Pierreodendron kerstingii

Details Top

Internal ID UUID64400134e92a6252470260
Scientific name Pierreodendron kerstingii
Authority (Engl.) Little
First published in Phytologia 3: 156 (1949)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Soft hardwood sawn timber, veneer, and plywood; planed lumber for joinery and interior fittings. Logs and lumber are traded under the regional names akom and akum (sometimes recorded as akom-kum or akum-kum). Trade flows are linked to West African coastal ports.

Wood and fiber:
The wood is used for high-value joinery and furniture, interior doors and frames, cabinetry, paneling and cladding, and flooring. It is also used for veneer, moldings, and turned items such as handles, brush backs, and laminated veneer lumber. Planing yields a smooth finish suitable for clear coatings. The timber can be converted to pulp for paper through mechanical or chemical processes when co-utilized with other hardwoods.

Properties relevant to use:
Specific gravity (air-dry) typically about 0.49–0.55; the wood dries readily and is relatively stable in service. Tangential shrinkage is lower than for many mahoganies, reducing risk of checking. Workability is good with standard woodworking tools; the wood holds nails and screws well and takes finishes readily. Color is reddish-brown to golden with interlocked grain and fine to medium texture, supporting clear finishing in furniture and interior applications.

Sustainability and sourcing:
The species is native to the Guineo-Congolian forest zone and adjacent savanna-forest mosaics in West Africa. Forests in parts of its range are under pressure from logging and land-use change. Sustainable sourcing is promoted through regional timber classifications and international timber trade controls such as the EU Timber Regulation and the Lacey Act, encouraging chain-of-custody documentation and verification of origin.

Synonyms Top

Scientific name Authority First published in
Mannia simarubopsis Pellegr. Bull. Soc. Bot. France 77: 665 (1930 publ. 1931)
Mannia kerstingii (Engl.) Harms Nat. Pflanzenfam. ed. 2 , 19a: 371 (1931)
Simarubopsis kerstingii Engl. Bot. Jahrb. Syst. 46: 280 (1911)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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
    • West Tropical Africa
      • Benin
      • Ghana
      • Ivory Coast
      • Liberia
      • Nigeria
      • Togo

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000474987
Tropicos 50088367
KEW urn:lsid:ipni.org:names:813984-1
The Plant List kew-2549737
Open Tree Of Life 6128070
IUCN Red List 32281
IPNI 813984-1
iNaturalist 185011
GBIF 5555208
Freebase /m/02xc65c
Wikipedia Pierreodendron_kerstingii

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
Title Authors Publication Released IDs
Aurantiamide Acetate, Quassinoids, and a Canthinone from the Stem Bark of Pierreodendron kerstingii Stephen A. Ampofo, Peter G. Waterman American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50041A043
Dehydroailanthinone, a new antileukemic quassinoid from Pierreodendron kerstingii. Kupchan SM, Lacadie JA J Org Chem 07-Mar-1975
doi:10.1021/JO00893A024
PMID:1133628

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 / Indolonaphthyridine alkaloids
6H-Indolo(3,2,1-de)(1,5)naphthyridin-6-one, 8-hydroxy- 6455362 Click to see C1=CC2=C(C(=C1)O)N3C(=O)C=CC4=NC=CC2=C43 236.22 unknown https://doi.org/10.1021/NP50041A043
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(4,5,17-Trihydroxy-14,18-dimethyl-6-methylidene-9,16-dioxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl) 2-methylbutanoate 4331397 Click to see 476.50 unknown https://doi.org/10.1021/JO00893A024
(4,5,17-Trihydroxy-6,14,18-trimethyl-9,16-dioxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl) 2-acetyloxy-2-methylbutanoate 3478825 Click to see 536.60 unknown https://doi.org/10.1021/JO00893A024
(4,5,17-Trihydroxy-6,14,18-trimethyl-9,16-dioxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl) 2-hydroxy-2-methylbutanoate 430508 Click to see 494.50 unknown https://doi.org/10.1021/JO00893A024
[(1S,4R,5R,6R,7S,8R,11R,13S,16S,17S,18S,19R)-4,5,16,17-tetrahydroxy-6,14,18-trimethyl-9-oxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl] (2S)-2-acetyloxy-2-methylbutanoate 49866282 Click to see 538.60 unknown https://doi.org/10.1021/NP50041A043
[(1S,4R,5R,6R,7S,8R,11R,13S,17S,18S,19R)-4,5,17-trihydroxy-6,14,18-trimethyl-9,16-dioxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl] (2R)-2-methylbutanoate 162919187 Click to see CCC(C)C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(=O)C=C5C)O)C)OC1=O)O)O)C 478.50 unknown https://doi.org/10.1021/JO00893A024
[(1S,4R,5R,6R,7S,8R,11R,13S,17S,18S,19R)-4,5,17-Trihydroxy-6,14,18-trimethyl-9,16-dioxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl] 2-hydroxy-2-methylbutanoate 12310232 Click to see 494.50 unknown https://doi.org/10.1021/NP50041A043
[(1S,4R,5R,6R,7S,8R,11R,17S,18S)-4,5,17-trihydroxy-6,14,18-trimethyl-9,16-dioxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl] 2-methylbutanoate 118701210 Click to see 478.50 unknown https://doi.org/10.1021/NP50041A043
[(1S,4R,5R,7S,8R,11R,13R,17S,18S,19R)-4,5,17-trihydroxy-14,18-dimethyl-6-methylidene-9,16-dioxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl] (2R)-2-methylbutanoate 162981997 Click to see 476.50 unknown https://doi.org/10.1021/JO00893A024
[(1S,4S,5R,6R,7S,8R,11R,13S,16S,17S,18S,19R)-4,5,16,17-tetrahydroxy-6,14,18-trimethyl-9-oxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl] (2S)-2-hydroxy-2-methylbutanoate 90469735 Click to see CCC(C)(C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(C=C5C)O)O)C)OC1=O)O)O)C)O 496.50 unknown https://doi.org/10.1021/NP50041A043
2'-Acetoxy-Glaucarubinone 49866280 Click to see CCC(C)(C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(=O)C=C5C)O)C)OC1=O)O)O)C)OC(=O)C 536.60 unknown https://doi.org/10.1021/JO00893A024
2'-Acetylglaucarubinone 303910 Click to see 536.60 unknown https://doi.org/10.1021/NP50041A043
Ailanthinone 428489 Click to see CCC(C)C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(=O)C=C5C)O)C)OC1=O)O)O)C 478.50 unknown https://doi.org/10.1021/NP50041A043
https://doi.org/10.1021/JO00893A024
Excelsin 49866283 Click to see 480.50 unknown https://doi.org/10.1021/NP50041A043
Glaucarubin 441794 Click to see 496.50 unknown https://doi.org/10.1021/NP50041A043
https://doi.org/10.1021/JO00893A024
Glaucarubinone 441796 Click to see CCC(C)(C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(=O)C=C5C)O)C)OC1=O)O)O)C)O 494.50 unknown https://doi.org/10.1021/NP50041A043
https://doi.org/10.1021/JO00893A024
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1021/NP50041A043
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1021/NP50041A043
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
[(2R)-2-[[[(2S)-2-benzamido-3-phenylpropanoyl]amino]methyl]-3-phenylpropyl] acetate 5321123 Click to see 458.50 unknown https://doi.org/10.1021/JO00893A024
https://doi.org/10.1021/NP50041A043
CID 13855373 13855373 Click to see CC(=O)OCC(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3 444.50 unknown https://doi.org/10.1021/JO00893A024
N-Benzoyl-1-phenylalanyl-1-phenylalaninol acetate 124319 Click to see CC(=O)OCC(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3 444.50 unknown https://doi.org/10.1021/NP50041A043

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