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Euchresta formosana

Euchresta formosana - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fd98ecf84a925118253
Scientific name Euchresta formosana
Authority (Hayata) Ohwi
First published in J. Jap. Bot.12: 659 (1936)

Description Top

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Synonyms Top

Scientific name Authority First published in
Euchresta formosana var. riukiuensis Ohwi J. Jap. Bot.12: 659 (1936)
Euchresta horsfieldii var. formosana Hayata Icon. Pl. Formosan.3: 81 (1913)

Common names Top

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Language Common/alternative name
Chinese 山豆根
Chinese 台湾山豆根
Chinese 臺灣山豆根

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000186114
Tropicos 13058181
KEW urn:lsid:ipni.org:names:494672-1
The Plant List ild-32518
Open Tree Of Life 280933
NCBI Taxonomy 256638
IPNI 494672-1
iNaturalist 736644
GBIF 2951878
EOL 643758

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
Tectorigenin: A Review of Its Sources, Pharmacology, Toxicity, and Pharmacokinetics Rong J, Fu F, Han C, Wu Y, Xia Q, Du D Molecules 05-Aug-2023
PMCID:PMC10421414
doi:10.3390/molecules28155904
PMID:37570873
Structure-Activity-Relationship and Mechanistic Insights for Anti-HIV Natural Products Kaur R, Sharma P, Gupta GK, Ntie-Kang F, Kumar D Molecules 29-Apr-2020
PMCID:PMC7249135
doi:10.3390/molecules25092070
PMID:32365518
New Records of Potent In-Vitro Antidiabetic Properties of Dalbergia tonkinensis Heartwood and the Bioactivity-Guided Isolation of Active Compounds Nguyen VB, Wang SL, Nhan NT, Nguyen TH, Nguyen NP, Nghi DH, Cuong NM Molecules 29-Jun-2018
PMCID:PMC6099635
doi:10.3390/molecules23071589
PMID:29966279
Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J Int J Mol Sci 14-May-2018
PMCID:PMC5983620
doi:10.3390/ijms19051459
PMID:29757986
Evolutionary response to the Qinghai-Tibetan Plateau uplift: phylogeny and biogeography of Ammopiptanthus and tribe Thermopsideae (Fabaceae) Shi W, Liu PL, Duan L, Pan BR, Su ZH PeerJ 31-Jul-2017
PMCID:PMC5541923
doi:10.7717/peerj.3607
PMID:28785518
Novel Approach to Classify Plants Based on Metabolite-Content Similarity Liu K, Abdullah AA, Huang M, Nishioka T, Altaf-Ul-Amin M, Kanaya S Biomed Res Int 09-Jan-2017
PMCID:PMC5253511
doi:10.1155/2017/5296729
PMID:28164123
The Constituents of <i>Euchresta Formosana</i> Wen‐Li Lo, Fang‐Rong Chang, Tian‐Jye Hsieh, Yang‐Chang Wu Wiley 01-May-2015
doi:10.1002/JCCS.200200066
In Vitro Antiproliferative Effect of Arthrocnemum indicum Extracts on Caco-2 Cancer Cells through Cell Cycle Control and Related Phenol LC-TOF-MS Identification Boulaaba M, Mkadmini K, Tsolmon S, Han J, Smaoui A, Kawada K, Ksouri R, Isoda H, Abdelly C Evid Based Complement Alternat Med 30-Sep-2013
PMCID:PMC3856152
doi:10.1155/2013/529375
PMID:24348703
Heartwood constituents ofPinus formosana Kung-Tsung Wang, K. C. Das, Yu-Yin Lin, B. Weinstein Springer Science and Business Media LLC 13-Sep-2005
doi:10.1007/BF02114110
Antiplatelet and anti-HIV constituents from Euchresta formosana. Lo WL, Wu CC, Chang FR, Wang WY, Khalil AT, Lee KH, Wu YC Nat Prod Res 01-Apr-2003
doi:10.1080/1478641031000103669
PMID:12713120
Phylogenetic analysis in genus Euchresta based on secondary metabolites Nobuyasu Matsuura, Munekazu Iinuma, Toshiyuki Tanaka Elsevier BV 10-Feb-2003
doi:10.1016/0305-1978(94)90075-2
Coumaronochromones and flavanones from Euchresta formosana roots. Lo WL, Chang FR, Hsieh TJ, Wu YC Phytochemistry 01-Aug-2002
doi:10.1016/S0031-9422(02)00017-1
PMID:12150810
Four flavonoids in the roots of Euchresta Formosana Mizuo Mizuno, Nobuyasu Matsuura, Toshiyuki Tanaka, Munekazu Iinuma, Feng-chi Ho Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)98260-8
Six flavanones from the roots of Euchresta formosana Mizuo Mizuno, Koh-Ich Tamura, Toshiyuki Tanaka, Munekazu Iinuma Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)98095-6
Coumaronochromones from the stems of Euschresta formosana Mizuo Mizuno, Toshiyuki Tanaka, Koh-Ichi Tamura, Munekazu Iinuma Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)98023-3

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 / Cytisine and derivatives
(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 https://doi.org/10.1055/S-2002-20248
1,2,3,4,5,6-Hexahydro-1,5-methano-pyrido[1,2-a][1,5]diazocin-8-one 683511 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1055/S-2002-20248
Pharmakon1600-01504027 6708720 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1080/1478641031000103669
> Alkaloids and derivatives / Lupin alkaloids / Matrine alkaloids
Matrine 91466 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown https://doi.org/10.1080/1478641031000103669
https://doi.org/10.1055/S-2002-20248
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1007/BF02114110
https://doi.org/10.1002/JCCS.200200066
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1007/BF02114110
https://doi.org/10.1080/1478641031000103669
https://doi.org/10.1002/JCCS.200200066
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol 100067 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1002/JCCS.200200066
Syringaresinol, (+)- 443023 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1007/BF02114110
https://doi.org/10.1002/JCCS.200200066
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Corchoionol C 137705650 Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C 224.30 unknown https://doi.org/10.1080/1478641031000103669
Vomifoliol 5280462 Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C 224.30 unknown https://doi.org/10.1080/1478641031000103669
> 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/BF02114110
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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 https://doi.org/10.1002/JCCS.200200066
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 https://doi.org/10.1002/JCCS.200200066
https://doi.org/10.1007/BF02114110
> Organoheterocyclic compounds / Isobenzofurans
[(1S,5R,6R)-5-[[(1R,3aR,7R,7aS)-7-hydroxy-3a,7-dimethyl-3-oxo-4,5,6,7a-tetrahydro-1H-2-benzofuran-1-yl]methyl]-7-methylidene-4-oxo-6-bicyclo[3.2.1]oct-2-enyl] acetate 162904392 Click to see CC(=O)OC1C(=C)C2CC1(C(=O)C=C2)CC3C4C(CCCC4(C)O)(C(=O)O3)C 388.50 unknown https://doi.org/10.1055/S-2002-20248
> Organoheterocyclic compounds / Tetrapyrroles and derivatives
methyl (3R,21S,22S)-16-ethenyl-11-ethyl-4-hydroxy-12,17,21,26-tetramethyl-22-[3-oxo-3-[(E,7S,11S)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate 136706892 Click to see CCC1=C(C2=NC1=CC3=C(C4=C(C(C(=C5C(C(C(=CC6=NC(=C2)C(=C6C)C=C)N5)C)CCC(=O)OCC=C(C)CCCC(C)CCCC(C)CCCC(C)C)C4=N3)C(=O)OC)O)C)C 871.20 unknown https://doi.org/10.1080/1478641031000103669
> Organoheterocyclic compounds / Tetrapyrroles and derivatives / Chlorins
methyl (3R,21S,22S)-16-ethenyl-11-ethyl-12,17,21,26-tetramethyl-4-oxo-22-[3-oxo-3-[(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaene-3-carboxylate 5459387 Click to see CCC1=C(C2=CC3=C(C(=C(N3)C=C4C(C(C(=N4)C5=C6C(=C(C(=N6)C=C1N2)C)C(=O)C5C(=O)OC)CCC(=O)OCC=C(C)CCCC(C)CCCC(C)CCCC(C)C)C)C)C=C)C 871.20 unknown https://doi.org/10.1080/1478641031000103669
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, octadecyl ester 149044 Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 446.70 unknown https://doi.org/10.1002/JCCS.200200066
Octadecyl ferulate 5320256 Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 446.70 unknown https://doi.org/10.1002/JCCS.200200066
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones
(2S)-5-hydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-8,8-dimethyl-2,3-dihydropyrano[2,3-h]chromen-4-one 162949514 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/10.1002/JCCS.200200066
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/10.1002/JCCS.200200066
> 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/S0031-9422(00)98260-8
(2S)-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 162848106 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/S0031-9422(00)98260-8
Euchrenone a12 42608046 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/S0031-9422(00)98260-8
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S)-2-(2,2-dimethylchromen-6-yl)-7-hydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 73355595 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC4=C(C=C3)OC(C=C4)(C)C)O)C 390.50 unknown https://doi.org/10.1016/S0031-9422(00)98095-6
(2S)-2-[2,2-dimethyl-8-(3-methylbut-2-enyl)chromen-6-yl]-7-hydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 5321396 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 https://doi.org/10.1016/0305-1978(95)00054-X
(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/S0031-9422(00)98260-8
(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/10.1002/JCCS.200200066
2-(2,2-Dimethyl-3,4-dihydrochromen-6-yl)-5,7-dihydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 22297222 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC4=C(C=C3)OC(CC4)(C)C)C 408.50 unknown https://doi.org/10.1016/S0031-9422(02)00017-1
2-(2,2-Dimethyl-3,4-dihydrochromen-6-yl)-7-hydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 74819342 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC4=C(C=C3)OC(CC4)(C)C)O)C 392.50 unknown https://doi.org/10.1002/JCCS.200200066
2-(4-Hydroxyphenyl)-5-hydroxy-2,3-dihydro-10-(3-methyl-2-butenyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:5,4-b']dipyran-4-one 13846826 Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C 406.50 unknown https://doi.org/10.1016/0305-1978(95)00054-X
5,7,4'-Trihydroxy-3',8-diprenylflavanone 10319282 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)98095-6
https://doi.org/10.1016/S0031-9422(02)00017-1
https://doi.org/10.1080/1478641031000103669
CID 14542254 14542254 Click to see CC(=CCC1=CC(=C(C=C1O)O)C2CC(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)C 424.50 unknown https://doi.org/10.1016/S0031-9422(00)98095-6
Euchrenone a11 42608045 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/S0031-9422(00)98260-8
Euchrenone a16 636551 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC4=C(C=C3)OC(CC4)(C)C)C 408.50 unknown https://doi.org/10.1016/S0031-9422(02)00017-1
Euchrenone a17 42607819 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC4=C(C=C3)OC(CC4)(C)C)O)C 392.50 unknown https://doi.org/10.1002/JCCS.200200066
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/S0031-9422(00)98095-6
Euchrenone a5 14769498 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC4=C(C=C3)OC(C=C4)(C)C)O)C 390.50 unknown https://doi.org/10.1016/S0031-9422(00)98095-6
Euchrenone a6 14769499 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/S0031-9422(00)98095-6
Euchrestaflavanone A 484588 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)98095-6
https://doi.org/10.1016/S0031-9422(02)00017-1
https://doi.org/10.1080/1478641031000103669
Euchrestaflavanone C 42608039 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/10.1016/S0031-9422(00)98095-6
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/BF02114110
https://doi.org/10.1002/JCCS.200200066
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 https://doi.org/10.1016/0305-1978(95)00054-X
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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/10.1080/1478641031000103669
https://doi.org/10.1055/S-2002-20248
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Isorhoifolin 9851181 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)O)O)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/0305-1978(94)90075-2
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(2S)-2-(2,2-dimethylchromen-6-yl)-8,8-dimethyl-2,3-dihydropyrano[2,3-f]chromen-4-one 73352581 Click to see CC1(C=CC2=C(O1)C=CC(=C2)C3CC(=O)C4=C(O3)C5=C(C=C4)OC(C=C5)(C)C)C 388.50 unknown https://doi.org/10.1016/S0031-9422(00)98095-6
Xambioona 14769500 Click to see CC1(C=CC2=C(O1)C=CC(=C2)C3CC(=O)C4=C(O3)C5=C(C=C4)OC(C=C5)(C)C)C 388.50 unknown https://doi.org/10.1016/S0031-9422(00)98095-6
> 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/10.1007/BF02114110
https://doi.org/10.1002/JCCS.200200066
> 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/S0031-9422(00)98095-6
https://doi.org/10.1080/1478641031000103669
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/S0031-9422(00)98095-6
Pterocarpin 454895 Click to see COC1=CC2=C(C=C1)C3C(CO2)C4=CC5=C(C=C4O3)OCO5 298.29 unknown https://doi.org/10.1080/1478641031000103669
Pterocarpin 1715306 Click to see COC1=CC2=C(C=C1)C3C(CO2)C4=CC5=C(C=C4O3)OCO5 298.29 unknown https://doi.org/10.1080/1478641031000103669
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/10.1080/1478641031000103669
https://doi.org/10.1055/S-2002-20248
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
11,17-Dihydroxy-7,7,20,20-tetramethyl-2,8,19,25-tetraoxahexacyclo[12.11.0.03,12.04,9.015,24.018,23]pentacosa-1(14),3(12),4(9),10,15,17,21,23-octaen-13-one 5317374 Click to see CC1(CCC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C6C(=C5O4)C=CC(O6)(C)C)O)O)C 434.40 unknown https://doi.org/10.1016/S0031-9422(02)00017-1
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/10.1002/JCCS.200200066
https://doi.org/10.1007/BF02114110
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/10.1080/1478641031000103669
https://doi.org/10.1055/S-2002-20248
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),4,6,8,13,19-heptaen-3-one 162821294 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)OC4=C5CCC(OC5=C(C=C34)O)(C)C)C 436.50 unknown https://doi.org/10.1055/S-2002-20248
Daidzein 5281708 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)O 254.24 unknown https://doi.org/10.1016/S0031-9422(02)00017-1
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/S0031-9422(00)98023-3
https://doi.org/10.1016/S0031-9422(00)98095-6
Flemiphyllin 44257286 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2=COC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C 474.60 unknown https://doi.org/10.1080/1478641031000103669
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown https://doi.org/10.1055/S-2002-20248
https://doi.org/10.1080/1478641031000103669
Tectorigenin 5281811 Click to see COC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1080/1478641031000103669
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(15S,16R)-5,7,15,16,20-pentahydroxy-17,17-dimethyl-6,8-bis(3-methylbut-2-enyl)-10,12,18-trioxapentacyclo[11.8.0.02,11.04,9.014,19]henicosa-1(21),2(11),4,6,8,13,19-heptaen-3-one 5317372 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)OC4=C5C(C(C(OC5=C(C=C34)O)(C)C)O)O)CC=C(C)C)O)C 536.60 unknown https://doi.org/10.1016/S0031-9422(02)00017-1
1,3,8-Trihydroxy-9-methoxy-2,4,7-tris(3-methylbut-2-enyl)-[1]benzofuro[2,3-b]chromen-11-one 163067573 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)OC4=C(C(=C(C=C34)OC)O)CC=C(C)C)CC=C(C)C)O)C 518.60 unknown https://doi.org/10.1080/1478641031000103669
https://doi.org/10.1055/S-2002-20248
1,3,8,9-Tetrahydroxy-2-(3-hydroxy-3-methylbutyl)-4,7-bis(3-methylbut-2-enyl)-[1]benzofuro[2,3-b]chromen-11-one 10346662 Click to see CC(=CCC1=C2C(=CC(=C1O)O)C3=C(O2)OC4=C(C(=C(C(=C4C3=O)O)CCC(C)(C)O)O)CC=C(C)C)C 522.60 unknown https://doi.org/10.1080/1478641031000103669
https://doi.org/10.1055/S-2002-20248
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/10.1080/1478641031000103669
https://doi.org/10.1055/S-2002-20248
10,23-Dihydroxy-6,6,20,20-tetramethyl-11-(3-methylbut-2-enyl)-5,13,15,21-tetraoxahexacyclo[12.11.0.03,12.04,9.016,25.017,22]pentacosa-1(14),3,9,11,16,18,22,24-octaen-2-one 10345944 Click to see CC(=CCC1=C2C(=C3C(=C1O)CCC(O3)(C)C)C(=O)C4=C(O2)OC5=C6C=CC(OC6=C(C=C45)O)(C)C)C 502.60 unknown https://doi.org/10.1080/1478641031000103669
https://doi.org/10.1055/S-2002-20248
10,23-Dihydroxy-6,6,20,20-tetramethyl-11-(3-methylbut-2-enyl)-5,13,15,21-tetraoxahexacyclo[12.11.0.03,12.04,9.016,25.017,22]pentacosa-1(14),3,9,11,16,22,24-heptaen-2-one 162821295 Click to see CC(=CCC1=C2C(=C3C(=C1O)CCC(O3)(C)C)C(=O)C4=C(O2)OC5=C6CCC(OC6=C(C=C45)O)(C)C)C 504.60 unknown https://doi.org/10.1055/S-2002-20248
11,17-Dihydroxy-7,7,20,20-tetramethyl-10-(3-methylbut-2-enyl)-2,8,19,25-tetraoxahexacyclo[12.11.0.03,12.04,9.015,24.018,23]pentacosa-1(14),3,5,9,11,15,17,21,23-nonaen-13-one 85617815 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=C(O3)OC5=C6C=CC(OC6=C(C=C45)O)(C)C)C=CC(O2)(C)C)C 500.50 unknown https://doi.org/10.1016/S0031-9422(02)00017-1
https://doi.org/10.1016/S0031-9422(00)98260-8
11,17-Dihydroxy-7,7,20,20-tetramethyl-4-(3-methylbut-2-enyl)-2,6,19,25-tetraoxahexacyclo[12.11.0.03,12.05,10.015,24.018,23]pentacosa-1(14),3(12),4,10,15,17,21,23-octaen-13-one 5317373 Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C5=CC(=C6C(=C5O4)C=CC(O6)(C)C)O)O)CCC(O2)(C)C)C 502.60 unknown https://doi.org/10.1080/1478641031000103669
https://doi.org/10.1016/S0031-9422(02)00017-1
11,17-Dihydroxy-7,7,20,20-tetramethyl-4-(3-methylbut-2-enyl)-2,6,19,25-tetraoxahexacyclo[12.11.0.03,12.05,10.015,24.018,23]pentacosa-1(14),3(12),4,8,10,15,17,21,23-nonaen-13-one 85617813 Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C5=CC(=C6C(=C5O4)C=CC(O6)(C)C)O)O)C=CC(O2)(C)C)C 500.50 unknown https://doi.org/10.1080/1478641031000103669
https://doi.org/10.1055/S-2002-20248
https://doi.org/10.1016/S0031-9422(00)98260-8
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/10.1002/JCCS.200200066
5,7,15,16,20-Pentahydroxy-17,17-dimethyl-6,8-bis(3-methylbut-2-enyl)-10,12,18-trioxapentacyclo[11.8.0.02,11.04,9.014,19]henicosa-1(21),2(11),4,6,8,13,19-heptaen-3-one 78384920 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)OC4=C5C(C(C(OC5=C(C=C34)O)(C)C)O)O)CC=C(C)C)O)C 536.60 unknown https://doi.org/10.1016/S0031-9422(02)00017-1
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/10.1002/JCCS.200200066
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/S0031-9422(02)00017-1
6,7,21-Trihydroxy-17,17-dimethyl-8,20-bis(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 163047260 Click to see CC(=CCC1=C2C(=CC(=C1O)O)C3=C(O2)OC4=C5C=CC(OC5=C(C(=C4C3=O)O)CC=C(C)C)(C)C)C 502.60 unknown https://doi.org/10.1080/1478641031000103669
https://doi.org/10.1055/S-2002-20248
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/10.1002/JCCS.200200066
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/10.1080/1478641031000103669
https://doi.org/10.1055/S-2002-20248
https://doi.org/10.1016/S0031-9422(00)98023-3
https://doi.org/10.1016/S0031-9422(00)98095-6
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/10.1080/1478641031000103669
https://doi.org/10.1055/S-2002-20248
https://doi.org/10.1016/S0031-9422(00)98023-3
https://doi.org/10.1016/S0031-9422(00)98095-6
Formosanatin A 636550 Click to see CC(=CCC1=C2C(=C(C(=C1O)CCC(C)(C)O)O)C(=O)C3=C(O2)OC4=C5C=CC(OC5=C(C=C34)O)(C)C)C 520.60 unknown https://doi.org/10.1080/1478641031000103669
https://doi.org/10.1016/S0031-9422(02)00017-1
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
2'-Hydroxybiochanin A 5282075 Click to see COC1=CC(=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O 300.26 unknown https://doi.org/10.1002/JCCS.200200066
2'-Hydroxyformononetin 5280551 Click to see COC1=CC(=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown https://doi.org/10.1080/1478641031000103669
3-(3,4-Dimethoxyphenyl)-7,8-dihydroxy-4H-1-benzopyran-4-one 13939417 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3O)O)OC 314.29 unknown https://doi.org/10.1002/JCCS.200200066
8-O-methylretusin 5319771 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3OC)O 298.29 unknown https://doi.org/10.1055/S-2002-20248
Biochanin A 5280373 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O 284.26 unknown https://doi.org/10.1080/1478641031000103669
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown https://doi.org/10.1007/BF02114110
https://doi.org/10.1080/1478641031000103669
https://doi.org/10.1002/JCCS.200200066
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
5-Deoxycajanin 11471620 Click to see COC1=CC2=C(C=C1)C(=O)C(=CO2)C3=C(C=C(C=C3)O)O 284.26 unknown https://doi.org/10.1002/JCCS.200200066

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