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Tephrosia villosa

Tephrosia villosa - 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 UUID643fdd2587ed4384391126
Scientific name Tephrosia villosa
Authority (L.) Pers.
First published in Syn. Pl.2: 329 (1807)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tephrosia incana (Roxb.) Sweet
Cracca villosa L. Sp. Pl.: 753 (1753)
Tephrosia incana (Roxb.) Wight & Arn.
Tephrosia villosa var. argentea Thwaites
Galega villosa (L.) L. Syst. Nat. ed. 10, 2: 1172 (1759)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Tephrosia villosa subsp. ehrenbergiana (Schweinf.) Brummitt Bol. Soc. Brot., sér. 2, 41: 225 (1968)
Tephrosia villosa subsp. villosa Unknown

Varieties (abbr. var.) Top

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Name Authority First published in
Tephrosia villosa var. daviesii Brummitt Bol. Soc. Brot., sér. 2, 41: 227 (1968)

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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Eritrea
      • Ethiopia
      • Somalia
      • Sudan
    • Northern Africa
      • Egypt
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zimbabwe
    • Southern Africa
      • Namibia
      • Northern Provinces
    • West Tropical Africa
      • Benin
      • Burkina
      • Ivory Coast
      • Senegal
      • Togo
    • Western Indian Ocean
      • Madagascar
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Lesser Sunda Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000204506
UNII 8QEE168DWE
USDA Plants TEVI8
Tropicos 13033607
KEW urn:lsid:ipni.org:names:1148851-2
The Plant List ild-5081
Open Tree Of Life 345230
NCBI Taxonomy 62125
IUCN Red List 19892432
IPNI 1148851-2
iNaturalist 138466
GBIF 5342176
EOL 688936
USDA GRIN 80183

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
Implementation of machine learning in DNA barcoding for determining the plant family taxonomy Riza LS, Zain MI, Izzuddin A, Prasetyo Y, Hidayat T, Abu Samah KA Heliyon 21-Sep-2023
PMCID:PMC10520734
doi:10.1016/j.heliyon.2023.e20161
PMID:37767518
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Anthelmintic Agents from African Medicinal Plants: Review and Prospects Jato J, Orman E, Duah Boakye Y, Oppong Bekoe E, Oppong Bekoe S, Asare-Nkansah S, Spiegler V, Hensel A, Liebau E, Agyare C Evid Based Complement Alternat Med 31-Dec-2022
PMCID:PMC9825222
doi:10.1155/2022/8023866
PMID:36624864
Use of Defensins to Develop Eco-Friendly Alternatives to Synthetic Fungicides to Control Phytopathogenic Fungi and Their Mycotoxins Leannec-Rialland V, Atanasova V, Chereau S, Tonk-Rügen M, Cabezas-Cruz A, Richard-Forget F J Fungi (Basel) 25-Feb-2022
PMCID:PMC8950385
doi:10.3390/jof8030229
PMID:35330231
Myco-Synergism Boosts Herbivory-Induced Maize Defense by Triggering Antioxidants and Phytohormone Signaling Batool R, Umer MJ, Wang Y, He K, Shabbir MZ, Zhang T, Bai S, Chen J, Wang Z Front Plant Sci 17-Feb-2022
PMCID:PMC8892192
doi:10.3389/fpls.2022.790504
PMID:35251075
Emerging Anthelmintic Resistance in Poultry: Can Ethnopharmacological Approaches Offer a Solution? Zirintunda G, Biryomumaisho S, Kasozi KI, Batiha GE, Kateregga J, Vudriko P, Nalule S, Olila D, Kajoba M, Matama K, Kwizera MR, Ghoneim MM, Abdelhamid M, Zaghlool SS, Alshehri S, Abdelgawad MA, Acai-Okwee J Front Pharmacol 14-Feb-2022
PMCID:PMC8883056
doi:10.3389/fphar.2021.774896
PMID:35237147
Status and consolidated list of threatened medicinal plants of India Gowthami R, Sharma N, Pandey R, Agrawal A Genet Resour Crop Evol 25-May-2021
PMCID:PMC8148398
doi:10.1007/s10722-021-01199-0
PMID:34054223
Plants in the Genus Tephrosia: Valuable Resources for Botanical Insecticides Zhang P, Qin D, Chen J, Zhang Z Insects 21-Oct-2020
PMCID:PMC7589259
doi:10.3390/insects11100721
PMID:33096762
Plant Defensins from a Structural Perspective Kovaleva V, Bukhteeva I, Kit OY, Nesmelova IV Int J Mol Sci 26-Jul-2020
PMCID:PMC7432377
doi:10.3390/ijms21155307
PMID:32722628
Defensins of Grasses: A Systematic Review Odintsova TI, Slezina MP, Istomina EA Biomolecules 10-Jul-2020
PMCID:PMC7407236
doi:10.3390/biom10071029
PMID:32664422
The potential of anti-malarial compounds derived from African medicinal plants: a review of pharmacological evaluations from 2013 to 2019 Bekono BD, Ntie-Kang F, Onguéné PA, Lifongo LL, Sippl W, Fester K, Owono LC Malar J 18-May-2020
PMCID:PMC7236213
doi:10.1186/s12936-020-03231-7
PMID:32423415
An Ethnobotanical Survey of a Dryland Botanical Garden and Its Environs in Kenya: The Mutomo Hill Plant Sanctuary Mutie FM, Gao LL, Kathambi V, Rono PC, Musili PM, Ngugi G, Hu GW, Wang QF Evid Based Complement Alternat Med 17-Mar-2020
PMCID:PMC7103046
doi:10.1155/2020/1543831
PMID:32256635
A novel recombinant javanicin with dual antifungal and anti-proliferative activities Orrapin S, Intorasoot A, Roytrakul S, Dechsupa N, Kantapan J, Onphat Y, Srimek C, Sitthidet Tharinjaroen C, Anukool U, Butr-Indr B, Phunpae P, Intorasoot S Sci Rep 05-Dec-2019
PMCID:PMC6895105
doi:10.1038/s41598-019-55044-7
PMID:31804594
Antidiabetic, antioxidant and antimicrobial activities of extracts of Tephrosia bracteolata leaves Egharevba GO, Dosumu OO, Oguntoye SO, Njinga NS, Dahunsi SO, Hamid AA, Anand A, Amtul Z, Priyanka U Heliyon 21-Aug-2019
PMCID:PMC6716168
doi:10.1016/j.heliyon.2019.e02275
PMID:31485511
In vivo and in vitro antidiabetic potentials of methanol extract of Tephrosia pumila against alloxan-induced diabetes in experimental animals Ramesh C, Rani AP Int J Health Sci (Qassim) 01-May-2019
PMCID:PMC6512151
PMID:31123434

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 7092730 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(00)95025-8
Lup-20(29)-en-3-one 323075 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(00)95025-8
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(00)95025-8
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1021/NP50095A015
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S)-7-[(2E)-3,7-dimethylocta-2,6-dienoxy]-8-[(2E)-3,7-dimethylocta-2,6-dienyl]-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 163190217 Click to see CC(=CCCC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)OCC=C(C)CCC=C(C)C)C)C 544.70 unknown https://doi.org/10.1080/14786410903020560
7-(3,7-Dimethylocta-2,6-dienoxy)-8-(3,7-dimethylocta-2,6-dienyl)-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 162843094 Click to see CC(=CCCC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)OCC=C(C)CCC=C(C)C)C)C 544.70 unknown https://doi.org/10.1080/14786410903020560
8-Prenylpinostrobin 14721597 Click to see CC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC)C 338.40 unknown https://doi.org/10.1016/0031-9422(80)83111-6
Tephrinone 156589 Click to see CC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC)C 338.40 unknown https://doi.org/10.1016/0031-9422(80)83111-6
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
4H-1-benzopyran-4-one, 7-[[(2E)-3,7-dimethyl-2,6-octadienyl]oxy]-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-, (2S)- 5716904 Click to see CC(=CCCC(=CCOC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O)C)C 408.50 unknown https://doi.org/10.1080/14786410903020560
7-(3,7-Dimethylocta-2,6-dienoxy)-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 77232705 Click to see CC(=CCCC(=CCOC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O)C)C 408.50 unknown https://doi.org/10.1080/14786410903020560
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5-hydroxy-7-methoxy-8-(2-methylprop-1-enyl)-2-phenyl-2,3-dihydrochromen-4-one 163065160 Click to see CC(=CC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC)C 324.40 unknown https://doi.org/10.1080/14786410903020560
5-Hydroxy-7-methoxy-8-(2-methylprop-1-enyl)-2-phenyl-2,3-dihydrochromen-4-one 163065159 Click to see CC(=CC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC)C 324.40 unknown https://doi.org/10.1080/14786410903020560
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Tephrosol 14704585 Click to see COC1=C(C=C2C(=C1)C3=C(C4=CC5=C(C=C4O3)OCO5)C(=O)O2)O 326.26 unknown https://doi.org/10.1016/0031-9422(80)83114-1
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
Medicarpin 336327 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.1016/0031-9422(80)85079-5
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids
(6R)-10-hydroxy-16,17-dimethoxy-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-1(13),3(11),4(8),9,14,16,18-heptaene-12,21-dione 101967043 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4=O)OC)OC)O 422.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
CID 99781 99781 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4=O)OC)OC 406.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
Rotenonone 442819 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4=O)OC)OC 406.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
Villosone 44257404 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4=O)OC)OC)O 422.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(1)Benzopyrano(3,4-b)furo(2,3-h)(1)benzopyran-6(12H)-one, 1,2-dihydro-8,9-dimethoxy-2-(1-methylethenyl)-, (R)- 99190 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC 392.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
(1R,14S)-11,14-dihydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),5,10,15,17,19-heptaen-13-one 162980813 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)C 426.40 unknown https://doi.org/10.1021/NP50095A015
(1R,6R,13R)-10,13-dihydroxy-16,17-dimethoxy-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one 51537291 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O 426.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
(1R,6S,13R)-10-hydroxy-16,17-dimethoxy-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one 145978778 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O 410.40 unknown https://doi.org/10.1016/0031-9422(80)83114-1
(1S,14R)-11,14-dihydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),5,10,15,17,19-heptaen-13-one 124355889 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)C 426.40 unknown https://doi.org/10.1021/NP50095A015
(1S,14S,22R)-11,22-dihydroxy-17,18-dimethoxy-7,7-dimethyl-2,21-dioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3,5,9,11,15,17,19-heptaen-13-one 162947671 Click to see CC1(CC2=CC(=C3C(=O)C4C(C(OC5=CC(=C(C=C45)OC)OC)O)OC3=C2C=C1)O)C 424.40 unknown https://doi.org/10.1016/0031-9422(80)83114-1
(1S,6R,13R,21S)-10,13,21-trihydroxy-16,17-dimethoxy-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one 98598071 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4C(OC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)O 442.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
(1S,6R,13S,21S)-10,21-dihydroxy-16,17-dimethoxy-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one 51669404 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4C(C3=O)C5=CC(=C(C=C5OC4O)OC)OC)O 426.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
(6R,21S)-10,21-dihydroxy-16,17-dimethoxy-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-1(13),3(11),4(8),9,14,16,18-heptaen-12-one 163083441 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4O)OC)OC)O 424.40 unknown https://doi.org/10.1016/S0031-9422(00)95025-8
(6R,21Z)-10-hydroxy-16,17-dimethoxy-21-(methoxymethylidene)-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-1(13),3(11),4(8),9,14,16,18-heptaen-12-one 163190118 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4=COC)OC)OC)O 450.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
(6R)-10-hydroxy-16,17-dimethoxy-21-methylidene-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-1(13),3(11),4(8),9,14,16,18-heptaen-12-one 163187729 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4=C)OC)OC)O 420.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
(6R)-16,17-dimethoxy-21-methylidene-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-1(13),3(11),4(8),9,14,16,18-heptaen-12-one 163043791 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4=C)OC)OC 404.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
(6R)-9,11-dihydroxy-2,3,6-trimethoxy-8-(3-methylbut-2-enyl)-6H-chromeno[3,4-b]chromen-12-one 162865458 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C(OC4=CC(=C(C=C43)OC)OC)OC)C 440.40 unknown https://doi.org/10.1021/NP50095A015
(6S,21S)-10,21-dihydroxy-16,17-dimethoxy-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-1(13),3(11),4(8),9,14,16,18-heptaen-12-one 163083440 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4O)OC)OC)O 424.40 unknown https://doi.org/10.1016/S0031-9422(00)95025-8
10-Hydroxy-16,17-dimethoxy-21-(methoxymethylidene)-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-1(13),3(11),4(8),9,14,16,18-heptaen-12-one 162884493 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4=COC)OC)OC)O 450.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
10-Hydroxy-16,17-dimethoxy-21-methylidene-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-1(13),3(11),4(8),9,14,16,18-heptaen-12-one 162846939 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4=C)OC)OC)O 420.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
11-Hydroxytephrosin 155725 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)C 426.40 unknown https://doi.org/10.1016/0031-9422(80)83114-1
12A-Dehydro-6-hydroxysumatrol 5459254 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4O)OC)OC)O 424.40 unknown https://doi.org/10.1016/S0031-9422(00)95025-8
16,17-Dimethoxy-21-methylidene-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-1(13),3(11),4(8),9,14,16,18-heptaen-12-one 163043790 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4=C)OC)OC 404.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
5-Hydroxy-8,9-dimethoxy-2-(prop-1-en-2-yl)-1,2,12,12a-tetrahydrofuro[2',3':7,8][1]benzopyrano[2,3-c][1]benzopyran-6(6aH)-one 3665545 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O 410.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
5'beta-Rotenone 5102 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC 394.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
6-Hydroxysumatrol 14427376 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4C(C3=O)C5=CC(=C(C=C5OC4O)OC)OC)O 426.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
Dehydrorotenone 303993 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC 392.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
Rotenone 6758 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC 394.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
Sumatrol 442824 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O 410.40 unknown https://doi.org/10.1016/0031-9422(80)83114-1
https://doi.org/10.1016/S0040-4039(01)83698-4
Villol 44257414 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4C(OC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)O 442.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
Villosinol 14704458 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O 426.40 unknown https://doi.org/10.1016/S0040-4039(01)83698-4
https://doi.org/10.1016/0031-9422(80)83114-1

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