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Turraeanthus africanus

Turraeanthus africanus - 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 UUID6440493f2f415806077737
Scientific name Turraeanthus africanus
Authority (Welw. ex C.DC.) Pellegr.
First published in Notul. Syst. (Paris) 2: 168 (1911)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Spanish apeya
Spanish avodiré
Spanish engan
Spanish lusamba
Spanish wansenwa
French avodiré
Japanese アボジラ
Japanese アボジレ
Japanese アボディレ
Ukrainian Аводіре
Ukrainian Турреантус африканський

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
      • Uganda
    • South Tropical Africa
      • Angola
    • West Tropical Africa
      • Ghana
      • Guinea
      • Ivory Coast
      • Liberia
      • Nigeria
      • Sierra Leone
    • 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-0001083600
Tropicos 20400596
KEW urn:lsid:ipni.org:names:579875-1
The Plant List kew-2517056
Open Tree Of Life 5747873
NCBI Taxonomy 1672009
IUCN Red List 33064
IPNI 579875-1
iNaturalist 182376
GBIF 4934740
Freebase /m/02y_y5y
EPPO TUUAF
USDA GRIN 401871
Wikipedia Turraeanthus_africanus

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
Chimpanzees select comfortable nesting tree species Lacroux C, Krief S, Douady S, Cornette R, Durand S, Aleeje A, Asalu E, Pouydebat E Sci Rep 07-Oct-2023
PMCID:PMC10560204
doi:10.1038/s41598-023-44192-6
PMID:37805595
Sesquiterpenoids from Meliaceae Family and Their Biological Activities Riyadi SA, Naini AA, Supratman U Molecules 20-Jun-2023
PMCID:PMC10302239
doi:10.3390/molecules28124874
PMID:37375428
Traditional knowledge of plants used in hunting and fishing practices among Baka hunter-gatherers of eastern Cameroon Fongnzossie EF, Ngansop MT, Oishi T, Biwole AB, Biye EH, Ichikawa M J Ethnobiol Ethnomed 03-Jan-2023
PMCID:PMC9808952
doi:10.1186/s13002-022-00571-3
PMID:36597154
Repellent activity against Anopheles gambiae of the leaves of nesting trees in the Sebitoli chimpanzee community of Kibale National Park, Uganda Lacroux C, Pouydebat E, Rossignol M, Durand S, Aleeje A, Asalu E, Chandre F, Krief S Malar J 27-Sep-2022
PMCID:PMC9513939
doi:10.1186/s12936-022-04291-7
PMID:36163024
Edge disturbance shapes liana diversity and abundance but not liana‐tree interaction network patterns in moist semi‐deciduous forests, Ghana Ofosu‐Bamfo B, Addo‐Fordjour P, Belford EJ Ecol Evol 20-Feb-2022
PMCID:PMC8859495
doi:10.1002/ece3.8585
PMID:35371433
No-reference quality assessment for image-based assessment of economically important tropical woods Rajagopal H, Mokhtar N, Tengku Mohmed Noor Izam TF, Wan Ahmad WK PLoS One 19-May-2020
PMCID:PMC7236984
doi:10.1371/journal.pone.0233320
PMID:32428043
Nature-derived compounds modulating Wnt/β-catenin pathway: a preventive and therapeutic opportunity in neoplastic diseases Sferrazza G, Corti M, Brusotti G, Pierimarchi P, Temporini C, Serafino A, Calleri E Acta Pharm Sin B 07-Jan-2020
PMCID:PMC7606110
doi:10.1016/j.apsb.2019.12.019
PMID:33163337
Rainfall seasonality and drought performance shape the distribution of tropical tree species in Ghana Amissah L, Mohren GM, Kyereh B, Agyeman VK, Poorter L Ecol Evol 30-Jul-2018
PMCID:PMC6144999
doi:10.1002/ece3.4384
PMID:30250725
The Effects of Drought and Shade on the Performance, Morphology and Physiology of Ghanaian Tree Species Amissah L, Mohren GM, Kyereh B, Poorter L PLoS One 02-Apr-2015
PMCID:PMC4383566
doi:10.1371/journal.pone.0121004
PMID:25836337
Cameroonian medicinal plants: a bioactivity versus ethnobotanical survey and chemotaxonomic classification Ntie-Kang F, Lifongo LL, Mbaze LM, Ekwelle N, Owono Owono LC, Megnassan E, Judson PN, Sippl W, Efange SM BMC Complement Altern Med 26-Jun-2013
PMCID:PMC3703288
doi:10.1186/1472-6882-13-147
PMID:23802859
Cameroonian Medicinal Plants: Pharmacology and Derived Natural Products Kuete V, Efferth T Front Pharmacol 25-Oct-2010
PMCID:PMC3153003
doi:10.3389/fphar.2010.00123
PMID:21833168
Revision of the afrotropical species of Zaprionus (Diptera, Drosophilidae), with descriptions of two new species and notes on internal reproductive structures and immature stages Yassin A, David JR Zookeys 23-Jul-2010
PMCID:PMC3088026
doi:10.3897/zookeys.51.380
PMID:21594121
Turrealabdane, turreanone and an antisalmonellal agent from Turraeanthus africanus. Djemgou PC, Gatsing D, Hegazy ME, El-Hamd Mohamed AH, Ngandeu F, Tane P, Ngadjui BT, Fotso S, Laatsch H Planta Med 01-Feb-2010
doi:10.1055/S-0029-1186038
PMID:19688688
Anticoccidial constituents from the stem bark of Turraeanthus africanus J. C. Vardamides, H. El Alaoui, D. L. Massoma, A. G. B. Azebaze, B. Ndemangou, V. T. Sielinou, M. Meyer, C. P. Vivares, Z. T. Fomum, A. E. Nkengfack Springer Science and Business Media LLC 03-Feb-2009
doi:10.1007/S10600-009-9196-2
Alkaloids from the Stem Bark of Turraeanthus africanus (Meliaceae). Juliette Catherine Vardamides, et al. et al. Wiley 05-Dec-2006
doi:10.1002/CHIN.200652203

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Secobenzophenanthridine alkaloids
Turraeanthin A 16079974 Click to see CN(C=O)C1=C(C=CC2=CC3=C(C=C21)OCO3)C4=CC(=C(C=C4OC)O)OC 381.40 unknown https://doi.org/10.1002/CHIN.200652203
https://doi.org/10.1248/CPB.54.1034
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
4-(4-Hydroxy-3-methylbutoxy)benzoic acid 25228448 Click to see CC(CCOC1=CC=C(C=C1)C(=O)O)CO 224.25 unknown https://doi.org/10.1007/S10600-009-9196-2
4-[(3S)-4-hydroxy-3-methylbutoxy]benzoic acid 163013653 Click to see CC(CCOC1=CC=C(C=C1)C(=O)O)CO 224.25 unknown https://doi.org/10.1007/S10600-009-9196-2
> Lignans, neolignans and related compounds / Furanoid lignans
5-[(3R,3aS,6S,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-1,3-benzodioxole 7059611 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1007/S10600-009-9196-2
Episesamin 5204 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1007/S10600-009-9196-2
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2E)-2-[2-[(1R,4aR,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]butanedial 45113574 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C 302.50 unknown https://doi.org/10.1055/S-2005-873164
(2S,3S,5R)-2-[[(1R,4aR,8aR)-5,5,8a-trimethyl-2-methylene-decalin-1-yl]methyl]-5-methoxy-tetrahydrofuran-3-carbaldehyde 16077659 Click to see CC1(CCCC2(C1CCC(=C)C2CC3C(CC(O3)OC)C=O)C)C 334.50 unknown https://doi.org/10.1055/S-2005-873164
[(E)-[(2R,5S)-2-[[(1R,4aR,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methyl]-5-methoxyoxolan-3-ylidene]methyl] acetate 163186748 Click to see CC(=O)OC=C1CC(OC1CC2C(=C)CCC3C2(CCCC3(C)C)C)OC 376.50 unknown https://doi.org/10.1055/S-2005-873164
[(E)-[(2R,5S)-2-[[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methyl]-5-acetyloxyoxolan-3-ylidene]methyl] acetate 162942138 Click to see CC(=O)OC=C1CC(OC1CC2C(=C)CCC3C2(CCCC3(C)C)C)OC(=O)C 404.50 unknown https://doi.org/10.1055/S-2005-873164
[(E)-[(2S,5R)-2-[[(1R,4aR,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methyl]-5-methoxyoxolan-3-ylidene]methyl] acetate 162998706 Click to see CC(=O)OC=C1CC(OC1CC2C(=C)CCC3C2(CCCC3(C)C)C)OC 376.50 unknown https://doi.org/10.1055/S-2005-873164
[(E)-[(2S,5R)-2-[[(1R,4aR,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methyl]-5-propan-2-yloxyoxolan-3-ylidene]methyl] acetate 162846762 Click to see CC(C)OC1CC(=COC(=O)C)C(O1)CC2C(=C)CCC3C2(CCCC3(C)C)C 404.60 unknown https://doi.org/10.1055/S-2005-873164
[2-[(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)methyl]-5-methoxyoxolan-3-ylidene]methyl acetate 162998705 Click to see CC(=O)OC=C1CC(OC1CC2C(=C)CCC3C2(CCCC3(C)C)C)OC 376.50 unknown https://doi.org/10.1055/S-2005-873164
[2-[(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)methyl]-5-propan-2-yloxyoxolan-3-ylidene]methyl acetate 162846761 Click to see CC(C)OC1CC(=COC(=O)C)C(O1)CC2C(=C)CCC3C2(CCCC3(C)C)C 404.60 unknown https://doi.org/10.1055/S-2005-873164
[5-acetyloxy-2-[(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)methyl]oxolan-3-ylidene]methyl acetate 72994268 Click to see CC(=O)OC=C1CC(OC1CC2C(=C)CCC3C2(CCCC3(C)C)C)OC(=O)C 404.50 unknown https://doi.org/10.1055/S-2005-873164
2-[(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)methyl]-5-methoxyoxolane-3-carbaldehyde 73001740 Click to see CC1(CCCC2(C1CCC(=C)C2CC3C(CC(O3)OC)C=O)C)C 334.50 unknown https://doi.org/10.1055/S-2005-873164
2-[2-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)ethylidene]butanedial 75094027 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C 302.50 unknown https://doi.org/10.1055/S-2005-873164
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
3-[2-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)ethyl]furan 13894513 Click to see CC1(CCCC2(C1CCC(=C)C2CCC3=COC=C3)C)C 286.50 unknown https://doi.org/10.1055/S-2005-873164
3-[2-[(1R,4aR,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethyl]furan 13894514 Click to see CC1(CCCC2(C1CCC(=C)C2CCC3=COC=C3)C)C 286.50 unknown https://doi.org/10.1055/S-2005-873164
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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/10.1055/S-0029-1186038
Lupeol 259846 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/10.1055/S-0029-1186038
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
9,19-Cyclolanost-25-en-3-ol, 24-methyl-, (3beta,24S)- 550205 Click to see CC(CCC(C)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 440.70 unknown https://doi.org/10.1055/S-0029-1186038
Cyclolaudenol 101729 Click to see CC(CCC(C)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 440.70 unknown https://doi.org/10.1055/S-0029-1186038
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1055/S-0029-1186038
https://doi.org/10.1007/S10600-009-9196-2
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1007/S10600-009-9196-2
https://doi.org/10.1055/S-0029-1186038
> Organoheterocyclic compounds / Heteroaromatic compounds
[2-[[(1R,4aR,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methyl]furan-3-yl]methyl acetate 162851521 Click to see CC(=O)OCC1=C(OC=C1)CC2C(=C)CCC3C2(CCCC3(C)C)C 344.50 unknown https://doi.org/10.1007/S10600-006-0033-6
[2-[[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methyl]furan-3-yl]methyl acetate 14658820 Click to see CC(=O)OCC1=C(OC=C1)CC2C(=C)CCC3C2(CCCC3(C)C)C 344.50 unknown https://doi.org/10.1055/S-2005-873164
https://doi.org/10.1055/S-0029-1186038
2-[(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)methyl]-3-methylfuran 14658823 Click to see CC1=C(OC=C1)CC2C(=C)CCC3C2(CCCC3(C)C)C 286.50 unknown https://doi.org/10.1055/S-2005-873164
2-[[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methyl]-3-methylfuran 14658824 Click to see CC1=C(OC=C1)CC2C(=C)CCC3C2(CCCC3(C)C)C 286.50 unknown https://doi.org/10.1055/S-2005-873164
> Organoheterocyclic compounds / Oxanes
(2R)-2-hydroxy-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]-2H-furan-5-one 163056971 Click to see C1C(C(C(C(O1)C2=CC(OC2=O)O)O)O)O 232.19 unknown https://doi.org/10.1055/S-0029-1186038
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
1-Hydroxy-3,5,6-trimethoxy-10-methyl-4-(3-methylbut-2-enyl)acridin-9-one 163049216 Click to see CC(=CCC1=C(C=C(C2=C1N(C3=C(C2=O)C=CC(=C3OC)OC)C)O)OC)C 383.40 unknown https://doi.org/10.1055/S-2005-873164
https://doi.org/10.1007/S10600-006-0033-6
https://doi.org/10.1055/S-0029-1186038
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Decarine 179640 Click to see COC1=C(C=CC2=C3C=CC4=CC5=C(C=C4C3=NC=C21)OCO5)O 319.30 unknown https://doi.org/10.1248/CPB.54.1034
https://doi.org/10.1002/CHIN.200652203
Oxynitidine 97597 Click to see CN1C2=C(C=CC3=CC4=C(C=C32)OCO4)C5=CC(=C(C=C5C1=O)OC)OC 363.40 unknown https://doi.org/10.1248/CPB.54.1034
https://doi.org/10.1002/CHIN.200652203
Turraeanthin B 16079975 Click to see CN1C2=C(C=CC3=CC4=C(C=C32)OCO4)C5=C(C1=O)C=C(C=C5OC)OC 363.40 unknown https://doi.org/10.1002/CHIN.200652203
https://doi.org/10.1248/CPB.54.1034

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