Pterocarpus angolensis - Unknown
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Internal ID UUID643fd70fd43e1013127160
Scientific name Pterocarpus angolensis
Authority DC.
First published in Prodr.2: 419 (1825)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pterocarpus bussei Harms Bot. Jahrb. Syst.33: 171 (1902)
Pterocarpus dekindtianus Harms Bot. Jahrb. Syst.30: 89 (1901)
Pterocarpus dekindtianus var. latifoliolatus De Wild. Ann. Mus. Congo Belge, Bot., sér. 4, 2: 78 (1913)

Common names Top

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Language Common/alternative name
English kiaat
English kiaat bloodwood
English mukwa
English bleedwood tree
Afrikaans bloedhoud
Afrikaans kiaat
Afrikaans bloedhout
Arabic توز مرجاني
Estonian angoola tiibviljak
Irish iorócó
Japanese ムニンガ
Japanese アンゴラカリン
Korean 키아트
Shona mubvamaropa
ts muvhangazi
Chinese 安哥拉紫檀

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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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
    • Southern Africa
      • Botswana
      • Caprivi Strip
      • Kwazulu-Natal
      • Namibia
      • Northern Provinces
      • Swaziland
    • West-central Tropical Africa
      • Congo
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000172643
Tropicos 13032356
KEW urn:lsid:ipni.org:names:516403-1
The Plant List ild-1884
Open Tree Of Life 507993
NCBI Taxonomy 182271
IUCN Red List 33190
IPNI 516403-1
iNaturalist 340243
GBIF 5349240
Freebase /m/0h0vsl
EOL 640047
USDA GRIN 30283
Wikipedia Pterocarpus_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
Phytochemicals from Pterocarpus angolensis DC and Their Cytotoxic Activities against Breast Cancer Cells Teclegeorgish ZW, Mokgalaka NS, Kemboi D, Krause RW, Siwe-Noundou X, Nyemba GR, Davison C, de la Mare JA, Tembu VJ Plants (Basel) 19-Jan-2024
PMCID:PMC10818308
doi:10.3390/plants13020301
PMID:38276759
Critical Review on the Use of Extractives of Naturally Durable Woods as Natural Wood Protectants Kirker GT, Hassan B, Mankowski ME, Eller FJ Insects 18-Jan-2024
PMCID:PMC10816604
doi:10.3390/insects15010069
PMID:38249075
In Vitro Cercaricidal Activity, Acute Toxicity, and GC/MS Analysis of Some Selected Ghanaian Medicinal Plants Osei-Mensah B, Boakye YD, Anyan WK, Agana TA, Aboagye EA, Bentil I, Lomotey ES, Adu F, Agyare C J Parasitol Res 15-Sep-2023
PMCID:PMC10516696
doi:10.1155/2023/4589424
PMID:37745984
Identification and Characterization of Diplodia parva and Diplodia crataegicola Causing Black Rot of Chinese Quince Kwon S, Kim J, Lee Y, Balaraju K, Jeon Y Plant Pathol J 01-Jun-2023
PMCID:PMC10265116
doi:10.5423/PPJ.OA.03.2023.0039
PMID:37291768
SmartWoodID—an image collection of large end-grain surfaces to support wood identification systems De Blaere R, Lievens K, Van Hassel D, Deklerck V, De Mil T, Hubau W, Van Acker J, Bourland N, Verwaeren J, Van den Bulcke J, Beeckman H Database (Oxford) 13-May-2023
PMCID:PMC10182821
doi:10.1093/database/baad034
PMID:37178209
The use of medicinal plants in common ophthalmic disorders: A systematic review with meta-analysis Alghamdi AH, Ahmed AA, Bashir M, Abdalgadir H, Khalid A, Gul S Heliyon 11-Apr-2023
PMCID:PMC10161615
doi:10.1016/j.heliyon.2023.e15340
PMID:37151714
Characterization of Pseudofusicoccum Species from Diseased Plantation-Grown Acacia mangium, Eucalyptus spp., and Pinus massoniana in Southern China Li G, Wu W, Lu L, Chen B, Chen S Pathogens 08-Apr-2023
PMCID:PMC10142214
doi:10.3390/pathogens12040574
PMID:37111460
Structural insights into a cooperative switch between one and two FimH bacterial adhesins binding pauci- and high-mannose type N-glycan receptors Krammer EM, Bridot C, Serna S, Echeverria B, Semwal S, Roubinet B, van Noort K, Wilbers RH, Bourenkov G, de Ruyck J, Landemarre L, Reichardt N, Bouckaert J J Biol Chem 20-Mar-2023
PMCID:PMC10127133
doi:10.1016/j.jbc.2023.104627
PMID:36944399
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
Antimicrobial Potential of Pithecellobium dulce Seed Extract against Pathogenic Bacteria: In Silico and In Vitro Evaluation Aldarhami A, Bazaid AS, Alhamed AS, Alghaith AF, Ahamad SR, Alassmrry YA, Alharazi T, Snoussi M, Qanash H, Alamri A, Badraoui R, Kadri A, Binsaleh NK, Alreshidi M Biomed Res Int 04-Feb-2023
PMCID:PMC9922195
doi:10.1155/2023/2848198
PMID:36785668
Pest categorisation of Lasiodiplodia pseudotheobromae Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Migheli Q, Vloutoglou I, Maiorano A, Streissl F, Reignault PL EFSA J 30-Jan-2023
PMCID:PMC9885757
doi:10.2903/j.efsa.2023.7737
PMID:36733438
Exposure Characterization of Wood Dust Particulate, Endotoxins, and (1–3)-β-d-Glucans, and Their Determinants in Mozambiquan Wood Processing Workers Chamba PS, Baatjies R, Singh TS, Cumbane AJ, Jeebhay MF Ann Work Expo Health 28-Jan-2023
PMCID:PMC10119701
doi:10.1093/annweh/wxac100
PMID:36715220
Molecular Level Sucrose Quantification: A Critical Review Lara-Cruz GA, Jaramillo-Botero A Sensors (Basel) 05-Dec-2022
PMCID:PMC9740140
doi:10.3390/s22239511
PMID:36502213
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
Changes in tree structure, composition and soil in different disturbance categories in Miombo and agroecosystems in Malawi, central Africa Nyirenda H Heliyon 16-Sep-2022
PMCID:PMC9508568
doi:10.1016/j.heliyon.2022.e10664
PMID:36164510

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Bis(2-ethylhexyl) phthalate 8343 Click to see CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC 390.60 unknown https://doi.org/10.1039/P19800002179
Diethylhexylphthalate 7057919 Click to see CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC 390.60 unknown https://doi.org/10.1039/P19800002179
> Phenylpropanoids and polyketides / Alpha-methyldeoxybenzoin flavonoids
(2r)-1-(2,4-Dihydroxyphenyl)-2-(4-methoxyphenyl)propan-1-one 821428 Click to see CC(C1=CC=C(C=C1)OC)C(=O)C2=C(C=C(C=C2)O)O 272.29 unknown https://doi.org/10.1039/P19800002179
(2R)-1-[4-[[(1R,4S,4aR,8aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-yl]oxy]-2-hydroxyphenyl]-2-(4-methoxyphenyl)propan-1-one 162928171 Click to see CC1=CC2C(CCC(C2CC1)(C)OC3=CC(=C(C=C3)C(=O)C(C)C4=CC=C(C=C4)OC)O)C(C)C 476.60 unknown https://doi.org/10.1039/P19800002179
(2R)-1-[4-[[(1S,4S,4aR,8aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-yl]oxy]-2-hydroxyphenyl]-2-(4-methoxyphenyl)propan-1-one 162928172 Click to see CC1=CC2C(CCC(C2CC1)(C)OC3=CC(=C(C=C3)C(=O)C(C)C4=CC=C(C=C4)OC)O)C(C)C 476.60 unknown https://doi.org/10.1039/P19800002179
(2S)-1-(2-hydroxy-4-methoxyphenyl)-2-(4-methoxyphenyl)propan-1-one 101668134 Click to see CC(C1=CC=C(C=C1)OC)C(=O)C2=C(C=C(C=C2)OC)O 286.32 unknown https://doi.org/10.1039/P19800002179
1-[4-[(1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-yl)oxy]-2-hydroxyphenyl]-2-(4-methoxyphenyl)propan-1-one 74978575 Click to see CC1=CC2C(CCC(C2CC1)(C)OC3=CC(=C(C=C3)C(=O)C(C)C4=CC=C(C=C4)OC)O)C(C)C 476.60 unknown https://doi.org/10.1039/P19800002179
4-O-Methylangolensin 14284966 Click to see CC(C1=CC=C(C=C1)OC)C(=O)C2=C(C=C(C=C2)OC)O 286.32 unknown https://doi.org/10.1039/P19800002179
Angolensin 3584988 Click to see CC(C1=CC=C(C=C1)OC)C(=O)C2=C(C=C(C=C2)O)O 272.29 unknown https://doi.org/10.1039/P19800002179
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Gallocatechin 65084 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1039/P19810000263
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Liquiritigenin 114829 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown https://doi.org/10.1039/P19810000263
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
5-(Acetyloxy)-3-[4-(acetyloxy)phenyl]-4-oxo-4H-chromen-7-yl acetate 623118 Click to see CC(=O)OC1=CC=C(C=C1)C2=COC3=C(C2=O)C(=CC(=C3)OC(=O)C)OC(=O)C 396.30 unknown https://doi.org/10.1039/P19810000263
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown https://doi.org/10.1039/P19810000263
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
[4-(5-Acetyloxy-6,7-dimethoxy-4-oxochromen-3-yl)phenyl] acetate 163034350 Click to see CC(=O)OC1=CC=C(C=C1)C2=COC3=CC(=C(C(=C3C2=O)OC(=O)C)OC)OC 398.40 unknown https://doi.org/10.1039/P19810000263
[4-(5-Acetyloxy-7-methoxy-4-oxochromen-3-yl)phenyl] acetate 162980719 Click to see CC(=O)OC1=CC=C(C=C1)C2=COC3=C(C2=O)C(=CC(=C3)OC)OC(=O)C 368.30 unknown https://doi.org/10.1039/P19810000263
7-O-Methyltectorigenin 5487785 Click to see COC1=C(C(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1039/P19810000263
Muningin 252471 Click to see COC1=C(C(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)O)OC)O 314.29 unknown https://doi.org/10.1039/JR9520000096
Prunetin 5281804 Click to see COC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)O)O 284.26 unknown https://doi.org/10.1016/S0031-9422(99)00526-9
https://doi.org/10.1039/P19810000263
https://doi.org/10.1039/JR9520003211
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
Odoratol 442440 Click to see COC1=CC=C(C=C1)CC(C(=O)C2=C(C=C(C=C2)OC)O)O 302.32 unknown https://doi.org/10.1039/P19810000263
Odoratol 42607724 Click to see COC1=CC=C(C=C1)CC(C(=O)C2=C(C=C(C=C2)OC)O)O 302.32 unknown https://doi.org/10.1039/P19810000263

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