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Uvaria kirkii

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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 UUID644046b9a0df6758921142
Scientific name Uvaria kirkii
Authority Oliv. ex Hook.f.
First published in Bot. Mag. 98: t. 6006 (1872)

Description Top

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Synonyms Top

Scientific name Authority First published in
Uvaria stuhlmannii Engl. Pflanzenw. Ost-Afrikas , C: 178 (1895)

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
    • South Tropical Africa
      • Mozambique

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001066196
Tropicos 1601765
KEW urn:lsid:ipni.org:names:75754-1
The Plant List tro-1601765
Open Tree Of Life 3867890
NCBI Taxonomy 2588161
IUCN Red List 158124
IPNI 75754-1
iNaturalist 444562
GBIF 3154309
EOL 304987
CMAUP NPO18276

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
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
Predicting the potential impacts of climate change on the endangered endemic annonaceae species in east africa Mkala EM, Mwanzia V, Nzei J, Oluoch WA, Ngarega BK, Wanga VO, Oulo MA, Ngarega BK, Munyao F, Kilingo FM, Rono P, Waswa EN, Mutinda ES, Ochieng CO, Mwachala G, Hu GW, Wang QF, Katunge JK, Victoire CI Heliyon 21-Jun-2023
PMCID:PMC10320037
doi:10.1016/j.heliyon.2023.e17405
PMID:37416643
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
Aboveground Carbon Storage and Its Links to Stand Structure, Tree Diversity and Floristic Composition in South-Eastern Tanzania McNicol IM, Ryan CM, Dexter KG, Ball SM, Williams M Ecosystems 06-Sep-2017
PMCID:PMC6438643
doi:10.1007/s10021-017-0180-6
PMID:30996655
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
7-Methuljuglone, Diuvaretin, and Benzyl Benzoates from the Root Bark of Uvaria kirkii M. H. H. Nkunya American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50042A028

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 / 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/10.1021/NP50042A028
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
Benzyl 2-methoxybenzoate 584904 Click to see COC1=CC=CC=C1C(=O)OCC2=CC=CC=C2 242.27 unknown https://doi.org/10.1021/NP50042A028
> Benzenoids / Naphthalenes / Naphthoquinones
7-Methyljuglone 26905 Click to see CC1=CC2=C(C(=O)C=CC2=O)C(=C1)O 188.18 unknown https://doi.org/10.1021/NP50042A028
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol 68171 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCO 382.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3beta-Acetoxytaraxasterane-20-ene-22-one 100936445 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(=O)C=C1C)C)C)C)(C)C)OC(=O)C)C 482.70 unknown via CMAUP database
alpha-Amyrenyl acetate 92842 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 468.80 unknown via CMAUP database
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
beta-Amyrone 12306160 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
methyl (1R,3aS,5aR,5bR,7aR,9S,10R,11aR,11bR,13aR,13bR)-9,10-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 21672694 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C(=O)OC 486.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
Diuvaretin 3085222 Click to see COC1=C(C(=C(C(=C1C(=O)CCC2=CC=CC=C2)O)CC3=CC=CC=C3O)O)CC4=CC=CC=C4O 484.50 unknown https://doi.org/10.1021/NP50042A028
Uvaretin 73447 Click to see COC1=C(C(=C(C(=C1)O)CC2=CC=CC=C2O)O)C(=O)CCC3=CC=CC=C3 378.40 unknown https://doi.org/10.1021/NP50042A028
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Kaempferol 3-neohesperidoside 5318761 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O 594.50 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database

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