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Macaranga barteri

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fe1ed49799089974284
Scientific name Macaranga barteri
Authority Müll.Arg.
First published in Flora 47: 535 (1864)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Macaranga heudelotii var. nitida Beille Mém. Soc. Bot. France 8: 79. 1908
Macaranga lancifolia Pax Bot. Jahrb. Syst. 43: 322 (1909)
Macaranga rowlandii Prain Bull. Misc. Inform. Kew 1910: 127 (1910)
Macaranga heudelotii A.Chev. Acta Hydrobiol. 1: 69x 1860-1861

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
      • Uganda
    • West Tropical Africa
      • Benin
      • Ghana
      • Guinea
      • Ivory Coast
      • Liberia
      • Nigeria
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Equatorial Guinea
      • Gabon
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000231826
Tropicos 12804194
KEW urn:lsid:ipni.org:names:351045-1
The Plant List kew-116322
Open Tree Of Life 289755
Observations.org 327725
NCBI Taxonomy 396451
IUCN Red List 144271689
IPNI 351045-1
iNaturalist 735245
GBIF 3074515
EOL 1155468
Elurikkus 363442

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
Nature’s Green Potential: Anticancer Properties of Plants of the Euphorbiaceae Family Jiménez-González V, Kowalczyk T, Piekarski J, Szemraj J, Rijo P, Sitarek P Cancers (Basel) 25-Dec-2023
PMCID:PMC10778523
doi:10.3390/cancers16010114
PMID:38201542
Ethnobotanical and ethnopharmacological survey of medicinal tree species used in the treatment of diseases by forest-fringe communities of Southwestern Ghana Asigbaase M, Adusu D, Musah AA, Anaba L, Nsor CA, Abugre S, Derkyi M Heliyon 14-Dec-2023
PMCID:PMC10788458
doi:10.1016/j.heliyon.2023.e23645
PMID:38226220
Pharmacological targeting of gastric mucosal barrier with traditional Chinese medications for repairing gastric mucosal injury Jia X, He Y, Li L, Xu D Front Pharmacol 08-Jun-2023
PMCID:PMC10285076
doi:10.3389/fphar.2023.1091530
PMID:37361204
Phytochemistry and pharmacology of natural prenylated flavonoids Lv HW, Wang QL, Luo M, Zhu MD, Liang HM, Li WJ, Cai H, Zhou ZB, Wang H, Tong SQ, Li XN Arch Pharm Res 14-Apr-2023
PMCID:PMC10101826
doi:10.1007/s12272-023-01443-4
PMID:37055613
Selective and clear-cut logging have varied imprints on tree community structure in a moist semi-deciduous forest in Ghana Addo-Fordjour P, Afram IS, Oppong J Heliyon 04-Nov-2022
PMCID:PMC9649955
doi:10.1016/j.heliyon.2022.e11393
PMID:36387494
West African medicinal plants and their constituent compounds as treatments for viral infections, including SARS-CoV-2/COVID-19 Popoola TD, Segun PA, Ekuadzi E, Dickson RA, Awotona OR, Nahar L, Sarker SD, Fatokun AA Daru 27-Apr-2022
PMCID:PMC9043090
doi:10.1007/s40199-022-00437-9
PMID:35476297
Sub-acute toxicity study on hydromethanolic leaves extract of Combretum hypopilinum (Combretaceae) Diels in Wistar rats Ahmad MH, Zezi AU, Anafi SB, Alshargi OY, Mohammed M, Mustapha S, Bala AA, Muhammad S, Julde SM, Wada AS, Jatau AI Toxicol Res 19-Apr-2022
PMCID:PMC9532474
doi:10.1007/s43188-022-00133-5
PMID:36277361
Molecular modelling identification of phytocompounds from selected African botanicals as promising therapeutics against druggable human host cell targets of SARS-CoV-2 Uhomoibhi JO, Shode FO, Idowu KA, Sabiu S J Mol Graph Model 12-Apr-2022
PMCID:PMC9002601
doi:10.1016/j.jmgm.2022.108185
PMID:35430474
Ethnobotanical Survey of Local Flora Used for Medicinal Purposes among Indigenous People in Five Areas in Lagos State, Nigeria Lawal IO, Rafiu BO, Ale JE, Majebi OE, Aremu AO Plants (Basel) 25-Feb-2022
PMCID:PMC8912796
doi:10.3390/plants11050633
PMID:35270103
Antiviral plant‐derived natural products to combat RNA viruses: Targets throughout the viral life cycle Owen L, Laird K, Shivkumar M Lett Appl Microbiol 25-Jan-2022
PMCID:PMC9544774
doi:10.1111/lam.13637
PMID:34953146
Wandering through southwestern Nigeria: An inventory of Yoruba useful angiosperm plants Ajao AA, Mukaila YO, Sabiu S Heliyon 25-Dec-2021
PMCID:PMC8733184
doi:10.1016/j.heliyon.2021.e08668
PMID:35024488
Potential Benefits of Antiviral African Medicinal Plants in the Management of Viral Infections: Systematic Review Beressa TB, Deyno S, Mtewa AG, Aidah N, Tuyiringire N, Lukubye B, Weisheit A, Tolo CU, Ogwang PE Front Pharmacol 24-Dec-2021
PMCID:PMC8740180
doi:10.3389/fphar.2021.682794
PMID:35002686
Structure, composition and diversity of restored forest ecosystems on mine-spoils in South-Western Ghana Nero BF PLoS One 14-Jun-2021
PMCID:PMC8202926
doi:10.1371/journal.pone.0252371
PMID:34125836
African Herbal Medicines: Adverse Effects and Cytotoxic Potentials with Different Therapeutic Applications Okaiyeto K, Oguntibeju OO Int J Environ Res Public Health 02-Jun-2021
PMCID:PMC8199769
doi:10.3390/ijerph18115988
PMID:34199632
Antiviral Activity Exerted by Natural Products against Human Viruses Musarra-Pizzo M, Pennisi R, Ben-Amor I, Mandalari G, Sciortino MT Viruses 04-May-2021
PMCID:PMC8147851
doi:10.3390/v13050828
PMID:34064347

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1021/NP8004634
https://doi.org/10.1055/S-0031-1273555
Methylgallic acid 20223962 Click to see CC1=C(C(=C(C=C1C(=O)O)O)O)O 184.15 unknown https://doi.org/10.1055/S-0031-1273555
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl Gallate 7428 Click to see 184.15 unknown https://doi.org/10.1021/NP8004634
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1055/S-0031-1273555
https://doi.org/10.1021/NP8004634
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(1,2,2,3,3,7,10,21,22,23,26,27,28,42,43-Pentadecahydroxy-13,18,31,39-tetraoxo-5,9,14,17,32,35,38,47-octaoxadecacyclo[42.2.1.04,12.06,10.012,46.015,34.016,37.019,24.025,30.040,45]heptatetraconta-19,21,23,25,27,29,40,42,44-nonaen-36-yl) 2,3,4-trihydroxybenzoate 162997997 Click to see 1102.80 unknown https://doi.org/10.1021/NP8004634
[(1R,4S,6S,7R,10S,12R,15R,16S,34R,36S,37R,46R)-1,2,2,3,3,7,10,21,22,23,26,27,28,42,43-pentadecahydroxy-13,18,31,39-tetraoxo-5,9,14,17,32,35,38,47-octaoxadecacyclo[42.2.1.04,12.06,10.012,46.015,34.016,37.019,24.025,30.040,45]heptatetraconta-19,21,23,25,27,29,40,42,44-nonaen-36-yl] 2,3,4-trihydroxybenzoate 163193625 Click to see C1C(C2C(O1)(CC34C5C6=C(C(=C(C=C6C(=O)OC7C8C(C(COC(=O)C9=CC(=C(C(=C9C1=C(C(=C(C=C1C(=O)O8)O)O)O)O)O)O)OC7OC(=O)C1=C(C(=C(C=C1)O)O)O)OC3=O)O)O)OC5(C(C(C4O2)(O)O)(O)O)O)O)O 1102.80 unknown https://doi.org/10.1021/NP8004634
[(1R,4S,6S,7S,10S,15R,16S,34R,36S,37R)-1,2,2,3,3,7,10,21,22,23,26,27,28,42,43-pentadecahydroxy-13,18,31,39-tetraoxo-9,14,17,32,35,38,47-heptaoxadecacyclo[42.2.1.04,12.06,10.012,46.015,34.016,37.019,24.025,30.040,45]heptatetraconta-19,21,23,25,27,29,40,42,44-nonaen-36-yl] 3,4,5-trihydroxybenzoate 45481550 Click to see 1100.80 unknown https://doi.org/10.1021/NP8004634
3-O-methyl-4-O-(beta-D-xylopyranosyl) ellagic acid 25156981 Click to see 448.30 unknown https://doi.org/10.1021/NP8004634
3-O-methylellagic acid 13915428 Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O)O 316.22 unknown https://doi.org/10.1021/NP8004634
6,7-Dihydroxy-14-methoxy-13-(3,4,5-trihydroxyoxan-2-yl)oxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione 162909069 Click to see 448.30 unknown https://doi.org/10.1021/NP8004634
Ellagic Acid 5281855 Click to see 302.19 unknown https://doi.org/10.1021/NP8004634
https://doi.org/10.1055/S-0031-1273555
Macabarterin 70697897 Click to see C1C(C2C(O1)(CC34C5C6=C(C(=C(C=C6C(=O)OC7C8C(C(COC(=O)C9=CC(=C(C(=C9C1=C(C(=C(C=C1C(=O)O8)O)O)O)O)O)O)OC7OC(=O)C1=CC(=C(C(=C1)O)O)O)OC3=O)O)O)OC5(C(C(C4O2)(O)O)(O)O)O)O)O 1102.80 unknown https://doi.org/10.1021/NP8004634

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