Scientific name	Authority	First published in
Vexibia alopecuroides	(L.) Yakovlev	Nauchyne Dokl. Vysshei Shkoly Biol. Nauki12: 54 (1973)
Sophora alopecuroides subsp. alopecuroides	L.
Goebelia alopecuroides var. alopecuroides	(L.) Bunge
Vexibiai alopecuroides	(L.) Yakovlev
Pseudosophora alopecuroides	(L.) Sweet	Hort. Brit., ed. 2: 122 (1830)
Vexibia alopecuroides subsp. alopecuroides	(L.) Yakovlev
Goebelia alopecuroides	(L.) Bunge ex Boiss.	Fl. Orient.2: 628 (1872)
Radiusia alopecuroides	(L.) Endl.	Cat. Hort. Vindob.2: 517 (1842)
Vexibia alopecuroides	(L.) W.A.Weber	Phytologia 62(5): 438. 1987
Pseudosophora alopecuroides	(L.) Galushko	Fl. Severn. Kavkaza Vopr. Ist. 3: 56. 1979
Sophora alopecuroides subsp. prodanii	Yakovlev
Sophora alopecuroides subsp. jaubertii	Borza
Goebelia alopecuroides var. tomentosa	Bunge

Common names Top

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Filter by language:

Language	Common/alternative name
Arabic	صفيراء ثعلبانية
Georgian	მაწაქი
Russian	Софора лисохвостовидная
Russian	Софора обыкновенная
Russian	Софора лисохвостная
Chinese	苦豆子
Chinese	苦豆子（苦豆草）
Chinese	苦豆根
Chinese	苦豆草

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Sophora alopecuroides subsp. tomentosa	(Boiss.) Bornm.	Beih. Bot. Centralbl.27(2): 347 (1910)
Sophora alopecuroides subsp. tomentosa	(Boiss.) Yakovlev	Vopr. Farmakogn. 4: 64. 1967 ; alt. title: Trudy Leningradsk. Khim.-Farm. Inst. 21: 64. 1967

Varieties (abbr. var.) Top

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Name	Authority	First published in
Sophora alopecuroides var. alopecuroides		Unknown

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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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
- Caucasus
  - Transcaucasus
- China
  - China North-central
  - China Southeast
  - Inner Mongolia
  - Qinghai
  - Tibet
  - Xinjiang
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Mongolia
  - Mongolia
- Siberia
  - Altay
  - West Siberia
- Western Asia
  - Afghanistan
  - Iran
  - Iraq
  - Lebanon-Syria
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Pakistan
  - West Himalaya

Europe click to expand
- Eastern Europe
  - East European Russia
  - Krym
  - South European Russia
  - Ukraine

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000213933
Tropicos	13032934
INPN	969317
KEW	urn:lsid:ipni.org:names:518788-1
The Plant List	ild-8998
Open Tree Of Life	571300
Observations.org	122496
NCBI Taxonomy	200492
IPNI	518788-1
GBIF	2959035
EPPO	SOBAL
EOL	704091
Elurikkus	341638
USDA GRIN	34945
CMAUP	NPO20471

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

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

Managing Opioid Withdrawal Symptoms During the Fentanyl Crisis: A Review

Weber AN, Trebach J, Brenner MA, Thomas MM, Bormann NL

Subst Abuse Rehabil

10-Apr-2024

PMCID:	PMC11016949
doi:	10.2147/SAR.S433358
PMID:	38623317

Inhibitory effect of aloperine on transient outward potassium currents in rat cardiac myocytes

Dong XN, Li MT

Front Pharmacol

28-Mar-2024

PMCID:	PMC11007096
doi:	10.3389/fphar.2024.1372973
PMID:	38606176

From immune checkpoints to therapies: understanding immune checkpoint regulation and the influence of natural products and traditional medicine on immune checkpoint and immunotherapy in lung cancer

Zhou Y, Wang F, Li G, Xu J, Zhang J, Gullen E, Yang J, Wang J

Front Immunol

15-Feb-2024

PMCID:	PMC10902058
doi:	10.3389/fimmu.2024.1340307
PMID:	38426097

A review of natural products targeting tumor immune microenvironments for the treatment of lung cancer

Yao P, Liang S, Liu Z, Xu C

Front Immunol

01-Feb-2024

PMCID:	PMC10867126
doi:	10.3389/fimmu.2024.1343316
PMID:	38361933

Sophoridine Counteracts Obesity via Src-Mediated Inhibition of VEGFR Expression and PI3K/AKT Phosphorylation

Sun J, Wang X, He Y, Tian X, Yuan T, Yang G, Yu T

Int J Mol Sci

19-Jan-2024

PMCID:	PMC10816114
doi:	10.3390/ijms25021206
PMID:	38279206

Pharmacokinetic, Tissue Distribution, Metabolite, and Toxicity Evaluation of the Matrine Derivative, (6aS, 10S, 11aR, 11bR, 11cS)-10-Methylaminododecahydro-3a, 7a-Diaza-benzo (de) Anthracene-8-thione

Li L, Lu F, Ding S, Wang X, Wang W, Zhang W, Xu W, Zhuang C, Miao Z, Ma X

Molecules

06-Jan-2024

PMCID:	PMC10820135
doi:	10.3390/molecules29020297
PMID:	38257210

Effects of Sophora alopecuroides in a High-Concentrate Diet on the Liver Immunity and Antioxidant Function of Lambs According to Transcriptome Analysis

An Y, Wang H, Gao A, Li S, Yang J, Li B, Lu H

Animals (Basel)

05-Jan-2024

PMCID:	PMC10812488
doi:	10.3390/ani14020182
PMID:	38254353

Matrine Targets BTF3 to Inhibit the Growth of Canine Mammary Tumor Cells

Feng Z, Sun N, Noor F, Sun P, Zhang H, Zhong J, Yin W, Fan K, Yang H, Zhang Z, Sun Y, Li H

Int J Mol Sci

30-Dec-2023

PMCID:	PMC10779273
doi:	10.3390/ijms25010540
PMID:	38203709

Potential Parasitoids for Biocontrol of the Ber Fruit Fly, Carpomya vesuviana Costa (Diptera: Tephritidae)

Amini A, Lotfalizadeh H, Peris-Felipo FJ, Rasplus JY

Life (Basel)

28-Dec-2023

PMCID:	PMC10821110
doi:	10.3390/life14010050
PMID:	38255665

Functional Trait Responses of Sophora alopecuroides L. Seedlings to Diverse Environmental Stresses in the Desert Steppe of Ningxia, China

Zhao J, Shi C, Wang L, Han X, Zhu Y, Liu J, Yang X

Plants (Basel)

25-Dec-2023

PMCID:	PMC10780927
doi:	10.3390/plants13010069
PMID:	38202378

An Overview of Traditional Chinese Medicine in the Treatment After Radical Resection of Hepatocellular Carcinoma

Peng Y, Wu X, Zhang Y, Yin Y, Chen X, Zheng D, Wang J

J Hepatocell Carcinoma

18-Dec-2023

PMCID:	PMC10743783
doi:	10.2147/JHC.S413996
PMID:	38143910

PacBio Full-Length Transcriptome Sequencing Reveals the Mechanism of Salt Stress Response in Sonneratia apetala

Chen B, Liu T, Yang Z, Yang S, Chen J

Plants (Basel)

14-Nov-2023

PMCID:	PMC10675792
doi:	10.3390/plants12223849
PMID:	38005746

Bacillus subtilis partially inhibits African swine fever virus infection in vivo and in vitro based on its metabolites arctiin and genistein interfering with the function of viral topoisomerase II

Lv C, Yang J, Zhao L, Zou Z, Kang C, Zhang Q, Wu C, Yang L, Cheng C, Zhao Y, Liao Q, Hu X, Li C, Sun X, Jin M

J Virol

06-Nov-2023

PMCID:	PMC10688316
doi:	10.1128/jvi.00719-23
PMID:	37929962

Transcriptome-Wide Analysis of Core Transcription Factors Associated with Defense Responses in Autotetraploid versus Diploid Rice under Saline Stress and Recovery

Wang Y, Meng W, Ye Y, Yu X, Chen H, Liu Y, Xu M, Wang N, Qi F, Lan Y, Xu Y, Ma J, Zhang C

Int J Mol Sci

05-Nov-2023

PMCID:	PMC10650042
doi:	10.3390/ijms242115982
PMID:	37958969

Pharmacological Activity of Matrine in Inhibiting Colon Cancer Cells VM Formation, Proliferation, and Invasion by Downregulating Claudin-9 Mediated EMT Process and MAPK Signaling Pathway

Du Q, Lin Y, Ding C, Wu L, Xu Y, Feng Q

Drug Des Devel Ther

11-Sep-2023

PMCID:	PMC10504061
doi:	10.2147/DDDT.S417077
PMID:	37719361

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
(6R,6aR,13S,13aS)-1,3,4,6,6a,7,8,9,10,12,13,13a-dodecahydro-2H-6,13-methanodipyrido[1,2-a:3',2'-e]azocine	442937	Click to see C1CCN2CC3CC(C2C1)C=C4C3NCCC4	232.36	unknown	https://doi.org/10.1007/BF00566104 https://doi.org/10.1007/BF00563812
(6R,7R,9R,11S)-16,17-Didehydro-9-de-2-piperidinylormosanine	139055730	Click to see C1CCN2CC3CC(C2C1)C=C4C3NCCC4	232.36	unknown	https://doi.org/10.1007/BF00566104 https://doi.org/10.1007/BF00563812
CID 10752071	10752071	Click to see C1CCN2CC3CC(C2C1)C=C4C3NCCC4	232.36	unknown	via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Anagyrine-type alkaloids
(1S,9S,10R,12R)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one	12299977	Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O	260.33	unknown	https://doi.org/10.1007/BF00580891
12-Hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one	621307	Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O	260.33	unknown	https://doi.org/10.1007/BF00580891
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(-)-Cytisine	22407	Click to see C1C2CNCC1C3=CC=CC(=O)N3C2	190.24	unknown	https://doi.org/10.1007/BF00580891 https://doi.org/10.1007/S10600-009-9360-8
(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/10.1007/BF00563949 https://doi.org/10.1007/BF00566104
(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,5R)-3,4,5,6-tetrahydro-1H-1,5-methanopyrido[1,2-a][1,5]diazocin-8(2H)-one	6713952	Click to see C1C2CNCC1C3=CC=CC(=O)N3C2	190.24	unknown	via CMAUP database
(1S,9S)-11-ethoxy-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one	162911612	Click to see CCON1CC2CC(C1)C3=CC=CC(=O)N3C2	234.29	unknown	https://doi.org/10.1007/BF00580891
11-Ethoxy-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one	162911611	Click to see CCON1CC2CC(C1)C3=CC=CC(=O)N3C2	234.29	unknown	https://doi.org/10.1007/BF00580891
Cytisinicline	10235	Click to see C1C2CNCC1C3=CC=CC(=O)N3C2	190.24	unknown	https://doi.org/10.1007/BF00580891 https://doi.org/10.1007/S10600-009-9360-8 https://doi.org/10.1007/BF00565158
Pharmakon1600-01504027	6708720	Click to see C1C2CNCC1C3=CC=CC(=O)N3C2	190.24	unknown	https://doi.org/10.1007/BF00565835 https://doi.org/10.1007/BF00566104
> Alkaloids and derivatives / Lupin alkaloids / Matrine alkaloids
(+)-Matrine	285698	Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1	248.36	unknown	https://doi.org/10.1007/S10600-009-9360-8 https://doi.org/10.1007/BF00580891 https://doi.org/10.1002/CBER.19330660707 https://doi.org/10.1007/BF01134626
(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	https://doi.org/10.1021/NP990351V
(1S,2R,9R,11S,17S)-11-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one	163010491	Click to see C1CC2C3CCCN4C3C(CC(C4)O)CN2C(=O)C1	264.36	unknown	https://doi.org/10.1007/BF00580891
(1S,2R,9R,17R)-13-oxido-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one	11874615	Click to see C1CC2C3CCC[N+]4(C3C(CCC4)CN2C(=O)C1)[O-]	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,9R,17S)-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one	7075140	Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1	248.36	unknown	https://doi.org/10.1007/BF01134626 https://doi.org/10.1007/BF00580891
(1S,2R,9S,17R)-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one	11881817	Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1	248.36	unknown	via CMAUP database
11-Hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one	163010490	Click to see C1CC2C3CCCN4C3C(CC(C4)O)CN2C(=O)C1	264.36	unknown	https://doi.org/10.1007/BF00580891
12beta-Hydroxysophoramine	12133309	Click to see C1CC2CN3C(C4C2N(C1)CCC4)C(C=CC3=O)O	262.35	unknown	https://doi.org/10.1021/NP990351V
13,14-Didehydrosophoridine	7605281	Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CCC4	246.35	unknown	https://doi.org/10.1007/BF01134626
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/10.1021/NP990351V
5-Hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one	78385079	Click to see C1CC2CN3C(CCC(C3=O)O)C4C2N(C1)CCC4	264.36	unknown	https://doi.org/10.1021/NP990351V
7,13-Diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one	618867	Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CCC4	246.35	unknown	https://doi.org/10.1007/BF01134626 https://doi.org/10.1007/S10600-009-9360-8 https://doi.org/10.1007/S10600-006-0054-1
Matridin-15-one, 12,13-didehydro-	3041752	Click to see C1CC2CN3C(C=CCC3=O)C4C2N(C1)CCC4	246.35	unknown	via CMAUP database
Matrine	91466	Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1	248.36	unknown	https://doi.org/10.1007/BF00563949 https://doi.org/10.1007/S10600-009-9360-8 https://doi.org/10.1007/BF00563650 https://doi.org/10.1016/0031-9422(91)80112-E https://doi.org/10.1007/BF01134626 https://doi.org/10.1007/BF00566104 https://doi.org/10.1016/S0021-9673(99)00758-X
N-Oxysophocarpine	618688	Click to see C1CC2CN3C(CC=CC3=O)C4C2[N+](C1)(CCC4)[O-]	262.35	unknown	via CMAUP database
Oxymatrine	114850	Click to see C1CC2C3CCC[N+]4(C3C(CCC4)CN2C(=O)C1)[O-]	264.36	unknown	https://doi.org/10.1007/BF00565835 https://doi.org/10.1007/BF00566104
Oxysophocarpine	161544	Click to see C1CC2CN3C(CC=CC3=O)C4C2[N+](C1)(CCC4)[O-]	262.35	unknown	https://doi.org/10.1007/BF00563949
Sophocarpidine	24721085	Click to see C1CC2CN3C(CC=CC3=O)C4C2[N+](C1)(CCC4)[O-]	262.35	unknown	https://doi.org/10.1007/BF00563949
Sophocarpine	115269	Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CCC4	246.35	unknown	https://doi.org/10.1007/BF00566104 https://doi.org/10.1007/BF00563650 https://doi.org/10.1007/S10600-009-9360-8 https://doi.org/10.1007/BF00563949 https://doi.org/10.1007/BF01134626 https://doi.org/10.1007/BF00563812 https://doi.org/10.1007/S10600-006-0054-1
Sophoridine	165549	Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1	248.36	unknown	https://doi.org/10.1007/BF00566104 https://doi.org/10.1007/S10600-009-9360-8 https://doi.org/10.1007/BF00563949 https://doi.org/10.1002/CBER.19330660707 https://doi.org/10.1007/BF01134626 https://doi.org/10.1007/BF00563812 https://doi.org/10.1016/S0021-9673(99)00758-X
> Benzenoids / Indanes
Pallidol	484757	Click to see C1=CC(=CC=C1C2C3C(C(C4=C3C=C(C=C4O)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)O	454.50	unknown	https://doi.org/10.1016/J.BMCL.2015.05.062
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
5-(3,8-Dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl)-3-methylpenta-2,4-dienoic acid	72833730	Click to see CC(=CC(=O)O)C=CC1(C2(CC(CC1(OC2)C)O)C)O	282.33	unknown	https://doi.org/10.1007/S10600-009-9360-8
Dihydrophaseic acid	11988272	Click to see CC(=CC(=O)O)C=CC1(C2(CC(CC1(OC2)C)O)C)O	282.33	unknown	https://doi.org/10.1007/S10600-009-9360-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1007/BF02249700
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1007/BF02249700
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Oxytocin injection	53477758	Click to see CCC(C)C1C(=O)NC(C(=O)NC(C(=O)NC(CSSCC(C(=O)NC(C(=O)N1)CC2=CC=C(C=C2)O)N)C(=O)N3CCCC3C(=O)NC(CC(C)C)C(=O)NCC(=O)N)CC(=O)N)CCC(=O)N	1007.20	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 C1CC(=O)C2=C1COCN2	139.15	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(E)-3-(2,2-dimethyl-4-oxo-3H-chromen-6-yl)prop-2-enoic acid	100951835	Click to see CC1(CC(=O)C2=C(O1)C=CC(=C2)C=CC(=O)O)C	246.26	unknown	https://doi.org/10.1016/J.BMCL.2015.05.062
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
cudraxanthone D	11611248	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C(=C(C=C3O)OC)C(C)(C)C=C)O)O)C	410.50	unknown	https://doi.org/10.1016/J.BMCL.2015.05.062
> Organoheterocyclic compounds / Diazanaphthalenes / Naphthyridines
1-Hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadeca-2,4-dien-6-one	85264774	Click to see C1CC2CN3C(=O)C=CC=C3C4(C2N(C1)CCC4)O	260.33	unknown	https://doi.org/10.1021/NP990351V
7alpha-Hydroxysophoramine	10777749	Click to see C1CC2CN3C(=O)C=CC=C3C4(C2N(C1)CCC4)O	260.33	unknown	https://doi.org/10.1021/NP990351V
CID 21769980	21769980	Click to see C1CC2CN3C(=O)C=CC=C3C4C2N(C1)CCC4	244.33	unknown	https://doi.org/10.1007/BF00566104 https://doi.org/10.1007/BF00565835 https://doi.org/10.1007/BF00563650 https://doi.org/10.1007/BF00563812
Neosophoramine	618327	Click to see C1CC2CN3C(=O)C=CC=C3C4C2N(C1)CCC4	244.33	unknown	https://doi.org/10.1002/CBER.19340670119 https://doi.org/10.1002/CBER.19330660707 https://doi.org/10.1007/S10600-009-9360-8
Sophoramine	169014	Click to see C1CC2CN3C(=O)C=CC=C3C4C2N(C1)CCC4	244.33	unknown	https://doi.org/10.1007/BF00563650 https://doi.org/10.1007/S10600-009-9360-8 https://doi.org/10.1007/BF00566104 https://doi.org/10.1007/BF00563812 https://doi.org/10.1021/NP990351V https://doi.org/10.1002/CBER.19330660707 https://doi.org/10.1002/CBER.19340670119
> Organoheterocyclic compounds / Diazinanes
(1S,3S,5S,7S,9S,11S)-3,7,11-trimethyl-2,6,10,13-tetrazatricyclo[7.3.1.05,13]tridecane	162901679	Click to see CC1CC2NC(CC3N2C(N1)CC(N3)C)C	224.35	unknown	https://doi.org/10.1007/BF00563994
1,4,7,9b-Tetraazaphenalene, dodecahydro-2,5,8-trimethyl-	72582	Click to see CC1CC2NC(CC3N2C(N1)CC(N3)C)C	224.35	unknown	https://doi.org/10.1007/BF00563994
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Nicotinic acid,[carboxyl-14C]	644263	Click to see C1=CC(=CN=C1)C(=O)O	125.10	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyrrolidinylpyridines
3-(1-Methylpyrrolidin-2-yl)pyridine	942	Click to see CN1CCCC1C2=CN=CC=C2	162.23	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolizines
6-(2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-ylmethylamino)-6-oxohexanoic acid	162979703	Click to see C1CCN2CCCC(C2C1)CNC(=O)CCCCC(=O)O	296.40	unknown	https://doi.org/10.1007/BF00566104
6-[[(1S,9aS)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-yl]methylamino]-6-oxohexanoic acid	162979704	Click to see C1CCN2CCCC(C2C1)CNC(=O)CCCCC(=O)O	296.40	unknown	https://doi.org/10.1007/BF00566104
9-(2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-ylmethylamino)-9-oxononanoic acid	162909508	Click to see C1CCN2CCCC(C2C1)CNC(=O)CCCCCCCC(=O)O	338.50	unknown	https://doi.org/10.1007/BF00566104
9-[[(1S,9aS)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-yl]methylamino]-9-oxononanoic acid	162909509	Click to see C1CCN2CCCC(C2C1)CNC(=O)CCCCCCCC(=O)O	338.50	unknown	https://doi.org/10.1007/BF00566104
butyl 5-(2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-ylmethylamino)-5-oxopentanoate	12125578	Click to see CCCCOC(=O)CCCC(=O)NCC1CCCN2C1CCCC2	338.50	unknown	https://doi.org/10.1007/BF00565158
butyl 5-[[(1R,9aR)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-yl]methylamino]-5-oxopentanoate	163049142	Click to see CCCCOC(=O)CCCC(=O)NCC1CCCN2C1CCCC2	338.50	unknown	https://doi.org/10.1007/BF00565158
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(1R,6S,7S,11R,12R,19R)-7-(3,5-dihydroxyphenyl)-6,11,19-tris(4-hydroxyphenyl)-5-oxapentacyclo[10.7.0.02,10.04,8.013,18]nonadeca-2,4(8),9,13(18),14,16-hexaene-9,15,17-triol	122184222	Click to see C1=CC(=CC=C1C2C3C(C(C4=C(C5=C(C=C34)OC(C5C6=CC(=CC(=C6)O)O)C7=CC=C(C=C7)O)O)C8=CC=C(C=C8)O)C9=C2C(=CC(=C9)O)O)O	680.70	unknown	https://doi.org/10.1016/J.BMCL.2015.05.062
(2R,3R,10R,11R)-16-(3,5-dihydroxyphenyl)-3,11,15-tris(4-hydroxyphenyl)-14-oxapentacyclo[10.7.0.02,10.04,9.013,17]nonadeca-1(19),4(9),5,7,12,17-hexaene-5,7,18-triol	122184223	Click to see C1=CC(=CC=C1C2C3C(C(C4=C5C(=C(C=C34)O)C(C(O5)C6=CC=C(C=C6)O)C7=CC(=CC(=C7)O)O)C8=CC=C(C=C8)O)C9=C2C(=CC(=C9)O)O)O	680.70	unknown	https://doi.org/10.1016/J.BMCL.2015.05.062
(2R,3R,7R)-7-(2,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-9-fluoro-4-hydroxy-2-(4-hydroxyphenyl)-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	122184220	Click to see C1C(OC2=C(C1=O)C(=C3C(C(OC3=C2F)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O)C6=C(C=C(C=C6)O)O	532.50	unknown	https://doi.org/10.1016/J.BMCL.2015.05.062
(2R,3R,7S)-3-(3,5-dihydroxyphenyl)-4-hydroxy-7-(4-hydroxy-2-methoxyphenyl)-2-(4-hydroxyphenyl)-9-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	162964577	Click to see CC(=CCC(CC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4)O)OC)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C(=C)C)C	664.70	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
(2R,3S,7S)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2,7-bis(4-hydroxyphenyl)-9-(3-methylbut-2-enyl)-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	162973297	Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=C(C=C4)O)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C	566.60	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
(2R,3S,7S)-3-(3,5-dihydroxyphenyl)-4-hydroxy-7-(4-hydroxy-2-methoxyphenyl)-2-(4-hydroxyphenyl)-9-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	101915837	Click to see CC(=CCC(CC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4)O)OC)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C(=C)C)C	664.70	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
(2R,3S,7S)-3-(3,5-dihydroxyphenyl)-4-hydroxy-7-(4-hydroxy-2-methoxyphenyl)-2-(4-hydroxyphenyl)-9-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	162964578	Click to see CC(=CCC(CC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4)O)OC)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C(=C)C)C	664.70	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
(2R,3S,7S)-7-(2,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(4-hydroxyphenyl)-9-(3-methylbut-2-enyl)-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	163093944	Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4)O)O)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C	582.60	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
(2R,3S,7S)-7-(2,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(4-hydroxyphenyl)-9-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	162987842	Click to see CC(=CCC(CC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4)O)O)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C(=C)C)C	650.70	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
(2R,3S,7S)-7-(2,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(4-hydroxyphenyl)-9-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	162987841	Click to see CC(=CCC(CC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4)O)O)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C(=C)C)C	650.70	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
(2S,3S,7S)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2,7-bis(4-hydroxyphenyl)-9-(3-methylbut-2-enyl)-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	101915835	Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=C(C=C4)O)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C	566.60	unknown	https://doi.org/10.1016/J.BMCL.2015.05.062 https://doi.org/10.1016/0031-9422(94)00720-E
(2S,3S,7S)-3-(3,5-dihydroxyphenyl)-4-hydroxy-7-(4-hydroxy-2-methoxyphenyl)-2-(4-hydroxyphenyl)-9-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	101915836	Click to see CC(=CCC(CC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4)O)OC)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C(=C)C)C	664.70	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
(2S,3S,7S)-3-(3,5-dihydroxyphenyl)-4-hydroxy-7-(4-hydroxy-2-methoxyphenyl)-2-(4-hydroxyphenyl)-9-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	162964579	Click to see CC(=CCC(CC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4)O)OC)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C(=C)C)C	664.70	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
(2S,3S,7S)-7-(2,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(4-hydroxyphenyl)-9-(3-methylbut-2-enyl)-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	101915838	Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4)O)O)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C	582.60	unknown	https://doi.org/10.1016/J.BMCL.2015.05.062 https://doi.org/10.1016/0031-9422(94)00720-E
(2S,3S,7S)-7-(2,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(4-hydroxyphenyl)-9-[(2,2,6,6-tetramethyloxan-3-yl)methyl]-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	122184219	Click to see CC1(CCC(C(O1)(C)C)CC2=C3C(=C(C4=C2OC(CC4=O)C5=C(C=C(C=C5)O)O)O)C(C(O3)C6=CC=C(C=C6)O)C7=CC(=CC(=C7)O)O)C	668.70	unknown	https://doi.org/10.1016/J.BMCL.2015.05.062
(2S,3S,7S)-7-(2,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(4-hydroxyphenyl)-9-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	162987839	Click to see CC(=CCC(CC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4)O)O)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C(=C)C)C	650.70	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
(2S,3S,7S)-7-(2,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(4-hydroxyphenyl)-9-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	162987840	Click to see CC(=CCC(CC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4)O)O)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C(=C)C)C	650.70	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
(2S,3S,7S)-7-(2,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-4-hydroxy-9-(5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl)-2-(4-hydroxyphenyl)-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	122184218	Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4)O)O)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O	668.70	unknown	https://doi.org/10.1016/J.BMCL.2015.05.062
3-(3,5-Dihydroxyphenyl)-4-hydroxy-2,7-bis(4-hydroxyphenyl)-9-(3-methylbut-2-enyl)-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	162973296	Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=C(C=C4)O)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C	566.60	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
3-(3,5-Dihydroxyphenyl)-4-hydroxy-7-(4-hydroxy-2-methoxyphenyl)-2-(4-hydroxyphenyl)-9-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	162964575	Click to see CC(=CCC(CC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4)O)OC)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C(=C)C)C	664.70	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
7-(2,4-Dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(4-hydroxyphenyl)-9-(3-methylbut-2-enyl)-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	163093943	Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4)O)O)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C	582.60	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
7-(2,4-Dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-4-hydroxy-2-(4-hydroxyphenyl)-9-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	9961130	Click to see CC(=CCC(CC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4)O)O)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C(=C)C)C	650.70	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
Alopecurone A	10032196	Click to see CC(=CCC(CC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4)O)O)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C(=C)C)C	650.70	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
Alopecurone B	10394489	Click to see CC(=CCC(CC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4)O)O)O)C(C(O2)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C(=C)C)C	650.70	unknown	https://doi.org/10.1016/J.BMCL.2015.05.062 https://doi.org/10.1016/0031-9422(94)00720-E
Epsilon-viniferin	5281728	Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O	454.50	unknown	https://doi.org/10.1016/0031-9422(94)00720-E https://doi.org/10.1016/0305-1978(95)00056-9
> Phenylpropanoids and polyketides / Aurone flavonoids
6,3',4'-Trihydroxyaurone	67111	Click to see C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C=C(C=C3)O)O)O	270.24	unknown	https://doi.org/10.1007/S10600-009-9360-8
Sulfuretin	5281295	Click to see C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C=C(C=C3)O)O)O	270.24	unknown	https://doi.org/10.1007/S10600-009-9360-8
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
(E)-3-phenyl-1-[5-[(2R)-piperidin-2-yl]-3,4-dihydro-2H-pyridin-1-yl]prop-2-en-1-one	101821131	Click to see C1CCNC(C1)C2=CN(CCC2)C(=O)C=CC3=CC=CC=C3	296.40	unknown	https://doi.org/10.1021/NP990351V
3-phenyl-1-(5-piperidin-2-yl-3,4-dihydro-2H-pyridin-1-yl)prop-2-en-1-one	583130	Click to see C1CCNC(C1)C2=CN(CCC2)C(=O)C=CC3=CC=CC=C3	296.40	unknown	https://doi.org/10.1021/NP990351V
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid	709	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1007/S10600-009-9360-8
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1007/S10600-009-9360-8
> Phenylpropanoids and polyketides / Coumarins and derivatives
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
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1S,3R,4R,11R,12R,15S,16S,17S)-17-(3,5-dihydroxyphenyl)-6,8-dihydroxy-4,12,16-tris(4-hydroxyphenyl)pentacyclo[13.2.1.02,13.03,11.05,10]octadeca-2(13),5(10),6,8-tetraene-14,18-dione	10055344	Click to see C1=CC(=CC=C1C2C(C3C4=C(C(C5C4C(C6=C5C=C(C=C6O)O)C7=CC=C(C=C7)O)C8=CC=C(C=C8)O)C(=O)C2C3=O)C9=CC(=CC(=C9)O)O)O	680.70	unknown	https://doi.org/10.1016/0031-9422(94)00720-E https://doi.org/10.1016/0305-1978(95)00056-9
> 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 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/10.1007/BF00574244
2-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-6-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one	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/10.1007/BF00574244
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-7-hydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	129360227	Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C(=C(C=C3)O)CC=C(C)C)O)C	392.50	unknown	https://doi.org/10.1007/BF00579498
(2S)-2-(2,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-9-(3-methylbut-2-enyl)-2,3,9,10-tetrahydropyrano[2,3-h]chromen-4-one	122184221	Click to see CC(=CCC1CC2=C(C=C(C3=C2OC(CC3=O)C4=C(C=C(C=C4)O)O)O)OC1(C)C)C	424.50	unknown	https://doi.org/10.1016/J.BMCL.2015.05.062
(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/10.1016/0031-9422(94)00720-E
(2S)-2-(2,4-dihydroxyphenyl)-7-hydroxy-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one	13831864	Click to see CC(=CCC(CC1=C(C=CC2=C1OC(CC2=O)C3=C(C=C(C=C3)O)O)O)C(=C)C)C	408.50	unknown	https://doi.org/10.1016/J.BMCL.2015.05.062
(2S)-7-hydroxy-2-(2-hydroxy-4-methoxyphenyl)-5-methoxy-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one	68103253	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)OC)O)C(=C)C)C	452.50	unknown	https://doi.org/10.1016/J.BMCL.2015.05.062
(2S)-7-hydroxy-2-(4-hydroxy-2-methoxyphenyl)-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one	101915839	Click to see CC(=CCC(CC1=C(C=CC2=C1OC(CC2=O)C3=C(C=C(C=C3)O)OC)O)C(=C)C)C	422.50	unknown	https://doi.org/10.1016/J.BMCL.2015.05.062
(S)-4',7-Dihydroxy-3',8-diprenylflavanone	480768	Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C(=C(C=C3)O)CC=C(C)C)O)C	392.50	unknown	https://doi.org/10.1007/BF00574244 https://doi.org/10.1007/BF00579498 https://doi.org/10.1016/0031-9422(94)00720-E
(S)-5,7-dihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)chroman-4-one	45272659	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)OC)C	354.40	unknown	https://doi.org/10.1016/J.BMCL.2015.05.062
2-(2,4-Dihydroxyphenyl)-7-hydroxy-5-methoxy-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one	5318882	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/10.1016/J.BMCL.2015.05.062
7-Hydroxy-2-(4-hydroxy-2-methoxyphenyl)-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one	74819345	Click to see CC(=CCC(CC1=C(C=CC2=C1OC(CC2=O)C3=C(C=C(C=C3)O)OC)O)C(=C)C)C	422.50	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
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/10.1007/BF00579498 https://doi.org/10.1007/BF02249700
Alopecurone G	42607826	Click to see CC(=CCC(CC1=C(C=CC2=C1OC(CC2=O)C3=C(C=C(C=C3)O)OC)O)C(=C)C)C	422.50	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
Glabrol	11596309	Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C(=C(C=C3)O)CC=C(C)C)O)C	392.50	unknown	https://doi.org/10.1007/BF00574244 https://doi.org/10.1007/BF00579498 https://doi.org/10.1016/0031-9422(94)00720-E
Isobavachin	193679	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/10.1007/BF00574244 https://doi.org/10.1016/J.BMCL.2015.05.062 https://doi.org/10.1007/BF00579498 https://doi.org/10.1007/BF02249700
Isokurarinone	5318581	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C	438.50	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
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/10.1016/J.BMCL.2015.05.062
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	https://doi.org/10.1016/J.BMCL.2015.05.062
leachianone A	44593449	Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C	438.50	unknown	https://doi.org/10.1007/BF00574244 https://doi.org/10.1016/J.BMCL.2015.05.062 https://doi.org/10.1016/0031-9422(94)00720-E
Marini	73198	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/10.1021/NP990567X https://doi.org/10.1016/0031-9422(94)00720-E
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/J.BMCL.2015.05.062
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/10.1007/BF00574244 https://doi.org/10.1016/0031-9422(94)00720-E https://doi.org/10.1016/J.BMCL.2015.05.062 https://doi.org/10.1016/S0944-7113(00)80089-6
Sophoranochromene	42607818	Click to see CC(=CCC1=CC(=CC2=C1OC(C=C2)(C)C)C3CC(=O)C4=C(O3)C(=C(C=C4)O)CC=C(C)C)C	458.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-2-(2,4-dihydroxyphenyl)-8-(2,7-dimethylocta-2,6-dien-3-yl)-5,7-dihydroxy-2,3-dihydrochromen-4-one	162998355	Click to see CC(=CCCC(=C(C)C)C1=C(C=C(C2=C1OC(CC2=O)C3=C(C=C(C=C3)O)O)O)O)C	424.50	unknown	https://doi.org/10.1007/BF02249700
2-(2,4-Dihydroxyphenyl)-8-(2,7-dimethylocta-2,6-dien-3-yl)-5,7-dihydroxy-2,3-dihydrochromen-4-one	162998354	Click to see CC(=CCCC(=C(C)C)C1=C(C=C(C2=C1OC(CC2=O)C3=C(C=C(C=C3)O)O)O)O)C	424.50	unknown	https://doi.org/10.1007/BF02249700
> Phenylpropanoids and polyketides / Flavonoids / Flavones
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	https://doi.org/10.1007/S10600-009-9360-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
CID 12309899	12309899	Click to see C1C(OC2=C(C1=O)C=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O	434.40	unknown	https://doi.org/10.1007/S10600-009-9360-8
Isocoreopsin	193124	Click to see C1C(OC2=C(C1=O)C=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O	434.40	unknown	https://doi.org/10.1007/S10600-009-9360-8
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
3-Hydroxy-8,9-methylenedioxypterocarpane	363863	Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5	284.26	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
Sophojaponicin	44257440	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	via CMAUP database
Sophoracarpan B	14704594	Click to see COC1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5	314.29	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
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/10.1007/BF00574244 https://doi.org/10.1007/BF00579498 https://doi.org/10.1016/J.BMCL.2015.05.062
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
2'-Hydroxygenistein	5282074	Click to see C1=CC(=C(C=C1O)O)C2=COC3=CC(=CC(=C3C2=O)O)O	286.24	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
Genistein	5280961	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O	270.24	unknown	https://doi.org/10.1007/BF02249700
Pseudobaptigenin	5281805	Click to see C1OC2=C(O1)C=C(C=C2)C3=COC4=C(C3=O)C=CC(=C4)O	282.25	unknown	https://doi.org/10.1007/S10600-009-9360-8
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(Z)-1-(2,4-dihydroxyphenyl)-3-(3,4-dihydroxyphenyl)prop-2-en-1-one	5315562	Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O)O	272.25	unknown	via CMAUP database
2',3,4,4'-tetrahydroxy Chalcone	2483	Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O)O	272.25	unknown	https://doi.org/10.1007/S10600-009-9360-8
Butein	5281222	Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O)O	272.25	unknown	https://doi.org/10.1007/S10600-009-9360-8
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
(E)-1-[2,4-dihydroxy-3-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]phenyl]-3-(2-hydroxyphenyl)prop-2-en-1-one	163185433	Click to see CC(=CCC(CC1=C(C=CC(=C1O)C(=O)C=CC2=CC=CC=C2O)O)C(=C)C)C	392.50	unknown	https://doi.org/10.1007/BF00579498
1-[2,4-Dihydroxy-3-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)phenyl]-3-(2-hydroxyphenyl)prop-2-en-1-one	73814661	Click to see CC(=CCC(CC1=C(C=CC(=C1O)C(=O)C=CC2=CC=CC=C2O)O)C(=C)C)C	392.50	unknown	https://doi.org/10.1007/BF00579498
Ammothamnidin	6247097	Click to see CC(=CCC(CC1=C(C=CC(=C1O)C(=O)C=CC2=C(C=C(C=C2)O)O)O)C(=C)C)C	408.50	unknown	https://doi.org/10.1007/BF00579498 https://doi.org/10.1016/J.BMCL.2015.05.062 https://doi.org/10.1007/BF00574244
> Phenylpropanoids and polyketides / Phenylpropanoic acids
Butanedioic acid, 2,3-dihydroxy-2-((4-hydroxyphenyl)methyl)-, (2R,3S)-	10038020	Click to see C1=CC(=CC=C1CC(C(C(=O)O)O)(C(=O)O)O)O	256.21	unknown	https://doi.org/10.1007/S10600-009-9360-8
Piscidic acid	120693	Click to see C1=CC(=CC=C1CC(C(C(=O)O)O)(C(=O)O)O)O	256.21	unknown	https://doi.org/10.1007/S10600-009-9360-8
> Phenylpropanoids and polyketides / Stilbenes
(1R,2S,3R)-2-(3,5-dihydroxyphenyl)-1-[(R)-hydroxy-(4-hydroxyphenyl)methyl]-3-(4-hydroxyphenyl)-2,3-dihydro-1H-indene-4,6-diol	60151313	Click to see C1=CC(=CC=C1C2C(C(C3=C2C(=CC(=C3)O)O)C(C4=CC=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O	472.50	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
(1R,2S,3R)-2-(3,5-dihydroxyphenyl)-1-[(S)-hydroxy-(4-hydroxyphenyl)methyl]-3-(4-hydroxyphenyl)-2,3-dihydro-1H-indene-4,6-diol	60151314	Click to see C1=CC(=CC=C1C2C(C(C3=C2C(=CC(=C3)O)O)C(C4=CC=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O	472.50	unknown	https://doi.org/10.1016/0031-9422(94)00720-E
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

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Sophora alopecuroides

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