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Vitex polygama

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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 UUID643ff09f7182b825224250
Scientific name Vitex polygama
Authority Cham.
First published in Linnaea 7: 371 (1832)

Description Top

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Synonyms Top

Scientific name Authority First published in
Vitex laciniosa Turcz. Bull. Soc. Imp. Naturalistes Moscou 36(II): 225 (1863)
Vitex polygama var. hirsuta Schauer Fl. Bras. 9: 300 (1851)
Vitex polygama var. holosericea Schauer Fl. Bras. 9: 300 (1851)
Casarettoa mollissima Walp. Repert. Bot. Syst. (Walpers) iv. 91 (1844).

Common names Top

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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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Southern South America
      • Paraguay
    • Western South America
      • Bolivia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000333372
Tropicos 33700492
KEW urn:lsid:ipni.org:names:865939-1
The Plant List kew-213715
Open Tree Of Life 5793056
IUCN Red List 148765619
IPNI 865939-1
iNaturalist 563930
GBIF 7309300
USDA GRIN 438867

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
Solution phase synthesis of a combinatorial library of chalcones and flavones as potent cathepsin V inhibitors. Alvim J Jr, Severino RP, Marques EF, Martinelli AM, Vieira PC, Fernandes JB, da Silva MF, Corrêa AG J Comb Chem 13-Sep-2010
doi:10.1021/CC100076K
PMID:20578711
Flavonas, lignanas e terpeno de Piper umbellata (Piperaceae) Debora Cristina Baldoqui, Vanderlan da S. Bolzani, Maysa Furlan, Massuo J. Kato, Márcia O. M. Marques FapUNIFESP (SciELO) 06-Aug-2009
doi:10.1590/S0100-40422009000500005
Enzymatic inhibitory activity and trypanocidal effects of extracts and compounds from Siphoneugena densiflora O. Berg and Vitex polygama Cham. Gallo MB, Marques AS, Vieira PC, da Silva MF, Fernandes JB, Silva M, Guido RV, Oliva G, Thiemann OH, Albuquerque S, Fairlamb AH Z Naturforsch C J Biosci 01-May-2008
PMCID:PMC3428908
doi:10.1515/ZNC-2008-5-611
PMID:18669023
Compounds from Vitex polygama active against kidney diseases. Gallo MB, Vieira PC, Fernandes JB, da Silva MF, Salimena-Pires FR J Ethnopharmacol 17-Jan-2008
doi:10.1016/J.JEP.2007.09.020
PMID:17981413
Bioactivity of extracts and isolated compounds from Vitex polygama (Verbenaceae) and Siphoneugena densiflora (Myrtaceae) against Spodoptera frugiperda (Lepidoptera: Noctuidae). Gallo MB, Rocha WC, da Cunha US, Diogo FA, da Silva FC, Vieira PC, Vendramim JD, Fernandes JB, da Silva MF, Batista-Pereira LG Pest Manag Sci 01-Nov-2006
doi:10.1002/PS.1278
PMID:16953496
2″-O-caffeoylorientin from Vitex polygama Suzana G Leitão, Franco Delle Monache Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00416-6
Ecdysteroids from two Brazilian Vitex species. dos Santos TC, Delle Monache F, Leitão SG Fitoterapia 01-Mar-2001
doi:10.1016/S0367-326X(00)00304-X
PMID:11295296

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
> 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://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
https://doi.org/10.1016/S0031-9422(98)00416-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aS,6bR,10S,11R,12aR)-10,11-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 10162403 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
2,3-Dihydroxyolean-12-en-28-oic acid 3694932 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
Jacarandic acid 13653335 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
NCGC00169714-02_C30H48O5_(2alpha,3alpha,5xi,9xi,18xi)-2,3,19-Trihydroxyurs-12-en-28-oic acid 11156036 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
(2S,3R,5R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3R)-2,3,6-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 11081347 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
(2S,3R,5R,9R,10R,11R,13R,14S,17R)-17-[(2S,3R)-3,6-dihydroxy-6-methylheptan-2-yl]-2,3,11,14-tetrahydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 101618910 Click to see CC(C1CCC2(C1(CC(C3C2=CC(=O)C4C3(CC(C(C4)O)O)C)O)C)O)C(CCC(C)(C)O)O 480.60 unknown https://doi.org/10.1016/S0367-326X(00)00304-X
(2S,3R,5S,10R,13R,14S,17S)-2,3,5,14-tetrahydroxy-10,13-dimethyl-17-[(2R,3R)-2,3,6-trihydroxy-6-methylheptan-2-yl]-1,2,3,4,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-6-one 10323567 Click to see CC12CCC3C(=CC(=O)C4(C3(CC(C(C4)O)O)C)O)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 496.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
17-(3,6-dihydroxy-6-methylheptan-2-yl)-2,3,11,14-tetrahydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 77199285 Click to see CC(C1CCC2(C1(CC(C3C2=CC(=O)C4C3(CC(C(C4)O)O)C)O)C)O)C(CCC(C)(C)O)O 480.60 unknown https://doi.org/10.1016/S0367-326X(00)00304-X
2,3,5,14-Tetrahydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-1,2,3,4,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-6-one 271604 Click to see CC12CCC3C(=CC(=O)C4(C3(CC(C(C4)O)O)C)O)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 496.60 unknown https://doi.org/10.1002/PS.1278
2beta,3beta,5beta,14,20,22R,25-Heptahydroxycholest-7-en-6-one 441833 Click to see CC12CCC3C(=CC(=O)C4(C3(CC(C(C4)O)O)C)O)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 496.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
https://doi.org/10.1002/PS.1278
Ajugasterone C 441826 Click to see CC(C)CCC(C(C)(C1CCC2(C1(CC(C3C2=CC(=O)C4C3(CC(C(C4)O)O)C)O)C)O)O)O 480.60 unknown https://doi.org/10.1016/S0367-326X(00)00304-X
Turkesterone 14376672 Click to see CC12CC(C3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O)O 496.60 unknown https://doi.org/10.1016/S0367-326X(00)00304-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
(2S,3R,10R,13R,17S)-2,3-dihydroxy-10,13-dimethyl-17-[(2R,3R)-2,3,6-trihydroxy-6-methylheptan-2-yl]-1,2,3,4,5,9,11,12,16,17-decahydrocyclopenta[a]phenanthren-6-one 162889695 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1=CCC2C(C)(C(CCC(C)(C)O)O)O 462.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
(2S,3R,5R,9R,10R,11R,13R,14S,17R)-2,3,11,14-tetrahydroxy-17-[(2S,3R)-3-hydroxy-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 162894070 Click to see CC(C)CCC(C(C)C1CCC2(C1(CC(C3C2=CC(=O)C4C3(CC(C(C4)O)O)C)O)C)O)O 464.60 unknown https://doi.org/10.1016/S0367-326X(00)00304-X
2,3-Dihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-1,2,3,4,5,9,11,12,16,17-decahydrocyclopenta[a]phenanthren-6-one 85449058 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1=CCC2C(C)(C(CCC(C)(C)O)O)O 462.60 unknown https://doi.org/10.1002/PS.1278
2,3,11,14-tetrahydroxy-17-(3-hydroxy-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 162894069 Click to see CC(C)CCC(C(C)C1CCC2(C1(CC(C3C2=CC(=O)C4C3(CC(C(C4)O)O)C)O)C)O)O 464.60 unknown https://doi.org/10.1016/S0367-326X(00)00304-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Trihydroxy bile acids, alcohols and derivatives
(1R,2R,4S,8R,10R,14S,17R,18R,20R)-14,20-dihydroxy-17-[(2S,3R)-3-hydroxy-6-methylheptan-2-yl]-2,6,6,18-tetramethyl-5,7-dioxapentacyclo[11.7.0.02,10.04,8.014,18]icos-12-en-11-one 162942303 Click to see CC(C)CCC(C(C)C1CCC2(C1(CC(C3C2=CC(=O)C4C3(CC5C(C4)OC(O5)(C)C)C)O)C)O)O 504.70 unknown https://doi.org/10.1016/S0367-326X(00)00304-X
14,20-Dihydroxy-17-(3-hydroxy-6-methylheptan-2-yl)-2,6,6,18-tetramethyl-5,7-dioxapentacyclo[11.7.0.02,10.04,8.014,18]icos-12-en-11-one 162942302 Click to see CC(C)CCC(C(C)C1CCC2(C1(CC(C3C2=CC(=O)C4C3(CC5C(C4)OC(O5)(C)C)C)O)C)O)O 504.70 unknown https://doi.org/10.1016/S0367-326X(00)00304-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
(2S,3R,10R,13R,14S,17S)-17-[(1R)-1-[(2R)-5,5-dimethyloxolan-2-yl]-1-hydroxyethyl]-2,3,14-trihydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 162864045 Click to see CC1(CCC(O1)C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)C 462.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
Shidasterone 15227299 Click to see CC1(CCC(O1)C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)C 462.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
https://doi.org/10.1002/PS.1278
Stachysterone D 634652 Click to see CC1(CCC(O1)C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)C 462.60 unknown https://doi.org/10.1002/PS.1278
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
Methacrylic Acid 4093 Click to see CC(=C)C(=O)O 86.09 unknown https://doi.org/10.1016/J.JEP.2007.09.020
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(3,4,5,6-Tetrahydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 85140196 Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)O)O)O)O)O)O 342.30 unknown https://doi.org/10.1002/PS.1278
[(2R,3S,4S,5R,6S)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 162947632 Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)O)O)O)O)O)O 342.30 unknown https://doi.org/10.1016/J.JEP.2007.09.020
6-O-caffeoyl-beta-glucose 101419460 Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)O)O)O)O)O)O 342.30 unknown https://doi.org/10.1016/J.JEP.2007.09.020
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
3-Methoxyminimiflorin 10433154 Click to see CC(=CCC1=C2C(=C(C3=C1OC(C(C3=O)OC)C4=CC=CC=C4O)O)C=CC(O2)(C)C)C 436.50 unknown https://doi.org/10.1021/CC100076K
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/S0031-9422(98)00416-6
https://doi.org/10.1021/CC100076K
> 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/10.1016/S0031-9422(98)00416-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 6426860 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(98)00416-6
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 4475102 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(98)00416-6
Isoorientin 114776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.JEP.2007.09.020
https://doi.org/10.1016/S0031-9422(98)00416-6
Isovitexin 162350 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(98)00416-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-8-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 100953245 Click to see C1=CC(=C(C=C1C=CC(=O)OC2C(C(C(OC2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)CO)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(98)00416-6
[(2S,3R,4S,5S,6S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-8-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 162971138 Click to see C1=CC(=C(C=C1C=CC(=O)OC2C(C(C(OC2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)CO)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(98)00416-6
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 154497137 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(98)00416-6
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 5378180 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(98)00416-6
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 154497677 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(98)00416-6
Homo-orientin 5382105 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(98)00416-6
Isocarlinoside 21576182 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC(=C(C=C4)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O 580.50 unknown https://doi.org/10.1016/J.JEP.2007.09.020
Isoschaftoside 3084995 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1016/J.JEP.2007.09.020
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1590/S0100-40422009000500005
https://doi.org/10.1016/S0031-9422(98)00416-6
Schaftoside 442658 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1016/J.JEP.2007.09.020
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(98)00416-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(98)00416-6
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 26339717 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(98)00416-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown https://doi.org/10.1016/S0031-9422(98)00416-6
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
Quercetin 3,3'-dimethyl ether 5316900 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)O 330.29 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 284.26 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Kaempferol 3,7,4'-trimethyl ether 5468749 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/

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