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Uvaria scheffleri

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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 UUID644046ba7fa98065823009
Scientific name Uvaria scheffleri
Authority Diels
First published in Bot. Jahrb. Syst. 41: 329 (1908)

Description Top

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Synonyms Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001066238
Tropicos 1601908
KEW urn:lsid:ipni.org:names:75922-1
The Plant List tro-1601908
Open Tree Of Life 3867785
NCBI Taxonomy 2588162
IPNI 75922-1
GBIF 3154338
EOL 304969
Elurikkus 366549

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
Antifungal Constituents of Piper crocatum and Their Activities as Ergosterol Biosynthesis Inhibitors Discovered via In Silico Study Using ADMET and Drug-Likeness Analysis Siswina T, Rustama MM, Sumiarsa D, Apriyanti E, Dohi H, Kurnia D Molecules 22-Nov-2023
PMCID:PMC10708292
doi:10.3390/molecules28237705
PMID:38067436
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
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
Antiplasmodial, antimalarial activities and toxicity of African medicinal plants: a systematic review of literature Tajbakhsh E, Kwenti TE, Kheyri P, Nezaratizade S, Lindsay DS, Khamesipour F Malar J 25-Aug-2021
PMCID:PMC8390284
doi:10.1186/s12936-021-03866-0
PMID:34433465
Antimicrobial Activity, in silico Molecular Docking, ADMET and DFT Analysis of Secondary Metabolites from Roots of Three Ethiopian Medicinal Plants Anza M, Endale M, Cardona L, Cortes D, Eswaramoorthy R, Zueco J, Rico H, Trelis M, Abarca B Adv Appl Bioinform Chem 20-Aug-2021
PMCID:PMC8384431
doi:10.2147/AABC.S323657
PMID:34447254
Conservation of Wild Food Plants and Their Potential for Combatting Food Insecurity in Kenya as Exemplified by the Drylands of Kitui County Mutie FM, Rono PC, Kathambi V, Hu GW, Wang QF Plants (Basel) 12-Aug-2020
PMCID:PMC7464302
doi:10.3390/plants9081017
PMID:32806636
Plants Used in Antivenom Therapy in Rural Kenya: Ethnobotany and Future Perspectives Omara T J Toxicol 16-Jun-2020
PMCID:PMC7315313
doi:10.1155/2020/1828521
PMID:32612650
Antimalarial Plants Used across Kenyan Communities Omara T Evid Based Complement Alternat Med 12-Jun-2020
PMCID:PMC7306085
doi:10.1155/2020/4538602
PMID:32617107
Anti-Fungal Efficacy and Mechanisms of Flavonoids Al Aboody MS, Mickymaray S Antibiotics (Basel) 26-Jan-2020
PMCID:PMC7168129
doi:10.3390/antibiotics9020045
PMID:31991883
Mannich base-connected syntheses mediated by ortho-quinone methides Barta P, Fülöp F, Szatmári I Beilstein J Org Chem 06-Mar-2018
PMCID:PMC5852458
doi:10.3762/bjoc.14.43
PMID:29623118
Medicinal Plants for the Treatment of Local Tissue Damage Induced by Snake Venoms: An Overview from Traditional Use to Pharmacological Evidence Félix-Silva J, Silva-Junior AA, Zucolotto SM, Fernandes-Pedrosa MD Evid Based Complement Alternat Med 21-Aug-2017
PMCID:PMC5585606
doi:10.1155/2017/5748256
PMID:28904556
Chalcone: A Privileged Structure in Medicinal Chemistry Zhuang C, Zhang W, Sheng C, Zhang W, Xing C, Miao Z Chem Rev 10-May-2017
PMCID:PMC6131713
doi:10.1021/acs.chemrev.7b00020
PMID:28488435
The potential of anti-malarial compounds derived from African medicinal plants, part II: a pharmacological evaluation of non-alkaloids and non-terpenoids Ntie-Kang F, Onguéné PA, Lifongo LL, Ndom JC, Sippl W, Mbaze LM Malar J 06-Mar-2014
PMCID:PMC3975711
doi:10.1186/1475-2875-13-81
PMID:24602358
Underestimating the Toxicological Challenges Associated with the Use of Herbal Medicinal Products in Developing Countries Neergheen-Bhujun VS Biomed Res Int 19-Sep-2013
PMCID:PMC3791562
doi:10.1155/2013/804086
PMID:24163821
Ethnodiagnostic Skills of the Digo Community for Malaria: A Lead to Traditional Bioprospecting Nguta JM, Mbaria JM, Gathumbi PK, Gakuya D, Kabasa JD, Kiama SG Front Pharmacol 24-Jun-2011
PMCID:PMC3125516
doi:10.3389/fphar.2011.00030
PMID:21738507

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
> Alkaloids and derivatives / Aporphines
Lanuginosine 97622 Click to see COC1=CC2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O 305.30 unknown https://doi.org/10.1007/S11418-009-0358-0
Oxoanolobine 135985965 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=C3C=CC(=C5)O 291.26 unknown https://doi.org/10.1007/S11418-009-0358-0
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Benzyl Benzoate 2345 Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2 212.24 unknown https://doi.org/10.1016/0031-9422(90)85438-L
https://doi.org/10.1007/S11418-009-0358-0
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2,4-Dimethoxy-6-methyl-3-propan-2-yl-phenol 178272 Click to see CC1=CC(=C(C(=C1O)OC)C(C)C)OC 210.27 unknown https://doi.org/10.1007/S11418-009-0358-0
https://doi.org/10.1016/J.PHYTOCHEM.2003.10.011
Hydroxyespintanol 16085790 Click to see CC(C)C1=C(C=C(C(=C1OC)O)CO)OC 226.27 unknown https://doi.org/10.1007/S11418-009-0358-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
3-(3,7,11-trimethyldodeca-2,6,10-trienyl)-1H-indole 366505 Click to see CC(=CCCC(=CCCC(=CCC1=CNC2=CC=CC=C21)C)C)C 321.50 unknown https://doi.org/10.1016/0031-9422(90)85438-L
3-Farnesylindole 49768248 Click to see CC(=CCCC(=CCCC(=CCC1CNC2=CC=CC=C12)C)C)C 323.50 unknown https://doi.org/10.1016/0031-9422(90)85438-L
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
5-Glutinen-3-ol 12309493 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(90)85438-L
Glutinol 9932254 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(90)85438-L
https://doi.org/10.1016/J.PHYTOCHEM.2003.10.011
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.10.011
https://doi.org/10.1016/0031-9422(90)85438-L
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(90)85438-L
https://doi.org/10.1016/J.PHYTOCHEM.2003.10.011
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.10.011
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
4-[6-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-3-hydroxybenzoic acid 85363635 Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(C=C(C=C3)C(=O)O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1007/S11418-009-0358-0
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Quinomethanes / O-quinomethanes
(2Z,6R)-6-hydroxy-2-[(E)-1-hydroxy-3-phenylprop-2-enylidene]-5-methoxy-6-methylcyclohex-4-ene-1,3-dione 163193836 Click to see CC1(C(=CC(=O)C(=C(C=CC2=CC=CC=C2)O)C1=O)OC)O 300.30 unknown https://doi.org/10.1007/S11418-009-0358-0
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes
(2S,4'aS,9'aS)-3',4'a,5',6,7',8-hexamethoxy-4',6',7-tri(propan-2-yl)spiro[3,4-dihydrochromene-2,1'-9,9a-dihydroxanthene]-2'-one 163044836 Click to see CC(C)C1=C(C=C2CCC3(C4CC5=CC(=C(C(=C5OC4(C(=C(C3=O)OC)C(C)C)OC)OC)C(C)C)OC)OC2=C1OC)OC 624.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.10.011
3',4'a,5',6,7',8-Hexamethoxy-4',6',7-tri(propan-2-yl)spiro[3,4-dihydrochromene-2,1'-9,9a-dihydroxanthene]-2'-one 5246770 Click to see CC(C)C1=C(C=C2CCC3(C4CC5=CC(=C(C(=C5OC4(C(=C(C3=O)OC)C(C)C)OC)OC)C(C)C)OC)OC2=C1OC)OC 624.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.10.011
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(2,6-dihydroxy-3,4-dimethoxyphenyl)-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 14585490 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C(=C(C=C2O)OC)OC)O)C3=CC=CC=C3 436.50 unknown https://doi.org/10.1016/0031-9422(90)85438-L
(2,6-dihydroxy-3,4-dimethoxyphenyl)-[(1R,5R,6R)-4-methyl-5-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 14585492 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C(=C(C=C3O)OC)OC)O 436.50 unknown https://doi.org/10.1016/0031-9422(90)85438-L
(2,6-dihydroxy-3,4-dimethoxyphenyl)-[(1S,2S,6S)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 101533038 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C(=C(C=C2O)OC)OC)O)C3=CC=CC=C3 436.50 unknown https://doi.org/10.1016/0031-9422(90)85438-L
(2,6-Dihydroxy-3,4-dimethoxyphenyl)-[3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 14585489 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C(=C(C=C2O)OC)OC)O)C3=CC=CC=C3 436.50 unknown https://doi.org/10.1016/0031-9422(90)85438-L
(2,6-Dihydroxy-3,4-dimethoxyphenyl)-[4-methyl-5-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 14585491 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C(=C(C=C3O)OC)OC)O 436.50 unknown https://doi.org/10.1016/0031-9422(90)85438-L
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2S)-5,7,8-trimethoxy-2-phenyl-2,3-dihydrochromen-4-one 162930791 Click to see COC1=CC(=C(C2=C1C(=O)CC(O2)C3=CC=CC=C3)OC)OC 314.30 unknown https://doi.org/10.1007/S11418-009-0358-0
(S)-5-Hydroxy-7,8-dimethoxy-2-phenylchroman-4-one 13963771 Click to see COC1=C(C2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)O)OC 300.30 unknown https://doi.org/10.1007/S11418-009-0358-0
5-Hydroxy-7,8-dimethoxyflavanone 13963770 Click to see COC1=C(C2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)O)OC 300.30 unknown https://doi.org/10.1007/S11418-009-0358-0
5,7,8-Trimethoxyflavanone 15380425 Click to see COC1=CC(=C(C2=C1C(=O)CC(O2)C3=CC=CC=C3)OC)OC 314.30 unknown https://doi.org/10.1007/S11418-009-0358-0
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2-Hydroxy-3,4,6-trimethoxyphenyl)-3-phenylprop-2-en-1-one 227450 Click to see COC1=CC(=C(C(=C1C(=O)C=CC2=CC=CC=C2)O)OC)OC 314.30 unknown https://doi.org/10.1007/S11418-009-0358-0
https://doi.org/10.1016/0031-9422(90)85438-L
2'-Hydroxy-3',4',6'-trimethoxychalcone 5354780 Click to see COC1=CC(=C(C(=C1C(=O)C=CC2=CC=CC=C2)O)OC)OC 314.30 unknown https://doi.org/10.1007/S11418-009-0358-0
https://doi.org/10.1016/0031-9422(90)85438-L

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