Scientific name	Authority	First published in
Scutellaria adamsii	A.Ham.	Esq. Monogr. Scutellaria : 34 (1832)
Scutellaria baicalensis f. albiflora	H.W.Jen & Y.J.Chang	J. Beijing Forest. Univ. 13(3): 3 (1991)
Scutellaria davurica	Pall. ex Ledeb.	Fl. Ross. 3: 397 (1849)
Scutellaria lanceolaria	Miq.	Ann. Mus. Bot. Lugduno-Batavi 2: 110 (1865)
Scutellaria macrantha	Fisch. ex Rchb.	Iconogr. Bot. Pl. Crit. 5: 52 (1827)
Scutellaria speciosa	Fisch. ex Turcz.	Bull. Soc. Imp. Naturalistes Moscou 24(II): 389 (1851)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	baikal skullcap
Azerbaijani	baykal başlıqotu
Belarusian	Шлёмнік байкальскі
Bulgarian	Шлемник байкалски
Bulgarian	байкалски шлемник
Czech	šišák bajkalský
German	baikalhelmkraut
German	baikal-helmkraut
Esperanto	bajkala skutelario
Estonian	baikali tihashein
French	scutellaire du baïkal
Japanese	黄岑
Japanese	黄苓
Japanese	コガネバナ
Japanese	オウゴン
Korean	황금
lzh	黃芩
Polish	tarczyca bajkalska
Russian	Шлемник байкальский
Thai	อึ่งงิ้ม
Vietnamese	hoàng cầm
Vietnamese	hoàng cầm (cây)
Chinese	黃芩
Chinese	黄岑
Chinese	黄芩子
Chinese	黄芩
Chinese	香水水草

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!

No variety added yet.

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!

Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

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
  - Inner Mongolia
  - Manchuria
- Eastern Asia
  - Korea
- Mongolia
  - Mongolia
- Russian Far East
  - Amur
  - Khabarovsk
  - Primorye
- Siberia
  - Buryatiya
  - Chita
  - Irkutsk

Asia-tropical click to expand
- Indo-China
  - Vietnam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000307642
UNII	6YF0M477I5
Tropicos	17604355
KEW	urn:lsid:ipni.org:names:458155-1
The Plant List	kew-188938
Open Tree Of Life	795166
Observations.org	122062
NCBI Taxonomy	65409
IPNI	458155-1
iNaturalist	565882
GBIF	7309014
Freebase	/m/03qcbsm
EPPO	SCDBA
Elurikkus	586527
USDA GRIN	33424
Wikipedia	Scutellaria_baicalensis
CMAUP	NPO28877

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_005771605.1	ASM577160v1	Chromosome	Shanghai Chen Shan Botanical Garden	2019-05-29	173.4x	368.76 Mb

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

Huang Lian Jie Du Decoction enhances the anti-tumor efficacy of immune checkpoint inhibitors by activating TLR7/8 signalling in melanoma

Liu S, Zhang Y, Zhu X, He S, Liu X, Lv X, Zuo F, Wu J

BMC Complement Med Ther

11-Apr-2024

PMCID:	PMC11007990
doi:	10.1186/s12906-024-04444-y
PMID:	38605368

Carbon Dots Derived from Curcumae Radix and Their Heartprotective Effect

Dong L, Zhao Y, Luo J, Li X, Wang S, Li M, Zou P, Kong H, Wang Q, Zhao Y, Qu H

Int J Nanomedicine

08-Apr-2024

PMCID:	PMC11012788
doi:	10.2147/IJN.S444125
PMID:	38617797

Deciphering the intricate linkage between the gut microbiota and Alzheimer's disease: Elucidating mechanistic pathways promising therapeutic strategies

Liang J, Wang Y, Liu B, Dong X, Cai W, Zhang N, Zhang H

CNS Neurosci Ther

07-Apr-2024

PMCID:	PMC10999574
doi:	10.1111/cns.14704
PMID:	38584341

Smart osteoclasts targeted nanomedicine based on amorphous CaCO3 for effective osteoporosis reversal

Yu B, Gao Q, Sheng S, Zhou F, Geng Z, Wei Y, Zhang H, Hu Y, Wang S, Huang J, Li M, Su J

J Nanobiotechnology

05-Apr-2024

PMCID:	PMC10996086
doi:	10.1186/s12951-024-02412-9
PMID:	38580995

Preparation, characterisation and in vitro anti-inflammatory activity of Baicalin microsponges

Li M, Gan J, Xu X, Zhang S, Li Y, Bian L, Dong Z

Heliyon

04-Apr-2024

PMCID:	PMC11015413
doi:	10.1016/j.heliyon.2024.e29151
PMID:	38617936

Baicalein improves renal interstitial fibrosis by inhibiting the ferroptosis in vivo and in vitro

Liang GQ, Mu W, Jiang CB

Heliyon

02-Apr-2024

PMCID:	PMC11004807
doi:	10.1016/j.heliyon.2024.e28954
PMID:	38601597

The complete chloroplast genome of Lagochilus ilicifolius Bunge ex Bentham, Labiat. Gen. 1834 (Lamiaceae) and its phylogenetic analysis

Hou WJ, Men WX, Xing YP, Yang YY, Xu L, Kang TG, Song YY

Mitochondrial DNA B Resour

02-Apr-2024

PMCID:	PMC10993758
doi:	10.1080/23802359.2024.2334013
PMID:	38586511

MYC Oncogene: A Druggable Target for Treating Cancers with Natural Products

Chan KI, Zhang S, Li G, Xu Y, Cui L, Wang Y, Su H, Tan W, Zhong Z

Aging Dis

01-Apr-2024

PMCID:	PMC10917530
doi:	10.14336/AD.2023.0520
PMID:	37450923

Research progress on the mechanism of TCM regulating intestinal microbiota in the treatment of DM mellitus

Ping Y, Liu J, Wang L, Qiu H, Zhang Y

Front Endocrinol (Lausanne)

27-Mar-2024

PMCID:	PMC11004430
doi:	10.3389/fendo.2024.1308016
PMID:	38601207

Recent advances in the potential effects of natural products from traditional Chinese medicine against respiratory diseases targeting ferroptosis

Chen T, Ding L, Zhao M, Song S, Hou J, Li X, Li M, Yin K, Li X, Wang Z

Chin Med

22-Mar-2024

PMCID:	PMC10958864
doi:	10.1186/s13020-024-00918-w
PMID:	38519984

Deciphering the dynamics of methicillin-resistant Staphylococcus aureus biofilm formation: from molecular signaling to nanotherapeutic advances

Aboelnaga N, Elsayed SW, Abdelsalam NA, Salem S, Saif NA, Elsayed M, Ayman S, Nasr M, Elhadidy M

Cell Commun Signal

22-Mar-2024

PMCID:	PMC10958940
doi:	10.1186/s12964-024-01511-2
PMID:	38519959

The effect of scutellaria baicalensis and its active ingredients on major depressive disorder: a systematic review and meta-analysis of literature in pre-clinical research

Ma Y, Zhou X, Zhang F, Huang C, Yang H, Chen W, Tao X

Front Pharmacol

20-Mar-2024

PMCID:	PMC10987764
doi:	10.3389/fphar.2024.1313871
PMID:	38572433

铁死亡在非小细胞肺癌中的作用及中药干预进展

GUO X, WANG T, XIA J, ZENG H, SHI W

Zhongguo Fei Ai Za Zhi

20-Mar-2024

PMCID:	PMC11002191
doi:	10.3779/j.issn.1009-3419.2024.101.06
PMID:	38590196

Mechanisms of Antibiotic Resistance and Developments in Therapeutic Strategies to Combat Klebsiella pneumoniae Infection

Li Y, Kumar S, Zhang L

Infect Drug Resist

19-Mar-2024

PMCID:	PMC10960543
doi:	10.2147/IDR.S453025
PMID:	38525477

Ultrasound-Assisted Multi-Enzyme Extraction for Highly Efficient Extraction of Polysaccharides from Ulva lactuca

Wang W, Li J, Lu F, Liu F

Foods

15-Mar-2024

PMCID:	PMC10969873
doi:	10.3390/foods13060891
PMID:	38540881

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
> Benzenoids / Benzene and substituted derivatives
3-Phenylfuran	518802	Click to see C1=CC=C(C=C1)C2=COC=C2	144.17	unknown	https://doi.org/10.1271/BBB1961.51.1449
Phenylethyl Alcohol	6054	Click to see C1=CC=C(C=C1)CCO	122.16	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Bis(2-ethylhexyl) phthalate	8343	Click to see CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC	390.60	unknown	https://doi.org/10.1271/BBB1961.51.1449
Dibutyl Phthalate	3026	Click to see CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC	278.34	unknown	https://doi.org/10.1271/BBB1961.51.1449
Dioctyl phthalate	8346	Click to see CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC	390.60	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid	243	Click to see C1=CC=C(C=C1)C(=O)O	122.12	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
3-Methoxybenzaldehyde	11569	Click to see COC1=CC=CC(=C1)C=O	136.15	unknown	via CMAUP database
p-Anisaldehyde	31244	Click to see COC1=CC=C(C=C1)C=O	136.15	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
2-Methylbenzyl alcohol	6994	Click to see CC1=CC=CC=C1CO	122.16	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
2,4-Dimethoxy-1-(1-propenyl)benzene	5314067	Click to see CC=CC1=C(C=C(C=C1)OC)OC	178.23	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
Phenylacetaldehyde	998	Click to see C1=CC=C(C=C1)CC=O	120.15	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Benzene and substituted derivatives / Styrenes
Benzylideneacetone	637759	Click to see CC(=O)C=CC1=CC=CC=C1	146.19	unknown	via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Elemicin	10248	Click to see COC1=CC(=CC(=C1OC)OC)CC=C	208.25	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Phenol	996	Click to see C1=CC=C(C=C1)O	94.11	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Phenols / Cresols / Ortho cresols
o-Cresol	335	Click to see CC1=CC=CC=C1O	108.14	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Phenols / Cresols / Para cresols
P-Cresol	2879	Click to see CC1=CC=C(C=C1)O	108.14	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Phenols / Methoxyphenols
2-Methoxy-4-vinylphenol	332	Click to see COC1=C(C=CC(=C1)C=C)O	150.17	unknown	https://doi.org/10.1271/BBB1961.51.1449
5-Ethenyl-2-methoxyphenol	10441857	Click to see COC1=C(C=C(C=C1)C=C)O	150.17	unknown	https://doi.org/10.1271/BBB1961.51.1449
Eugenol	3314	Click to see COC1=C(C=CC(=C1)CC=C)O	164.20	unknown	https://doi.org/10.1271/BBB1961.51.1449
Guaiacol	460	Click to see COC1=CC=CC=C1O	124.14	unknown	https://doi.org/10.1271/BBB1961.51.1449
Isoeugenol	853433	Click to see CC=CC1=CC(=C(C=C1)O)OC	164.20	unknown	https://doi.org/10.1271/BBB1961.51.1449
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Phenols / Methoxyphenols / Gingerdiols
[4]-Gingerdiol	5318276	Click to see CCCC(CC(CCC1=CC(=C(C=C1)O)OC)O)O	268.35	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Docosane	12405	Click to see CCCCCCCCCCCCCCCCCCCCCC	310.60	unknown	https://doi.org/10.1271/BBB1961.51.1449
Dodecane	8182	Click to see CCCCCCCCCCCC	170.33	unknown	https://doi.org/10.1271/BBB1961.51.1449
Eicosane	8222	Click to see CCCCCCCCCCCCCCCCCCCC	282.50	unknown	https://doi.org/10.1271/BBB1961.51.1449
Heneicosane	12403	Click to see CCCCCCCCCCCCCCCCCCCCC	296.60	unknown	https://doi.org/10.1271/BBB1961.51.1449
Heptacosane	11636	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC	380.70	unknown	https://doi.org/10.1271/BBB1961.51.1449
Heptadecane	12398	Click to see CCCCCCCCCCCCCCCCC	240.50	unknown	https://doi.org/10.1271/BBB1961.51.1449
Hexacosane	12407	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC	366.70	unknown	https://doi.org/10.1271/BBB1961.51.1449
Hexadecane	11006	Click to see CCCCCCCCCCCCCCCC	226.44	unknown	https://doi.org/10.1271/BBB1961.51.1449
Nonadecane	12401	Click to see CCCCCCCCCCCCCCCCCCC	268.50	unknown	https://doi.org/10.1271/BBB1961.51.1449
Octadecane	11635	Click to see CCCCCCCCCCCCCCCCCC	254.50	unknown	https://doi.org/10.1271/BBB1961.51.1449
Pentacosane	12406	Click to see CCCCCCCCCCCCCCCCCCCCCCCCC	352.70	unknown	https://doi.org/10.1271/BBB1961.51.1449
Pentadecane	12391	Click to see CCCCCCCCCCCCCCC	212.41	unknown	https://doi.org/10.1271/BBB1961.51.1449
Tetracosane	12592	Click to see CCCCCCCCCCCCCCCCCCCCCCCC	338.70	unknown	https://doi.org/10.1271/BBB1961.51.1449
Tetradecane	12389	Click to see CCCCCCCCCCCCCC	198.39	unknown	https://doi.org/10.1271/BBB1961.51.1449
Tricosane	12534	Click to see CCCCCCCCCCCCCCCCCCCCCCC	324.60	unknown	https://doi.org/10.1271/BBB1961.51.1449
Tridecane	12388	Click to see CCCCCCCCCCCCC	184.36	unknown	https://doi.org/10.1271/BBB1961.51.1449
Undecane	14257	Click to see CCCCCCCCCCC	156.31	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl palmitate	8181	Click to see CCCCCCCCCCCCCCCC(=O)OC	270.50	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid	11005	Click to see CCCCCCCCCCCCCC(=O)O	228.37	unknown	https://doi.org/10.1271/BBB1961.51.1449
Oleic Acid	445639	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	https://doi.org/10.1271/BBB1961.51.1449
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	https://doi.org/10.1271/BBB1961.51.1449
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid	2969	Click to see CCCCCCCCCC(=O)O	172.26	unknown	https://doi.org/10.1271/BBB1961.51.1449
Heptanoic Acid	8094	Click to see CCCCCCC(=O)O	130.18	unknown	https://doi.org/10.1271/BBB1961.51.1449
Nonanoic acid	8158	Click to see CCCCCCCCC(=O)O	158.24	unknown	https://doi.org/10.1271/BBB1961.51.1449
Octanoic acid	379	Click to see CCCCCCCC(=O)O	144.21	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,4bR,7R,9R,10aR)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-9-ol	13966170	Click to see CC1(CCC2C(=C1)C(CC3C2(CCCC3(C)CO)C)O)C=C	304.50	unknown	via CMAUP database
(1R,4aS,4bS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid	11870275	Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C	302.50	unknown	via CMAUP database
18-Nordehydroabiet-4(19)-ene	44268166	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(=C)C3CC2)C	254.40	unknown	via CMAUP database
7-Dehydroabietanone	11289118	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)C)C	284.40	unknown	via CMAUP database
7-Oxodehydroabietinol	15715176	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)CO)C	300.40	unknown	via CMAUP database
Abieta-8,11,13-trien-15-ol	101586702	Click to see CC1(CCCC2(C1CCC3=C2C=CC(=C3)C(C)(C)O)C)C	286.50	unknown	via CMAUP database
Abieta-8,11,13-trien-7alpha-ol	21764434	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C)C	286.50	unknown	via CMAUP database
Abietatriene	6432211	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C)C	270.50	unknown	via CMAUP database
Anticopalic acid	11808890	Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)C)C	304.50	unknown	via CMAUP database
Anticopalic acid methyl ester	11290126	Click to see CC(=CC(=O)OC)CCC1C(=C)CCC2C1(CCCC2(C)C)C	318.50	unknown	via CMAUP database
Ethyl abietate	61182	Click to see CCOC(=O)C1(CCCC2(C1CC=C3C2CCC(=C3)C(C)C)C)C	330.50	unknown	via CMAUP database
Ferruginol	442027	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1271/BBB1961.51.1449
Isopimara-7,15-diene	13969536	Click to see CC1(CCCC2(C1CC=C3C2CCC(C3)(C)C=C)C)C	272.50	unknown	via CMAUP database
Pimarol	12314285	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C	288.50	unknown	via CMAUP database
Sandaracopimaradiene	443469	Click to see CC1(CCCC2(C1CCC3=CC(CCC32)(C)C=C)C)C	272.50	unknown	via CMAUP database
Sandaracopimarinol	12314286	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C	288.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids
[(1S,4S,5R,6R,9S,14R)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxo-7-tetracyclo[7.5.1.01,5.010,12]pentadeca-2,7-dienyl]methyl hexadecanoate	5318035	Click to see CCCCCCCCCCCCCCCC(=O)OCC1=CC2C3C(C3(C)C)CC(C4(C2=O)C=C(C(C4(C1O)O)O)C)C	586.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geranylacetone	1549778	Click to see CC(=CCCC(=CCCC(=O)C)C)C	194.31	unknown	https://doi.org/10.1271/BBB1961.51.1449
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	via CMAUP database
(+)-3-Carene	443156	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	via CMAUP database
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
Borneol, (-)-	1201518	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-beta-Phellandrene	443161	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	via CMAUP database
(+)-beta-Phellandrene	442484	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	via CMAUP database
[4-(Prop-1-en-2-yl)cyclohexyl]methanol	519954	Click to see CC(=C)C1CCC(CC1)CO	154.25	unknown	via CMAUP database
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1271/BBB1961.51.1449
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene	1796220	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	via CMAUP database
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene	134779875	Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	https://doi.org/10.1271/BBB1961.51.1449
6-Methoxygossypol	3085061	Click to see CC1=CC2=C(C(=C(C(=C2C(C)C)O)O)C=O)C(=C1C3=C(C4=C(C=C3C)C(=C(C(=C4C=O)O)OC)C(C)C)O)O	532.60	unknown	via CMAUP database
6,10,14-Trimethylpentadecan-2-one	10408	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=O)C	268.50	unknown	https://doi.org/10.1271/BBB1961.51.1449
alpha-Cubebene	442359	Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	https://doi.org/10.1271/BBB1961.51.1449
Caryophyllene,alpha + beta mixt.	5354499	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1271/BBB1961.51.1449
delta-Cadinol	3084311	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene	6918391	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
beta-EUDESMOL	91457	Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O	222.37	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
(1S,3Z,6S,7E,11R,12R,13S,17S)-1,4,8,14,14,17-hexamethyltricyclo[9.8.0.012,17]nonadeca-3,7-diene-6,13-diol	163189028	Click to see CC1=CC(CC(=CCC2(CCC3(CCC(C(C3C2CC1)O)(C)C)C)C)C)O	374.60	unknown	https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[(1R,2S,3R,4R,4aS,8aR)-2-benzoyloxy-3-hydroxy-3,4,8a-trimethyl-8-methylidene-4-[2-(5-oxo-2H-furan-3-yl)ethyl]-1,2,4a,5,6,7-hexahydronaphthalen-1-yl] benzoate	102247117	Click to see CC1(C2CCCC(=C)C2(C(C(C1(C)O)OC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4)C)CCC5=CC(=O)OC5	558.70	unknown	https://doi.org/10.1016/0031-9422(96)00380-9
[2-benzoyloxy-3-hydroxy-3,4,8a-trimethyl-8-methylidene-4-[2-(5-oxo-2H-furan-3-yl)ethyl]-1,2,4a,5,6,7-hexahydronaphthalen-1-yl] benzoate	162905592	Click to see CC1(C2CCCC(=C)C2(C(C(C1(C)O)OC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4)C)CCC5=CC(=O)OC5	558.70	unknown	https://doi.org/10.1016/0031-9422(96)00380-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(24S)-Lanosta-9(11)-ene-3beta,24,25-triol	101121169	Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C	460.70	unknown	via CMAUP database
16-Oxo-21-episerratenediol	101280208	Click to see CC1(C2CCC3(CC4=CC(=O)C5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C	456.70	unknown	via CMAUP database
21-Episerratenediol	12309682	Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C	442.70	unknown	via CMAUP database
21-Episerratenediol 3-methyl ether	101280203	Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)O)(C)C)C)C	456.70	unknown	via CMAUP database
3beta-Methoxy-21-oxoserratene	14830066	Click to see CC1(C2CCC3(CC4=CCC5C(C(=O)CCC5(C4CCC3C2(CCC1OC)C)C)(C)C)C)C	454.70	unknown	via CMAUP database
Serratenediol 3-methyl ether	21672660	Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)O)(C)C)C)C	456.70	unknown	via CMAUP database
Serratenediol dimethyl ether	101280202	Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)OC)(C)C)C)C	470.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesta-4,6-dien-3-one	3034666	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2C=CC4=CC(=O)CCC34C)C	382.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(8R,9S,10S,13R,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	51051617	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CCC4C3(CC=C(C4)O)C)C	400.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
Campesteryl ferulate	15056832	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C=CC5=CC(=C(C=C5)O)OC)C)C	576.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(10R,13S)-3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-17-[1-[5-methyl-6-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]ethyl]-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one	11968816	Click to see CC1CCC(OC1OC2C(C(C(C(O2)C)O)O)O)C(C)C3CCC4C3(CCC5C4CC(=O)C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C	887.10	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8R,9R,10S,13R,14R,17R)-17-[(E,2R,5R)-5-ethyl-6-methylhept-3-en-2-yl]-3,10,13-trimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene	50930798	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)C)C)C)C(C)C	410.70	unknown	via CMAUP database
(3S,8R,9R,10S,13R,14S,17R)-17-[(2R,5S)-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	636741	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one	12943207	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C=CC4=CC(=O)CCC34C)C)C(C)C	410.70	unknown	via CMAUP database
Stigmast-4-en-3-one	5484202	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	412.70	unknown	via CMAUP database
Stigmasta-3,5-dien-7-one	12444466	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC=C4)C)C)C(C)C	410.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
2-Butenedioic acid	723	Click to see C(=CC(=O)O)C(=O)O	116.07	unknown	https://doi.org/10.1007/S10600-008-0023-Y
Fumaric Acid	444972	Click to see C(=CC(=O)O)C(=O)O	116.07	unknown	https://doi.org/10.1007/S10600-008-0023-Y
Malonic acid	867	Click to see C(C(=O)O)C(=O)O	104.06	unknown	https://doi.org/10.1007/S10600-008-0023-Y
Succinic Acid	1110	Click to see C(CC(=O)O)C(=O)O	118.09	unknown	https://doi.org/10.1007/S10600-008-0023-Y
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Citric Acid	311	Click to see C(C(=O)O)C(CC(=O)O)(C(=O)O)O	192.12	unknown	https://doi.org/10.1007/S10600-008-0023-Y
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(2S)-2-Hydroxybutanedioic acid	222656	Click to see C(C(C(=O)O)O)C(=O)O	134.09	unknown	https://doi.org/10.1007/S10600-008-0023-Y
Malic Acid	525	Click to see C(C(C(=O)O)O)C(=O)O	134.09	unknown	https://doi.org/10.1007/S10600-008-0023-Y
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid	1794427	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
Chlorogensaure	12310830	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
cis-Chlorogenic acid	1794425	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
2-(Hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxane-3,4,5-triol	4961358	Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O	300.30	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
D-Alt(a1-2a)L-Psif	53301851	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	via CMAUP database
Salidroside	159278	Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O	300.30	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
4-[4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]butan-2-one	10172008	Click to see CC(=O)CCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O	326.34	unknown	via CMAUP database
Suffruticoside A	9986231	Click to see CC(=O)C1=C(C=C(C=C1)OC)OC2C(C(C(C(O2)COC3C(C(CO3)(COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)O)O	612.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
(3R,4R,5R)-2-[(3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyperoxy-5-(hydroxymethyl)oxolane-3,4-diol	91884769	Click to see C(C1C(C(C(O1)OOOC2C(C(C(O2)CO)O)O)O)O)O	314.24	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
DL-Tartaric acid	875	Click to see C(C(C(=O)O)O)(C(=O)O)O	150.09	unknown	https://doi.org/10.1007/S10600-008-0023-Y
Mesotartaric acid	447315	Click to see C(C(C(=O)O)O)(C(=O)O)O	150.09	unknown	https://doi.org/10.1007/S10600-008-0023-Y
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Methylfurfural	12097	Click to see CC1=CC=C(O1)C=O	110.11	unknown	https://doi.org/10.1271/BBB1961.51.1449
Pyrrole-2-carboxaldehyde	13854	Click to see C1=CNC(=C1)C=O	95.10	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Sebacaldehyde	3016433	Click to see C(CCCCC=O)CCCC=O	170.25	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
(E)-beta-Damascone	5374527	Click to see CC=CC(=O)C1=C(CCCC1(C)C)C	192.30	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
2-Acetylpyrrole	14079	Click to see CC(=O)C1=CC=CN1	109.13	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
2-Hydroxyacetophenone	68490	Click to see C1=CC=C(C=C1)C(=O)CO	136.15	unknown	https://doi.org/10.1271/BBB1961.51.1449
4'-Methoxyacetophenone	7476	Click to see CC(=O)C1=CC=C(C=C1)OC	150.17	unknown	https://doi.org/10.1271/BBB1961.51.1449
Acetophenone	7410	Click to see CC(=O)C1=CC=CC=C1	120.15	unknown	https://doi.org/10.1271/BBB1961.51.1449
Benzoylacetone	7166	Click to see CC(=O)CC(=O)C1=CC=CC=C1	162.18	unknown	via CMAUP database
Paeonol	11092	Click to see CC(=O)C1=C(C=C(C=C1)OC)O	166.17	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organoheterocyclic compounds / Benzofurans / Benzofuranones
Butylphthalide	61361	Click to see CCCCC1C2=CC=CC=C2C(=O)O1	190.24	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,6-Dihydroxy-3,5,7-trimethoxyxanthen-9-one	5316837	Click to see COC1=CC(=C2C(=C1)OC3=C(C(=C(C=C3C2=O)OC)O)OC)O	318.28	unknown	via CMAUP database
6,8-Dihydroxy-9-oxoxanthen-4-olate	25200626	Click to see C1=CC2=C(C(=C1)[O-])OC3=CC(=CC(=C3C2=O)O)O	243.19	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
Mellein	28516	Click to see CC1CC2=C(C(=CC=C2)O)C(=O)O1	178.18	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Pentylfuran	19602	Click to see CCCCCC1=CC=CO1	138.21	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Indole	798	Click to see C1=CC=C2C(=C1)C=CN2	117.15	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
3-Dihydrocadambine	162138	Click to see COC(=O)C1=COC(C2C1CC3C4=C(CCN3CC2O)C5=CC=CC=C5N4)OC6C(C(C(C(O6)CO)O)O)O	546.60	unknown	via CMAUP database
> Organoheterocyclic compounds / Isobenzofurans
3-N-Butyl-4,5-dihydrophthalide	173843	Click to see CCCCC1C2=C(C=CCC2)C(=O)O1	192.25	unknown	https://doi.org/10.1271/BBB1961.51.1449
Cnidilide	160710	Click to see CCCCC1C2CCC=CC2C(=O)O1	194.27	unknown	https://doi.org/10.1271/BBB1961.51.1449
Ligustilide	5319022	Click to see CCCC=C1C2=C(C=CCC2)C(=O)O1	190.24	unknown	https://doi.org/10.1271/BBB1961.51.1449
Sedanolide	5018391	Click to see CCCCC1C2CCCC=C2C(=O)O1	194.27	unknown	https://doi.org/10.1271/BBB1961.51.1449
Senkyunolide A	3085257	Click to see CCCCC1C2=C(C=CCC2)C(=O)O1	192.25	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organoheterocyclic compounds / Isocoumarans / Isobenzofuranones
Butylidene phthalide	62368	Click to see CCCC=C1C2=CC=CC=C2C(=O)O1	188.22	unknown	https://doi.org/10.1271/BBB1961.51.1449
Butylidenephthalide	5352899	Click to see CCCC=C1C2=CC=CC=C2C(=O)O1	188.22	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
gamma-Caprolactone	12756	Click to see CCC1CCC(=O)O1	114.14	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organoheterocyclic compounds / Naphthopyrans
13-Vinyl-16,17-dinor-14-oxaabietane	102594798	Click to see CC1(CCCC2(C1CCC3C2CCC(O3)(C)C=C)C)C	276.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Piperidines
beta-Skytanthine	442552	Click to see CC1CCC2C1CN(CC2C)C	167.29	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Maltol	8369	Click to see CC1=C(C(=O)C=CO1)O	126.11	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Phenylpropanoids and polyketides / Aurone flavonoids
(2Z)-2-benzylidene-4,5,6-trihydroxy-1-benzofuran-3-one	5322048	Click to see C1=CC=C(C=C1)C=C2C(=O)C3=C(O2)C=C(C(=C3O)O)O	270.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-Phenyl-propenal	307	Click to see C1=CC=C(C=C1)C=CC=O	132.16	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[5-Hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate	73157771	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)OC)O)O)O)O)O	638.60	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	74027662	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	638.60	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside	132274946	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1248/CPB.50.896 https://doi.org/10.1016/S0031-9422(99)00306-4
Acteoside;Kusaginin;TJC160	354009	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/S0031-9422(96)00443-8
beta-D-Glucopyranoside, 2-(3-hydroxy-4-methoxyphenyl)ethyl 3-O-(6-deoxy-alpha-L-mannopyranosyl)-, 4-[3-(4-hydroxy-3-methoxyphenyl)-2-propenoate], (E)-	72725940	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)OC)O)O)O)O)O	652.60	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
Jionoside D	9895632	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)OC)O)O)O)O)O	638.60	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
Leucosceptoside A	10394343	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	638.60	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
Martynoside	5319292	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)OC)O)O)O)O)O	652.60	unknown	https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1016/S0031-9422(96)00443-8
Verbascoside	5281800	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1248/CPB.50.896 https://doi.org/10.1016/S0031-9422(96)00443-8 https://doi.org/10.1016/S0031-9422(99)00306-4
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Cupressuflavone	5281609	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O)O	538.50	unknown	https://doi.org/10.1111/J.1600-0609.2009.01365.X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(+)-Epicatechin	182232	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
(2R,3S)-2-(2,6-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol	163014180	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=C(C=CC=C3O)O)O	290.27	unknown	https://doi.org/10.1248/CPB.33.2411
2-(2,6-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol	163014179	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=C(C=CC=C3O)O)O	290.27	unknown	https://doi.org/10.1248/CPB.33.2411
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+/-)-Eriodictyol	11095	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	288.25	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7
(2R)-2-(3,4-dihydroxyphenyl)-7-hydroxy-4-oxo-2,3-dihydrochromen-5-olate	25200419	Click to see C1C(OC2=CC(=CC(=C2C1=O)[O-])O)C3=CC(=C(C=C3)O)O	287.24	unknown	via CMAUP database
(2S)-dihydrotricetin	440836	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C(=C3)O)O)O	304.25	unknown	via CMAUP database
(S)-2,3-Dihydro-5,7-dihydroxy-8-methyl-2-phenyl-4-benzopyrone	6453244	Click to see CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3	270.28	unknown	via CMAUP database
2,3,3,5,6-Pentahydroxy-2-phenylchromen-4-one	54231395	Click to see C1=CC=C(C=C1)C2(C(C(=O)C3=C(O2)C=CC(=C3O)O)(O)O)O	304.25	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3857833/
2',5,6',7-Tetrahydroxyflavanone	42607849	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=C(C=CC=C3O)O	288.25	unknown	https://doi.org/10.1007/BF00630621 https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1248/CPB.30.1792 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X
4H-1-Benzopyran-4-one, 2-(2,6-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-, (2S)-	157671	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=C(C=CC=C3O)O	288.25	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1007/BF00630621 https://doi.org/10.1248/CPB.30.1792 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X
Carthamidin	188308	Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)O)O)C3=CC=C(C=C3)O	288.25	unknown	via CMAUP database
Dihydrobaicalein	9816931	Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)O)O)C3=CC=CC=C3	272.25	unknown	via CMAUP database
Eriodictyol	440735	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	288.25	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7
Strobopinin	442520	Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O	270.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2S,3R)-2-(2,6-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one	86311089	Click to see C1=CC(=C(C(=C1)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	304.25	unknown	https://doi.org/10.1007/BF00630621 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q
2-(2,6-Dihydroxyphenyl)-3,5,7-trihydroxychroman-4-one	71307292	Click to see C1=CC(=C(C(=C1)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	304.25	unknown	https://doi.org/10.1007/BF00630621 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X https://doi.org/10.1016/0031-9422(95)00200-Q
2',3,5,7-Tetrahydroxyflavanone	3082330	Click to see C1=CC=C(C(=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	288.25	unknown	via CMAUP database
4H-1-Benzopyran-4-one, 2-(2,6-dihydroxyphenyl)-2,3-dihydro-3,5,7-trihydroxy-, (2R,3R)-	157633	Click to see C1=CC(=C(C(=C1)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	304.25	unknown	https://doi.org/10.1111/J.2042-7158.1997.TB06119.X
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(2,6-Dihydroxyphenyl)-5,6,7,8-tetrahydroxychromen-4-one	141059302	Click to see C1=CC(=C(C(=C1)O)C2=CC(=O)C3=C(C(=C(C(=C3O2)O)O)O)O)O	318.23	unknown	https://doi.org/10.1248/CPB.33.2411
5,7-dihydroxy-2-[2-hydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one	102445445	Click to see C1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
5,7-Dihydroxy-2-[2-hydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one	74977417	Click to see C1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
5,7,2'-Trihydroxyflavone	5322064	Click to see C1=CC=C(C(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1248/CPB.40.531
5,7,2',3'-Tetrahydroxyflavone	5321864	Click to see C1=CC(=C(C(=C1)O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	286.24	unknown	https://doi.org/10.1248/CPB.40.531
5,7,2',5'-Tetrahydroxyflavone	5487756	Click to see C1=CC(=C(C=C1O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	286.24	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X
5,7,2',6'-Tetrahydroxyflavone	5321865	Click to see C1=CC(=C(C(=C1)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	286.24	unknown	https://doi.org/10.1007/BF00630621 https://doi.org/10.1248/CPB.40.531 https://doi.org/10.1055/S-2001-15810 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q
7-Hydroxy-4-oxo-2-phenylchromen-5-olate	25200543	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)[O-]	253.23	unknown	via CMAUP database
7,3',4'-Trihydroxyflavone	5322065	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)O)O	270.24	unknown	via CMAUP database
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1248/YAKUSHI1947.104.5_529
Baicalein	5281605	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O	270.24	unknown	https://doi.org/10.1006/JMCC.1999.1021 https://doi.org/10.1252/KAKORONBUNSHU.22.287 https://doi.org/10.1007/BF00040133 https://doi.org/10.1016/S0031-9422(96)00443-8 https://doi.org/10.1016/J.JPBA.2010.04.019 https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1055/S-2007-969712 https://doi.org/10.1248/CPB.40.531 https://doi.org/10.1055/S-2007-969517 https://doi.org/10.1248/CPB.33.4894 https://doi.org/10.1055/S-2004-815489 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/S0176-1617(00)80282-5 https://doi.org/10.1248/CPB.35.3494 https://doi.org/10.1055/S-2001-15810 https://doi.org/10.1016/S0378-8741(97)00045-7 https://doi.org/10.1248/CPB.50.896 https://doi.org/10.1016/S0304-4165(99)00152-X https://doi.org/10.1158/1078-0432.CCR-04-1974 https://doi.org/10.1515/ZNC-1997-11-1215 https://doi.org/10.1021/NP980163P https://doi.org/10.1016/S0021-9673(01)87399-4 https://doi.org/10.1007/BF02976430 https://doi.org/10.1016/0003-2670(94)80134-7 https://doi.org/10.1016/S0021-9673(98)00906-6 https://doi.org/10.1055/S-2006-958036 https://doi.org/10.1248/BPB.21.1067 https://doi.org/10.1248/CPB.33.2411 https://doi.org/10.1248/BPB.31.838 https://doi.org/10.1248/YAKUSHI1947.107.4_315 https://doi.org/10.1248/CPB.32.5051 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X https://doi.org/10.1055/S-0029-1243121 https://doi.org/10.1016/S0039-9140(00)00514-2 https://doi.org/10.1111/J.1600-0609.2009.01365.X https://doi.org/10.1055/S-2006-957517 https://doi.org/10.1248/YAKUSHI1947.105.2_148 https://doi.org/10.1007/BF02277510 https://doi.org/10.1002/CHIN.200333219 https://doi.org/10.1055/S-0029-1243111
Chrysin	5281607	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	254.24	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8 https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1055/S-2007-969712 https://doi.org/10.1248/YAKUSHI1947.104.5_529 https://doi.org/10.1007/BF02976430 https://doi.org/10.1248/CPB.33.2411 https://doi.org/10.1248/CPB.32.5051 https://doi.org/10.1111/J.1600-0609.2009.01365.X https://doi.org/10.1248/YAKUSHI1947.105.2_148
Isoscutellarein	5281665	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)O)O	286.24	unknown	https://doi.org/10.1248/YAKUSHI1947.104.5_529
Norwogonin	5281674	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)O	270.24	unknown	https://doi.org/10.1248/YAKUSHI1947.103.6_607 https://doi.org/10.1016/S0176-1617(00)80282-5
Scutellarein	5281697	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O)O	286.24	unknown	https://doi.org/10.1248/YAKUSHI1947.104.5_529 https://doi.org/10.1055/S-0029-1243121
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,7,4'-Trihydroxyflavone	5281611	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C=C3)O)O)O	270.24	unknown	https://doi.org/10.1111/J.1600-0609.2009.01365.X
Galangin	5281616	Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1111/J.1600-0609.2009.01365.X
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1016/S0039-9140(00)00514-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-Dihydroxy-2-phenyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-(3,4,5-trihydroxyoxan-2-yl)chromen-4-one	73829976	Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=CC=C4)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O	548.50	unknown	https://doi.org/10.1016/S0031-9422(00)82692-8 https://doi.org/10.1016/S0031-9422(96)00443-8
Apigenin 6-C-alpha-L-arabinopyranoside-8-C-beta-D-glucopyranoside	44257699	Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O	564.50	unknown	via CMAUP database
Chrysin 6-C-arabinoside 8-C-glucoside	21722008	Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=CC=C4)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O	548.50	unknown	https://doi.org/10.1016/S0031-9422(00)82692-8 https://doi.org/10.1016/S0031-9422(96)00443-8
Chrysin 6-C-glucoside 8-C-arabinoside	21722007	Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=CC=C5)O)O)O	548.50	unknown	https://doi.org/10.1016/S0031-9422(00)82692-8 https://doi.org/10.1016/S0031-9422(96)00443-8
CID 44715843	44715843	Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=CC=C5)O)O)O	548.50	unknown	https://doi.org/10.1016/S0031-9422(00)82692-8 https://doi.org/10.1016/S0031-9422(96)00443-8
Corymboside	13644660	Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O	564.50	unknown	https://doi.org/10.1016/S0031-9422(00)82692-8
Isoschaftoside	3084995	Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O	564.50	unknown	https://doi.org/10.1016/S0031-9422(00)82692-8
Schaftoside	442658	Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O	564.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2R,3R,4S,5R,6S)-6-(5,6-dihydroxy-4-oxo-2-phenylchromen-7-yl)oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	69717682	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	446.40	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
(3S,4S,6S)-6-(5,6-dihydroxy-4-oxo-2-phenylchromen-7-yl)oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	44258403	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	446.40	unknown	via CMAUP database
3,4,5-Trihydroxy-6-(5-hydroxy-8-methoxy-4-oxo-2-phenylchromen-7-yl)oxyoxane-2-carboxylic acid	12004622	Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)OC4C(C(C(C(O4)C(=O)O)O)O)O	460.40	unknown	https://doi.org/10.1248/CPB.32.5051 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1078/0944711041495173 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X https://doi.org/10.1016/S0304-4165(99)00152-X https://doi.org/10.1016/S0031-9422(96)00443-8 https://doi.org/10.1002/CHIN.200333219 https://doi.org/10.1002/(SICI)1099-1573(199909)13:6<479::AID-PTR484>3.0.CO;2-M
6-(5,6-Dihydroxy-4-oxo-2-phenylchromen-7-yl)oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	3807559	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	446.40	unknown	https://doi.org/10.1016/J.JPBA.2010.04.019 https://doi.org/10.15281/JPLANTRES1887.36.1 https://doi.org/10.1055/S-0029-1243121 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1111/J.2042-7158.1997.TB06119.X https://doi.org/10.1016/S0031-9422(96)00443-8 https://doi.org/10.1055/S-2006-958036
Apigenin-7-o-glucuronide	12912214	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	446.40	unknown	https://doi.org/10.1248/YAKUSHI1947.104.5_529
Baicalin	64982	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	446.40	unknown	https://doi.org/10.1055/S-2001-15810 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X https://doi.org/10.1016/S0304-4165(99)00152-X https://doi.org/10.1016/0306-3623(95)02143-4 https://doi.org/10.1055/S-2006-958036 https://doi.org/10.1055/S-2006-961769 https://doi.org/10.1055/S-2004-815489 https://doi.org/10.1248/BPB.31.838 https://doi.org/10.15281/JPLANTRES1887.36.1 https://doi.org/10.1016/J.JPBA.2010.04.019 https://doi.org/10.1016/0003-2670(94)80134-7 https://doi.org/10.1007/BF00040133 https://doi.org/10.1016/S0039-9140(00)00514-2 https://doi.org/10.1002/CHIN.200333219 https://doi.org/10.1055/S-2007-969517 https://doi.org/10.1016/S0021-9673(98)00906-6 https://doi.org/10.1248/CPB.33.4894 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1111/J.1600-0609.2009.01365.X https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1016/S0378-8741(97)00045-7 https://doi.org/10.1248/YAKUSHI1947.105.2_148 https://doi.org/10.1007/BF02277510 https://doi.org/10.1252/KAKORONBUNSHU.22.287 https://doi.org/10.1078/0944711041495173 https://doi.org/10.1248/YAKUSHI1947.107.4_315 https://doi.org/10.1248/CPB.33.2411 https://doi.org/10.1248/CPB.50.896 https://doi.org/10.1055/S-0029-1243121 https://doi.org/10.1515/ZNC-1997-11-1215 https://doi.org/10.1248/CPB.32.5051 https://doi.org/10.1248/CPB.35.3494
Baicalin methyl ester	15223582	Click to see COC(=O)C1C(C(C(C(O1)OC2=C(C(=C3C(=C2)OC(=CC3=O)C4=CC=CC=C4)O)O)O)O)O	460.40	unknown	https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q
Chrysin 7-glucuronide	44257628	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O	430.40	unknown	via CMAUP database
Dihydrobaicalin	14135325	Click to see C1C(OC2=CC(=C(C(=C2C1=O)O)O)OC3C(C(C(C(O3)C(=O)O)O)O)O)C4=CC=CC=C4	448.40	unknown	https://doi.org/10.1248/YAKUSHI1947.103.6_607
Glychionide A	11597485	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O	446.40	unknown	via CMAUP database
Methyl 6-(5,6-dihydroxy-4-oxo-2-phenylchromen-7-yl)oxy-3,4,5-trihydroxyoxane-2-carboxylate	72747690	Click to see COC(=O)C1C(C(C(C(O1)OC2=C(C(=C3C(=C2)OC(=CC3=O)C4=CC=CC=C4)O)O)O)O)O	460.40	unknown	https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q
Oroxindin	3084961	Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)OC4C(C(C(C(O4)C(=O)O)O)O)O	460.40	unknown	https://doi.org/10.1248/CPB.33.4894 https://doi.org/10.1248/CPB.32.5051 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1007/BF00040133 https://doi.org/10.1016/0003-2670(94)80134-7 https://doi.org/10.1248/CPB.35.3494 https://doi.org/10.1002/PTR.1216 https://doi.org/10.1078/0944711041495173 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X https://doi.org/10.1248/YAKUSHI1947.107.4_315 https://doi.org/10.1016/S0304-4165(99)00152-X https://doi.org/10.1016/S0031-9422(96)00443-8 https://doi.org/10.1002/(SICI)1099-1573(199909)13:6<479::AID-PTR484>3.0.CO;2-M https://doi.org/10.1248/YAKUSHI1947.105.2_148
Oroxylin A glucoronide	14655552	Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=CC=C3)OC4C(C(C(C(O4)C(=O)O)O)O)O	460.40	unknown	https://doi.org/10.1016/0003-2670(94)80134-7 https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1248/CPB.35.3494 https://doi.org/10.1248/YAKUSHI1947.105.2_148
oroxylin A glucuronide	44567248	Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=CC=C3)OC4C(C(C(C(O4)C(=O)O)O)O)O	460.40	unknown	https://doi.org/10.1016/S0021-9673(01)87399-4 https://doi.org/10.1078/0944711041495173
Scutellarin	185617	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O	462.40	unknown	via CMAUP database
Scutellarin(1-)	29927686	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)[O-])O)O)O)O)O)O	461.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-8-O-glucuronides
ISOSCUTELLAREIN 8-O-beta-D-GLUCURONIDE	14332450	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O	462.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
8-methoxy-2-phenyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5319440	Click to see COC1=C2C(=C(C=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C=C(O2)C4=CC=CC=C4	430.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-Dihydroxyphenyl)-3-(beta-D-glucopyranosyloxy)-5-hydroxy-7-(beta-D-glucopyranosyloxy)-2,3-dihydro-4H-1-benzopyran-4-one	5317187	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O	628.50	unknown	via CMAUP database
5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	5353588	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O	608.50	unknown	https://doi.org/10.1111/J.1600-0609.2009.01365.X
7-[(4,8-Dihydroxy-7-oxo-2,6-dioxabicyclo[3.2.1]octan-3-yl)oxy]-5,6-dihydroxy-2-phenylchromen-4-one	69755698	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C5C(C(O4)C(=O)O5)O)O)O)O	428.30	unknown	https://doi.org/10.1248/CPB.33.2411
7-[[(1S,3S,4R,5S,8R)-4,8-dihydroxy-7-oxo-2,6-dioxabicyclo[3.2.1]octan-3-yl]oxy]-5,6-dihydroxy-2-phenylchromen-4-one	162921922	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C5C(C(O4)C(=O)O5)O)O)O)O	428.30	unknown	https://doi.org/10.1248/CPB.33.2411
Oroxin A	5320313	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1248/YAKUSHI1947.105.2_148
wogonin 7-O-glucoside	51136398	Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)OC4C(C(C(C(O4)CO)O)O)O	446.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
(2R)-2-(2,6-dihydroxyphenyl)-3,4-dihydro-2H-chromene-5,7-diol	124708188	Click to see C1CC2=C(C=C(C=C2OC1C3=C(C=CC=C3O)O)O)O	274.27	unknown	https://doi.org/10.1248/CPB.33.2411
2',5,6',7-Tetrahydroxyflavane	92043131	Click to see C1CC2=C(C=C(C=C2OC1C3=C(C=CC=C3O)O)O)O	274.27	unknown	https://doi.org/10.1248/CPB.33.2411
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 2-O-methylated flavonoids
5-Hydroxy-2-(2-hydroxy-6-methoxyphenyl)-6,7,8-trimethylchromen-4-one	162904250	Click to see CC1=C(C(=C2C(=O)C=C(OC2=C1C)C3=C(C=CC=C3OC)O)O)C	326.30	unknown	https://doi.org/10.1016/0031-9422(95)00200-Q
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
4',5-Dihydroxy-3'-methoxyflavon-7-olate(1-)	25203524	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)[O-]	299.25	unknown	via CMAUP database
Geraldone	5281618	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C=C3)O)O	284.26	unknown	https://doi.org/10.1111/J.1600-0609.2009.01365.X
Quercetagetin 3-methyl ether	5320475	Click to see COC1=C(OC2=C(C1=O)C(=C(C(=C2)O)O)O)C3=CC(=C(C=C3)O)O	332.26	unknown	via CMAUP database
Tricin	5281702	Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	330.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin	5280442	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	284.26	unknown	via CMAUP database
Diosmetin	5281612	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	https://doi.org/10.1111/J.1600-0609.2009.01365.X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
7,2',6'-Trihydroxy-5-methoxyflavanone	5322075	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=C(C=CC=C3O)O)O	302.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
(2s)-5,7,4'-Trihydroxy-6-methoxyflavanone	46893290	Click to see COC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)O)O	302.28	unknown	https://doi.org/10.1248/YAKUSHI1947.100.12_1220
5,7,2'-Trihydroxy-6-methoxyflavone	5322076	Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=CC=C3O)O	300.26	unknown	https://doi.org/10.1248/CPB.40.531
5,7,4'-Trihydroxy-6-methoxyflavanone	5322074	Click to see COC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)O)O	302.28	unknown	via CMAUP database
Dihydrooroxylin A	5316733	Click to see COC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O	286.28	unknown	https://doi.org/10.1248/YAKUSHI1947.105.2_148
Oroxylin A	5320315	Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=CC=C3)O	284.26	unknown	https://doi.org/10.1055/S-2001-15810 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X https://doi.org/10.1016/S0021-9673(01)87399-4 https://doi.org/10.1055/S-2007-969712 https://doi.org/10.1007/BF02976430 https://doi.org/10.1016/0003-2670(94)80134-7 https://doi.org/10.1055/S-2007-969517 https://doi.org/10.1007/BF00630621 https://doi.org/10.5586/ASBP.1999.015 https://doi.org/10.1002/MC.20570 https://doi.org/10.1002/PTR.1216 https://doi.org/10.1021/NP9003036 https://doi.org/10.1016/S0378-8741(97)00045-7 https://doi.org/10.1248/YAKUSHI1947.105.2_148 https://doi.org/10.1016/S0176-1617(00)80282-5 https://doi.org/10.1007/BF02277510 https://doi.org/10.1248/CPB.51.339 https://doi.org/10.1248/CPB.33.2411 https://doi.org/10.1055/S-2006-957517 https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1248/CPB.40.531 https://doi.org/10.1248/CPB.35.3494 https://doi.org/10.1016/S0006-2952(03)00233-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R,3R)-2-(2,6-dimethoxyphenyl)-3,5,7-trimethoxy-2,3-dihydrochromen-4-one	162958441	Click to see COC1C(OC2=C(C1=O)C(=CC(=C2)OC)OC)C3=C(C=CC=C3OC)OC	374.40	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7
2-(2,6-Dimethoxyphenyl)-3,5,7-trimethoxy-2,3-dihydrochromen-4-one	162958440	Click to see COC1C(OC2=C(C1=O)C(=CC(=C2)OC)OC)C3=C(C=CC=C3OC)OC	374.40	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7
2-(3,4-dimethoxyphenyl)-6,7-dimethoxy-4H-chromene-3,4-diol	5316834	Click to see COC1=C(C=C(C=C1)C2=C(C(C3=CC(=C(C=C3O2)OC)OC)O)O)OC	360.40	unknown	via CMAUP database
5-hydroxy-2-[2-hydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-6,7-dimethoxychromen-4-one	102445447	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=C(C=CC=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)OC	492.40	unknown	https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1016/S0031-9422(96)00443-8
5-hydroxy-2-[2-hydroxy-6-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-6,7-dimethoxychromen-4-one	163049058	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=C(C=CC=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)OC	492.40	unknown	https://doi.org/10.1016/0031-9422(95)00200-Q
5-Hydroxy-2-[2-hydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-6,7-dimethoxychromen-4-one	74977825	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=C(C=CC=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)OC	492.40	unknown	https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1016/S0031-9422(96)00443-8
5,8-Dihydroxy-6,7-dimethoxyflavone	153441	Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=CC=C3)O)OC	314.29	unknown	via CMAUP database
5,8,2'-Trihydroxy-6,7-dimethoxyflavone	156993	Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=CC=C3O)O)OC	330.29	unknown	https://doi.org/10.1248/YAKUSHI1947.100.12_1220
5,8,2'-Trihydroxy-7-methoxyflavone	156992	Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=CC=C3O)O	300.26	unknown	https://doi.org/10.1248/YAKUSHI1947.100.12_1220
Chrysosplenetin	5281608	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O	374.30	unknown	https://doi.org/10.1111/J.1600-0609.2009.01365.X
Salvigenin	161271	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O	328.30	unknown	https://doi.org/10.1248/YAKUSHI1947.104.5_529
Tectochrysin	5281954	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O	268.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-(5-hydroxy-7,8-dimethoxy-4-oxochromen-2-yl)-3-methoxyphenoxy]oxane-2-carboxylic acid	14825641	Click to see COC1=C(C(=CC=C1)OC2C(C(C(C(O2)C(=O)O)O)O)O)C3=CC(=O)C4=C(O3)C(=C(C=C4O)OC)OC	520.40	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
(2S,3S,4S,5R)-2,3,4,5-Tetrahydroxy-5-(5-hydroxy-8-methoxy-4-oxo-2-phenyl-4H-chromen-7-yl)-6-oxohexanoic acid	29927693	Click to see COC1=C2C(=C(C=C1C(C=O)(C(C(C(C(=O)O)O)O)O)O)O)C(=O)C=C(O2)C3=CC=CC=C3	460.40	unknown	via CMAUP database
(5-hydroxy-8-methoxy-4-oxo-2-phenylchromen-7-yl) (2S,3S,4S,5R)-2,3,4,5-tetrahydroxy-6-oxohexanoate	163052805	Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)OC(=O)C(C(C(C(C=O)O)O)O)O	460.40	unknown	https://doi.org/10.1248/CPB.33.2411
(5-Hydroxy-8-methoxy-4-oxo-2-phenylchromen-7-yl) 2,3,4,5-tetrahydroxy-6-oxohexanoate	163052804	Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)OC(=O)C(C(C(C(C=O)O)O)O)O	460.40	unknown	https://doi.org/10.1248/CPB.33.2411
3,4,5-Trihydroxy-6-[2-(5-hydroxy-7,8-dimethoxy-4-oxochromen-2-yl)-3-methoxyphenoxy]oxane-2-carboxylic acid	14825640	Click to see COC1=C(C(=CC=C1)OC2C(C(C(C(O2)C(=O)O)O)O)O)C3=CC(=O)C4=C(O3)C(=C(C=C4O)OC)OC	520.40	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
4'-Hydroxywogonin	5322078	Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=C(C=C3)O)O)O	300.26	unknown	https://doi.org/10.1248/CPB.38.3488
5-hydroxy-2-[2-hydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-6,7,8-trimethoxychromen-4-one	162869198	Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=C(C=CC=C3OC4C(C(C(C(O4)CO)O)O)O)O)OC)OC	522.50	unknown	https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q
5-hydroxy-2-[2-hydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7,8-dimethoxychromen-4-one	101932172	Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=C(C=CC=C3OC4C(C(C(C(O4)CO)O)O)O)O)OC	492.40	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
5-hydroxy-2-[2-hydroxy-6-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-6,7,8-trimethoxychromen-4-one	162869199	Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=C(C=CC=C3OC4C(C(C(C(O4)CO)O)O)O)O)OC)OC	522.50	unknown	https://doi.org/10.1016/0031-9422(95)00200-Q
5-Hydroxy-2-[2-hydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7,8-dimethoxychromen-4-one	133561455	Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=C(C=CC=C3OC4C(C(C(C(O4)CO)O)O)O)O)OC	492.40	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
5-Hydroxy-7,8-dimethoxyflavone	188316	Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=CC=C3)OC	298.29	unknown	via CMAUP database
5,2'-Dihydroxy-6,7,8,3'-tetramethoxy flavone	15896301	Click to see COC1=CC=CC(=C1O)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O	374.30	unknown	https://doi.org/10.1016/S0031-9422(99)00306-4
5,2',5'-Trihydroxy-6,7,8-trimethoxyflavone	21721900	Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=C(C=CC(=C3)O)O)OC)OC	360.30	unknown	via CMAUP database
5,2',5'-Trihydroxy-7,8-dimethoxyflavone	21122623	Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=C(C=CC(=C3)O)O)OC	330.29	unknown	https://doi.org/10.1248/CPB.40.531
5,7-dihydroxy-2-[3-hydroxy-2-methoxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-8-methoxychromen-4-one	102445446	Click to see COC1=C(C=CC(=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC4C(C(C(C(O4)CO)O)O)O)O	508.40	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1016/S0031-9422(96)00443-8
5,7-Dihydroxy-2-[3-hydroxy-2-methoxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-8-methoxychromen-4-one	74977898	Click to see COC1=C(C=CC(=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC4C(C(C(C(O4)CO)O)O)O)O	508.40	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1016/S0031-9422(96)00443-8
5,7-Dihydroxy-6,8-dimethoxyflavone	11609345	Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=CC=C3)OC)O	314.29	unknown	via CMAUP database
5,7-Dihydroxy-6,8,2',3'-tetramethoxyflavone	5316833	Click to see COC1=CC=CC(=C1OC)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O	374.30	unknown	via CMAUP database
5,7,2'-Trihydroxy-6,8-dimethoxyflavone	9818878	Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=CC=C3O)OC)O	330.29	unknown	https://doi.org/10.1055/S-2002-36357
5,7,2'-Trihydroxy-8,6'-dimethoxyflavone	5322060	Click to see COC1=CC=CC(=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC)O	330.29	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1248/CPB.40.531
5,7,2',3'-Tetrahydroxy-8,6'-dimethoxyflavone	21718608	Click to see COC1=C(C(=C(C=C1)O)O)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC	346.30	unknown	https://doi.org/10.1055/S-2007-969712
5,7,3',4'-Tetrahydroxy-6,8-dimethoxyflavone	5321859	Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC)O	346.30	unknown	via CMAUP database
6,2'-Dihydroxy-5,7,8,6'-tetramethoxyflavone	10872445	Click to see COC1=CC=CC(=C1C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)O)OC)OC)O	374.30	unknown	https://doi.org/10.1055/S-2002-36357
Ganhuangenin	5271991	Click to see COC1=C(C=CC(=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC)O)O	346.30	unknown	https://doi.org/10.1055/S-0029-1243111 https://doi.org/10.1055/S-2001-15810 https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1007/BF00630621 https://doi.org/10.1002/(SICI)1099-1573(199808)12:5<340::AID-PTR316>3.0.CO;2-U https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1002/(SICI)1099-1573(199909)13:6<479::AID-PTR484>3.0.CO;2-M https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1248/CPB.33.3982
Rivularin (flavone)	13889022	Click to see COC1=CC=CC(=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)OC)O	344.30	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1248/CPB.40.531 https://doi.org/10.1016/S0031-9422(96)00443-8
Scutevulin	5321205	Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3O)O)O	300.26	unknown	via CMAUP database
Skullcapflavone I	5320399	Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=CC=C3O)OC	314.29	unknown	https://doi.org/10.1055/S-2001-15810 https://doi.org/10.1016/S0031-9422(96)00443-8 https://doi.org/10.1248/CPB.40.531 https://doi.org/10.1248/YAKUSHI1947.107.10_827 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1006/JMCC.1999.1021
Skullcapflavone II	124211	Click to see COC1=CC=CC(=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O	374.30	unknown	https://doi.org/10.1016/S0378-8741(97)00045-7 https://doi.org/10.1248/CPB.33.2411 https://doi.org/10.1055/S-2007-969517 https://doi.org/10.1248/BPB.31.838 https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1248/CPB.32.5051 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1007/BF02976430 https://doi.org/10.1016/J.ETAP.2014.12.002 https://doi.org/10.1016/0031-9422(95)00200-Q https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1352373/ https://doi.org/10.1055/S-2007-969712 https://doi.org/10.1248/CPB.40.531 https://doi.org/10.1248/CPB.35.3494 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X https://doi.org/10.1158/1078-0432.CCR-04-1974 https://doi.org/10.1055/S-2006-957517 https://doi.org/10.1006/JMCC.1999.1021 https://doi.org/10.1016/S0031-9422(96)00443-8 https://doi.org/10.1248/YAKUSHI1947.105.2_148
Tenaxin I	159029	Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=CC=C3O)OC)OC	344.30	unknown	https://doi.org/10.1248/CPB.40.531 https://doi.org/10.1016/S0031-9422(96)00443-8
Viscidulin II	5322059	Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=C(C=CC=C3O)O)OC	330.29	unknown	https://doi.org/10.1248/CPB.40.531
Wogonin	5281703	Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)O	284.26	unknown	https://doi.org/10.1006/JMCC.1999.1021 https://doi.org/10.1007/BF00040133 https://doi.org/10.1016/S0031-9422(96)00443-8 https://doi.org/10.1016/J.JPBA.2010.04.019 https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1055/S-2007-969712 https://doi.org/10.1248/CPB.40.531 https://doi.org/10.1248/CPB.51.339 https://doi.org/10.1055/S-2007-969517 https://doi.org/10.1016/S0006-2952(02)01347-3 https://doi.org/10.1002/(SICI)1099-1573(199808)12:5<340::AID-PTR316>3.0.CO;2-U https://doi.org/10.1248/YAKUSHI1947.104.5_529 https://doi.org/10.1248/CPB.33.4894 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/S0176-1617(00)80282-5 https://doi.org/10.1248/CPB.35.3494 https://doi.org/10.1055/S-2001-15810 https://doi.org/10.1016/S0378-8741(97)00045-7 https://doi.org/10.1248/CPB.50.896 https://doi.org/10.1016/S0304-4165(99)00152-X https://doi.org/10.1158/1078-0432.CCR-04-1974 https://doi.org/10.1007/BF02980087 https://doi.org/10.1515/ZNC-1997-11-1215 https://doi.org/10.1016/S0021-9673(01)87399-4 https://doi.org/10.1055/S-2006-961769 https://doi.org/10.1007/BF02976430 https://doi.org/10.1002/(SICI)1099-1573(199909)13:6<479::AID-PTR484>3.0.CO;2-M https://doi.org/10.1016/0003-2670(94)80134-7 https://doi.org/10.1016/S0021-9673(98)00906-6 https://doi.org/10.1055/S-2006-958036 https://doi.org/10.1248/CPB.33.2411 https://doi.org/10.1248/BPB.31.838 https://doi.org/10.1248/YAKUSHI1947.107.4_315 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X https://doi.org/10.1248/CPB.32.5051 https://doi.org/10.1055/S-0029-1243121 https://doi.org/10.5586/ASBP.1999.015 https://doi.org/10.1248/YAKUSHI1947.105.2_148 https://doi.org/10.1007/BF02277510 https://doi.org/10.15281/JPLANTRES1887.36.1 https://doi.org/10.1002/CHIN.200333219
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid C-glycosides
5,7-dihydroxy-3-(4-hydroxyphenyl)-8-[(2S,3R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	44257269	Click to see C1=CC(=CC=C1C2=COC3=C(C(=C(C(=C3C2=O)O)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O	594.50	unknown	via CMAUP database
Puerarin	5281807	Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O	416.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Iridin	5281777	Click to see COC1=CC(=CC(=C1OC)O)C2=COC3=CC(=C(C(=C3C2=O)O)OC)OC4C(C(C(C(O4)CO)O)O)O	522.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
2',7-Dihydroxy-4',5'-dimethoxyisoflavone	5316763	Click to see COC1=C(C=C(C(=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O)OC	314.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(2E)-1-(2,4-Dihydroxy-6-methoxyphenyl)-3-(2,6-dihydroxyphenyl)-2-propen-1-one	5321869	Click to see COC1=CC(=CC(=C1C(=O)C=CC2=C(C=CC=C2O)O)O)O	302.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Combretastatin A4	5351344	Click to see COC1=C(C=C(C=C1)C=CC2=CC(=C(C(=C2)OC)OC)OC)O	316.30	unknown	via CMAUP database
Pinosylvin methyl ether	5281719	Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2	226.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Woodorien	192694	Click to see COC(=O)C1=CC(=C(C=C1)O)OC2C(C(C(C(O2)CO)O)O)O	330.29	unknown	via CMAUP database

Biological Material Top

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.

Scutellaria baicalensis

Table of Contents

Details Top

Description 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

Biological Material Top

Contributors Top

Collections Top