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Vepris nobilis

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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 UUID643ffaaac9bea841201300
Scientific name Vepris nobilis
Authority (Delile) Mziray
First published in Symb. Bot. Upsal. 30(1): 74 (1992)

Description Top

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Synonyms Top

Scientific name Authority First published in
Toddalia nobilis Hook.f. ex Oliv. Fl. Trop. Afr. 1: 306 (1868)
Teclea diversifolia Lanza Lav. Reale Ist. Bot. Palermo 5: 7 (1934)
Teclea nobilis Delile Ann. Sci. Nat., Bot. , sér. 2, 20: 90 (1843)
Aspidostigma acuminatum Hochst. Flora 27: 18 (1844)
Cranzia nobilis Kuntze Revis. Gen. Pl. 1: 99 (1891)

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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Djibouti
      • Eritrea
      • Ethiopia
      • Somalia
      • Sudan
    • South Tropical Africa
      • Malawi
      • Zambia
      • Zimbabwe
    • West-central Tropical Africa
      • Burundi
      • Rwanda
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000420153
Tropicos 50052221
KEW urn:lsid:ipni.org:names:969503-1
The Plant List kew-2454487
Open Tree Of Life 5747655
NCBI Taxonomy 1220089
IUCN Red List 153944693
IPNI 969503-1
iNaturalist 147401
GBIF 3834246
EOL 5625882
CMAUP NPO12078
Wikipedia Vepris_nobilis

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
Ethnoveterinary medicinal plants and their utilization by indigenous and local communities of Dugda District, Central Rift Valley, Ethiopia Oda BK, Lulekal E, Warkineh B, Asfaw Z, Debella A J Ethnobiol Ethnomed 09-Mar-2024
PMCID:PMC10924356
doi:10.1186/s13002-024-00665-0
PMID:38461267
Medicinal Plants Used by Oromo Community in Kofale District, West-Arsi Zone, Oromia Regional State, Ethiopia Nuro GB, Tolossa K, Giday M J Exp Pharmacol 05-Mar-2024
PMCID:PMC10929209
doi:10.2147/JEP.S449496
PMID:38476311
Ethnobotanical study of wild edible plants in Dibatie district, Metekel zone, Benishangul Gumuz Regional State, western Ethiopia Anbessa B, Lulekal E, Getachew P, Hymete A J Ethnobiol Ethnomed 27-Feb-2024
PMCID:PMC10900549
doi:10.1186/s13002-024-00671-2
PMID:38413982
Ethnoveterinary medicinal plants and their utilization by the people of Soro District, Hadiya Zone, southern Ethiopia Hankiso M, Asfaw Z, Warkineh B, Abebe A, Sisay B, Debella A J Ethnobiol Ethnomed 22-Feb-2024
PMCID:PMC10885532
doi:10.1186/s13002-024-00651-6
PMID:38389077
A comprehensive review of antimalarial medicinal plants used by Tanzanians Kacholi DS Pharm Biol 25-Jan-2024
PMCID:PMC10812860
doi:10.1080/13880209.2024.2305453
PMID:38270178
Determinants of plant community along environmental gradients in Geramo forest, the western escarpment of the rift valley of Ethiopia Getaneh ZA, Demissew S, Woldu Z, Aynekulu E PLoS One 27-Nov-2023
PMCID:PMC10681247
doi:10.1371/journal.pone.0294324
PMID:38011089
Ectoparasite Fauna of Rodents and Shrews with Their Spatial, Temporal, and Dispersal along a Degradation Gradient in Mabira Central Forest Reserve Babyesiza WS, Mpagi J, Ssuuna J, Akoth S, Katakweba A J Parasitol Res 28-Oct-2023
PMCID:PMC10625493
doi:10.1155/2023/7074041
PMID:37928436
Medicinal plants of the upper Aswa River catchment of northern Uganda - a cultural crossroads Masters ET J Ethnobiol Ethnomed 27-Oct-2023
PMCID:PMC10605377
doi:10.1186/s13002-023-00620-5
PMID:37884931
Potential of medicinal plants as antimalarial agents: a review of work done at Kenya Medical Research Institute Irungu B, Okari E, Nyangi M, Njeru S, Koech L Front Pharmacol 20-Oct-2023
PMCID:PMC10623325
doi:10.3389/fphar.2023.1268924
PMID:37927601
Chimpanzees select comfortable nesting tree species Lacroux C, Krief S, Douady S, Cornette R, Durand S, Aleeje A, Asalu E, Pouydebat E Sci Rep 07-Oct-2023
PMCID:PMC10560204
doi:10.1038/s41598-023-44192-6
PMID:37805595
In Vitro Cercaricidal Activity, Acute Toxicity, and GC/MS Analysis of Some Selected Ghanaian Medicinal Plants Osei-Mensah B, Boakye YD, Anyan WK, Agana TA, Aboagye EA, Bentil I, Lomotey ES, Adu F, Agyare C J Parasitol Res 15-Sep-2023
PMCID:PMC10516696
doi:10.1155/2023/4589424
PMID:37745984
Ethnobotanical study of nutraceutical plants used to manage opportunistic infections associated with HIV/AIDS in Acholi sub-region, Northern Uganda Ikinyom N, Lamwaka AV, Malagala AT, Ndyomugyenyi EK Trop Med Health 01-Sep-2023
PMCID:PMC10472741
doi:10.1186/s41182-023-00540-w
PMID:37658427
Furoquinoline Alkaloids: Insights into Chemistry, Occurrence, and Biological Properties Szewczyk A, Pęczek F Int J Mol Sci 15-Aug-2023
PMCID:PMC10454094
doi:10.3390/ijms241612811
PMID:37628986
Ethnobotanical study of underutilized wild edible plants and threats to their long-term existence in Midakegn District, West Shewa Zone, Central Ethiopia Guzo S, Lulekal E, Nemomissa S J Ethnobiol Ethnomed 14-Jul-2023
PMCID:PMC10347739
doi:10.1186/s13002-023-00601-8
PMID:37452368
Root and branch hydraulic functioning and trait coordination across organs in drought-deciduous and evergreen tree species of a subtropical highland forest Schönauer M, Hietz P, Schuldt B, Rewald B Front Plant Sci 12-Jun-2023
PMCID:PMC10291250
doi:10.3389/fpls.2023.1127292
PMID:37377798

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
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl petroselinate 5362717 Click to see CCCCCCCCCCCC=CCCCCC(=O)OC 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
p-Mentha-1,3,8-triene 176983 Click to see CC1=CC=C(CC1)C(=C)C 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
1-(4-hydroxy-3a-methyl-7-methylidene-2,3,4,5,6,7a-hexahydro-1H-inden-1-yl)-2-methylpropan-1-one 73880654 Click to see CC(C)C(=O)C1CCC2(C1C(=C)CCC2O)C 236.35 unknown https://doi.org/10.1021/NP0106485
Teclenone A 637008 Click to see CC(C)C(=O)C1CCC2(C1C(=C)CCC2O)C 236.35 unknown https://doi.org/10.1021/NP0106485
Teclenone B 10354116 Click to see CC(C)C(=O)C1CCC2(C1C(=C)CCC2O)C 236.35 unknown https://doi.org/10.1021/NP0106485
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
CID 11953937 11953937 Click to see CC=C(C)C(=O)OC1CC(=CCC(C(=CC2C1C(=C)C(=O)O2)C)O)C 346.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Icariside F2 14079045 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)(CO)O 402.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Apiole 10659 Click to see COC1=C2C(=C(C(=C1)CC=C)OC)OCO2 222.24 unknown via CMAUP database
Myristicin 4276 Click to see COC1=CC(=CC2=C1OCO2)CC=C 192.21 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
1-Hydroxy-2,3,6,7-tetramethoxy-10-methylacridin-9-one 163041408 Click to see CN1C2=CC(=C(C=C2C(=O)C3=C(C(=C(C=C31)OC)OC)O)OC)OC 345.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
Arborinine 5281832 Click to see CN1C2=CC=CC=C2C(=O)C3=C(C(=C(C=C31)OC)OC)O 285.29 unknown https://doi.org/10.1002/CHIN.200413167
https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
> Organoheterocyclic compounds / Quinolines and derivatives / Dihydrofuranoquinolines
(2S)-2-(2-hydroxypropan-2-yl)-9-methyl-2,3-dihydrofuro[2,3-b]quinolin-4-one 638263 Click to see CC(C)(C1CC2=C(O1)N(C3=CC=CC=C3C2=O)C)O 259.30 unknown https://doi.org/10.1016/0031-9422(88)83170-4
(3R)-3-hydroxy-2,2,9-trimethyl-3H-furo[2,3-b]quinolin-4-one 162913263 Click to see CC1(C(C2=C(O1)N(C3=CC=CC=C3C2=O)C)O)C 245.27 unknown https://doi.org/10.1016/0031-9422(88)83170-4
3-hydroxy-2,2,9-trimethyl-3H-furo[2,3-b]quinolin-4-one 162913262 Click to see CC1(C(C2=C(O1)N(C3=CC=CC=C3C2=O)C)O)C 245.27 unknown https://doi.org/10.1016/0031-9422(88)83170-4
Isoplatydesmine 11219133 Click to see CC(C)(C1CC2=C(O1)N(C3=CC=CC=C3C2=O)C)O 259.30 unknown https://doi.org/10.1016/0031-9422(88)83170-4
https://doi.org/10.1002/CHIN.200413167
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
(2R)-1-(4,7-dimethoxyfuro[2,3-b]quinolin-6-yl)oxy-3-methoxy-3-methylbutan-2-ol 163033709 Click to see CC(C)(C(COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC)O)OC 361.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
(2R)-1-(4,7-dimethoxyfuro[2,3-b]quinolin-6-yl)oxy-3-methylbutane-2,3-diol 162911907 Click to see CC(C)(C(COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC)O)O 347.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.08.012
(2S)-1-(4,7-dimethoxyfuro[2,3-b]quinolin-6-yl)oxy-3-methoxy-3-methylbutan-2-ol 163033708 Click to see CC(C)(C(COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC)O)OC 361.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
(2S)-1-(4,7-dimethoxyfuro[2,3-b]quinolin-6-yl)oxy-3-methylbutane-2,3-diol 25157866 Click to see CC(C)(C(COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC)O)O 347.40 unknown https://doi.org/10.1016/0031-9422(88)83170-4
(2S)-3-chloro-1-(4,7-dimethoxyfuro[2,3-b]quinolin-6-yl)oxy-3-methylbutan-2-ol 162998818 Click to see CC(C)(C(COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC)O)Cl 365.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
[(2R)-1-(4,7-dimethoxyfuro[2,3-b]quinolin-6-yl)oxy-3-hydroxy-3-methylbutan-2-yl] acetate 38346088 Click to see CC(=O)OC(COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC)C(C)(C)O 389.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.08.012
3-Chloro-1-(4,7-dimethoxyfuro[2,3-b]quinolin-6-yl)oxy-3-methylbutan-2-ol 11428548 Click to see CC(C)(C(COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC)O)Cl 365.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
4,6-Dimethoxy-7-(3-methylbut-2-enoxy)furo[2,3-b]quinoline 13970974 Click to see CC(=CCOC1=C(C=C2C(=C1)N=C3C(=C2OC)C=CO3)OC)C 313.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
https://doi.org/10.1016/0031-9422(88)83170-4
6-[(3,3-Dimethyloxiran-2-yl)methoxy]-4,7-dimethoxyfuro[2,3-b]quinoline 11404711 Click to see CC1(C(O1)COC2=C(C=C3C(=C2)C(=C4C=COC4=N3)OC)OC)C 329.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.023
https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
6-[[(2R)-3,3-dimethyloxiran-2-yl]methoxy]-4,7-dimethoxyfuro[2,3-b]quinoline 163091449 Click to see CC1(C(O1)COC2=C(C=C3C(=C2)C(=C4C=COC4=N3)OC)OC)C 329.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
https://doi.org/10.1016/J.PHYTOCHEM.2004.12.023
7-[(3,3-Dimethyloxiran-2-yl)methoxy]-4,6-dimethoxyfuro[2,3-b]quinoline 11461631 Click to see CC1(C(O1)COC2=C(C=C3C(=C2)N=C4C(=C3OC)C=CO4)OC)C 329.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
7-[[(2R)-3,3-dimethyloxiran-2-yl]methoxy]-4,6-dimethoxyfuro[2,3-b]quinoline 162860005 Click to see CC1(C(O1)COC2=C(C=C3C(=C2)N=C4C(=C3OC)C=CO4)OC)C 329.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
7-[[(2R)-3,3-dimethyloxiran-2-yl]methoxy]-4,8-dimethoxyfuro[2,3-b]quinoline 23629251 Click to see CC1(C(O1)COC2=C(C3=C(C=C2)C(=C4C=COC4=N3)OC)OC)C 329.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
7-[[(2S)-3,3-dimethyloxiran-2-yl]methoxy]-4,8-dimethoxyfuro[2,3-b]quinoline 163035693 Click to see CC1(C(O1)COC2=C(C3=C(C=C2)C(=C4C=COC4=N3)OC)OC)C 329.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
7-Isopentenyloxy-gamma-fagarine 12110169 Click to see CC(=CCOC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC)C 313.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
Anhydroevoxine 161441 Click to see CC1(C(O1)COC2=C(C3=C(C=C2)C(=C4C=COC4=N3)OC)OC)C 329.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
Flindersiamine 68221 Click to see COC1=C2C=COC2=NC3=C(C4=C(C=C31)OCO4)OC 273.24 unknown https://doi.org/10.1016/0031-9422(88)83170-4
https://doi.org/10.1002/CHIN.200413167
Furo[2,3-b]quinoline, 4,6-dimethoxy-8-[(3-methyl-2-butenyl)oxy]- 641762 Click to see CC(=CCOC1=CC(=CC2=C1N=C3C(=C2OC)C=CO3)OC)C 313.30 unknown https://doi.org/10.1002/CHIN.200413167
https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
Kokusagine 5318829 Click to see COC1=C2C=COC2=NC3=C1C=CC4=C3OCO4 243.21 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
https://doi.org/10.1002/CHIN.200413167
Kokusaginine 10227 Click to see COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1016/J.PHYTOL.2011.08.012
https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
Maculine 68232 Click to see COC1=C2C=COC2=NC3=CC4=C(C=C31)OCO4 243.21 unknown https://doi.org/10.1002/CHIN.200413167
https://doi.org/10.1016/0031-9422(88)83170-4
https://doi.org/10.1016/J.PHYTOL.2011.08.012
Methylnkolbisine 11360412 Click to see CC(C)(C(COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC)O)OC 361.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
Nkolbisine 157014 Click to see CC(C)(C(COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC)O)O 347.40 unknown https://doi.org/10.1016/0031-9422(88)83170-4
Pteleine 159650 Click to see COC1=CC2=C(C=C1)N=C3C(=C2OC)C=CO3 229.23 unknown https://doi.org/10.1002/CHIN.200413167
https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1002/CHIN.200413167
https://doi.org/10.1016/J.PHYTOL.2011.08.012
https://doi.org/10.1016/0031-9422(88)83170-4
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
(S)-Edulinine 356087 Click to see CC(C)(C(CC1=C(C2=CC=CC=C2N(C1=O)C)OC)O)O 291.34 unknown https://doi.org/10.1016/0031-9422(88)83170-4
3-[(2S)-2,3-dihydroxy-3-methylbutyl]-4-methoxy-1-methylquinolin-2-one 10902387 Click to see CC(C)(C(CC1=C(C2=CC=CC=C2N(C1=O)C)OC)O)O 291.34 unknown https://doi.org/10.1016/0031-9422(88)83170-4
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
7-methoxy-2,2-dimethyl-6H-pyrano[3,2-c]quinolin-5-one 14166104 Click to see CC1(C=CC2=C(O1)C3=C(C(=CC=C3)OC)NC2=O)C 257.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
Ribalinine 932818 Click to see CC1(C(CC2=C(O1)N(C3=CC=CC=C3C2=O)C)O)C 259.30 unknown https://doi.org/10.1016/0031-9422(88)83170-4
https://doi.org/10.1002/CHIN.200413167
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Isoimperatorin 68081 Click to see CC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Cnidilin 821449 Click to see CC(=CCOC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC)C 300.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-5-hydroxy-2-(4-hydroxyphenyl)-7-(3-methylbut-2-enoxy)-2,3-dihydrochromen-4-one 162842343 Click to see CC(=CCOC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O)C 340.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
5,4'-Dihydroxy-7-O-prenylflavanone 12110170 Click to see CC(=CCOC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O)C 340.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.013
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
6''-Acetylapiin 10531745 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)OC5C(C(CO5)(CO)O)O)O)O 606.50 unknown via CMAUP database
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
Apiin 5280746 Click to see C1C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)(CO)O 564.50 unknown via CMAUP database
Diosmetin 7-O-beta-D-glucopyranoside 11016019 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown via CMAUP database
Graveobioside A 101248035 Click to see C1C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)CO)O)O)O)(CO)O 580.50 unknown via CMAUP database
Malonylapiin 5280803 Click to see C1C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)COC(=O)CC(=O)O)O)O)O)(CO)O 650.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown via CMAUP database

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