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Terminalia macroptera

Terminalia macroptera - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643ff939a5380807046409
Scientific name Terminalia macroptera
Authority Guill. & Perr.
First published in Fl. Seneg. Tent. : 276 (1832)

Description Top

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Synonyms Top

Scientific name Authority First published in
Myrobalanus macroptera Kuntze Revis. Gen. Pl. 1: 237 (1891)
Terminalia chevalieri Diels Bot. Jahrb. Syst. 39: 510 (1907)
Terminalia adamanensis Engl. & Diels Monogr. Afrik. Pflanzen-Fam. 4: 11 (1900)
Terminalia claessensii De Wild. Pl. Bequaert. 4: 343 (1928)
Terminalia dawei Rolfe J. Linn. Soc., Bot. 37: 516 (1906)

Common names Top

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Language Common/alternative name
Bambara wɔlɔba
dag kɔrilangbɔŋ
Chinese 大翅榄仁

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000408824
Tropicos 8200096
KEW urn:lsid:ipni.org:names:171217-1
The Plant List kew-2434416
Open Tree Of Life 6120077
NCBI Taxonomy 2871447
IUCN Red List 61990252
IPNI 171218-1
iNaturalist 506924
GBIF 3699999
Freebase /m/0kfwwpn
EPPO TEMMA
USDA GRIN 36343
Wikipedia Terminalia_macroptera

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
Woody Species Composition, Structure, and Status of Regeneration in Pugnido Forest, Gambella Region, Western Ethiopia Masresha G, Melkamu Y, Mulu G Scientifica (Cairo) 04-Apr-2024
PMCID:PMC11008979
doi:10.1155/2024/3961434
PMID:38605976
Anti-diabetic and anti-inflammatory bioactive hits from Coriaria intermedia Matsum. stem and Dracontomelon dao (Blanco) Merr. & Rolfe bark through bioassay-guided fractionation and liquid chromatography-tandem mass spectrometry Fabian MC, Astorga RM, Atis AA, Pilapil LA, Hernandez CC Front Pharmacol 08-Mar-2024
PMCID:PMC10957545
doi:10.3389/fphar.2024.1349725
PMID:38523640
Classification, biosynthesis, and biological functions of triterpene esters in plants Liu J, Yin X, Kou C, Thimmappa R, Hua X, Xue Z Plant Commun 13-Feb-2024
PMCID:PMC11009366
doi:10.1016/j.xplc.2024.100845
PMID:38356259
Polyherbal Combinations Used by Traditional Health Practitioners against Mental Illnesses in Bamako, Mali, West Africa Moussavi N, Mounkoro PP, Dembele SM, Ballo NN, Togola A, Diallo D, Sanogo R, Wangensteen H, Paulsen BS Plants (Basel) 04-Feb-2024
PMCID:PMC10857219
doi:10.3390/plants13030454
PMID:38337987
Antimalarial and Antioxidant Activities of Ethanolic Stem Bark Extract of Terminalia macroptera in Swiss Albino Mice Infected with Plasmodium berghei Sidiki NN, Nadia NA, Cedric Y, Guy-Armand GN, Sandra TN, Kevin TD, Azizi MA, Payne VK J Parasitol Res 03-Jul-2023
PMCID:PMC10332924
doi:10.1155/2023/3350293
PMID:37435530
Medical Ethnobotany of the Bissau-Guinean Community of Migrants Living in Northern Italy and Comparison with the Ethnopharmacology of Guinea-Bissau Sambù A, Cornara L, Catarino L, Indjai B, Biagi M, Giordani P Plants (Basel) 08-May-2023
PMCID:PMC10181441
doi:10.3390/plants12091909
PMID:37176967
Structures, Sources, Identification/Quantification Methods, Health Benefits, Bioaccessibility, and Products of Isorhamnetin Glycosides as Phytonutrients Wang H, Chen L, Yang B, Du J, Chen L, Li Y, Guo F Nutrients 18-Apr-2023
PMCID:PMC10143801
doi:10.3390/nu15081947
PMID:37111165
New Inonotus Polysaccharides: Characterization and Anticomplementary Activity of Inonotus rheades Mycelium Polymers Olennikov DN, Gornostai TG Polymers (Basel) 01-Mar-2023
PMCID:PMC10007321
doi:10.3390/polym15051257
PMID:36904498
Drug discovery inspired by bioactive small molecules from nature Kim S, Lim SW, Choi J Anim Cells Syst (Seoul) 21-Dec-2022
PMCID:PMC9809404
doi:10.1080/19768354.2022.2157480
PMID:36605590
Latitudinal variation in the woody species diversity and population structure of Lannea microcarpa Engl. and K. Krause in Burkina Faso Tinguéri B, Dimobe K, Lankoandé B, Boussim JI, Ouédraogo A Heliyon 04-Jun-2022
PMCID:PMC9192807
doi:10.1016/j.heliyon.2022.e09625
PMID:35711998
Ethnopharmacological Study of Medicinal Plants Used for the Treatment of Cardiovascular Diseases and Their Associated Risk Factors in sub-Saharan Africa Odukoya JO, Odukoya JO, Mmutlane EM, Ndinteh DT Plants (Basel) 23-May-2022
PMCID:PMC9143319
doi:10.3390/plants11101387
PMID:35631812
Traditional Medicine Utilisation Among Pregnant Women in Sub-saharan African Countries: A Systematic Review of Literature Mudonhi N, Nunu WN Inquiry 04-May-2022
PMCID:PMC9073130
doi:10.1177/00469580221088618
PMID:35506677
Local perception of ecosystem services and their conservation in Sudanian savannas of Burkina Faso (West Africa) Nabaloum A, Goetze D, Ouédraogo A, Porembski S, Thiombiano A J Ethnobiol Ethnomed 19-Feb-2022
PMCID:PMC8858500
doi:10.1186/s13002-022-00508-w
PMID:35183193
Anti-HCV Tannins From Plants Traditionally Used in West Africa and Extracted With Green Solvents Bamba M, Bordage S, Sahuc ME, Moureu S, Samaillie J, Roumy V, Vauchel P, Dimitrov K, Rouillé Y, Dubuisson J, Tra Bi FH, Séron K, Sahpaz S Front Pharmacol 28-Jan-2022
PMCID:PMC8831738
doi:10.3389/fphar.2021.789688
PMID:35153750
Ethnobotanical and Phytochemical Profiling of Medicinal Plants from Burkina Faso Used to Increase Physical Performance Sama H, Traoré M, Guenné S, Séré I, Hilou A, Dicko MH Medicines (Basel) 28-Jan-2022
PMCID:PMC8878663
doi:10.3390/medicines9020010
PMID:35200754

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 / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8R,8aR,9S,10R,11R,12aR,14bS)-8,10,11-trihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 102005082 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 666.80 unknown https://doi.org/10.1080/10575630108041255
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bR)-10,11-dihydroxy-2,2,6a,6b,9,12a-hexamethyl-9-[(3,4,5-trihydroxybenzoyl)oxymethyl]-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162982681 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)COC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C)C)C2C1)C)C(=O)O)C 640.80 unknown https://doi.org/10.1016/S0031-9422(98)00154-X
(4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-2,2,6a,6b,9,12a-hexamethyl-9-[(3,4,5-trihydroxybenzoyl)oxymethyl]-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 15385514 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)COC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C)C)C2C1)C)C(=O)O)C 640.80 unknown https://doi.org/10.1016/S0031-9422(98)00154-X
(4aS,6aS,6aS,6bR,10R,11R,12aS,14bR)-10,11-dihydroxy-12a-(hydroxymethyl)-2,2,6a,6b,9,9-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 182035 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)CO)C)C2C1)C)C(=O)O)C 488.70 unknown https://doi.org/10.1016/S0031-9422(98)00154-X
Arjugenin 12444386 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1O)C)C(=O)O)C 504.70 unknown https://doi.org/10.1016/S0031-9422(98)00154-X
Arjunglucoside I 14658050 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 666.80 unknown https://doi.org/10.1016/S0031-9422(98)00154-X
Arjunic Acid 15385516 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1O)C)C(=O)O)C 488.70 unknown https://doi.org/10.1016/S0031-9422(98)00154-X
Sericic Acid 124214 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1O)C)C(=O)O)C 504.70 unknown https://doi.org/10.1016/S0031-9422(98)00154-X
Sericoside 76972524 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 666.80 unknown https://doi.org/10.1016/S0031-9422(98)00154-X
Terminolic acid 12314613 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1)C)C(=O)O)C 504.70 unknown https://doi.org/10.1016/S0031-9422(98)00154-X
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(10R,11R,13R,14R,15S)-3,4,5,11,20,21,22-heptahydroxy-8,17-dioxo-13-[(3,4,5-trihydroxybenzoyl)oxymethyl]-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-14-yl] 3,4,5-trihydroxy-2-(6,7,13,14-tetrahydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4(16),5,7,11,13-hexaen-5-yl)benzoate 101589226 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C8C9=C7C(=O)OC1=C9C(=CC(=C1O)O)C(=O)O8)O)O)O)O)O 1086.70 unknown https://doi.org/10.1021/NP000506V
[(10S,11S,12R,13R,15R)-3,4,5,11,13,21,22,23,26,27,38,39-dodecahydroxy-8,18,30,35-tetraoxo-9,14,17,29,36-pentaoxaoctacyclo[29.8.0.02,7.010,15.019,24.025,34.028,33.032,37]nonatriaconta-1(39),2,4,6,19,21,23,25,27,31,33,37-dodecaen-12-yl] 3,4,5-trihydroxybenzoate 101136622 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C6C7=C5C(=O)OC8=C(C(=C(C9=C(C(=C(C=C9C(=O)O1)O)O)O)C(=C78)C(=O)O6)O)O)O)O)O)O)O 934.60 unknown https://doi.org/10.1021/NP000506V
CID 16129869 16129869 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C8C9=C7C(=O)OC2=C(C(=C(C3=C(C(=C(C=C3C(=O)O1)O)O)O)C(=C92)C(=O)O8)O)O)O)O)O)O)O 1084.70 unknown https://doi.org/10.1021/NP000506V
Isoterchebulin 16143735 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C8C9=C7C(=O)OC2=C9C(=CC(=C2OC2=C(C(=C(C=C2C(=O)O1)O)O)O)O)C(=O)O8)O)O)O)O)O 1084.70 unknown https://doi.org/10.1021/NP000506V
Punicacortein C 16129720 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C4C5=C3C(=O)OC6=C(C(=C(C7=C(C(=C(C=C7C(=O)O1)O)O)O)C(=C56)C(=O)O4)O)O)O)O)O)O)O)C8C9C(C1=C(C(=C(C(=C1C(=O)O9)C1=C(C(=C(C=C1C(=O)O8)O)O)O)O)O)O)O)O 1084.70 unknown https://doi.org/10.1021/NP000506V
Punicalagin 44584733 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C8C9=C7C(=O)OC2=C(C(=C(C3=C(C(=C(C=C3C(=O)O1)O)O)O)C(=C92)C(=O)O8)O)O)O)O)O)O)O 1084.70 unknown https://doi.org/10.1021/NP000506V
terflavin B 44584734 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)O)OC(=O)C3=CC(=C(C(=C3C4=C(C(=C5C6=C4C(=O)OC7=C6C(=CC(=C7O)O)C(=O)O5)O)O)O)O)O 784.50 unknown https://doi.org/10.1021/NP000506V

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