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Internal ID UUID644022eb26d0a805729249
Scientific name Uvaria cherrevensis
Authority (Pierre ex Finet & Gagnep.) L.L.Zhou, Y.C.F.Su & R.M.K.Saunders
First published in Syst. Biodivers. 7: 255 (2009)

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Synonyms Top

Scientific name Authority First published in
Ellipeia cherrevensis Pierre ex Finet & Gagnep. Mém. Soc. Bot. France 4: 76 (1906)
Ellipeiopsis cherrevensis (Pierre ex Finet & Gagnep.) R.E.Fr. Ark. Bot. , prepr., a.s., 3: 41 (1953)

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000744955
KEW urn:lsid:ipni.org:names:77101188-1
Open Tree Of Life 1088660
NCBI Taxonomy 672959
IPNI 77101188-1
GBIF 6308635
EOL 303687
CMAUP NPO14742

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Machine Learning and In Vitro Chemical Screening of Potential α-Amylase and α-Glucosidase Inhibitors from Thai Indigenous Plants Srisongkram T, Waithong S, Thitimetharoch T, Weerapreeyakul N Nutrients 09-Jan-2022
PMCID:PMC8781461
doi:10.3390/nu14020267
PMID:35057448
Oxygenated Cyclohexene Derivatives from the Stem and Root Barks of Uvaria pandensis Maeda G, Gilissen PJ, Rudenko A, van der Wal J, Bourgard C, Gupta AK, Sunnerhagen P, Munissi JJ, Nyandoro SS, Erdélyi M J Nat Prod 22-Nov-2021
PMCID:PMC8713284
doi:10.1021/acs.jnatprod.1c00811
PMID:34802242
Crystal structure of 5-[(benzo­yloxy)meth­yl]-5,6-dihy­droxy-4-oxo­cyclo­hex-2-en-1-yl benzoate Leepasert T, Saparpakorn P, Chainok K, Duangthongyou T Acta Crystallogr E Crystallogr Commun 19-Jun-2020
PMCID:PMC7336786
doi:10.1107/S2056989020007793
PMID:32695459

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 / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Pterodonoic acid 11054003 Click to see CC1=C2CC(CCC2(CCC1=O)C)C(=C)C(=O)O 248.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
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 via CMAUP database
Isokaempferide 5280862 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 300.26 unknown via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
4',5,7-Trihydroxy-3,6-dimethoxyflavone 5352032 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 330.29 unknown via CMAUP database
Jaceidin 5464461 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3,4',5,6,7-Pentamethoxyflavone 521171 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC 372.40 unknown via CMAUP database
4'-Hydroxy-3,5,6,7-tetramethoxyflavone 13983731 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)OC)OC 358.30 unknown via CMAUP database
Jaranol 5318869 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 314.29 unknown via CMAUP database
Pachypodol 5281677 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)OC)O 344.30 unknown via CMAUP database
Penduletin 5320462 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)OC 344.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3-Methoxytangeretin 11741814 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)OC 402.40 unknown via CMAUP database

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