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Tetracera boiviniana

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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 UUID644043bb3770a497498833
Scientific name Tetracera boiviniana
Authority Baill.
First published in Adansonia 7: 300 (1867)

Description Top

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Synonyms Top

No known synonyms.

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-0001045864
Tropicos 10900223
KEW urn:lsid:ipni.org:names:317366-1
The Plant List tro-10900223
Open Tree Of Life 5503421
NCBI Taxonomy 1389779
IUCN Red List 157974
IPNI 317366-1
GBIF 5680727

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
Phytochemicals as Immunomodulatory Molecules in Cancer Therapeutics Paudel S, Mishra N, Agarwal R Pharmaceuticals (Basel) 26-Nov-2023
PMCID:PMC10746110
doi:10.3390/ph16121652
PMID:38139779
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
Ethnobotanical study of plants used by the traditional healers to treat malaria in Mogovolas district, northern Mozambique Manuel L, Bechel A, Noormahomed EV, Hlashwayo DF, Madureira MD Heliyon 18-Dec-2020
PMCID:PMC7753128
doi:10.1016/j.heliyon.2020.e05746
PMID:33364508
A Pentacyclic Triterpene from Ligustrum lucidum Targets γ-Secretase Luo W, Ip FC, Fu G, Cheung K, Tian Y, Hu Y, Sinha A, Cheng EY, Wu X, Bustos V, Greengard P, Li YM, Sinha SC, Ip NY ACS Chem Neurosci 03-Sep-2020
PMCID:PMC8325170
doi:10.1021/acschemneuro.0c00389
PMID:32786303
Targeting DNA Polymerase β for Therapeutic Intervention Goellner EM, Svilar D, Almeida KH, Sobol RW Curr Mol Pharmacol 01-Jan-2012
PMCID:PMC3894524
PMID:22122465
Hypericum lanceolatum (Hypericaceae) as a potential source of new anti-malarial agents: a bioassay-guided fractionation of the stem bark Zofou D, Kowa TK, Wabo HK, Ngemenya MN, Tane P, Titanji VP Malar J 17-Jun-2011
PMCID:PMC3131257
doi:10.1186/1475-2875-10-167
PMID:21682873
Cancer Preventive Agents 9. Betulinic Acid Derivatives as Potent Cancer Chemopreventive Agents Nakagawa-Goto K, Yamada K, Taniguchi M, Tokuda H, Lee KH Bioorg Med Chem Lett 18-May-2009
PMCID:PMC2747314
doi:10.1016/j.bmcl.2009.05.050
PMID:19481937
Screening of Tanzanian medicinal plants for anti-Candida activity Runyoro DK, Matee MI, Ngassapa OD, Joseph CC, Mbwambo ZH BMC Complement Altern Med 30-Mar-2006
PMCID:PMC1481531
doi:10.1186/1472-6882-6-11
PMID:16571139
Biotransformation of the Antimelanoma Agent Betulinic Acid by Bacillus megaterium ATCC 13368 Chatterjee P, Kouzi SA, Pezzuto JM, Hamann MT Appl Environ Microbiol 01-Sep-2000
PMCID:PMC92230
doi:10.1128/aem.66.9.3850-3855.2000
PMID:10966400
DNA polymerase beta inhibitors from Tetracera boiviniana. Ma J, Starck SR, Hecht SM J Nat Prod 01-Dec-1999
doi:10.1021/NP990326P
PMID:10654414

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 / Triterpenoids
(4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-11-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-(3-phenylprop-2-enoyloxy)-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 163035428 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=CC=C6)O)C)C)C2C1)C)C(=O)O)C 602.80 unknown https://doi.org/10.1021/NP990326P
11-Hydroxy-10-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 75110902 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1)C)C(=O)O)C 618.80 unknown https://doi.org/10.1021/NP990326P
3-beta-O-(cis-p-Coumaroyl)maslinic acid 101001054 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1)C)C(=O)O)C 618.80 unknown https://doi.org/10.1021/NP990326P
3-beta-O-(trans-p-Coumaroyl)maslinic acid 14335962 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1)C)C(=O)O)C 618.80 unknown https://doi.org/10.1021/NP990326P
3-cis-p-Coumaroyl maslinic acid 16664518 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=CC=C6)O)C)C)C2C1)C)C(=O)O)C 602.80 unknown https://doi.org/10.1021/NP990326P
3-trans-p-Coumaroyl maslinic acid 16664517 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=CC=C6)O)C)C)C2C1)C)C(=O)O)C 602.80 unknown https://doi.org/10.1021/NP990326P
9-Hydroxy-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-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1021/NP990326P
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 https://doi.org/10.1021/NP990326P

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