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Alstonia boonei

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

Ethnobotanical Use Top

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General Uses 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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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
Helicobacter pylori infection in humans and phytotherapy, probiotics, and emerging therapeutic interventions: a review Liu M, Gao H, Miao J, Zhang Z, Zheng L, Li F, Zhou S, Zhang Z, Li S, Liu H, Sun J Front Microbiol 10-Jan-2024
PMCID:PMC10806011
doi:10.3389/fmicb.2023.1330029
PMID:38268702
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
Medicinal plants used for management of diabetes and hypertension in Ghana Asafo-Agyei T, Appau Y, Barimah KB, Asase A Heliyon 29-Nov-2023
PMCID:PMC10703729
doi:10.1016/j.heliyon.2023.e22977
PMID:38076168
Buruli ulcer in Africa: Geographical distribution, ecology, risk factors, diagnosis, and indigenous plant treatment options – A comprehensive review Osei-Owusu J, Aidoo OF, Eshun F, Gaikpa DS, Dofuor AK, Vigbedor BY, Turkson BK, Ochar K, Opata J, Opoku MJ, Ninsin KD, Borgemeister C Heliyon 15-Nov-2023
PMCID:PMC10686891
doi:10.1016/j.heliyon.2023.e22018
PMID:38034712
Correction: Phytochemical analysis, in vitro and in silico effects from Alstonia boonei De Wild stem bark on selected digestive enzymes and adipogenesis in 3T3‑L1 preadipocytes Anyanwu GO, Ejike UD, Gyebi GA, Rauf K, Nisar-Ur-Rehman, Iqbal J, Zaib S, Usunobun U, Onyeneke EC, Alotaibi BS, El-Saber Batiha G BMC Complement Med Ther 28-Oct-2023
PMCID:PMC10612388
doi:10.1186/s12906-023-04236-w
PMID:37898774
Phytochemical analysis, in vitro and in silico effects from Alstonia boonei De Wild stem bark on selected digestive enzymes and adipogenesis in 3T3-L1 preadipocytes Anyanwu GO, Ejike UD, Gyebi GA, Rauf K, Nisar-Ur-Rehman, Iqbal J, Zaib S, Usunobun U, Onyeneke EC, Alotaibi BS, Batiha GE BMC Complement Med Ther 20-Oct-2023
PMCID:PMC10588189
doi:10.1186/s12906-023-04202-6
PMID:37864233
Antispasmodic Effect of Alstonia boonei De Wild. and Its Constituents: Ex Vivo and In Silico Approaches Akinmurele OJ, Sonibare MA, Elujoba AA, Ogunlakin AD, Yeye OE, Gyebi GA, Ojo OA, Alanzi AR Molecules 13-Oct-2023
PMCID:PMC10609272
doi:10.3390/molecules28207069
PMID:37894548
Cytotoxic Activity of Wild Plant and Callus Extracts of Ageratina pichinchensis and 2,3-Dihydrobenzofuran Isolated from a Callus Culture Sánchez-Ramos M, Encarnación-García JG, Marquina-Bahena S, Sánchez-Carranza JN, Bernabé-Antonio A, Domínguez-Villegas V, Cabañas-García E, Cruz-Sosa F Pharmaceuticals (Basel) 03-Oct-2023
PMCID:PMC10609924
doi:10.3390/ph16101400
PMID:37895871
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

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 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 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 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 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 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 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 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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