Details Top

Internal ID UUID643fd8ea60da8072463947
Scientific name Deguelia scandens
Authority Aubl.
First published in Hist. Pl. Guiane2: 750 (1775)

Ethnobotanical Use Top

Write a new one!
No ethnobotanical data added yet. Help us by writing one.

General Uses Top

Suggest a correction!

Common products:
Root material of Deguelia scandens is processed into dried root chips, crude rotenone extracts, and purified rotenone crystals. These materials are the primary commercial forms used as the basis for insecticidal and piscicidal formulations.

Industrial and craft applications:
Rotenone extracted from the roots serves as a broad‑spectrum insecticide for fruit, vegetable, ornamental, and greenhouse crops. It is employed in integrated pest‑management programs where its rapid knock‑down effect on insects such as aphids, whiteflies, thrips and certain beetles is valued. Historically the same extract has been used as a fish poison (piscicide) in subsistence fisheries, where the compound immobilizes fish through mitochondrial disruption. Modern applications include dusts, wettable powders, and emulsifiable concentrates designed for spray or bait applications in organic and conventional agriculture.

Properties relevant to use:
Rotenone (C₂₃H₂₂O₆, molecular weight 394 g mol⁻¹) is a non‑water‑soluble, crystalline tetranortriterpenoid with a water solubility of ~0.05 g L⁻¹ but high solubility in organic solvents such as ethanol, acetone and dichloromethane. Its octanol‑water partition coefficient (log P ≈ 3.2) confers good penetration into insect cuticles. The compound inhibits mitochondrial complex I, causing oxidative stress and rapid paralysis in target insects and fish. Rotenone is photolabile, degrading under UV exposure, which influences formulation stability and packaging requirements. Root material typically contains 0.2–0.6 % rotenone by dry weight.

Standards and regulation:
Rotenone is registered as a restricted‑use pesticide in the United States (EPA registration) and is listed under the European Union Plant Protection Products Regulation (Reg. (EU) 528/2012). The EU sets maximum residue limits (MRLs) for rotenone on food crops, and US regulations impose label requirements for aquatic toxicity (GHS classification H400: very toxic to aquatic life). Analytical methods for rotenone residues are validated according to ISO 17025 and GLP guidelines, ensuring compliance with national food‑safety monitoring programs.

Sustainability and sourcing:
Commercial supplies have historically depended on wild harvest of roots from tropical forests in Southeast Asia. Overharvest has raised concerns about depletion of natural populations and loss of habitat. Sustainable practices include controlled cultivation in agroforestry systems, standardized harvesting cycles, and certification schemes such as FairWild that verify responsible collection. Research into domestication and propagation of Deguelia scandens aims to reduce pressure on wild stocks while maintaining a steady supply of rotenone for agricultural use.

Synonyms Top

Scientific name Authority First published in
Phyllocarpus pterocarpus (DC.) Endl. ex B.D.Jacks. Index Kew.2: 513 (1895)
Derris pterocarpus (DC.) Killip J. Washington Acad. Sci.26: 360 (1936)
Lonchocarpus pterocarpus DC. Prodr.2: 260 (1825)
Derris guianensis Benth. J. Proc. Linn. Soc., Bot.4(Suppl.): 106 (1860)
Pterocarpus guianensis Kuntze Revis. Gen. Pl.1: 203 (1891)
Lonchocarpus scandens (Aubl.) Ducke Trop. Woods 69: 5 (1942)
Derris scandens (Aubl.) Pittier Contr. U.S. Natl. Herb. 20: 41 (1917)

Common names Top

Add a new one! Suggest a correction!
No common names added yet.

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000182170
Tropicos 13017512
INPN 633041
KEW urn:lsid:ipni.org:names:491205-1
The Plant List ild-28265
IUCN Red List 19892317
IPNI 77181-2
iNaturalist 139331
GBIF 2960243
EOL 640296
USDA GRIN 13393

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)!
Title Authors Publication Released IDs
Estudo químico de Derris negrensis M. N. Lima Vasconcelos, J. G. Soares Maia FapUNIFESP (SciELO) 04-Jul-2017
doi:10.1590/1809-43921976061059
Vapor-phase toxicity of Derris scandens Benth.-derived constituents against four stored-product pests. Hymavathi A, Devanand P, Suresh Babu K, Sreelatha T, Pathipati UR, Madhusudana Rao J J Agric Food Chem 09-Mar-2011
doi:10.1021/JF104411H
PMID:21314138
A new prenylated isoflavone from Derris scandens Benth. Babu TH, Tiwari AK, Rao VR, Ali AZ, Rao JM, Babu KS J Asian Nat Prod Res 01-Jul-2010
doi:10.1080/10286020.2010.486378
PMID:20628945
A new benzil derivative from Derris scandens: Structure-insecticidal activity study. Sreelatha T, Hymavathi A, Rama Subba Rao V, Devanand P, Usha Rani P, Madhusudana Rao J, Suresh Babu K Bioorg Med Chem Lett 15-Jan-2010
doi:10.1016/J.BMCL.2009.11.103
PMID:19969457
Prenylated Isoflavones from Derris scandens Mayuree Chuankamnerdkarn, Somyote Sutthivaiyakit, Nopporn Thasana, Somchai Pisutjaroenpong The Japan Institute of Heterocyclic Chemistry 09-Mar-2009
doi:10.3987/COM-02-9544
Prenylated Isoflavones from Derris scandens. Mayuree Chuankamnerdkarn, Somyote Sutthivaiyakit, Nopporn Thasana, Somchai Pisutjaroenpong Wiley 30-Jun-2005
doi:10.1002/CHIN.200305216
SCANDENIN—A CONSTITUENT OF THE ROOTS OF DERRIS SCANDENS E. P. CLARK American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/JO01193A012
Anti-inflammatory isoflavonoids from the stems of Derris scandens. Laupattarakasem P, Houghton PJ, Hoult JR Planta Med 01-Jun-2004
doi:10.1055/S-2004-827147
PMID:15229800
The extractives from Derris scandens. Part II. The isolation of osajin and two new isoflavones, scandenone and scandinone Andrew Pelter, P. Stainton Royal Society of Chemistry (RSC) 20-Apr-2004
doi:10.1039/J39660000701
A benzil and isoflavone derivatives from Derris scandens Benth. Mahabusarakam W, Deachathai S, Phongpaichit S, Jansakul C, Taylor WC Phytochemistry 01-Apr-2004
doi:10.1016/J.PHYTOCHEM.2004.03.006
PMID:15110702
Flavonoids from Derris species Raimundo Braz Filho, Otto R. Gottiieb, Ayssor P. Mourão, Arnaldo I.Da Rocha, Francisco Souza Oliveira Elsevier BV 12-Feb-2003
doi:10.1016/S0031-9422(00)98664-3
Isoflavone glycosides from Derris scandens. Rukachaisirikul V, Sukpondma Y, Jansakul C, Taylor WC Phytochemistry 01-Aug-2002
doi:10.1016/S0031-9422(02)00163-2
PMID:12150808
Six diprenylisoflavones, derrisisoflavones A–F, from Derris scandens Toshikazu Sekine, Miyuki Inagaki, Fumio Ikegami, Yuichi Fujii, Nijsiri Ruangrungsi Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00103-X
Four isoflavones and two 3-aryl coumarins from stems of Derris scandens M.Narayana Rao, G.L.David Krupadanam, G. Srimannarayana Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(94)85038-0

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
nigrospoxydon B 25016663 Click to see CC(C)CC(C(=O)OC1C(C(C=C(C1=O)CO)O)O)OC(CC2=CC=CC=C2)C(=O)OC 450.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
Senegalensin 124035 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)CC=C(C)C)O)C 408.50 unknown https://doi.org/10.1002/CHIN.200305216
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
Isolaxifolin 15677602 Click to see 404.50 unknown https://doi.org/10.1021/JF104411H
https://doi.org/10.1016/J.BMCL.2009.11.103
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chrysoeriol 5280666 Click to see 300.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Retusin 5352005 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC 358.30 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Flemichapparin C 11088179 Click to see 310.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Maackiain 91510 Click to see 284.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
3-Hydroxy-8,9-methylenedioxypterocarpane 363863 Click to see 284.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
Anhydropisatin 11822566 Click to see 296.27 unknown https://doi.org/10.1016/S0031-9422(00)98664-3
https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
Dehydromaackiain 14730797 Click to see 282.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
> Phenylpropanoids and polyketides / Isoflavonoids / Hydroxyisoflavonoids
Lonchocarpic acid 54683839 Click to see 434.50 unknown https://doi.org/10.1021/JO01193A012
Robustic acid 54677407 Click to see CC1(C=CC2=C(O1)C=C3C(=C2OC)C(=C(C(=O)O3)C4=CC=C(C=C4)OC)O)C 380.40 unknown https://doi.org/10.1016/0031-9422(94)85038-0
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
5,7-Dihydroxy-3-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one 5317480 Click to see 338.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
Genistein 5280961 Click to see 270.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
https://doi.org/10.1021/JF104411H
https://doi.org/10.1016/J.BMCL.2009.11.103
https://doi.org/10.1055/S-2004-827147
Isolupabigenin 26238934 Click to see 406.50 unknown https://doi.org/10.1016/0031-9422(94)85038-0
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(2S)-4-hydroxy-6-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-g]chromen-5-one 162842930 Click to see 422.50 unknown https://doi.org/10.3987/COM-02-9544
(2S)-4-hydroxy-6-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-5-one 163014265 Click to see 422.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
(8R)-3-(4-hydroxyphenyl)-8-(2-hydroxypropan-2-yl)-5-methoxy-6-(3-methylbut-2-enyl)-8,9-dihydrofuro[2,3-h]chromen-4-one 162896478 Click to see 436.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
(8S)-3-(4-hydroxyphenyl)-8-(2-hydroxypropan-2-yl)-5-methoxy-6-(3-methylbut-2-enyl)-8,9-dihydrofuro[2,3-h]chromen-4-one 162896477 Click to see CC(=CCC1=C2C(=C3C(=C1OC)C(=O)C(=CO3)C4=CC=C(C=C4)O)CC(O2)C(C)(C)O)C 436.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
(8S)-8-(2-hydroxypropan-2-yl)-5-methoxy-3-(4-methoxyphenyl)-6-(3-methylbut-2-enyl)-8,9-dihydrofuro[2,3-h]chromen-4-one 162910931 Click to see 450.50 unknown https://doi.org/10.1080/10286020.2010.486378
2-Hydroxy-5-(5-hydroxy-2,2-dimethyl-6-oxopyrano[3,2-g]chromen-7-yl)benzaldehyde 11132244 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC(=C(C=C4)O)C=O)C 364.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
https://doi.org/10.3987/COM-02-9544
3-(4-Hydroxyphenyl)-8-(2-hydroxypropan-2-yl)-5-methoxy-6-(3-methylbut-2-enyl)-8,9-dihydrofuro[2,3-h]chromen-4-one 10094562 Click to see 436.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
4-Hydroxy-6-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-g]chromen-5-one 195652 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/10.3987/COM-02-9544
5-Hydroxy-7-(4-hydroxyphenyl)-10-(3-methoxy-3-methylbutyl)-2,2-dimethylpyrano[3,2-g]chromen-6-one 101674022 Click to see 436.50 unknown https://doi.org/10.1016/0031-9422(94)85038-0
5-hydroxy-7-[(2S,3R)-3-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-yl]-2,2-dimethylpyrano[3,2-g]chromen-6-one 163040776 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC5=C(C=C4)OC(C5O)C(C)(C)O)C 436.50 unknown https://doi.org/10.3987/COM-02-9544
5-hydroxy-7-[(2S,3S)-3-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-yl]-2,2-dimethylpyrano[3,2-g]chromen-6-one 163040777 Click to see 436.50 unknown https://doi.org/10.3987/COM-02-9544
5-Hydroxy-7-[3-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-yl]-2,2-dimethylpyrano[3,2-g]chromen-6-one 11826241 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC5=C(C=C4)OC(C5O)C(C)(C)O)C 436.50 unknown https://doi.org/10.3987/COM-02-9544
5-Methoxy-3-(4-methoxyphenyl)-8,8-dimethyl-6-(3-methylbut-2-en-1-yl)-4h,8h-pyrano[2,3-f]chromen-4-one 228559 Click to see 432.50 unknown https://doi.org/10.1080/10286020.2010.486378
5,7-Dihydroxy-3-(3-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-6-(3-methylbut-2-enyl)chromen-4-one 10502340 Click to see 422.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
5,7-dihydroxy-3-[(3R)-3-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl]-6-(3-methylbut-2-enyl)chromen-4-one 162946951 Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC4=C(C=C3)OC(C(C4)O)(C)C)O)C 422.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
5,7-dihydroxy-3-[4-hydroxy-3-[(2R)-2-hydroxy-3-methylbut-3-enyl]phenyl]-6-(3-methylbut-2-enyl)chromen-4-one 124355945 Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC(=C(C=C3)O)CC(C(=C)C)O)O)C 422.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
5,7-dihydroxy-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]chromen-4-one 162873519 Click to see CC(=CCC1=C(C=CC(=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)CC(C(=C)C)O)O)O)C 422.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
5,7-dihydroxy-8-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)chromen-4-one 124355949 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)CC(C(=C)C)O)O)C 422.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
5,7-dihydroxy-8-[(2S)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)chromen-4-one 124355950 Click to see 422.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
6-(2-Hydroxy-3-methylbut-3-enyl)-3-(4-hydroxyphenyl)-5-methoxy-8,8-dimethylpyrano[2,3-h]chromen-4-one 46854087 Click to see 434.50 unknown https://doi.org/10.1080/10286020.2010.486378
6-(2,3-Dimethylbut-3-enyl)-5,7-dihydroxy-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]chromen-4-one 162928841 Click to see CC(CC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC(=C(C=C3)O)CC=C(C)C)O)C(=C)C 420.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)-5-methoxy-8,8-dimethylpyrano[2,3-h]chromen-4-one 163023016 Click to see 434.50 unknown https://doi.org/10.1080/10286020.2010.486378
6-[(2S)-2,3-dimethylbut-3-enyl]-5,7-dihydroxy-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]chromen-4-one 162928842 Click to see 420.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
6,8-Diprenylgenistein 480783 Click to see 406.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
https://doi.org/10.1080/10286020.2010.486378
https://doi.org/10.1016/0031-9422(94)85038-0
7-(2,2-Dimethylchromen-6-yl)-5-hydroxy-2,2-dimethylpyrano[3,2-g]chromen-6-one 154497638 Click to see 402.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
7-Hydroxy-3-[4-hydroxy-3-(2-hydroxy-3-methylbut-3-enyl)phenyl]-5-methyl-6-(3-methylbut-2-enyl)chromen-4-one 162986488 Click to see CC1=C(C(=CC2=C1C(=O)C(=CO2)C3=CC(=C(C=C3)O)CC(C(=C)C)O)O)CC=C(C)C 420.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
7-hydroxy-3-[4-hydroxy-3-[(2R)-2-hydroxy-3-methylbut-3-enyl]phenyl]-5-methyl-6-(3-methylbut-2-enyl)chromen-4-one 162986489 Click to see 420.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
7-Hydroxy-6-(2-hydroxy-3-methylbut-3-enyl)-3-(4-hydroxyphenyl)-5-methoxy-8-(3-methylbut-2-enyl)chromen-4-one 10789057 Click to see CC(=CCC1=C(C(=C(C2=C1OC=C(C2=O)C3=CC=C(C=C3)O)OC)CC(C(=C)C)O)O)C 436.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
7-Hydroxy-6-(2-hydroxy-3-methylbutyl)-3-(4-hydroxyphenyl)-5-methoxy-8-(3-methylbut-2-enyl)chromen-4-one 163042072 Click to see CC(C)C(CC1=C(C2=C(C(=C1O)CC=C(C)C)OC=C(C2=O)C3=CC=C(C=C3)O)OC)O 438.50 unknown https://doi.org/10.1080/10286020.2010.486378
7-hydroxy-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)-5-methoxy-8-(3-methylbut-2-enyl)chromen-4-one 162980008 Click to see 436.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
7-hydroxy-6-[(2S)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)-5-methoxy-8-(3-methylbut-2-enyl)chromen-4-one 162980007 Click to see CC(=CCC1=C(C(=C(C2=C1OC=C(C2=O)C3=CC=C(C=C3)O)OC)CC(C(=C)C)O)O)C 436.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
7-hydroxy-6-[(2S)-2-hydroxy-3-methylbutyl]-3-(4-hydroxyphenyl)-5-methoxy-8-(3-methylbut-2-enyl)chromen-4-one 163042073 Click to see 438.50 unknown https://doi.org/10.1080/10286020.2010.486378
7-Hydroxy-8-(2-hydroxy-3-methylbut-3-enyl)-3-(4-hydroxyphenyl)-5-methoxy-6-(3-methylbut-2-enyl)chromen-4-one 10574933 Click to see 436.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
7-hydroxy-8-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)-5-methoxy-6-(3-methylbut-2-enyl)chromen-4-one 163043317 Click to see 436.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
8-(2-Hydroxypropan-2-yl)-5-methoxy-3-(4-methoxyphenyl)-6-(3-methylbut-2-enyl)-8,9-dihydrofuro[2,3-h]chromen-4-one 11812414 Click to see 450.50 unknown https://doi.org/10.1080/10286020.2010.486378
8-hydroxy-5-methoxy-7-(4-methoxyphenyl)-2,2-dimethylpyrano[3,2-g]chromen-6-one 168996 Click to see 380.40 unknown https://doi.org/10.1016/0031-9422(94)85038-0
Chandalone 12302850 Click to see 404.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
Derrisisoflavone A 10070758 Click to see 420.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
https://doi.org/10.1080/10286020.2010.486378
Derrisisoflavone B 10812165 Click to see 422.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
Erysenegalensein E 15478903 Click to see 422.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
Euchrenone b10 402594 Click to see 422.50 unknown https://doi.org/10.3987/COM-02-9544
Lupalbigenin 10001388 Click to see 406.50 unknown https://doi.org/10.1016/J.BMCL.2009.11.103
https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
https://doi.org/10.1016/S0031-9422(99)00103-X
https://doi.org/10.1055/S-2004-827147
https://doi.org/10.1021/JF104411H
https://doi.org/10.1016/0031-9422(94)85038-0
https://doi.org/10.3987/COM-02-9544
Lupinisoflavone G 14237661 Click to see 422.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
https://doi.org/10.3987/COM-02-9544
Lupinisol A 14237668 Click to see 422.50 unknown https://doi.org/10.1016/S0031-9422(99)00103-X
https://doi.org/10.3987/COM-02-9544
Osajin 95168 Click to see 404.50 unknown https://doi.org/10.1016/J.BMCL.2009.11.103
https://doi.org/10.1021/JF104411H
https://doi.org/10.1039/J39660000701
https://doi.org/10.1080/10286020.2010.486378
https://doi.org/10.1016/0031-9422(94)85038-0
Osajin 4'-methyl ether 24721108 Click to see 418.50 unknown https://doi.org/10.1080/10286020.2010.486378
Robustone 5983661 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC5=C(C=C4)OCO5)C 364.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
Scandinone 634141 Click to see CC(=CCC1=C2C(=C3C(=C1OC)C(=O)C(=CO3)C4=CC=C(C=C4)O)C=CC(O2)(C)C)C 418.50 unknown https://doi.org/10.1021/JF104411H
https://doi.org/10.1016/S0031-9422(99)00103-X
https://doi.org/10.1016/J.BMCL.2009.11.103
https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
https://doi.org/10.1039/J39660000701
https://doi.org/10.1080/10286020.2010.486378
Warangalone 5379679 Click to see 404.50 unknown https://doi.org/10.1016/J.BMCL.2009.11.103
https://doi.org/10.1021/JF104411H
https://doi.org/10.1039/J39660000701
https://doi.org/10.1080/10286020.2010.486378
https://doi.org/10.1016/0031-9422(94)85038-0
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 163018227 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C(=O)C(=CO4)C5=CC=C(C=C5)O)O)O)O)O)O)O 562.50 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 163018229 Click to see 562.50 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
3-(4-Hydroxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 163018226 Click to see 562.50 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
3-(4-methoxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4R,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162897034 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C(=O)C(=CO4)C5=CC=C(C=C5)OC)O)O)O)O)O)O 576.50 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
3-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162897033 Click to see 576.50 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
3-(4-methoxyphenyl)-7-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 154497130 Click to see 430.40 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
3-(4-methoxyphenyl)-7-[(2S,4S,5R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44257215 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O 430.40 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
3-(4-Methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 162897031 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C(=O)C(=CO4)C5=CC=C(C=C5)OC)O)O)O)O)O)O 576.50 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162927140 Click to see 578.50 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
5-Hydroxy-3-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 146160904 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC=C(C4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/J.BMCL.2009.11.103
https://doi.org/10.1055/S-2004-827147
https://doi.org/10.1016/S0031-9422(02)00163-2
5-hydroxy-3-(4-methoxyphenyl)-7-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 163095601 Click to see 592.50 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
5-hydroxy-6-methoxy-3-(4-methoxyphenyl)-7-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 163194136 Click to see 622.60 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
5-hydroxy-6-methoxy-3-(4-methoxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162857599 Click to see 622.60 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
5-hydroxy-6-methoxy-3-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 10031836 Click to see 622.60 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
5-Hydroxy-6-methoxy-3-(4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 162857598 Click to see 622.60 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
6-methoxy-3-(4-methoxyphenyl)-7-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 163189288 Click to see 606.60 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
6-methoxy-3-(4-methoxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162891222 Click to see 606.60 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
6-methoxy-3-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 10483813 Click to see 606.60 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
6-Methoxy-3-(4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 162891221 Click to see 606.60 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
7-hydroxy-3-(4-methoxyphenyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 10366267 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
7-hydroxy-3-(4-methoxyphenyl)-8-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163023401 Click to see 446.40 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
7-Hydroxy-3-(4-methoxyphenyl)-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163023400 Click to see 446.40 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
7-methoxy-3-(4-methoxyphenyl)-8-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162994831 Click to see 606.60 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
7-methoxy-3-(4-methoxyphenyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 10366980 Click to see 460.40 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
7-methoxy-3-(4-methoxyphenyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 25087693 Click to see 606.60 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
7-methoxy-3-(4-methoxyphenyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 10348695 Click to see 606.60 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
7-Methoxy-3-(4-methoxyphenyl)-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163011067 Click to see 460.40 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
7-Methoxy-3-(4-methoxyphenyl)-8-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 162994830 Click to see 606.60 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
8-hydroxy-3-(4-methoxyphenyl)-7-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 163195600 Click to see 592.50 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
8-hydroxy-3-(4-methoxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162911580 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C4=C(C=C3)C(=O)C(=CO4)C5=CC=C(C=C5)OC)O)O)O)O)O)O)O 592.50 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
8-hydroxy-3-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 10054171 Click to see 592.50 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
8-Hydroxy-3-(4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 162911579 Click to see 592.50 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
8-methoxy-3-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 131637615 Click to see 460.40 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
8-methoxy-3-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 9986123 Click to see 606.60 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
8-Methoxy-3-(4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 137796491 Click to see 460.40 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
8-Methoxy-3-(4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 162949910 Click to see 606.60 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
Npc198030 3733033 Click to see 430.40 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
Ononin 442813 Click to see 430.40 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
Sphaerobioside 76315025 Click to see 578.50 unknown https://doi.org/10.1021/JF104411H
https://doi.org/10.1016/J.BMCL.2009.11.103
https://doi.org/10.1055/S-2004-827147
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-O-Methylorobol 5319744 Click to see COC1=C(C=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O 300.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
7,8-Dihydroxy-4'-methoxyisoflavone 5481240 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3O)O 284.26 unknown https://doi.org/10.1016/S0031-9422(02)00163-2
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Santal 9926336 Click to see 300.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
4-Hydroxy-6-(2-hydroxy-3-methylbut-3-enyl)-3-(4-hydroxyphenyl)-5-methoxy-8,8-dimethylpyrano[2,3-h]chromen-2-one 163047803 Click to see CC(=C)C(CC1=C2C(=C3C(=C1OC)C(=C(C(=O)O3)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)O 450.50 unknown https://doi.org/10.1080/10286020.2010.486378
4-hydroxy-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)-5-methoxy-8,8-dimethylpyrano[2,3-h]chromen-2-one 163047804 Click to see 450.50 unknown https://doi.org/10.1080/10286020.2010.486378
4,5-Dimethoxy-3-(4-methoxyphenyl)-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-2-one 21676221 Click to see 462.50 unknown https://doi.org/10.1016/0031-9422(94)85038-0
https://doi.org/10.1080/10286020.2010.486378
5-Hydroxy-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-8,8-dimethylpyrano[2,3-h]chromen-4-one 11441072 Click to see 404.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
5-Hydroxy-3',4'-methylenedioxy-6'',6''-dimethylpyrano[2'',3'':7,8]isoflavone 14502737 Click to see 364.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
Scandenin 54676535 Click to see CC(=CCC1=C2C(=C3C(=C1OC)C(=C(C(=O)O3)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C 434.50 unknown https://doi.org/10.1021/JF104411H
https://doi.org/10.1016/J.BMCL.2009.11.103
https://doi.org/10.1021/JO01193A012
https://doi.org/10.1055/S-2004-827147
Scandenin A 76329518 Click to see 448.50 unknown https://doi.org/10.1021/JF104411H
https://doi.org/10.1016/J.BMCL.2009.11.103
Ulexone A 14583600 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=CO2)C3=CC4=C(C=C3)OC(C=C4)(C)C)C 404.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
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/10.1590/1809-43921976061059
> Phenylpropanoids and polyketides / Stilbenes
1-[5-Hydroxy-7-methoxy-2,2-dimethyl-8-(3-methylbut-2-enyl)chromen-6-yl]-2-(4-hydroxyphenyl)ethane-1,2-dione 76315983 Click to see CC(=CCC1=C2C(=C(C(=C1OC)C(=O)C(=O)C3=CC=C(C=C3)O)O)C=CC(O2)(C)C)C 422.50 unknown https://doi.org/10.1016/J.BMCL.2009.11.103
Derrisdione A 76308776 Click to see 422.50 unknown https://doi.org/10.1016/J.BMCL.2009.11.103
Scandione 643011 Click to see 316.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.006
https://doi.org/10.1016/0031-9422(94)85038-0

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.