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Uvaria angolensis

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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 UUID643ffa1e98167652887230
Scientific name Uvaria angolensis
Authority Welw. ex Oliv.
First published in Fl. Trop. Afr. 1: 23 (1868)

Description Top

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Synonyms Top

Scientific name Authority First published in
Uva angolensis Kuntze Revis. Gen. Pl. 1: 7 (1891)
Uvaria bukobensis Engl. Pflanzenw. Ost-Afrikas , C: 178 (1895)
Uvaria variabilis De Wild. Pl. Bequaert. 1: 461 (1922)

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
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Angola
      • Zambia
    • West Tropical Africa
      • Ivory Coast
      • Nigeria
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Rwanda
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000415894
Tropicos 1601211
KEW urn:lsid:ipni.org:names:75563-1
The Plant List kew-2447595
Open Tree Of Life 614239
NCBI Taxonomy 672961
IUCN Red List 146198634
IPNI 75563-1
iNaturalist 486554
GBIF 3154217
EPPO UVAAN
EOL 1053984

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
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
Lipid composition and antioxidant activities of some underused wild plants seeds from Burundi Niyukuri J, Raiti J, Ntakarutimana V, Hafidi A Food Sci Nutr 01-Nov-2020
PMCID:PMC7802583
doi:10.1002/fsn3.1969
PMID:33473275
Structure-Activity-Relationship and Mechanistic Insights for Anti-HIV Natural Products Kaur R, Sharma P, Gupta GK, Ntie-Kang F, Kumar D Molecules 29-Apr-2020
PMCID:PMC7249135
doi:10.3390/molecules25092070
PMID:32365518
Dihydrochalcones: Methods of Acquisition and Pharmacological Properties—A First Systematic Review Stompor M, Broda D, Bajek-Bil A Molecules 05-Dec-2019
PMCID:PMC6943545
doi:10.3390/molecules24244468
PMID:31817526
A New Benzopyranyl Cadenane Sesquiterpene and Other Antiplasmodial and Cytotoxic Metabolites from Cleistochlamys kirkii Nyandoro SS, Maeda G, Munissi JJ, Gruhonjic A, Fitzpatrick PA, Lindblad S, Duffy S, Pelletier J, Pan F, Puttreddy R, Avery VM, Erdélyi M Molecules 29-Jul-2019
PMCID:PMC6695775
doi:10.3390/molecules24152746
PMID:31362371
Metabolic engineering of Saccharomyces cerevisiae for de novo production of dihydrochalcones with known antioxidant, antidiabetic, and sweet tasting properties Eichenberger M, Lehka BJ, Folly C, Fischer D, Martens S, Simón E, Naesby M Metab Eng 01-Jan-2017
PMCID:PMC5249241
doi:10.1016/j.ymben.2016.10.019
PMID:27810393
Revision of the African genus Uvariastrum (Annonaceae) Couvreur TL PhytoKeys 16-Jan-2014
PMCID:PMC3921557
doi:10.3897/phytokeys.33.5907
PMID:24526846
Massive structural and compositional changes over two decades in forest fragments near Kampala, Uganda Bulafu C, Baranga D, Mucunguzi P, Telford RJ, Vandvik V Ecol Evol 12-Sep-2013
PMCID:PMC3810876
doi:10.1002/ece3.747
PMID:24198941
Chemistry of the Annonaceae, Part 18. Benzylated Indoles and Dihydrochalcones in Uvaria angolensis from Tanzania Ilias Muhammad, Peter G. Waterman American Chemical Society (ACS) 30-May-2007
doi:10.1021/NP50040A009
New Dihydrochalcones and Flavanones From Uvaria Angolensis Charles D. Hufford, Babajide O. Oguntimein American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50021A016
Angoluvarin, an antimicrobial dihydrochalcone from Uvaria angolensis Charles D. Hufford, Babajide O. Oguntimein, James N. Shoolery American Chemical Society (ACS) 12-Mar-2005
doi:10.1021/JO00232A045
Chemistry of the annonaceae. Structures of uvarindoles A—D, four new benzylated indole alkaloids from Uvaria angolensis Peter G. Waterman, Ilias Mohammad Royal Society of Chemistry (RSC) 30-Mar-2004
doi:10.1039/C39840001280
Cytotoxic C-benzylated dihydrochalcones from Uvaria acuminata. Ichimaru M, Nakatani N, Takahashi T, Nishiyama Y, Moriyasu M, Kato A, Mathenge SG, Juma FD, Nganga JN Chem Pharm Bull (Tokyo) 01-Jan-2004
doi:10.1248/CPB.52.138
PMID:14709883
A novel phenanthrenolide and C-benzyl dihydrochalcones from Uvaria puguensis. Makangara JJ, Jonker SA, Nkunya MH Nat Prod Lett 01-Aug-2002
doi:10.1080/10575630290020604
PMID:12168763
Dihydrochalcones from Uvaria angolensis Charles D. Hufford, Babajide O. Oguntimein Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(80)83036-6

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/NP50040A009
> Benzenoids / Benzene and substituted derivatives / Phenethylamines / Amphetamines and derivatives
Uvarindole D 180620 Click to see C1=CC=C(C(=C1)CC2(C(=O)C3=CC=CC=C3N2CC4=CC=CC=C4O)CC5=CC=CC=C5O)O 451.50 unknown https://doi.org/10.1039/C39840001280
https://doi.org/10.1021/NP50040A009
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R)-1-[(1R,3aS,5aR,11aS,11bS)-3a,11a-dimethyl-1,2,3,4,5,5a,6,11b-octahydrocyclopenta[c]xanthen-1-yl]-2-methylpropan-1-ol 162929114 Click to see CC(C)C(C1CCC2(C1C3(C(CC2)CC4=CC=CC=C4O3)C)C)O 328.50 unknown https://doi.org/10.1021/NP50058A009
(1S,10R,13S,16S,17E)-1,13-dimethyl-16-propan-2-yl-2-oxatricyclo[8.8.0.03,8]octadeca-3,5,7,17-tetraen-13-ol 14138736 Click to see CC(C)C1CCC(CCC2CC3=CC=CC=C3OC2(C=C1)C)(C)O 328.50 unknown https://doi.org/10.1021/NP50058A009
1-(3a,11a-Dimethyl-1,2,3,3a,4,5,5a,6,11a,11b-decahydrocyclopenta[c]xanthen-1-yl)-2-methylpropan-1-ol 189475 Click to see CC(C)C(C1CCC2(C1C3(C(CC2)CC4=CC=CC=C4O3)C)C)O 328.50 unknown https://doi.org/10.1021/NP50058A009
Uvarisesquiterpene A 6443359 Click to see CC(C)C1CCC(CCC2CC3=CC=CC=C3OC2(C=C1)C)(C)O 328.50 unknown https://doi.org/10.1021/NP50058A009
Uvarisesquiterpene B 189474 Click to see CC(C)C1=CCC2(CCC3CC4=CC=CC=C4OC3(C2C1)C)C 310.50 unknown https://doi.org/10.1021/NP50058A009
> Organoheterocyclic compounds / Indoles and derivatives / Benzoylindoles
Uvarindole C 185374 Click to see C1=CC=C(C(=C1)CC2=C(NC3=CC=CC=C32)C(=O)C4=CC=CC=C4O)O 343.40 unknown https://doi.org/10.1039/C39840001280
https://doi.org/10.1021/NP50040A009
> Organoheterocyclic compounds / Indoles and derivatives / N-alkylindoles
Phenol, 2,2',2''-1H-indole-1,2,3-triyltris(methylene))tris- 185372 Click to see C1=CC=C(C(=C1)CC2=C(N(C3=CC=CC=C32)CC4=CC=CC=C4O)CC5=CC=CC=C5O)O 435.50 unknown https://doi.org/10.1021/NP50040A009
https://doi.org/10.1039/C39840001280
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(2R)-7-hydroxy-8-[(2-hydroxyphenyl)methyl]-5-methoxy-2-phenyl-2,3-dihydrochromen-4-one 162847252 Click to see COC1=C2C(=O)CC(OC2=C(C(=C1)O)CC3=CC=CC=C3O)C4=CC=CC=C4 376.40 unknown https://doi.org/10.1021/NP50021A016
1-Propanone, 1-(2,4-dihydroxy-3-((2-hydroxyphenyl)methyl)-6-methoxy-5-methylphenyl)-3-phenyl- 158308 Click to see CC1=C(C(=C(C(=C1OC)C(=O)CCC2=CC=CC=C2)O)CC3=CC=CC=C3O)O 392.40 unknown https://doi.org/10.1021/NP50021A016
Angoluvarin 639275 Click to see COC1=C(C(=C(C(=C1)O)CC2=C(C=CC(=C2)CC3=CC=CC=C3O)O)O)C(=O)CCC4=CC=CC=C4 484.50 unknown https://doi.org/10.1021/JO00232A045
Chamuvaritin 100418 Click to see C1C2=CC=CC=C2OC3=C(C(=C(C(=C31)O)C(=O)CCC4=CC=CC=C4)O)CC5=CC=CC=C5O 452.50 unknown https://doi.org/10.1021/NP50040A009
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/10.1080/10575630290020604
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/10.1016/0031-9422(80)83036-6
https://doi.org/10.1248/CPB.52.138
https://doi.org/10.1021/NP50040A009
Uvarindole B 185373 Click to see C1=CC=C(C(=C1)CC2=CC3=C(C=C2)N(C(=C3CC4=CC=CC=C4O)CC5=CC=CC=C5O)CC6=CC=CC=C6O)O 541.60 unknown https://doi.org/10.1021/NP50040A009
https://doi.org/10.1039/C39840001280
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
(2s)-7-Hydroxy-5-methoxy-6,8-dimethyl flavanone 101890693 Click to see CC1=C(C(=C(C2=C1OC(CC2=O)C3=CC=CC=C3)OC)C)O 298.30 unknown https://doi.org/10.1021/NP50021A016
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
Angoletin 131162 Click to see CC1=C(C(=C(C(=C1O)C(=O)CCC2=CC=CC=C2)OC)C)O 300.30 unknown https://doi.org/10.1016/0031-9422(80)83036-6
Uvangoletin 6483649 Click to see COC1=CC(=CC(=C1C(=O)CCC2=CC=CC=C2)O)O 272.29 unknown https://doi.org/10.1016/0031-9422(80)83036-6
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Flavokawain B 5356121 Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=CC=C2)O 284.31 unknown https://doi.org/10.1021/NP50021A016

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