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Alstonia boonei

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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 UUID644039b292bc0999021297
Scientific name Alstonia boonei
Authority De Wild.
First published in Repert. Spec. Nov. Regni Veg. 13: 382 (1914)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 板凳木

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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No forms added yet.

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
    • West Tropical Africa
      • Benin
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cabinda
      • 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-0000951936
UNII 03HE649U3E
Tropicos 1800022
KEW urn:lsid:ipni.org:names:76511-1
The Plant List kew-7007
Open Tree Of Life 364332
NCBI Taxonomy 84857
IUCN Red List 60760752
IPNI 76511-1
GBIF 5535759
Freebase /m/010phfdv
EOL 6848242
USDA GRIN 417467
Wikipedia Alstonia_boonei

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
Ethnobotanical study and vulnerability of medicinal plants used against the symptoms of COVID-19 in the Lomié subdivision, East Region of Cameroon Ngamsou Abdel K, Mala WA, Chimi PM, Funwi FP, Engoulou C, Messi Effa JA, Kouoguem Kamdem ME, Nzoyeuem Djonko F, Landry Fokoua U, Brice Adounga S, Marguerite Mbolo M Heliyon 21-Mar-2024
PMCID:PMC10999872
doi:10.1016/j.heliyon.2024.e28247
PMID:38590891
In vitro activities and mechanisms of action of anti-cancer molecules from African medicinal plants: a systematic review Adico MD, Bayala B, Zoure AA, Lagarde A, Bazie JT, Traore L, Buñay J, Yonli AT, Djigma F, Bambara HA, Baron S, Simporé J, Lobaccaro JM Am J Cancer Res 15-Mar-2024
PMCID:PMC10998760
doi:10.62347/AUHB5811
PMID:38590420
Evaluation of packaging, labels, and some physicochemical properties of herbal antimalarial products on the Ghanaian market Amekyeh H, Kumadoh D, Adongo DW, Orman E, Abubakar S, Dwamena A, Aggrey MO Heliyon 28-Feb-2024
PMCID:PMC10920373
doi:10.1016/j.heliyon.2024.e27032
PMID:38463810
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
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
Preventive Action of Beta-Carotene against the Indoxyl Sulfate-Induced Renal Dysfunction in Male Adult Zebrafish via Regulations of Mitochondrial Inflammatory and β-Carotene Oxygenase-2 Actions Muthuraman A, Sayem AS, Meenakshisundaram S, Ali N, Ahmad SF, AlAsmari AF, Nishat S, Lim KG, Paramaswaran Y Biomedicines 27-Sep-2023
PMCID:PMC10603961
doi:10.3390/biomedicines11102654
PMID:37893028
Anti-inflammatory natural products modulate interleukins and their related signaling markers in inflammatory bowel disease: A systematic review Gandhi GR, Mohana T, Athesh K, Hillary VE, Vasconcelos AB, Farias de Franca MN, Montalvão MM, Ceasar SA, Jothi G, Sridharan G, Gurgel RQ, Xu B J Pharm Anal 22-Sep-2023
PMCID:PMC10785269
doi:10.1016/j.jpha.2023.09.012
PMID:38223446
Indigenous medicinal plants used in folk medicine for malaria treatment in Kwara State, Nigeria: an ethnobotanical study Evbuomwan IO, Stephen Adeyemi O, Oluba OM BMC Complement Med Ther 16-Sep-2023
PMCID:PMC10504731
doi:10.1186/s12906-023-04131-4
PMID:37716985
Herbs Used in Antimalarial Medicines: A Study in the Greater Accra Region of Ghana Nortey NN, Korsah S, Tagoe M, Apenteng JA, Owusu FA, Oppong J, Attah AE, Allotey S Evid Based Complement Alternat Med 19-Aug-2023
PMCID:PMC10460277
doi:10.1155/2023/6697078
PMID:37636997
The Aqueous Stem Bark Extract of Alstonia boonei Exhibits Anticataract Activity in Sprague Dawley Rat Amanfo AF, Kyei S, Boakye YD, Akoto CO, Addo JK, Yeboah KO, Osafo N Scientifica (Cairo) 01-Aug-2023
PMCID:PMC10409581
doi:10.1155/2023/5524137
PMID:37560323
Participation of Oxidative Stress in the Activity of Compounds Isolated from Eleutherine plicata Herb Gomes AR, Cruz JN, Castro AL, Cordovil Brigido HP, Varela EL, Vale VV, Carneiro LA, Ferreira GG, Percario S, Dolabela MF Molecules 20-Jul-2023
PMCID:PMC10385196
doi:10.3390/molecules28145557
PMID:37513429
Ethnobotanical Survey and Cercaricidal Activity Screening of Medicinal Plants Used for Schistosomiasis Treatment in Atwima-Nwabiagya District, Ashanti Region, Ghana Asante-Kwatia E, Gyimah L, Forkuo AD, Anyan WK, Gbemu MA, Armah FA, Mensah AY J Parasitol Res 19-Jul-2023
PMCID:PMC10372336
doi:10.1155/2023/6707157
PMID:37520159
Phytopharmaceutical practices of traditional health practitioners in Burkina Faso: a cross-sectional study Ouoba K, Lehmann H, Zongo A, Semdé R, Pabst JY BMC Complement Med Ther 30-Jun-2023
PMCID:PMC10311739
doi:10.1186/s12906-023-04055-z
PMID:37391813
In vitro nematocidal potential of hydro-ethanolic and aqueous extracts of Calotropis procera (Aiton) W.T. Aiton, 1811 (Apocynaceae) and Faidherbia albida (Delile) A. Chev., 1934 (Fabacae) against Onchocerca ochengi and Caenorhabditiselegans Mamat A, Lame Y, Sabine Adeline FY, Yvette N, Ndode Herman ON, Arnold Roger BN, Dieudonné N Heliyon 18-May-2023
PMCID:PMC10209015
doi:10.1016/j.heliyon.2023.e16379
PMID:37251817

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
> Alkaloids and derivatives / Strychnos alkaloids
Curan-17-oic acid, 2,16-didehydro-19-hydroxy-, methyl ester, (20xi)- 541842 Click to see CC(C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C(=O)OC)O 340.40 unknown https://doi.org/10.1016/S0031-9422(00)84144-8
Echitamidine 10991442 Click to see CC(C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C(=O)OC)O 340.40 unknown https://doi.org/10.1016/S0031-9422(00)84144-8
methyl (1R,11S,12S,17S)-8-formyl-12-[(1S)-1-hydroxyethyl]-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carboxylate 162895080 Click to see CC(C1CN2CCC34C2CC1C(=C3N(C5=CC=CC=C45)C=O)C(=O)OC)O 368.40 unknown https://doi.org/10.1016/S0031-9422(00)84144-8
Methyl 12-(1-hydroxypropan-2-yl)-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carboxylate 5317005 Click to see CC(CO)C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C(=O)OC 354.40 unknown https://doi.org/10.1016/S0031-9422(00)84144-8
Methyl 8-formyl-12-(1-hydroxyethyl)-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carboxylate 162895079 Click to see CC(C1CN2CCC34C2CC1C(=C3N(C5=CC=CC=C45)C=O)C(=O)OC)O 368.40 unknown https://doi.org/10.1016/S0031-9422(00)84144-8
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 345510 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(72)80114-6
[(3S,4aR,6aS,6bR,8aR,12aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 162928471 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(72)80114-6
4,4,6a,6b,8a,11,11,14b-Octamethyl-1,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-octadecahydro-2H-picen-3-one 612782 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(72)80114-6
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.3109/13880209.2014.898078
https://doi.org/10.4314/BCSE.V11I2.71725
beta-Amyrone 12306160 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(72)80114-6
Epilupeol 5270628 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(72)80114-6
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(72)80114-6
Lupeol acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1002/PTR.2650070227
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(72)80114-6
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(72)80114-6
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
CID 11953926 11953926 Click to see CC=C1C[N+]2(CCC34C2(C(CC1C3(CO)C(=O)OC)O)NC5=CC=CC=C45)C 385.50 unknown https://doi.org/10.3109/13880208409070663
methyl (1S,9R,12R,18R)-13-ethylidene-10-hydroxy-18-(hydroxymethyl)-15-methyl-8-aza-15-azoniapentacyclo[10.5.1.01,9.02,7.09,15]octadeca-2,4,6-triene-18-carboxylate 137795385 Click to see CC=C1C[N+]2(CCC34C2(C(CC1C3(CO)C(=O)OC)O)NC5=CC=CC=C45)C 385.50 unknown https://doi.org/10.3109/13880208409070663

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