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Internal ID UUID643fe29fa49cf302773022
Scientific name Maprounea africana
Authority Müll.Arg.
First published in Prodr. 15(2): 1191 (1866)

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Synonyms Top

Scientific name Authority First published in
Maprounea africana var. benguelensis Pax & K.Hoffm. Pflanzenr. IV, 147, V: 180. 1912
Maprounea africana var. cinnamomea Pax & K.Hoffm. Pflanzenr. IV, 147, V: 179. 1912
Maprounea africana var. leucosperma Pax & K.Hoffm. Pflanzenr. IV, 147, V: 179. 1912
Maprounea africana var. obtusa (Pax) Pax & K.Hoffm. Pflanzenr. IV, 147, V: 180. 1912
Maprounea africana var. orientalis Pax & K.Hoffm. Pflanzenr. IV, 147, V: 179. 1912

Common names Top

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Language Common/alternative name
Chinese 非洲头序桕

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Maprounea africana var. africana Unknown
Maprounea africana var. gracilis Pax & K.Hoffm. Pflanzenr. , IV, 147, V: 179 (1912)

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Tanzania
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Caprivi Strip
    • West Tropical Africa
      • Benin
      • Nigeria
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000236256
Tropicos 12803117
KEW urn:lsid:ipni.org:names:352049-1
The Plant List kew-120517
Open Tree Of Life 210323
NCBI Taxonomy 316848
IPNI 352049-1
iNaturalist 589646
GBIF 3054670
EOL 1154530

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
Use of Multi-Date and Multi-Spectral UAS Imagery to Classify Dominant Tree Species in the Wet Miombo Woodlands of Zambia Shamaoma H, Chirwa PW, Zekeng JC, Ramoelo A, Hudak AT, Handavu F, Syampungani S Sensors (Basel) 16-Feb-2023
PMCID:PMC9960281
doi:10.3390/s23042241
PMID:36850838
The Main Protease of SARS-CoV-2 as a Target for Phytochemicals against Coronavirus Issa SS, Sokornova SV, Zhidkin RR, Matveeva TV Plants (Basel) 17-Jul-2022
PMCID:PMC9319234
doi:10.3390/plants11141862
PMID:35890496
Antidiabetic Medicinal Plants Used in Democratic Republic of Congo: A Critical Review of Ethnopharmacology and Bioactivity Data Kasali FM, Kadima JN, Peter EL, Mtewa AG, Ajayi CO, Tusiimire J, Tolo CU, Ogwang PE, Weisheit A, Agaba AG Front Pharmacol 27-Oct-2021
PMCID:PMC8579071
doi:10.3389/fphar.2021.757090
PMID:34776975
Emerging paradigms of viral diseases and paramount role of natural resources as antiviral agents Sagaya Jansi R, Khusro A, Agastian P, Alfarhan A, Al-Dhabi NA, Arasu MV, Rajagopal R, Barcelo D, Al-Tamimi A Sci Total Environ 07-Nov-2020
PMCID:PMC7833357
doi:10.1016/j.scitotenv.2020.143539
PMID:33234268
Evaluation of Antimycobacterial and Synergistic Activity of Plants Selected Based on Cheminformatic Parameters Rahgozar N, Khaniki GB, Sardari S Iran Biomed J 01-Nov-2018
PMCID:PMC6305812
doi:10.29252/.22.6.401
PMID:29510602
First large-scale ethnobotanical survey in the province of Uíge, northern Angola Lautenschläger T, Monizi M, Pedro M, Mandombe JL, Bránquima MF, Heinze C, Neinhuis C J Ethnobiol Ethnomed 25-Jul-2018
PMCID:PMC6060550
doi:10.1186/s13002-018-0238-3
PMID:30045744
Ethnobotanical survey of herbs used in the management of diabetes mellitus in Southern Katanga Area/DR Congo Amuri B, Maseho M, Simbi L, Duez P, Byanga K Pan Afr Med J 18-Jul-2018
PMCID:PMC6294981
doi:10.11604/pamj.2018.30.218.11718
PMID:30574237
Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J Int J Mol Sci 14-May-2018
PMCID:PMC5983620
doi:10.3390/ijms19051459
PMID:29757986
Recent progress in the antiviral activity and mechanism study of pentacyclic triterpenoids and their derivatives Xiao S, Tian Z, Wang Y, Si L, Zhang L, Zhou D Med Res Rev 19-Jan-2018
PMCID:PMC7168445
doi:10.1002/med.21484
PMID:29350407
Bershacolone, an unprecedented diterpene cyclobutene from Maprounea africana Matthew W. Bernart, Yoel Kashman, Mark Tischler, John H. Cardellina, Michael R. Boyd Elsevier BV 25-Jul-2002
doi:10.1016/0040-4039(93)88059-R
Role of Human Immunodeficiency Virus (HIV) Type 1 Envelope in the Anti-HIV Activity of the Betulinic Acid Derivative IC9564 Holz-Smith SL, Sun IC, Jin L, Matthews TJ, Lee KH, Chen CH Antimicrob Agents Chemother 01-Jan-2001
PMCID:PMC90240
doi:10.1128/AAC.45.1.60-66.2001
PMID:11120945
Natural Products as Antiviral Agents El Sayed KA 01-Jan-2000
PMCID:PMC7147881
doi:10.1016/S1572-5995(00)80051-4
Plant Products as Antimicrobial Agents Cowan MM Clin Microbiol Rev 01-Oct-1999
PMCID:PMC88925
doi:10.1128/cmr.12.4.564
PMID:10515903
Maprouneacin, a new daphnane diterpenoid with potent antihyperglycemic activity from Maprounea africana. Carney JR, Krenisky JM, Williamson RT, Luo J, Carlson TJ, Hsu VL, Moswa JL J Nat Prod 01-Feb-1999
doi:10.1021/NP980356C
PMID:10075783
A reinvestigation of Maprounea triterpenes. Beutler JA, Kashman Y, Tischler M, Cardellina JH 2nd, Gray GN, Currens MJ, Wall ME, Wani MC, Boyd MR J Nat Prod 01-Jul-1995
doi:10.1021/NP50121A008
PMID:7561897

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 / Diterpenoids / Cembrane diterpenoids
(1R,2Z,6Z,10Z)-8-Hydroxy-3,7,11,15,15-pentamethylbicyclo[12.1.0]pentadeca-2,6,10-triene-4,9-dione 6444299 Click to see CC1=CC(=O)C(C(=CCC(=O)C(=CC2C(C2(C)C)CC1)C)C)O 316.40 unknown https://doi.org/10.1021/NP50105A020
https://doi.org/10.1021/NP50121A008
Koumbalone A 5469801 Click to see CC1=CC(=O)C(C(=CCC(=O)C(=CC2C(C2(C)C)CC1)C)C)O 316.40 unknown https://doi.org/10.1021/NP50121A008
https://doi.org/10.1021/NP50105A020
Koumbalone B 5469802 Click to see 316.40 unknown https://doi.org/10.1021/NP50105A020
https://doi.org/10.1021/NP50121A008
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(4aS,6aR,6bR,8aR,10S,12aR,14aS,14bR)-10-hydroxy-2,2,6b,9,9,12a,14a-heptamethyl-1,3,4,5,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydropicene-4a-carboxylic acid 637268 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C(=O)O)C 456.70 unknown https://doi.org/10.1021/NP50115A001
https://doi.org/10.1021/NP50028A019
Aleuritolic Acid 161527 Click to see 456.70 unknown https://doi.org/10.1021/NP50115A001
https://doi.org/10.1021/NP50028A019
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Maprounic acid B805169K075 338181 Click to see 456.70 unknown https://doi.org/10.1021/NP50028A019
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(1R,4E,7S,8E,10R,11R,13R)-7-hydroxy-10-(hydroxymethyl)-4,8,11,15-tetramethylbicyclo[11.2.0]pentadeca-4,8,14-trien-6-one 162903381 Click to see 318.40 unknown https://doi.org/10.1016/0040-4039(93)88059-R
7-Hydroxy-10-(hydroxymethyl)-4,8,11,15-tetramethylbicyclo[11.2.0]pentadeca-4,8,14-trien-6-one 3481814 Click to see 318.40 unknown https://doi.org/10.1016/0040-4039(93)88059-R
Bershacolone 5469800 Click to see CC1CC2C=C(C2CCC(=CC(=O)C(C(=CC1CO)C)O)C)C 318.40 unknown https://doi.org/10.1021/NP50121A008
https://doi.org/10.1016/0040-4039(93)88059-R
> Organoheterocyclic compounds / Dioxepanes / 1,3-dioxepanes
[(1S,2R,6S,7S,8R,10S,11S,12R,14S,16S,17S,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4-methyl-17-(3-methylbutanoyloxy)-16-[(2R)-2-methyloxiran-2-yl]-14-[(1E,3E)-nona-1,3-dienyl]-5-oxo-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-18-yl]methyl 3-methylbutanoate 162970647 Click to see CCCCCC=CC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C7(CO7)C)OC(=O)CC(C)C)COC(=O)CC(C)C)C=C(C6=O)C)O)O)CO 744.90 unknown https://doi.org/10.1021/NP980356C
[(2R,7S,8R,10S,11S,12R,14S,16S,17S,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4-methyl-17-(3-methylbutanoyloxy)-16-[(2R)-2-methyloxiran-2-yl]-14-[(1E,3E)-nona-1,3-dienyl]-5-oxo-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-18-yl]methyl 3-methylbutanoate 163186079 Click to see 744.90 unknown https://doi.org/10.1021/NP980356C
[6,7-Dihydroxy-8-(hydroxymethyl)-4-methyl-17-(3-methylbutanoyloxy)-16-(2-methyloxiran-2-yl)-14-nona-1,3-dienyl-5-oxo-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-18-yl]methyl 3-methylbutanoate 74030552 Click to see 744.90 unknown https://doi.org/10.1021/NP980356C
Maprouneacin 44558999 Click to see 744.90 unknown https://doi.org/10.1021/NP980356C

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