxy-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	163041858	Click to see	454.50	unknown	https://doi.org/10.1021/NP060189D
(2S)-2-(2,4-dihydroxy-5-methoxyphenyl)-5,7-dihydroxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	163041857	Click to see	454.50	unknown	https://doi.org/10.1021/NP060189D
(2S)-2-(2,4-dihydroxyphenyl)-5-hydroxy-7-(3-methylbut-2-enoxy)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	162995311	Click to see CC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=C(C=C(C=C3)O)O)O)OCC=C(C)C)C	424.50	unknown	https://doi.org/10.1021/NP060189D
(2S)-2-(2,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	163011881	Click to see	370.40	unknown	https://doi.org/10.1016/S0031-9422(02)00671-4
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3-methylbut-2-enyl)-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	162960095	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)CC(CC=C(C)C)C(=C)C)O)C	492.60	unknown	https://doi.org/10.1055/S-2006-957906 https://doi.org/10.1248/CPB.33.3231
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(E)-3-methylbut-1-enyl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	163014511	Click to see	424.50	unknown	https://doi.org/10.1248/BPB.31.908
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one	9910234	Click to see	424.50	unknown	https://doi.org/10.1016/J.PHYMED.2007.09.022
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2R)-2-[(2S)-1-hydroxypropan-2-yl]-5-methylhex-4-enyl]-2,3-dihydrochromen-4-one	162989710	Click to see	442.50	unknown	https://doi.org/10.1021/NP990051D
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-2,3-dihydrochromen-4-one	44563159	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O	442.50	unknown	https://doi.org/10.1021/NP990051D https://doi.org/10.1007/BF02973946 https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1055/S-2003-40643 https://doi.org/10.1055/S-2006-957906
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-2,3-dihydrochromen-4-one	160193092	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O	442.50	unknown	https://doi.org/10.1021/NP990051D
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	6565899	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C	424.50	unknown	https://doi.org/10.1007/7081_2009_128 https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1021/NP990567X https://doi.org/10.1021/NP990051D https://doi.org/10.1016/J.BMC.2008.05.080 https://doi.org/10.1055/S-2006-957906
(2S)-2-(2,4-dihydroxyphenyl)-7-hydroxy-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	26209050	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C	438.50	unknown	via CMAUP database
(2S)-2'-methoxykurarinone	11982641	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C	452.50	unknown	https://doi.org/10.1021/NP990567X https://doi.org/10.1021/NP990051D https://doi.org/10.1016/J.BMC.2008.05.080 https://doi.org/10.1007/S12272-011-0206-0
(2S)-5,7-dihydroxy-2-(2-hydroxyphenyl)-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	162957435	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O)C(=C)C)C	408.50	unknown	https://doi.org/10.1021/NP990051D https://doi.org/10.1248/CPB.33.3231
(2S)-5,7-dihydroxy-2-(4-hydroxy-2-methoxyphenyl)-8-[(2R)-2-[(2R)-1-hydroxypropan-2-yl]-5-methylhex-4-enyl]-2,3-dihydrochromen-4-one	154496855	Click to see CC(CO)C(CC=C(C)C)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC	456.50	unknown	https://doi.org/10.1021/NP990051D
(2S)-5,7-dihydroxy-2-(4-hydroxy-2-methoxyphenyl)-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-2,3-dihydrochromen-4-one	154496854	Click to see	456.50	unknown	https://doi.org/10.1021/NP990051D
(2S)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	14258999	Click to see	370.40	unknown	via CMAUP database
(2S)-5,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-2-(2-hydroxyphenyl)-2,3-dihydrochromen-4-one	44563122	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O	426.50	unknown	https://doi.org/10.1021/NP990051D
(2S)-5,7-dihydroxy-8-[(2S)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-2-(2-hydroxyphenyl)-2,3-dihydrochromen-4-one	160245721	Click to see	426.50	unknown	https://doi.org/10.1021/NP990051D
(2S)-7-hydroxy-2-(4-hydroxy-2-methoxyphenyl)-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one	60039901	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C	452.50	unknown	via CMAUP database
(2S)-Euchrenone A7	44593508	Click to see	340.40	unknown	https://doi.org/10.1016/S0031-9422(02)00671-4
(2S)-Isoxanthohumol	9928523	Click to see	354.40	unknown	via CMAUP database
(3R)-2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-6-(3-hydroxy-3-methylbutyl)-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one	5318844	Click to see CC(=CCC(CC1=C2C(=C(C(=C1O)CCC(C)(C)O)O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C	526.60	unknown	https://doi.org/10.1080/14786419.2017.1297992 https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1007/BF02973946 https://doi.org/10.1055/S-2003-40643
(3R)-2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-6-(3-methylbut-2-enyl)-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one	5318900	Click to see	508.60	unknown	https://doi.org/10.1080/14786419.2017.1297992 https://doi.org/10.1248/YAKUSHI1947.105.11_1034 https://doi.org/10.1007/BF02973946 https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1055/S-2003-40643
(3R)-2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	5318899	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)CC=C(C)C)O)C	440.50	unknown	https://doi.org/10.1080/14786419.2017.1297992 https://doi.org/10.1248/YAKUSHI1947.105.11_1034 https://doi.org/10.1007/BF02973946 https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1055/S-2003-40643
2-(2,4-Dihydroxy-5-methoxyphenyl)-5,7-dihydroxy-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one	16083183	Click to see	454.50	unknown	https://doi.org/10.1021/NP060189D
2-(2,4-Dihydroxyphenyl)-3,5,7-trihydroxy-6-(3-hydroxy-3-methylbutyl)-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one	78385167	Click to see	526.60	unknown	https://doi.org/10.1055/S-2006-957906
2-(2,4-Dihydroxyphenyl)-3,5,7-trihydroxy-6-(3-methylbut-2-enyl)-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one	53463122	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)CC(CC=C(C)C)C(=C)C)O)C	508.60	unknown	https://doi.org/10.1055/S-2006-957906
2-(2,4-Dihydroxyphenyl)-3,5,7-trihydroxy-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	73829916	Click to see	440.50	unknown	https://doi.org/10.1055/S-2006-957906
2-(2,4-Dihydroxyphenyl)-3,5,7-trihydroxy-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one	85200255	Click to see	440.50	unknown	https://doi.org/10.1055/S-2005-871302 https://doi.org/10.1021/NP990051D https://doi.org/10.1016/S0031-9422(02)00671-4 https://doi.org/10.1007/S12272-011-0206-0
2-(2,4-Dihydroxyphenyl)-3,7-dihydroxy-8-(5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl)-5-methoxy-2,3-dihydrochromen-4-one	5318897	Click to see	472.50	unknown	https://doi.org/10.1080/14786419.2017.1297992 https://doi.org/10.1007/BF02973946 https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1021/NP990051D https://doi.org/10.1055/S-2003-40643 https://doi.org/10.1016/S0887-2333(00)00041-2 https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1055/S-2004-815545 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3196987/ https://doi.org/10.1248/YAKUSHI1947.105.11_1034 https://doi.org/10.1021/NP980103J https://doi.org/10.1248/YAKUSHI1947.105.8_736 https://doi.org/10.1055/S-2006-957906 https://doi.org/10.1016/J.BMC.2007.03.011
2-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-6-(3-methylbut-1-enyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	163014510	Click to see	424.50	unknown	https://doi.org/10.1248/BPB.31.908
2-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	9979767	Click to see	424.50	unknown	https://doi.org/10.1055/S-2006-957906
2-(2,4-Dihydroxyphenyl)-7-hydroxy-8-(5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl)-5-methoxy-2,3-dihydrochromen-4-one	185720	Click to see	456.50	unknown	https://doi.org/10.1248/BPB.31.908 https://doi.org/10.1021/NP990051D https://doi.org/10.1248/BPB.31.154 https://doi.org/10.1055/S-2006-957906 https://doi.org/10.1016/J.PHYMED.2007.09.022 https://doi.org/10.1016/J.BMC.2008.05.080 https://doi.org/10.1021/NP980103J https://doi.org/10.1007/S12272-011-0206-0
2-(4-Hydroxyphenyl)-5-methoxy-8-(3-methylbut-2-enyl)-4-oxo-2,3-dihydrochromen-7-olate	25200491	Click to see	353.40	unknown	via CMAUP database
2'-Methoxykurarinone	25252741	Click to see	452.50	unknown	https://doi.org/10.1021/NP990567X https://doi.org/10.1021/NP990051D https://doi.org/10.1211/JPP.60.9.0016 https://doi.org/10.1089/JMF.2009.1333 https://doi.org/10.1016/J.BMC.2008.05.080 https://doi.org/10.1007/S12272-011-0206-0 https://doi.org/10.1248/BPB.31.1964
3,5-Dihydroxy-2-(7-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-8,8-dimethyl-2,3,9,10-tetrahydropyrano[2,3-h]chromen-4-one	72812477	Click to see	440.50	unknown	https://doi.org/10.1002/HLCA.200490230
5,7-Dihydroxy-2-(2-hydroxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	85290220	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O)C	340.40	unknown	https://doi.org/10.1021/NP990051D
5,7-Dihydroxy-2-(2-hydroxyphenyl)-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one	5318890	Click to see	408.50	unknown	via CMAUP database
5,7-Dihydroxy-2-(4-hydroxy-2-methoxyphenyl)-8-(5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl)-2,3-dihydrochromen-4-one	85252194	Click to see	456.50	unknown	https://doi.org/10.1021/NP990051D
5,7-Dihydroxy-8-(5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl)-2-(2-hydroxyphenyl)-2,3-dihydrochromen-4-one	25252740	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O	426.50	unknown	https://doi.org/10.1021/NP990051D https://doi.org/10.1016/J.BMC.2008.05.080
7-Hydroxy-2-(4-hydroxyphenyl)-5-methoxy-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one	73105202	Click to see	422.50	unknown	https://doi.org/10.1021/NP990051D
7-Hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	11609510	Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)C	324.40	unknown	https://doi.org/10.1016/S0031-9422(02)00671-4
Alopecurone G	42607826	Click to see	422.50	unknown	https://doi.org/10.1177/1934578X1000501210
CID 102004745	102004745	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)CC(CC=C(C)C)C(=C)C)O)C	492.60	unknown	https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1007/BF02973946 https://doi.org/10.1055/S-2003-40643 https://doi.org/10.1055/S-2006-957906 https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1248/CPB.33.3231
CID 133612300	133612300	Click to see	454.50	unknown	https://doi.org/10.1007/7081_2009_128 https://doi.org/10.1248/YAKUSHI1947.105.8_736 https://doi.org/10.1515/ZNC-1992-7-808
Euchrenone a7	10291003	Click to see	340.40	unknown	https://doi.org/10.1016/S0031-9422(02)00671-4
Isobavachin	193679	Click to see	324.40	unknown	https://doi.org/10.1016/S0031-9422(02)00671-4
Isokurarinone	124355878	Click to see	438.50	unknown	https://doi.org/10.1002/PTR.2650040607 https://doi.org/10.1248/CPB.34.2094
Isoxanthohumol	513197	Click to see	354.40	unknown	https://doi.org/10.1016/J.BMC.2008.05.080 https://doi.org/10.1248/YAKUSHI1947.105.11_1034 https://doi.org/10.1007/7081_2009_128 https://doi.org/10.1248/YAKUSHI1947.90.4_463 https://doi.org/10.1248/CPB.34.2094
Kenusanone I	42608020	Click to see	370.40	unknown	https://doi.org/10.1016/S0031-9422(02)00671-4
kosamol Q	85172366	Click to see	442.50	unknown	https://doi.org/10.1021/NP990051D
kosamol R	74819350	Click to see	422.50	unknown	https://doi.org/10.1021/NP990051D
Kurarinol	44563198	Click to see	456.50	unknown	https://doi.org/10.1007/BF02973946 https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1248/BPB.31.908 https://doi.org/10.1021/NP990051D https://doi.org/10.1016/J.BMC.2008.05.080 https://doi.org/10.1055/S-2003-40643 https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1055/S-2004-815545 https://doi.org/10.1007/S12272-011-0206-0 https://doi.org/10.1021/NP980103J https://doi.org/10.1055/S-2006-957906 https://doi.org/10.1248/BPB.31.154 https://doi.org/10.1016/J.PHYMED.2007.09.022
Kurarinone	10812923	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C	438.50	unknown	https://doi.org/10.1055/S-2008-1034285 https://doi.org/10.1177/1934578X1000501210
Kurarinone	11982640	Click to see	438.50	unknown	https://doi.org/10.1248/BPB.31.908 https://doi.org/10.1021/NP990567X https://doi.org/10.1021/NP990051D https://doi.org/10.1016/J.BMC.2008.05.080 https://doi.org/10.1021/NP040069A https://doi.org/10.1007/S12272-011-0206-0 https://doi.org/10.1248/BPB.29.1911 https://doi.org/10.1248/BPB.26.1348 https://doi.org/10.1055/S-2006-957906 https://doi.org/10.1016/J.BMC.2007.03.011
Kurarinone [M+H]+	5318882	Click to see	438.50	unknown	https://doi.org/10.1248/BPB.31.908 https://doi.org/10.1002/PTR.2650040607 https://doi.org/10.1016/0378-8741(90)90100-8 https://doi.org/10.1007/BF02973946 https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1016/0378-8741(90)90053-V https://doi.org/10.1055/S-2004-815545 https://doi.org/10.1016/J.BMC.2008.05.080 https://doi.org/10.1248/BPB.29.1911 https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1016/S0367-326X(00)00165-9 https://doi.org/10.1021/NP990567X https://doi.org/10.1016/J.BMC.2007.03.011 https://doi.org/10.1021/NP990051D https://doi.org/10.1016/J.PHYMED.2007.09.022 https://doi.org/10.2174/187153011796429790 https://doi.org/10.1248/BPB.26.1348 https://doi.org/10.1016/S0887-2333(00)00041-2 https://doi.org/10.1055/S-2003-40643 https://doi.org/10.1080/14786419.2017.1297992 https://doi.org/10.1055/S-2006-957906 https://doi.org/10.1007/S12272-011-0206-0 https://doi.org/10.1021/NP040069A
Kushenol A	44563121	Click to see	408.50	unknown	https://doi.org/10.1248/CPB.33.3231
Kushenol B	5318891	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)CC(CC=C(C)C)C(=C)C)O)C	492.60	unknown	https://doi.org/10.1080/14786419.2017.1297992 https://doi.org/10.1007/BF02973946 https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1055/S-2003-40643 https://doi.org/10.1055/S-2006-957906 https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1248/CPB.33.3231
Kushenol E	127234	Click to see	424.50	unknown	https://doi.org/10.1007/BF02973946 https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1248/BPB.31.908 https://doi.org/10.1055/S-2003-40643 https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1248/YAKUSHI1947.105.8_736 https://doi.org/10.1055/S-2006-957906
Kushenol H	44584091	Click to see	472.50	unknown	https://doi.org/10.1021/NP990051D https://doi.org/10.1055/S-2006-957906 https://doi.org/10.1021/NP980103J
Kushenol I	20832634	Click to see	454.50	unknown	https://doi.org/10.1021/NP990051D https://doi.org/10.1007/S12272-011-0206-0
Kushenol L	21721878	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)CC=C(C)C)O)C	440.50	unknown	https://doi.org/10.1248/YAKUSHI1947.105.11_1034 https://doi.org/10.1177/1934578X1000501210 https://doi.org/10.1007/BF02973946 https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1055/S-2003-40643 https://doi.org/10.1055/S-2006-957906
Kushenol M	180948	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)CC(CC=C(C)C)C(=C)C)O)C	508.60	unknown	https://doi.org/10.1248/YAKUSHI1947.105.11_1034 https://doi.org/10.1007/BF02973946 https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1055/S-2003-40643 https://doi.org/10.1055/S-2006-957906
Kushenol N	10253436	Click to see	454.50	unknown	via CMAUP database
Kushenol P	10742453	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC	456.50	unknown	via CMAUP database
Kushenol R	42607847	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=CC=C3O)C(=C)C)C	422.50	unknown	https://doi.org/10.1021/NP990051D
Kushenol S	10854625	Click to see	340.40	unknown	https://doi.org/10.1021/NP990051D
Kushenol U	42608062	Click to see	422.50	unknown	https://doi.org/10.1021/NP990051D
Kushenol W	42608033	Click to see	386.40	unknown	https://doi.org/10.1021/NP990051D
Kushenol X	10599228	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C	440.50	unknown	via CMAUP database
KushenolK	44428630	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O	472.50	unknown	https://doi.org/10.1248/YAKUSHI1947.105.11_1034 https://doi.org/10.1055/S-2004-815545 https://doi.org/10.1007/BF02973946 https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1055/S-2006-957906 https://doi.org/10.1016/J.BMC.2007.03.011 https://doi.org/10.1021/NP980103J
KushenolX	124413655	Click to see	440.50	unknown	https://doi.org/10.1055/S-2005-871302 https://doi.org/10.1021/NP990051D https://doi.org/10.1007/S12272-011-0206-0
Leachianone A	44593449	Click to see	438.50	unknown	https://doi.org/10.1055/S-2005-871302 https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1021/NP990567X https://doi.org/10.1055/S-2008-1034285 https://doi.org/10.1021/NP990051D https://doi.org/10.1016/J.BMC.2008.05.080 https://doi.org/10.1016/S0887-2333(00)00041-2 https://doi.org/10.1177/1934578X1000501210
Leachianone G	5275227	Click to see	356.40	unknown	https://doi.org/10.1248/BPB.31.908 https://doi.org/10.1021/NP990051D https://doi.org/10.1016/S0031-9422(02)00671-4
leachianone G(1-)	25201713	Click to see	355.40	unknown	via CMAUP database
Lehmannin	4359200	Click to see	408.50	unknown	https://doi.org/10.1515/ZNC-1991-3-402
Marini	73198	Click to see	424.50	unknown	https://doi.org/10.1016/J.BMC.2008.05.080 https://doi.org/10.1055/S-2005-871302 https://doi.org/10.1248/BPB.29.1911 https://doi.org/10.1016/S0031-9422(02)00111-5 https://doi.org/10.1016/J.BMC.2007.03.011 https://doi.org/10.1021/NP990051D https://doi.org/10.1248/BPB.26.1348 https://doi.org/10.1016/S0887-2333(00)00041-2 https://doi.org/10.1055/S-2006-957906 https://doi.org/10.1007/S12272-011-0206-0 https://doi.org/10.1248/BPB.31.908 https://doi.org/10.1248/CPB.34.2094
Neokurarinol	102090469	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC	470.60	unknown	via CMAUP database
Norkurarinol	12146484	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O	442.50	unknown	https://doi.org/10.1021/NP990051D https://doi.org/10.1055/S-2006-957906
Npc187837	5318581	Click to see	438.50	unknown	https://doi.org/10.1055/S-2005-871302 https://doi.org/10.1021/NP990051D https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1016/J.BMC.2008.05.080
Npc301322	381851	Click to see	454.50	unknown	https://doi.org/10.1080/14786419.2017.1297992 https://doi.org/10.1007/BF02973946 https://doi.org/10.1248/YAKUSHI1947.106.1_22 https://doi.org/10.1021/NP990051D https://doi.org/10.1055/S-2003-40643 https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1007/S12272-011-0206-0 https://doi.org/10.1271/BBB.120739 https://doi.org/10.1055/S-2006-957906 https://doi.org/10.1016/J.BMC.2007.03.011
Sophoraflavanone B	480764	Click to see	340.40	unknown	https://doi.org/10.1177/1934578X1000501210 https://doi.org/10.1016/S0031-9422(02)00671-4
Sophoraflavanone B	509245	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)O)C	340.40	unknown	https://doi.org/10.1016/S0031-9422(02)00671-4
Sophoraflavanone G	72936	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C	424.50	unknown	https://doi.org/10.1248/BPB.29.1911 https://doi.org/10.1248/BPB.26.1348 https://doi.org/10.1016/0378-8741(90)90053-V https://doi.org/10.1007/BF02973946 https://doi.org/10.1248/BPB.31.908 https://doi.org/10.1016/S0031-9422(02)00111-5 https://doi.org/10.1016/S0031-9422(02)00671-4 https://doi.org/10.1002/PTR.2650040607 https://doi.org/10.1055/S-2003-40643 https://doi.org/10.1016/0378-8741(90)90100-8 https://doi.org/10.1055/S-2008-1034285 https://doi.org/10.1177/1934578X1000501210 https://doi.org/10.1016/S0887-2333(00)00041-2 https://doi.org/10.1007/BF02976197 https://doi.org/10.1515/ZNC-1992-7-808 https://doi.org/10.1021/NP990567X https://doi.org/10.1055/S-2006-957906 https://doi.org/10.1080/14786419.2017.1297992 https://doi.org/10.1016/J.BMC.2007.03.011 https://doi.org/10.1016/0305-1978(95)00056-9 https://doi.org/10.1248/YAKUSHI1947.105.11_1034 https://doi.org/10.1055/S-2005-871302 https://doi.org/10.1007/S12272-011-0206-0
Sophoraflavanone L	16083180	Click to see	424.50	unknown	https://doi.org/10.1021/NP060189D
Sophoranochromene	42607818	Click to see	458.60	unknown	via CMAUP database
Sophoranon	4482007	Click to see	460.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Flavanone	10251	Click to see C1C(OC2=CC=CC=C2C1=O)C3=CC=CC=C3	224.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
Norartocarpetin	5481970	Click to see	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 3-prenylated flavones
2-[3-[(1S,5S,6S)-6-(2,4-dihydroxybenzoyl)-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3,7-dihydroxychromen-4-one	162921495	Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C(C=CC(=C4O)C5=C(C(=O)C6=C(O5)C=C(C=C6)O)O)O	624.60	unknown	https://doi.org/10.1021/NP990051D https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1248/CPB.33.3231 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3196987/ https://doi.org/10.1016/J.BMC.2008.05.080
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
2-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-6-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)chromen-4-one	5318895	Click to see	422.50	unknown	https://doi.org/10.1007/BF02977714 https://doi.org/10.1248/YAKUSHI1947.105.8_736
Licoflavonol	5481964	Click to see	354.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
2-(2,4-Dihydroxyphenyl)-3,5,7-trihydroxy-8-(5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl)chromen-4-one	5318896	Click to see	456.50	unknown	https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1248/YAKUSHI1947.105.8_736
2-(2,4-Dihydroxyphenyl)-3,5,7-trihydroxy-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)chromen-4-one	5318892	Click to see	438.50	unknown	https://doi.org/10.1055/S-2005-871302 https://doi.org/10.1248/BPB.31.908 https://doi.org/10.1002/PTR.2650040607 https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1248/CPB.33.3231 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3196987/
2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]chromen-4-one	133562402	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C	438.50	unknown	https://doi.org/10.1248/CPB.33.3231
3-Hydroxy-2-(4-hydroxyphenyl)-5-methoxy-8,8-dimethyl-9,10-dihydropyrano[2,3-h]chromen-4-one	11451469	Click to see	368.40	unknown	https://doi.org/10.1002/HLCA.200490230
3,5,7-trihydroxy-2-(4-hydroxyphenyl)-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]chromen-4-one	124355926	Click to see	422.50	unknown	https://doi.org/10.1007/S12272-011-0206-0
3,5,7-trihydroxy-2-(4-hydroxyphenyl)-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]chromen-4-one	124355925	Click to see	422.50	unknown	https://doi.org/10.1021/NP060189D
5-Hydroxy-4-(4-hydroxyphenyl)-10,10,16,16-tetramethyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1,4,7,13-tetraen-6-one	11327657	Click to see	422.50	unknown	https://doi.org/10.1002/HLCA.200490230
7-Hydroxy-2-(4-hydroxy-2-methoxyphenyl)-8-(5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl)-5-methoxychromen-4-one	5320098	Click to see	468.50	unknown	https://doi.org/10.1021/NP990051D https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3196987/
8-Lavandulylkaempferol	16083184	Click to see	422.50	unknown	https://doi.org/10.1142/S0192415X10007944 https://doi.org/10.1021/NP060189D https://doi.org/10.1007/BF02977897
8-Prenylkaempferol	5318624	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)C	354.40	unknown	https://doi.org/10.1055/S-2005-871302 https://doi.org/10.1248/YAKUSHI1947.90.4_463
Isoanhydroicaritin	5322079	Click to see CC(=CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)OC)C	368.40	unknown	https://doi.org/10.1248/YAKUSHI1947.90.4_463
Kushenol C	5481237	Click to see	438.50	unknown	https://doi.org/10.1055/S-2005-871302 https://doi.org/10.1248/CPB.33.3231 https://doi.org/10.1002/PTR.2650040607 https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1248/BPB.31.908 https://doi.org/10.1248/YAKUSHI1947.105.8_736 https://doi.org/10.1515/ZNC-1992-7-808
Kushenol G	44259516	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)O	456.50	unknown	https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1248/YAKUSHI1947.105.8_736
Sophoflavescenol	9929189	Click to see CC(=CCC1=C2C(=C(C=C1O)OC)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)C	368.40	unknown	https://doi.org/10.1021/NP980103J
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin	5280805	Click to see	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2R,3S)-3-hydroxy-2-(4-methoxyphenyl)-7-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one	154496850	Click to see	580.50	unknown	https://doi.org/10.1248/YAKUSHI1947.105.11_1034
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	13093776	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	via CMAUP database
2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	71541772	Click to see	430.40	unknown	via CMAUP database
2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	5318902	Click to see	562.50	unknown	https://doi.org/10.1248/YAKUSHI1947.106.1_22
3-hydroxy-2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one	5318898	Click to see COC1=CC=C(C=C1)C2C(C(=O)C3=C(O2)C=C(C=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O	580.50	unknown	https://doi.org/10.1248/YAKUSHI1947.105.11_1034
3-Hydroxy-2-(4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one	78385180	Click to see COC1=CC=C(C=C1)C2C(C(=O)C3=C(O2)C=C(C=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O	580.50	unknown	https://doi.org/10.1248/YAKUSHI1947.105.11_1034
7-(alpha-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one	12304095	Click to see	432.40	unknown	via CMAUP database
Apigenin 7-O-glucoside	5280704	Click to see	432.40	unknown	https://doi.org/10.1515/ZNC-1992-7-808
Luteolin 7-galactoside	5291488	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/JA01651A057
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/JA01651A057 https://doi.org/10.1515/ZNC-1992-7-808
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Hesperetin	72281	Click to see COC1=C(C=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O	302.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Xanthomicrol	73207	Click to see	344.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Maackiain	91510	Click to see	284.26	unknown	https://doi.org/10.1002/PTR.2650040607 https://doi.org/10.1177/1934578X1000501210 https://doi.org/10.1021/NP990567X https://doi.org/10.1016/S0367-326X(00)00165-9 https://doi.org/10.1055/S-2005-871302 https://doi.org/10.1021/NP990051D https://doi.org/10.1007/S12272-011-0206-0
(-)-Maackiain 3-O-glucoside	4485132	Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6	446.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2704566/ https://doi.org/10.1021/NP980103J https://doi.org/10.1248/BPB.31.154
(-)-Maackiain-3-O-glucosyl-6''-O-malonate	23724669	Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)OC5=CC6=C(C=C25)OCO6	532.40	unknown	https://doi.org/10.1016/0031-9422(91)84251-M
(+)-Maackiain	161298	Click to see	284.26	unknown	https://doi.org/10.1016/J.BMC.2007.03.011
(+)-Medicarpin	73067	Click to see	270.28	unknown	https://doi.org/10.1007/S12272-011-0206-0
(1S,12S)-16-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaene	373519	Click to see	298.29	unknown	https://doi.org/10.1016/J.BMC.2007.03.011
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[[(1S,12S)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-16-yl]oxy]oxane-3,4,5-triol	6326060	Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6	446.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2704566/
(6aR,11aR)-3-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-8,9-diol	361910	Click to see	286.28	unknown	via CMAUP database
(6aR,11aR)-3,9-Dimethoxy-6H-benzofuro(3,2-c)(1)benzopyran-6a(11aH)-ol	442828	Click to see	300.30	unknown	https://doi.org/10.1016/J.BMC.2007.03.011
(6aR,11aR)-8-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol	21676223	Click to see COC1=C(C=C2C(=C1)C3COC4=C(C3O2)C=CC(=C4)O)O	286.28	unknown	https://doi.org/10.1248/CPB.33.3231
(6aS,11aS)-8-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol	154496847	Click to see COC1=C(C=C2C(=C1)C3COC4=C(C3O2)C=CC(=C4)O)O	286.28	unknown	https://doi.org/10.1248/CPB.33.3231
(6S,6aR,11aS)-6,9-dimethoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-ol	162889965	Click to see COC1C2C(C3=C(O1)C=C(C=C3)O)OC4=C2C=CC(=C4)OC	300.30	unknown	https://doi.org/10.1007/S12272-011-0206-0
3-Hydroxy-8,9-methylenedioxypterocarpane	363863	Click to see	284.26	unknown	https://doi.org/10.1007/S12272-011-0206-0 https://doi.org/10.1016/J.BMC.2007.03.011 https://doi.org/10.1055/S-2005-871302 https://doi.org/10.1021/NP990051D https://doi.org/10.1021/NP990567X https://doi.org/10.1515/ZNC-1992-7-808
3-Methoxy-8,9-methylenedioxypterocarpan	454895	Click to see COC1=CC2=C(C=C1)C3C(CO2)C4=CC5=C(C=C4O3)OCO5	298.29	unknown	https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1016/S0367-326X(00)00165-9 https://doi.org/10.1016/J.BMC.2007.03.011
6'-Malonyltrifolirhizin	14841223	Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)OC5=CC6=C(C=C25)OCO6	532.40	unknown	https://doi.org/10.1016/0031-9422(91)84251-M
9-Methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-ol	623060	Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O	270.28	unknown	https://doi.org/10.1007/S12272-011-0206-0
CID 44428627	44428627	Click to see COC1=CC2=C(C=C1)C3C(CO2)(C4=C(O3)C=C(C=C4)OC)O	300.30	unknown	https://doi.org/10.1007/S12272-011-0206-0
Kushenin	5318889	Click to see	286.28	unknown	https://doi.org/10.1248/CPB.33.3231
Pterocarpin	1715306	Click to see	298.29	unknown	https://doi.org/10.1016/S0367-326X(00)00165-9 https://doi.org/10.1248/CPB.34.2094
Sophojaponicin	44257440	Click to see	446.40	unknown	via CMAUP database
Trifolirhizin	442827	Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6	446.40	unknown	https://doi.org/10.1248/BPB.31.154 https://doi.org/10.1021/NP980103J https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1016/S0367-326X(00)00165-9 https://doi.org/10.1007/BF02977714 https://doi.org/10.1515/ZNC-1992-7-808 https://doi.org/10.1002/PTR.2650040607 https://doi.org/10.1007/BF02973946 https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1515/ZNC-1991-3-402
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
3',4',7-Trihydroxyisoflavone	5284648	Click to see	270.24	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.04.003
5,7-Dihydroxy-3-(6-hydroxy-1,3-benzodioxol-5-yl)chromen-4-one	157010141	Click to see C1OC2=C(O1)C=C(C(=C2)C3=COC4=CC(=CC(=C4C3=O)O)O)O	314.25	unknown	https://doi.org/10.1016/S0031-9422(02)00671-4
Genistein	5280961	Click to see	270.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
(3R)-5,7-dihydroxy-3-(6-hydroxy-1,3-benzodioxol-5-yl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	101238023	Click to see CC(=CCC1=C(C2=C(C=C1O)OCC(C2=O)C3=CC4=C(C=C3O)OCO4)O)C	384.40	unknown	https://doi.org/10.1016/S0031-9422(02)00671-4
5,7-Dihydroxy-3-(6-hydroxy-1,3-benzodioxol-5-yl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	162994107	Click to see CC(=CCC1=C(C2=C(C=C1O)OCC(C2=O)C3=CC4=C(C=C3O)OCO4)O)C	384.40	unknown	https://doi.org/10.1016/S0031-9422(02)00671-4
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 3-prenylated isoflavanones
Sophoraisoflavanone A	442822	Click to see CC(=CCC1=C(C=CC(=C1OC)C2COC3=CC(=CC(=C3C2=O)O)O)O)C	370.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
5,7-Dihydroxy-3-(6-hydroxy-1,3-benzodioxol-5-yl)-6-(3-methylbut-2-enyl)chromen-4-one	101238024	Click to see	382.40	unknown	https://doi.org/10.1016/S0031-9422(02)00671-4
Alpinumisoflavone	5490139	Click to see	336.30	unknown	https://doi.org/10.1016/S0031-9422(02)00671-4
Lupalbigenin	10001388	Click to see	406.50	unknown	https://doi.org/10.1016/S0031-9422(02)00111-5
Luteone	5281797	Click to see	354.40	unknown	https://doi.org/10.1016/S0031-9422(02)00671-4
Wighteone	5281814	Click to see	338.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(1,3-benzodioxol-5-yl)-7-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one	102131643	Click to see	576.50	unknown	via CMAUP database
3-(3,4-Dihydroxyphenyl)-7-(((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2h-pyran-2-yl) oxy)-4h-chromen-4-one	68607439	Click to see	432.40	unknown	via CMAUP database
3-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	73603979	Click to see	578.50	unknown	via CMAUP database
3-(4-methoxyphenyl)-7-[(2S,4S,5R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	44257215	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O	430.40	unknown	https://doi.org/10.1002/PTR.2650040607
3'-Methoxy-4'-hydroxy-7-(6-O-(D-apio-beta-D-furanosyl)-beta-D-glucopyranosyloxy)isoflavone	102131642	Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)O	578.50	unknown	via CMAUP database
7-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-3-(3-hydroxy-4-methoxyphenyl)chromen-4-one	73603978	Click to see	578.50	unknown	via CMAUP database
Calycosin 7-O-xylosylglucoside	73603980	Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O	578.50	unknown	via CMAUP database
Daidzein 7-O-apiosyl-(1->6)-glucoside	20055730	Click to see	548.50	unknown	via CMAUP database
Kushenol O	44257224	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O	562.50	unknown	https://doi.org/10.1248/YAKUSHI1947.106.1_22
Ononin	442813	Click to see	430.40	unknown	https://doi.org/10.1002/PTR.2650040607
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Calycosin	5280448	Click to see	284.26	unknown	https://doi.org/10.1016/S0031-9422(02)00671-4
Koparin	5318834	Click to see COC1=C(C(=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O)O	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Biochanin A	5280373	Click to see	284.26	unknown	via CMAUP database
CID 10378473	10378473	Click to see	271.24	unknown	via CMAUP database
Formononetin	5280378	Click to see	268.26	unknown	https://doi.org/10.1007/BF02973946 https://doi.org/10.1007/BF02977714 https://doi.org/10.1248/CPB.21.2733 https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1177/1934578X1000501210 https://doi.org/10.1016/S0367-326X(00)00165-9 https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1016/J.BMC.2007.03.011 https://doi.org/10.1021/NP990567X
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-3-(2,4-dihydroxyphenyl)-1-[(3R)-5-hydroxy-7-methoxy-2,2-dimethyl-3-(3-methylbut-2-enyl)-3,4-dihydrochromen-6-yl]prop-2-en-1-one	163193946	Click to see	438.50	unknown	https://doi.org/10.1021/NP060189D
(E)-3-(2,4-dihydroxyphenyl)-1-[(3S)-5-hydroxy-7-methoxy-2,2-dimethyl-3-(3-methylbut-2-enyl)-3,4-dihydrochromen-6-yl]prop-2-en-1-one	163050493	Click to see	438.50	unknown	https://doi.org/10.1021/NP060189D
3-(2,4-Dihydroxyphenyl)-1-[5-hydroxy-7-methoxy-2,2-dimethyl-3-(3-methylbut-2-enyl)-3,4-dihydrochromen-6-yl]prop-2-en-1-one	73236930	Click to see	438.50	unknown	https://doi.org/10.1021/NP060189D
Cyclokuraridin	16083181	Click to see CC(=CCC1CC2=C(C(=C(C=C2OC1(C)C)OC)C(=O)C=CC3=C(C=C(C=C3)O)O)O)C	438.50	unknown	https://doi.org/10.1021/NP060189D
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
(E)-1-[2,4-dihydroxy-3-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-6-methoxyphenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one	163065327	Click to see	456.50	unknown	https://doi.org/10.1248/BPB.31.908 https://doi.org/10.1248/BPB.31.154
(E)-1-[2,4-dihydroxy-3-[(2S)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-6-methoxyphenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one	154496845	Click to see	456.50	unknown	https://doi.org/10.1248/CPB.21.2733
(E)-1-[2,4-dihydroxy-6-methoxy-3-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]phenyl]-3-(4-hydroxy-2-methoxyphenyl)prop-2-en-1-one	163028044	Click to see	452.50	unknown	https://doi.org/10.1248/CPB.33.3231
(E)-1-[2,4-dihydroxy-6-methoxy-3-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]phenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one	124303655	Click to see	438.50	unknown	https://doi.org/10.1248/CPB.19.2126
(E)-1-[2,4-dihydroxy-6-methoxy-3-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]phenyl]-3-(4-hydroxy-2-methoxyphenyl)prop-2-en-1-one	154496849	Click to see	452.50	unknown	https://doi.org/10.1248/CPB.33.3231
(Z)-1-[2,4-dihydroxy-6-methoxy-3-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)phenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one	102340315	Click to see	438.50	unknown	https://doi.org/10.1080/14786419.2017.1297992 https://doi.org/10.1007/BF02973946 https://doi.org/10.1002/PTR.2650040607 https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1248/BPB.31.908 https://doi.org/10.1248/CPB.19.2126 https://doi.org/10.1055/S-2008-1034285 https://doi.org/10.1055/S-2003-40643 https://doi.org/10.1055/S-2004-815545 https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<51::AID-PTR949>3.0.CO;2-H https://doi.org/10.1248/BPB.26.1348 https://doi.org/10.1016/0305-1978(95)00056-9 https://doi.org/10.1016/S0367-326X(00)00165-9 https://doi.org/10.1021/NP980103J https://doi.org/10.1055/S-2006-957906
1-[2,4-Dihydroxy-3-(5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl)-6-methoxyphenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one	71438140	Click to see	456.50	unknown	https://doi.org/10.1248/BPB.31.908 https://doi.org/10.1248/BPB.31.154
1-[2,4-Dihydroxy-6-methoxy-3-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)phenyl]-3-(4-hydroxy-2-methoxyphenyl)prop-2-en-1-one	78385179	Click to see	452.50	unknown	https://doi.org/10.1248/CPB.33.3231
1-{2,4-Dihydroxy-6-methoxy-3-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]phenyl}-3-(2,4-dihydroxyphenyl)prop-2-en-1-one	75026053	Click to see CC(=CCC(CC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=C(C=C(C=C2)O)O)O)C(=C)C)C	438.50	unknown	https://doi.org/10.1248/BPB.31.908 https://doi.org/10.1248/BPB.26.1348 https://doi.org/10.1055/S-2006-957906 https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1016/J.BMC.2007.03.011 https://doi.org/10.1007/S12272-011-0206-0 https://doi.org/10.1021/NP980103J
2',4',6',4-Tetrahydroxy-3'-prenylchalcone	189267	Click to see	340.40	unknown	https://doi.org/10.1248/YAKUSHI1947.90.4_463
3-hydroxy-6-[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]-5-methoxy-2-(3-methylbut-2-en-1-yl)phenolate	25245735	Click to see CC(=CCC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=C(C=C2)O)[O-])C	353.40	unknown	via CMAUP database
Desmethylxanthohumol	6443339	Click to see	340.40	unknown	https://doi.org/10.1248/YAKUSHI1947.90.4_463
Isocordoin	6251270	Click to see CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=CC=C2)O)C	308.40	unknown	via CMAUP database
Kuraridin	44428631	Click to see	438.50	unknown	https://doi.org/10.1248/BPB.31.908 https://doi.org/10.1248/BPB.26.1348 https://doi.org/10.1055/S-2006-957906 https://doi.org/10.1248/CPB.34.2094 https://doi.org/10.1016/J.BMC.2007.03.011 https://doi.org/10.1007/S12272-011-0206-0 https://doi.org/10.1021/NP980103J
Kuraridinol	5318880	Click to see	456.50	unknown	https://doi.org/10.1248/BPB.31.908 https://doi.org/10.1248/BPB.31.154 https://doi.org/10.1248/CPB.21.2733 https://doi.org/10.1248/CPB.34.2094
Kushenol D	5318893	Click to see	452.50	unknown	https://doi.org/10.1002/PTR.2650040607 https://doi.org/10.1248/CPB.33.3231
Npc239	9954815	Click to see	438.50	unknown	via CMAUP database
Xanthohumol	639665	Click to see CC(=CCC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=C(C=C2)O)O)C	354.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retrochalcones
2-Hydroxychalcone	5367146	Click to see	224.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavones
2H-1-Benzopyran-2-one, 4-(3,4-dihydroxyphenyl)-6-hydroxy-7-methoxy-	5318262	Click to see	300.26	unknown	via CMAUP database
6,7-Dimethoxy-4-phenylcoumarin	1235191	Click to see	282.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
1-[2,4-dihydroxy-6-methoxy-3-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]phenyl]-2-(2,4-dihydroxyphenyl)ethane-1,2-dione	162984338	Click to see	440.50	unknown	https://doi.org/10.1021/NP060189D
Oxynarcotine	5320347	Click to see CNCCC1=CC2=C(C(=C1CC(=O)C3=C(C(=C(C=C3)OC)OC)C(=O)O)OC)OCO2	431.40	unknown	via CMAUP database
Sophoradione	16083185	Click to see CC(=CCC(CC1=C(C(=C(C=C1O)OC)C(=O)C(=O)C2=C(C=C(C=C2)O)O)O)C(=C)C)C	440.50	unknown	https://doi.org/10.1021/NP060189D
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
1-(3-hydroxy-4-methoxyphenyl)-2-[2-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]ethane-1,2-dione	73603972	Click to see	582.50	unknown	via CMAUP database
1-[4-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-2-hydroxyphenyl]-2-(3-hydroxy-4-methoxyphenyl)ethane-1,2-dione	73603983	Click to see COC1=C(C=C(C=C1)C(=O)C(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O)O)O	582.50	unknown	via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Sophora flavescens

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top