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Euchresta japonica

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fdacae70bc304841321
Scientific name Euchresta japonica
Authority Hook.f. ex Regel
First published in Gartenflora40: 321 (1865)

Description Top

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Synonyms Top

Scientific name Authority First published in
Euchresta japonica Benth. ex Oliv. J. Linn. Soc., Bot. 9: 164. 1865 [1867 publ. 1865]
Euchresta japonica Oliv.
Euchresta trifoliolata Merr. Philipp. J. Sci.21: 496 (1922)

Common names Top

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Language Common/alternative name
Japanese サンズコン
lzh 山豆根
Chinese 山豆根
Chinese 三小叶山豆根
Chinese 三叶山豆根
Chinese 一种维管植物

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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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
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000192259
Tropicos 13067023
KEW urn:lsid:ipni.org:names:328804-2
The Plant List ild-38820
Open Tree Of Life 280934
NCBI Taxonomy 256639
IPNI 328804-2
iNaturalist 635725
GBIF 2951881
EOL 643246
USDA GRIN 16118
Wikipedia Euchresta_japonica

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
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
Research progress of sophoridine’s pharmacological activities and its molecular mechanism: an updated review Chen Y, Wang X, Ye D, Yang Z, Shen Q, Liu X, Chen C, Chen X Front Pharmacol 16-Jun-2023
PMCID:PMC10311568
doi:10.3389/fphar.2023.1126636
PMID:37397472
Sophoridine alleviates hyperalgesia and anxiety-like behavior in an inflammatory pain mouse model induced by complete freund’s adjuvant Rong Z, Yang L, Chen Y, Qin Y, Cheng CY, Zhao J, Li LF, Ma X, Wu YM, Liu SB, Liang YN, Zhao MG Mol Pain 19-May-2023
PMCID:PMC10201643
doi:10.1177/17448069231177634
PMID:37207346
Research Progress on Autophagy Regulation by Active Ingredients of Traditional Chinese Medicine in the Treatment of Acute Lung Injury Dong JY, Yin HL, Hao H, Liu Y J Inflamm Res 17-Apr-2023
PMCID:PMC10120836
doi:10.2147/JIR.S398203
PMID:37092134
Natural flavonoids derived from herbal medicines are potential anti-atherogenic agents by inhibiting oxidative stress in endothelial cells Li RL, Wang LY, Duan HX, Qian D, Zhang Q, He LS, Li XP Front Pharmacol 24-Feb-2023
PMCID:PMC10001913
doi:10.3389/fphar.2023.1141180
PMID:36909175
The application of gargle containing honeysuckle and semen oroxyli to reduce the pain and complications after uvulopalatopharyngoplasty Ren L, Li J, Miao Z, Yan R, Li Q, Zhang R, Rong T, Dong X Front Pharmacol 17-Oct-2022
PMCID:PMC9619035
doi:10.3389/fphar.2022.974233
PMID:36324688
Progress in ICP-MS Analysis of Minerals and Heavy Metals in Traditional Medicine Chen W, Yang Y, Fu K, Zhang D, Wang Z Front Pharmacol 28-Jun-2022
PMCID:PMC9274010
doi:10.3389/fphar.2022.891273
PMID:35837276
Anti-tumor pharmacology of natural products targeting mitosis Huang M, Liu C, Shao Y, Zhou S, Hu G, Yin S, Pu W, Yu H Cancer Biol Med 15-Jun-2022
PMCID:PMC9257311
doi:10.20892/j.issn.2095-3941.2022.0006
PMID:35699421
Research Progress on Natural Products' Therapeutic Effects on Atrial Fibrillation by Regulating Ion Channels He J, Li S, Ding Y, Tong Y, Li X Cardiovasc Ther 22-Mar-2022
PMCID:PMC8964196
doi:10.1155/2022/4559809
PMID:35387267
Update and New Insights on Future Cancer Drug Candidates From Plant-Based Alkaloids Tilaoui M, Ait Mouse H, Zyad A Front Pharmacol 16-Dec-2021
PMCID:PMC8716855
doi:10.3389/fphar.2021.719694
PMID:34975465
Improving the Physicochemical and Biopharmaceutical Properties of Active Pharmaceutical Ingredients Derived from Traditional Chinese Medicine through Cocrystal Engineering Guan D, Xuan B, Wang C, Long R, Jiang Y, Mao L, Kang J, Wang Z, Chow SF, Zhou Q Pharmaceutics 15-Dec-2021
PMCID:PMC8704577
doi:10.3390/pharmaceutics13122160
PMID:34959440
Neochlorogenic acid: an anti-HIV active compound identified by screening of Cortex Mori [Morus Alba L. (Moraceae)] Li J, Dou L, Chen S, Zhou H, Mou F Pharm Biol 29-Oct-2021
PMCID:PMC8567877
doi:10.1080/13880209.2021.1995005
PMID:34714196
Herbal Medicine, Gut Microbiota, and COVID-19 Chen Z, Lv Y, Xu H, Deng L Front Pharmacol 07-Jul-2021
PMCID:PMC8293616
doi:10.3389/fphar.2021.646560
PMID:34305582
Quantitative and Molecular Similarity Analyses of the Metabolites of Cold- and Hot-Natured Chinese Herbs Guo J, Wang J, Iino K, Tomita M, Soga T Evid Based Complement Alternat Med 05-Mar-2021
PMCID:PMC7954617
doi:10.1155/2021/6646507
PMID:33747108
The complete chloroplast genome of a Korean endemic species Sophora koreensis, Nakai Ramekar RV, Cheong EJ, Lee H, Park KC, Kwak M, Choi IY Mitochondrial DNA B Resour 29-Jul-2020
PMCID:PMC7782127
doi:10.1080/23802359.2020.1797579
PMID:33458061

Phytochemical Profile Top

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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 / Anagyrine-type alkaloids
(1R,9R,10R,12R)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 15939858 Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O 260.33 unknown https://doi.org/10.1248/CPB.28.546
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/10.1248/CPB.28.546
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(-)-Cytisine 22407 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1248/CPB.28.546
(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/10.1248/CPB.28.546
(1R)-1,2,3,4,5,6-Hexahydro-1,5-methano-8H-pyrido[1,2-a][1,5]diazocin-8-one 1278189 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1248/CPB.28.546
Cytisine, N-formyl- 589870 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)C=O 218.25 unknown https://doi.org/10.1248/CPB.28.546
Cytisinicline 10235 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1248/CPB.28.546
N-Formylcytisine, (-)- 6604689 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)C=O 218.25 unknown https://doi.org/10.1248/CPB.28.546
N-Methylcytisine 234566 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1248/CPB.28.546
> Alkaloids and derivatives / Lupin alkaloids / Matrine alkaloids
(+)-Matrine 285698 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown https://doi.org/10.1248/CPB.28.546
(5beta,6beta,7beta,11alpha)-Matridin-15-one 638232 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown https://doi.org/10.1248/CPB.28.546
Sophoridine 165549 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown https://doi.org/10.1248/CPB.28.546
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl 14-oxooctadecanoate 13991164 Click to see CCCCC(=O)CCCCCCCCCCCCC(=O)OC 312.50 unknown https://doi.org/10.1016/0031-9422(80)85077-1
> 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/10.1016/0031-9422(80)85077-1
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/10.1016/0031-9422(80)85077-1
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones
(2R)-5-hydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-8,8-dimethyl-2,3-dihydropyrano[2,3-h]chromen-4-one 162949515 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C4=C(C=C3O)OC(C=C4)(C)C)O)C 406.50 unknown https://doi.org/10.1016/0031-9422(88)80454-0
Euchrenone a2 14134103 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C4=C(C=C3O)OC(C=C4)(C)C)O)C 406.50 unknown https://doi.org/10.1016/0031-9422(88)80454-0
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2R)-5-hydroxy-2-(7-hydroxy-2,2-dimethylchromen-6-yl)-8,8-dimethyl-6-(3-methylbut-2-enyl)-2,3-dihydropyrano[2,3-h]chromen-4-one 162848105 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=C(C=C5C(=C4)C=CC(O5)(C)C)O)O)C 488.60 unknown https://doi.org/10.1016/0031-9422(92)90058-X
(S)-2-(2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl)-5,7-dihydroxy-6-(3-methylbut-2-enyl)chroman-4-one 44419446 Click to see CC(=CCC1=CC(=C(C=C1O)O)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)C 424.50 unknown https://doi.org/10.1016/0031-9422(80)85077-1
5,7-Dihydroxy-2-(7-hydroxy-2,2-dimethylchromen-6-yl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 14886039 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C4C(=C3)C=CC(O4)(C)C)O)O)C 422.50 unknown https://doi.org/10.1016/0031-9422(80)85077-1
5,7-Dihydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-6-(3-methylbut-2-enyl)chroman-4-one 480769 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)C 408.50 unknown https://doi.org/10.1016/0031-9422(80)85077-1
cudraflavanone A 21721847 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C4C(=C3)C=CC(O4)(C)C)O)O)C 422.50 unknown https://doi.org/10.1016/0031-9422(80)85077-1
Macarangaflavanone B 14309760 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)C 408.50 unknown https://doi.org/10.1016/0031-9422(80)85077-1
> 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/10.1016/0031-9422(92)90058-X
(2S)-2-(2,2-dimethylchromen-6-yl)-5,7-dihydroxy-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 162919555 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC4=C(C=C3)OC(C=C4)(C)C)CC=C(C)C)O)C 474.60 unknown https://doi.org/10.1248/CPB.37.195
(2S)-5,7-dihydroxy-2-(7-hydroxy-2,2-dimethylchromen-6-yl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 21721849 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C4C(=C3)C=CC(O4)(C)C)O)C 422.50 unknown https://doi.org/10.3987/R-1984-05-0997
(8R)-5-hydroxy-8-(7-hydroxy-2,2-dimethylchromen-6-yl)-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one 163015656 Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C5C(=C4)C=CC(O5)(C)C)O)O)C=CC(O2)(C)C)C 488.60 unknown https://doi.org/10.1016/0031-9422(92)90058-X
(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/10.1016/0031-9422(92)90058-X
https://doi.org/10.1016/0031-9422(92)90052-R
3,5,7-Trihydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 14542251 Click to see CC(=CCC1=C(C=CC(=C1)C2C(C(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)O)C 424.50 unknown https://doi.org/10.1016/0031-9422(92)90052-R
4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-(4-hydroxy-3-(3-methyl-2-butenyl)phenyl)-6,8-bis(3-methyl-2-butenyl)-, (2S)- 158519 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(C(=C(C(=C3O2)CC=C(C)C)O)CC=C(C)C)O)O)C 476.60 unknown https://doi.org/10.1016/0031-9422(88)80454-0
Amorilin 14134104 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(C(=C(C(=C3O2)CC=C(C)C)O)CC=C(C)C)O)O)C 476.60 unknown https://doi.org/10.1016/0031-9422(88)80454-0
Euchrenone a3 45269666 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C4C(=C3)C=CC(O4)(C)C)O)CC=C(C)C)O)C 490.60 unknown https://doi.org/10.1016/0031-9422(92)90058-X
Euchrenone a4 14284690 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC4=C(C=C3)OC(C=C4)(C)C)CC=C(C)C)O)C 474.60 unknown https://doi.org/10.1248/CPB.37.195
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/10.1016/0031-9422(92)90052-R
Lespedezaflavanone C 14542252 Click to see CC(=CCC1=C(C=CC(=C1)C2C(C(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)O)C 424.50 unknown https://doi.org/10.1016/0031-9422(92)90052-R
https://doi.org/10.1016/0031-9422(92)90058-X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1016/0031-9422(80)85077-1
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1016/0031-9422(80)85077-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Rhoifolin 5282150 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/0305-1978(94)90075-2
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(2R)-2-(2,2-dimethylchromen-6-yl)-5-hydroxy-8,8-dimethyl-2,3-dihydropyrano[2,3-h]chromen-4-one 162896041 Click to see CC1(C=CC2=C(O1)C=CC(=C2)C3CC(=O)C4=C(O3)C5=C(C=C4O)OC(C=C5)(C)C)C 404.50 unknown https://doi.org/10.1016/0031-9422(88)80454-0
Euchrenone a1 42607936 Click to see CC1(C=CC2=C(O1)C=CC(=C2)C3CC(=O)C4=C(O3)C5=C(C=C4O)OC(C=C5)(C)C)C 404.50 unknown https://doi.org/10.1016/0031-9422(88)80454-0
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Medicagol 5319322 Click to see C1OC2=C(O1)C=C3C(=C2)C4=C(O3)C5=C(C=C(C=C5)O)OC4=O 296.23 unknown https://doi.org/10.1016/0031-9422(80)85077-1
> 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(80)85077-1
Maackiain 91510 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(80)85077-1
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
5,7,20-Trihydroxy-17,17-dimethyl-8-(3-methylbut-2-enyl)-10,12,18-trioxapentacyclo[11.8.0.02,11.04,9.014,19]henicosa-1(21),2(11),4,6,8,13,15,19-octaen-3-one 15138440 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)OC4=C5C=CC(OC5=C(C=C34)O)(C)C)C 434.40 unknown https://doi.org/10.1016/0031-9422(92)90052-R
https://doi.org/10.1016/0031-9422(92)90058-X
Euchretin B 15138441 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)OC4=C(C(=C(C=C34)O)O)CC=C(C)C)C 436.50 unknown https://doi.org/10.1016/0031-9422(92)90058-X
https://doi.org/10.1016/0031-9422(92)90052-R
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(2R)-4-hydroxy-6-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-g]chromen-5-one 132988923 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)CC(O2)C(C)(C)O)C 422.50 unknown https://doi.org/10.1016/0031-9422(92)90058-X
1,3,8,9-Tetrahydroxy-2,4-bis(3-methylbut-2-enyl)-[1]benzofuro[2,3-b]chromen-11-one 15138438 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)OC4=CC(=C(C=C43)O)O)CC=C(C)C)O)C 436.50 unknown https://doi.org/10.1016/0031-9422(92)90052-R
https://doi.org/10.1016/0031-9422(92)90058-X
3-[2,4-Dihydroxy-3-(3-methylbut-2-enyl)phenyl]-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one 101620891 Click to see CC(=CCC1=C(C=CC(=C1O)C2=COC3=C4C=CC(OC4=C(C(=C3C2=O)O)CC=C(C)C)(C)C)O)C 488.60 unknown https://doi.org/10.1016/0031-9422(92)90058-X
5-Hydroxy-3-(8-hydroxy-5-methoxy-2,2-dimethylchromen-6-yl)-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one 101621397 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=CC(=C5C(=C4OC)C=CC(O5)(C)C)O)C=CC(O2)(C)C)C 516.60 unknown https://doi.org/10.1016/0031-9422(92)90058-X
5-Hydroxy-3-[4-hydroxy-2-methoxy-3-(3-methylbut-2-enyl)phenyl]-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one 101620888 Click to see CC(=CCC1=C(C=CC(=C1OC)C2=COC3=C4C=CC(OC4=C(C(=C3C2=O)O)CC=C(C)C)(C)C)O)C 502.60 unknown https://doi.org/10.1016/0031-9422(92)90058-X
5-Hydroxy-7-[4-hydroxy-2-methoxy-3-(3-methylbut-2-enyl)phenyl]-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-g]chromen-6-one 101620887 Click to see CC(=CCC1=C(C=CC(=C1OC)C2=COC3=C(C2=O)C(=C4C=CC(OC4=C3CC=C(C)C)(C)C)O)O)C 502.60 unknown https://doi.org/10.1016/0031-9422(92)90058-X
5,7-Dihydroxy-3-(4-hydroxy-2-methoxyphenyl)-6,8-bis(3-methylbut-2-enyl)chromen-4-one 101620890 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=C(C=C(C=C3)O)OC)CC=C(C)C)O)C 436.50 unknown https://doi.org/10.1016/0031-9422(92)90058-X
5,7-Dihydroxy-3-[4-hydroxy-2-methoxy-3-(3-methylbut-2-enyl)phenyl]-6,8-bis(3-methylbut-2-enyl)chromen-4-one 101620889 Click to see CC(=CCC1=C(C=CC(=C1OC)C2=COC3=C(C(=C(C(=C3C2=O)O)CC=C(C)C)O)CC=C(C)C)O)C 504.60 unknown https://doi.org/10.1016/0031-9422(92)90058-X
5,7,2',4'-Tetrahydroxy-6,8,3'-triprenylisoflavone 44257319 Click to see CC(=CCC1=C(C=CC(=C1O)C2=COC3=C(C(=C(C(=C3C2=O)O)CC=C(C)C)O)CC=C(C)C)O)C 490.60 unknown https://doi.org/10.1016/0031-9422(88)80700-3
6,7,21-Trihydroxy-17,17-dimethyl-20-(3-methylbut-2-enyl)-10,12,18-trioxapentacyclo[11.8.0.03,11.04,9.014,19]henicosa-1(21),3(11),4,6,8,13,15,19-octaen-2-one 15138439 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=C(O3)OC5=CC(=C(C=C54)O)O)C=CC(O2)(C)C)C 434.40 unknown https://doi.org/10.1016/0031-9422(92)90058-X
https://doi.org/10.1016/0031-9422(92)90052-R
6,8-Diprenylgenistein 480783 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)CC=C(C)C)O)C 406.50 unknown https://doi.org/10.1016/0031-9422(80)85077-1
Euchrenone b1 25224570 Click to see CC(=CCC1=C(C=CC(=C1)C2=COC3=C(C(=C(C(=C3C2=O)O)CC=C(C)C)O)CC=C(C)C)O)C 474.60 unknown https://doi.org/10.1016/0031-9422(88)80700-3
Euchrenone b3 44257323 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=CC5=C(C=C4OC)OCO5)C=CC(O2)(C)C)C 462.50 unknown https://doi.org/10.1016/0031-9422(88)80700-3
Euchrenone b4 14284691 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC4=C(C=C3OC)OCO4)CC=C(C)C)O)C 464.50 unknown https://doi.org/10.1248/CPB.37.195
Euchrenone b5 14284692 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC4=C(C=C3O)OCO4)CC=C(C)C)O)C 450.50 unknown https://doi.org/10.1248/CPB.37.195
Euchretin A 10368763 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)OC4=C5C=CC(OC5=C(C=C34)O)(C)C)CC=C(C)C)O)C 502.60 unknown https://doi.org/10.1016/0031-9422(92)90058-X
https://doi.org/10.1016/0031-9422(92)90052-R
https://doi.org/10.3987/COM-88-4552
Euchretin C 44260102 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)OC4=C(C(=C(C=C34)O)O)CC=C(C)C)CC=C(C)C)O)C 504.60 unknown https://doi.org/10.1016/0031-9422(92)90058-X
https://doi.org/10.1016/0031-9422(92)90052-R
Osajin 95168 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=CC=C(C=C4)O)C=CC(O2)(C)C)C 404.50 unknown https://doi.org/10.1016/0031-9422(80)85077-1
Warangalone 5379679 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C 404.50 unknown https://doi.org/10.1016/0031-9422(80)85077-1

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