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Internal ID UUID644012e035772605864385
Scientific name Combretum psidioides
Authority Welw.
First published in Bol. Ann. Conselho Ultram. Lisb. May 1856 , 24: 249 (1856)

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Synonyms Top

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Common names Top

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Language Common/alternative name
English peeling bushwillow
English savanna bushwillow
Afrikaans skilferboswilg

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Combretum psidioides subsp. dinteri (Schinz, De Wild. & T.Durand) Exell Mitt. Bot. Staatssamml. München 4: 3. 1961 (1961)
Combretum psidioides subsp. grandifolium (F.Hoffm.) Jordaan Bothalia 41: 147 (2011)
Combretum psidioides subsp. kwinkiti (De Wild.) Exell Mitt. Bot. Staatssamml. München 4: 4. 1961 (1961)
Combretum psidioides subsp. psidioides
Combretum psidioides subsp. psilophyllum Wickens Kew Bull. 26: 39 (1971)

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
      • Kenya
      • Tanzania
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Caprivi Strip
      • Namibia
    • West-central Tropical Africa
      • Burundi
      • Congo
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000616684
Tropicos 8200378
KEW urn:lsid:ipni.org:names:170394-1
The Plant List kew-2732946
Open Tree Of Life 538017
NCBI Taxonomy 507422
IUCN Red List 143714606
IPNI 170394-1
iNaturalist 582594
GBIF 7327073

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
Therapeutic Potential and Predictive Pharmaceutical Modeling of Stilbenes in Cannabis sativa O’Croinin C, Garcia Guerra A, Doschak MR, Löbenberg R, Davies NM Pharmaceutics 12-Jul-2023
PMCID:PMC10386382
doi:10.3390/pharmaceutics15071941
PMID:37514127
Effect of fire on the palatability of plants in an African woodland savanna: varying impacts depending on plant functional groups Stolter C, Joubert DF, Uunona N, Nghalipo E, Amputu V, Felton AM PeerJ 19-Jan-2022
PMCID:PMC8783561
doi:10.7717/peerj.12721
PMID:35111393
Antiplasmodial, antimalarial activities and toxicity of African medicinal plants: a systematic review of literature Tajbakhsh E, Kwenti TE, Kheyri P, Nezaratizade S, Lindsay DS, Khamesipour F Malar J 25-Aug-2021
PMCID:PMC8390284
doi:10.1186/s12936-021-03866-0
PMID:34433465
HPLC-DAD and UHPLC/QTOF-MS Analysis of Polyphenols in Extracts of the African Species Combretum padoides, C. zeyheri and C. psidioides Related to Their Antimycobacterial Activity Fyhrquist P, Salih EY, Helenius S, Laakso I, Julkunen-Tiitto R Antibiotics (Basel) 29-Jul-2020
PMCID:PMC7460068
doi:10.3390/antibiotics9080459
PMID:32751268
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
First large-scale ethnobotanical survey in the province of Uíge, northern Angola Lautenschläger T, Monizi M, Pedro M, Mandombe JL, Bránquima MF, Heinze C, Neinhuis C J Ethnobiol Ethnomed 25-Jul-2018
PMCID:PMC6060550
doi:10.1186/s13002-018-0238-3
PMID:30045744
The charcoal trap: Miombo forests and the energy needs of people Kutsch WL, Merbold L, Ziegler W, Mukelabai MM, Muchinda M, Kolle O, Scholes RJ Carbon Balance Manag 19-Aug-2011
PMCID:PMC3189094
doi:10.1186/1750-0680-6-5
PMID:21854587
Chemical constituents of the combretaceae. Part III. Substituted phenanthrenes, 9,10-dihydrophenanthrenes, and bibenzyls from the heartwood of Combretum psidioides R. M. Letcher, L. R. M. Nhamo Royal Society of Chemistry (RSC) 23-Apr-2004
doi:10.1039/P19720002941

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 / Phenanthrenes and derivatives / Hydrophenanthrenes
2-Hydroxy-3,5,7-trimethoxy-9,10-dihydrophenanthrene 71437517 Click to see COC1=CC2=C(C3=CC(=C(C=C3CC2)O)OC)C(=C1)OC 286.32 unknown https://doi.org/10.1039/P19720002941
2,5-Phenanthrenediol, 9,10-dihydro-3,7-dimethoxy- 182231 Click to see COC1=CC2=C(C3=CC(=C(C=C3CC2)O)OC)C(=C1)O 272.29 unknown https://doi.org/10.1039/P19720002941
2,7-Phenanthrenediol, 9,10-dihydro-3,4,6-trimethoxy- 181637 Click to see COC1=C(C=C2CCC3=CC(=C(C(=C3C2=C1)OC)OC)O)O 302.32 unknown https://doi.org/10.1039/P19720002941
3,6,7-Trimethoxy-9,10-dihydrophenanthrene-2,5-diol 14135385 Click to see COC1=C(C(=C2C(=C1)CCC3=CC(=C(C=C32)OC)O)O)OC 302.32 unknown https://doi.org/10.1039/P19720002941
5,6-Dimethoxy-9,10-dihydrophenanthrene-2,3,7-triol 154013145 Click to see COC1=C(C=C2CCC3=CC(=C(C=C3C2=C1OC)O)O)O 288.29 unknown https://doi.org/10.1039/P19720002941
5,6,7-Trimethoxy-9,10-dihydrophenanthrene-2,3-diol 14049973 Click to see COC1=C(C(=C2C(=C1)CCC3=CC(=C(C=C32)O)O)OC)OC 302.32 unknown https://doi.org/10.1039/P19720002941
6,7-Dimethoxy-9,10-dihydrophenanthrene-2,3,5-triol 53438747 Click to see COC1=C(C(=C2C(=C1)CCC3=CC(=C(C=C32)O)O)O)OC 288.29 unknown https://doi.org/10.1039/P19720002941
9,10-Dihydro-3,5,6,7-tetramethoxyphenanthren-2-ol 14049974 Click to see COC1=C(C(=C2C(=C1)CCC3=CC(=C(C=C32)OC)O)OC)OC 316.30 unknown https://doi.org/10.1039/P19720002941
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
2,7-Phenanthrenediol, 3,4,6-trimethoxy- 356766 Click to see COC1=C(C=C2C=CC3=CC(=C(C(=C3C2=C1)OC)OC)O)O 300.30 unknown https://doi.org/10.1039/P19720002941
3,5,6,7-Tetramethoxyphenanthrene-2-ol 11141545 Click to see COC1=C(C(=C2C(=C1)C=CC3=CC(=C(C=C32)OC)O)OC)OC 314.30 unknown https://doi.org/10.1039/P19720002941
5,6-Dimethoxyphenanthrene-2,3,7-triol 140299698 Click to see COC1=C(C=C2C=CC3=CC(=C(C=C3C2=C1OC)O)O)O 286.28 unknown https://doi.org/10.1039/P19720002941
5,6,7-Trimethoxyphenanthrene-2,3-diol 162982396 Click to see COC1=C(C(=C2C(=C1)C=CC3=CC(=C(C=C32)O)O)OC)OC 300.30 unknown https://doi.org/10.1039/P19720002941
6,7-Dimethoxyphenanthrene-2,3,5-triol 22753769 Click to see COC1=C(C(=C2C(=C1)C=CC3=CC(=C(C=C32)O)O)O)OC 286.28 unknown https://doi.org/10.1039/P19720002941
Isobatatasin I 442708 Click to see COC1=CC(=C2C(=C1)C=CC3=CC(=C(C=C32)OC)O)OC 284.31 unknown https://doi.org/10.1039/P19720002941
> Phenylpropanoids and polyketides / Stilbenes
4,4'-Dihydroxy-3,5-dimethoxydihydrostilbene 442701 Click to see COC1=CC(=CC(=C1O)OC)CCC2=CC=C(C=C2)O 274.31 unknown https://doi.org/10.1039/P19720002941
5-[2-(4-Hydroxy-phenyl)-ethyl]-2,3-dimethoxy-phenol 22753767 Click to see COC1=CC(=CC(=C1OC)O)CCC2=CC=C(C=C2)O 274.31 unknown https://doi.org/10.1039/P19720002941
Isoamoenylin 3084744 Click to see COC1=CC(=CC(=C1OC)OC)CCC2=CC=C(C=C2)O 288.34 unknown https://doi.org/10.1039/P19720002941

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