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Details Top

Internal ID UUID643fdeac2d90b546130918
Scientific name Pericopsis angolensis
Authority (Baker) Meeuwen
First published in Bull. Jard. Bot. État Bruxelles32: 216 (1962)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pericopsis angolensis var. subtomentosa (De Wild.) Meeuwen
Afrormosia angolensis (Baker) De Wild.
Ormosia angolensis Baker D.Oliver & auct. suc. (eds.), Fl. Trop. Afr.2: 255 (1871)
Afrormosia angolensis (Baker) Harms H.G.A.Engler & K.A.E.Prantl, Nat. Pflanzenfam., Nachtr. 3: 159 (1906)

Common names Top

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Language Common/alternative name
Chinese 安哥拉柚木豆

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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Name Authority First published in
Pericopsis angolensis f. angolensis Unknown
Pericopsis angolensis f. brasseuriana (De Wild.) Brummitt Kew Bull.21: 244 (1967)
Pericopsis angolensis f. intermedia Yakovlev Novosti Sist. Vyssh. Rast.8: 180 (1971)

Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Tanzania
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • West-central Tropical Africa
      • Burundi
      • Congo
      • Rwanda
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000212075
Tropicos 13059758
KEW urn:lsid:ipni.org:names:513072-1
The Plant List ild-7153
Open Tree Of Life 3919927
NCBI Taxonomy 1899197
IUCN Red List 146223839
IPNI 513072-1
iNaturalist 428538
GBIF 2940400
EOL 702851
USDA GRIN 437157
CMAUP NPO9522
PFAF Pericopsis angolensis
Wikipedia Pericopsis_angolensis

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
Preserving Ethnoveterinary Medicine (EVM) along the Transhumance Routes in Southwestern Angola: Synergies between International Cooperation and Academic Research Solazzo D, Moretti MV, Tchamba JJ, Rafael MF, Tonini M, Fico G, Basterrecea T, Levi S, Marini L, Bruschi P Plants (Basel) 28-Feb-2024
PMCID:PMC10933900
doi:10.3390/plants13050670
PMID:38475516
Data on fungal abundance and diversity in copper and cobalt contaminated tailing soils in Kitwe, Zambia Dusengemungu L, Gwanama C, Mubemba B Data Brief 12-Dec-2023
PMCID:PMC10770708
doi:10.1016/j.dib.2023.109951
PMID:38186741
Medicinal Uses of the Fabaceae Family in Zimbabwe: A Review Maroyi A Plants (Basel) 10-Mar-2023
PMCID:PMC10051751
doi:10.3390/plants12061255
PMID:36986943
Use of Multi-Date and Multi-Spectral UAS Imagery to Classify Dominant Tree Species in the Wet Miombo Woodlands of Zambia Shamaoma H, Chirwa PW, Zekeng JC, Ramoelo A, Hudak AT, Handavu F, Syampungani S Sensors (Basel) 16-Feb-2023
PMCID:PMC9960281
doi:10.3390/s23042241
PMID:36850838
Ethnomedicinal plants used for treatment of snakebites in Tanzania – a systematic review Mogha NG, Kalokora OJ, Amir HM, Kacholi DS Pharm Biol 07-Oct-2022
PMCID:PMC9553154
doi:10.1080/13880209.2022.2123942
PMID:36205572
Medicinal plants used for the management of respiratory diseases in Zimbabwe: Review and perspectives potential management of COVID-19 Nyagumbo E, Pote W, Shopo B, Nyirenda T, Chagonda I, Mapaya RJ, Maunganidze F, Mavengere WN, Mawere C, Mutasa I, Kademeteme E, Maroyi A, Taderera T, Bhebhe M Phys Chem Earth (2002) 21-Sep-2022
PMCID:PMC9489988
doi:10.1016/j.pce.2022.103232
PMID:36161239
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
Root Nodule Rhizobia From Undomesticated Shrubs of the Dry Woodlands of Southern Africa Can Nodulate Angolan Teak Pterocarpus angolensis, an Important Source of Timber Bünger W, Sarkar A, Grönemeyer JL, Zielinski J, Revermann R, Hurek T, Reinhold-Hurek B Front Microbiol 28-Jan-2021
PMCID:PMC7876412
doi:10.3389/fmicb.2021.611704
PMID:33584615
Savanna tree evolutionary ages inform the reconstruction of the paleoenvironment of our hominin ancestors Davies TJ, Daru BH, Bezeng BS, Charles-Dominique T, Hempson GP, Kabongo RM, Maurin O, Muasya AM, van der Bank M, Bond WJ Sci Rep 24-Jul-2020
PMCID:PMC7381606
doi:10.1038/s41598-020-69378-0
PMID:32709951
Evaluation of the relative roles of the Tabanidae and Glossinidae in the transmission of trypanosomosis in drug resistance hotspots in Mozambique Mulandane FC, Snyman LP, Brito DR, Bouyer J, Fafetine J, Van Den Abbeele J, Oosthuizen M, Delespaux V, Neves L Parasit Vectors 29-Apr-2020
PMCID:PMC7189697
doi:10.1186/s13071-020-04087-1
PMID:32349788
Field data on Vegetation Structure and Effects of Human Use of the Dambos Ecosystem in Northern Mozambique Mbanze AA, Mário AM, Rivaes R, Ribeiro-Barros AI, Ribeiro NS Data Brief 12-Sep-2019
PMCID:PMC6811917
doi:10.1016/j.dib.2019.104454
PMID:31667226
Diversification of African Tree Legumes in Miombo–Mopane Woodlands Maquia I, Catarino S, Pena AR, Brito DR, Ribeiro NS, Romeiras MM, Ribeiro-Barros AI Plants (Basel) 20-Jun-2019
PMCID:PMC6631767
doi:10.3390/plants8060182
PMID:31226765
Conservation and sustainable use of the medicinal Leguminosae plants from Angola Catarino S, Duarte MC, Costa E, Carrero PG, Romeiras MM PeerJ 23-May-2019
PMCID:PMC6535223
doi:10.7717/peerj.6736
PMID:31198619
Data for developing allometric models and evaluating carbon stocks of the Zambezi Teak Forests in Zambia Ngoma J, Moors E, Kruijt B, Speer JH, Vinya R, Chidumayo EN, Leemans R Data Brief 28-Feb-2018
PMCID:PMC5854870
doi:10.1016/j.dib.2018.02.057
PMID:29556519
Traditional uses of plants in a rural community of Mozambique and possible links with Miombo degradation and harvesting sustainability Bruschi P, Mancini M, Mattioli E, Morganti M, Signorini MA J Ethnobiol Ethnomed 23-Jul-2014
PMCID:PMC4112836
doi:10.1186/1746-4269-10-59
PMID:25056487

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 / Lupin alkaloids / Anagyrine-type alkaloids
Anagyrin 71056954 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/0031-9422(88)83116-9
Thermopsine 92768 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/0031-9422(88)83116-9
Thermospine 638234 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/0031-9422(88)83116-9
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(1R,9R)-11-methyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 1747617 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1039/P19760000186
(1R)-1,2,3,4,5,6-Hexahydro-1,5-methano-8H-pyrido[1,2-a][1,5]diazocin-8-one 1278189 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1016/0031-9422(88)83116-9
Citizin 22407 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1016/0031-9422(88)83116-9
Cytisine, N-formyl- 589870 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)C=O 218.25 unknown https://doi.org/10.1016/0031-9422(88)83116-9
Cytisinicline 10235 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1016/0031-9422(88)83116-9
N-Formylcytisine, (-)- 6604689 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)C=O 218.25 unknown https://doi.org/10.1016/0031-9422(88)83116-9
N-Methylcytisine 234566 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1016/0031-9422(88)83116-9
Pharmakon1600-01504027 6708720 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1016/0031-9422(88)83116-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown via CMAUP database
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown via CMAUP database
Hexacosanoic acid 10469 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 396.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,10aS)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-ol 40522879 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)O)C 272.40 unknown via CMAUP database
(1R,4aS,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid 7075030 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown via CMAUP database
(1R,4aS,9R,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1,9-diol 21604174 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)O)C 288.40 unknown via CMAUP database
(1R,4aS,9R,10aR)-9-hydroxy-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carbaldehyde 10425915 Click to see CC1(CCCC2(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)C)C=O 316.40 unknown via CMAUP database
(1R,4aS,9S,10aR)-1-(hydroxymethyl)-7-(1-hydroxy-1-methyl-ethyl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol 3009626 Click to see CC1(CCCC2(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)C)CO 318.40 unknown via CMAUP database
(1R,4aS,9S,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1,9-diol 100982592 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)O)C 288.40 unknown via CMAUP database
(1S,4aS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-ol 26183496 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)O)C 272.40 unknown via CMAUP database
(1S,4aS,10aS)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-ol 26183495 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)O)C 272.40 unknown via CMAUP database
15-Hydroxy-7-oxodehydroabietic acid 14017925 Click to see CC12CCCC(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)(C)C(=O)O 330.40 unknown via CMAUP database
15-Hydroxydehydroabietic Acid 14487943 Click to see CC12CCCC(C1CCC3=C2C=CC(=C3)C(C)(C)O)(C)C(=O)O 316.40 unknown via CMAUP database
15,18-Dihydroxyabieta-8,11,13-trien-7-one 3009631 Click to see CC1(CCCC2(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)C)CO 316.40 unknown via CMAUP database
18-Nor-4,15-dihydroxyabieta-8,11,13-trien-7-one 3009629 Click to see CC12CCCC(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)(C)O 302.40 unknown via CMAUP database
18-Norabieta-8,11,13-trien-4-ol 15605917 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)O)C 272.40 unknown via CMAUP database
7-Oxodehydroabietinol 15715176 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)CO)C 300.40 unknown via CMAUP database
7alpha-Hydroxydehydroabieticacid 13370053 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C(=O)O)C 316.40 unknown via CMAUP database
7alpha,15-Dihydroxydehydroabietic acid 12047563 Click to see CC12CCCC(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)(C)C(=O)O 332.40 unknown via CMAUP database
7Beta-Hydroxydehydroabietic Acid 13370052 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C(=O)O)C 316.40 unknown via CMAUP database
7beta,15-Dihydroxydehydroabietic acid 21626423 Click to see CC12CCCC(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)(C)C(=O)O 332.40 unknown via CMAUP database
Aquilarabietic acid H 71578077 Click to see CC(=C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C(=O)O)C 314.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
Ammodendrine 442625 Click to see CC(=O)N1CCCC(=C1)C2CCCCN2 208.30 unknown https://doi.org/10.1016/0031-9422(88)83116-9
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, octadecyl ester 149044 Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 446.70 unknown via CMAUP database
Docosylferulate 54370069 Click to see CCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 502.80 unknown via CMAUP database
Hexacosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 20980932 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 558.90 unknown via CMAUP database
Icosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 149045 Click to see CCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 474.70 unknown via CMAUP database
Tetracosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 54412038 Click to see CCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 530.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Pinobanksin 73202 Click to see C1=CC=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
3,9-Dimethoxypterocarpan 454892 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC 284.31 unknown via CMAUP database
Medicarpin 336327 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.1039/P19760000186
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
8-O-methylretusin 5319771 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3OC)O 298.29 unknown https://doi.org/10.1039/P19760000186
> Phenylpropanoids and polyketides / Stilbenes
3,5-Dimethoxystilbene 5316874 Click to see COC1=CC(=CC(=C1)C=CC2=CC=CC=C2)OC 240.30 unknown via CMAUP database
Cis-3,5-Dimethoxystilbene 13556468 Click to see COC1=CC(=CC(=C1)C=CC2=CC=CC=C2)OC 240.30 unknown via CMAUP database
Piceatannol 667639 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O 244.24 unknown via CMAUP database
Pinosylvin methyl ether 5281719 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database

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