Ekebergia pterophylla

Details Top

Internal ID UUID644018fe505d2585374443
Scientific name Ekebergia pterophylla
Authority Hofmeyr
First published in J. Bot. 63: 57 (1925)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Solid wood from the heartwood is marketed as a durable construction timber for flooring, decking, interior framing, and high‑end furniture.
- Charcoal derived from the species is used for domestic heating and cooking in parts of southern Africa.

Industrial and craft applications:
- Structural timbers are employed in house framing, roof trusses, and exterior cladding where termite resistance is required.
- The dense, fine‑grained wood is suitable for tool handles, carving, turnery, and specialty craft items such as musical instrument components.
- Charcoal production involves traditional pit‑kiln carbonisation, yielding a high‑carbon product valued for its clean burn and high calorific value.

Colorants and tanning:
- The inner bark contains high levels of condensed tannins (proanthocyanidins), which are extracted and used in leather tanning as a natural brown mordant.
- The same tannin extracts serve as a natural dye for protein fibers, producing a stable brown shade without synthetic chemicals.

Wood and fiber:
- Wood is processed into sawn timber, veneer, and plywood for interior and exterior applications requiring strength and stability.
- Wood fibers are used for pulp in small‑scale paper production, contributing cellulose with a moderate lignin content that facilitates chemical pulping.

Properties relevant to use:
- Wood density averages 0.78–0.85 g cm⁻³, with a modulus of rupture of 90–110 MPa, providing good load‑bearing capacity.
- Natural durability is high (Class 1–2) due to extractives and high tannin content, conferring resistance to termites and fungal decay.
- Tannins in bark are classified as condensed proanthocyanidins, with pH‑dependent astringency useful for leather processing.

Standards and regulation:
- In South Africa, timber grading follows SANS 1831 (structural timber) and SANS 1128 (timber quality), aligning with ISO 13061‑1/2 for solid wood testing.
- Export of raw timber and charcoal must comply with ISPM 15 (phytosanitary treatment) and national export licensing requirements.
- The species is not listed under CITES, but national forest regulations require sustainable harvesting plans.

Sustainability and sourcing:
- Ekebergia pterophylla occurs across southern Africa, with IUCN assessing it as “Least Concern” globally, though regional declines are noted due to habitat conversion.
- Sustainable management recommendations include selective harvesting, promotion of natural regeneration, and the development of small‑scale plantations to reduce pressure on wild populations.
- Certification schemes (e.g., FSC) are increasingly applied to timber harvested for commercial use, ensuring traceability and responsible forest stewardship.

Synonyms Top

Scientific name Authority First published in
Trichilia alata N.E.Br. Bull. Misc. Inform. Kew 1896: 160 (1896)
Trichilia pterophylla C.DC. Bull. Herb. Boissier 2: 581 (1894)

Common names Top

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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
    • Southern Africa
      • Cape Provinces
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000663640
Tropicos 20400491
KEW urn:lsid:ipni.org:names:578379-1
The Plant List kew-2784954
Open Tree Of Life 1076020
NCBI Taxonomy 992690
IUCN Red List 146446590
IPNI 578379-1
iNaturalist 584385
GBIF 3851159
Wikipedia Ekebergia_pterophylla

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
The Ethnobotany and Chemistry of South African Meliaceae: A Review Oyedeji-Amusa MO, Sadgrove NJ, Van Wyk BE Plants (Basel) 28-Aug-2021
PMCID:PMC8466584
doi:10.3390/plants10091796
PMID:34579329
A Review of Plant-Based Therapies for the Treatment of Urinary Tract Infections in Traditional Southern African Medicine Cock I, Mavuso N, Van Vuuren S Evid Based Complement Alternat Med 29-Jul-2021
PMCID:PMC8346297
doi:10.1155/2021/7341124
PMID:34367307
Fungal Planet description sheets: 1182–1283 Crous PW, Cowan DA, Maggs-Kölling G, Yilmaz N, Thangavel R, Wingfield MJ, Noordeloos ME, Dima B, Brandrud TE, Jansen GM, Morozova OV, Vila J, Shivas RG, Tan YP, Bishop-Hurley S, Lacey E, Marney TS, Larsson E, Le Floch G, Lombard L, Nodet P, Hubka V, Alvarado P, Berraf-Tebbal A, Reyes JD, Delgado G, Eichmeier A, Jordal JB, Kachalkin AV, Kubátová A, Maciá-Vicente JG, Malysheva EF, Papp V, Rajeshkumar KC, Sharma A, Spetik M, Szabóová D, Tomashevskaya MA, Abad JA, Abad ZG, Alexandrova AV, Anand G, Arenas F, Ashtekar N, Balashov S, Bañares Á, Baroncelli R, Bera I, Biketova AY, Blomquist CL, Boekhout T, Boertmann D, Bulyonkova TM, Burgess TI, Carnegie AJ, Cobo-Diaz JF, Corriol G, Cunnington JH, da Cruz MO, Damm U, Davoodian N, de A. Santiago AL, Dearnaley J, de Freitas LW, Dhileepan K, Dimitrov R, Di Piazza S, Fatima S, Fuljer F, Galera H, Ghosh A, Giraldo A, Glushakova AM, Gorczak M, Gouliamova DE, Gramaje D, Groenewald M, Gunsch CK, Gutiérrez A, Holdom D, Houbraken J, Ismailov AB, Istel Ł, Iturriaga T, Jeppson M, Jurjević Ž, Kalinina LB, Kapitonov VI, Kautmanová I, Khalid AN, Kiran M, Kiss L, Kovács Á, Kurose D, Kušan I, Lad S, Læssøe T, Lee HB, Luangsa-ard JJ, Lynch M, Mahamedi AE, Malysheva VF, Mateos A, Matočec N, Mešić A, Miller AN, Mongkolsamrit S, Moreno G, Morte A, Mostowfizadeh-Ghalamfarsa R, Naseer A, Navarro-Ródenas A, Nguyen TT, Noisripoom W, Ntandu JE, Nuytinck J, Ostrý V, Pankratov TA, Pawłowska J, Pecenka J, Pham TH, Polhorský A, Pošta A, Raudabaugh DB, Reschke K, Rodríguez A, Romero M, Rooney-Latham S, Roux J, Sandoval-Denis M, Smith MT, Steinrucken TV, Svetasheva TY, Tkalčec Z, van der Linde EJ, v.d. Vegte M, Vauras J, Verbeken A, Visagie CM, Vitelli JS, Volobuev SV, Weill A, Wrzosek M, Zmitrovich IV, Zvyagina EA, Groenewald JZ Persoonia 13-Jul-2021
PMCID:PMC9311394
doi:10.3767/persoonia.2021.46.11
PMID:35935893
Furo[3,2-c]coumarins carrying carbon substituents at C-2 and/or C-3. Isolation, biological activity, synthesis and reaction mechanisms Cortés I, Cala LJ, Bracca AB, Kaufman TS RSC Adv 10-Sep-2020
PMCID:PMC9056730
doi:10.1039/d0ra06930b
PMID:35515056
Foliar secretory structures in Ekebergia capensis (Meliaceae) Tilney PM, Nel M, van Wyk AE Heliyon 01-Mar-2018
PMCID:PMC5842367
doi:10.1016/j.heliyon.2018.e00541
PMID:29527579
Astrotricoumarin, an antiproliferative 4′-hydroxy-2′,3′-dihydroprenylated methylcoumarin from an Astrotrichilia sp. from the Madagascar Dry Forest[] Harinantenaina L, Brodie PJ, Callmander MW, Randrianaivo R, Rakotonandrasana S, Rasamison VE, Rakotobe E, Kingston DG Nat Prod Commun 01-Sep-2011
PMCID:PMC3183991
PMID:21941893
Limonoids from Ekebergia pterophylla Anne R.H. Taylor, David A.H. Taylor Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84126-6
Limonoids from Ekebergia pterophylla seed Anne R.H. Kehrli, David A.H. Taylor, Margaret Niven Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)89029-9
Coumarins from Ekebergia pterophylla Dulcie A. Mulholland, Serge E. Iourine, David A.H. Taylor, Francis M. Dean Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(97)00783-8

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 / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Atraric Acid 78435 Click to see 196.20 unknown https://doi.org/10.1016/S0031-9422(97)00783-8
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aS,6aR,6aR,6bR,8aR,12aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,14a-tetradecahydropicen-3-ol 154497735 Click to see CC1(CCC2(CCC3(C(C2C1)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)00783-8
3-Oxo-olean-12-en-28-oic acid 12313702 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C(=O)O)C 454.70 unknown https://doi.org/10.1016/S0031-9422(97)00783-8
4,4,6a,6b,8a,11,11,14b-Octamethyl-1,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-octadecahydro-2H-picen-3-one 612782 Click to see 424.70 unknown https://doi.org/10.1016/S0031-9422(97)00783-8
beta-Amyrenol 225689 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(97)00783-8
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)00783-8
beta-Amyrone 12306160 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(97)00783-8
Beta-Sitosteryl Acetate 5354503 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(97)00783-8
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/10.1016/S0031-9422(97)00783-8
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/10.1016/S0031-9422(97)00783-8
Npc155187 521199 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(97)00783-8
Oleanonic Acid 12313704 Click to see 454.70 unknown https://doi.org/10.1016/S0031-9422(97)00783-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(97)00783-8
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/10.1016/S0031-9422(97)00783-8
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(97)00783-8
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
Ekebergin 101710313 Click to see CC(C)CC(=O)OC1C(C(C(C2(C1OC34C(C(=O)OC(C3(CCC2C4=C)C)C5=COC=C5)OC(=O)C)C)CC(=O)OC)(C)C)O 630.70 unknown https://doi.org/10.1016/S0031-9422(00)84126-6
methyl 2-[(1S,3R,4S,5S,7S,8S,9R,12S,13S,16S)-4,16-diacetyloxy-13-(furan-3-yl)-5-hydroxy-6,6,8,12-tetramethyl-17-methylidene-15-oxo-2,14-dioxatetracyclo[7.7.1.01,12.03,8]heptadecan-7-yl]acetate 163002256 Click to see 588.60 unknown https://doi.org/10.1016/S0031-9422(00)84126-6
methyl 2-[(1S,3S,5R,7S,8S,9R,12S,13S,16S)-5,16-diacetyloxy-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-15-oxo-2,14-dioxatetracyclo[7.7.1.01,12.03,8]heptadecan-7-yl]acetate 162844995 Click to see 572.60 unknown https://doi.org/10.1016/S0031-9422(00)84126-6
Methyl 2-[4,16-diacetyloxy-13-(furan-3-yl)-5-hydroxy-6,6,8,12-tetramethyl-17-methylidene-15-oxo-2,14-dioxatetracyclo[7.7.1.01,12.03,8]heptadecan-7-yl]acetate 14466043 Click to see 588.60 unknown https://doi.org/10.1016/S0031-9422(00)84126-6
Methyl 2-[5,16-diacetyloxy-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-15-oxo-2,14-dioxatetracyclo[7.7.1.01,12.03,8]heptadecan-7-yl]acetate 162844994 Click to see 572.60 unknown https://doi.org/10.1016/S0031-9422(00)84126-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1S,3R,4S,5S,7S,8S,9R,12S,13S,16S)-13-(furan-3-yl)-5,16-dihydroxy-7-(2-methoxy-2-oxoethyl)-6,6,8,12-tetramethyl-17-methylidene-15-oxo-2,14-dioxatetracyclo[7.7.1.01,12.03,8]heptadecan-4-yl] (E)-2-methylbut-2-enoate 163188598 Click to see CC=C(C)C(=O)OC1C(C(C(C2(C1OC34C(C(=O)OC(C3(CCC2C4=C)C)C5=COC=C5)O)C)CC(=O)OC)(C)C)O 586.70 unknown https://doi.org/10.1016/0031-9422(90)89029-9
[13-(Furan-3-yl)-5,16-dihydroxy-7-(2-methoxy-2-oxoethyl)-6,6,8,12-tetramethyl-17-methylidene-15-oxo-2,14-dioxatetracyclo[7.7.1.01,12.03,8]heptadecan-4-yl] 2-methylbut-2-enoate 162843440 Click to see 586.70 unknown https://doi.org/10.1016/0031-9422(90)89029-9
methyl 2-[(1S,3R,4S,5S,7S,8S,9R,12S,13S)-4-acetyloxy-13-(furan-3-yl)-5-hydroxy-6,6,8,12-tetramethyl-17-methylidene-15-oxo-2,14-dioxatetracyclo[7.7.1.01,12.03,8]heptadecan-7-yl]acetate 163193594 Click to see 530.60 unknown https://doi.org/10.1016/S0031-9422(00)84126-6
Methyl 2-[4-acetyloxy-13-(furan-3-yl)-5-hydroxy-6,6,8,12-tetramethyl-17-methylidene-15-oxo-2,14-dioxatetracyclo[7.7.1.01,12.03,8]heptadecan-7-yl]acetate 14466040 Click to see 530.60 unknown https://doi.org/10.1016/S0031-9422(00)84126-6
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
(2R)-9-methyl-2-prop-1-en-2-yl-2,3-dihydrofuro[3,2-c]chromen-4-one 162882794 Click to see 242.27 unknown https://doi.org/10.1016/S0031-9422(97)00783-8
(2S)-9-methyl-2-prop-1-en-2-yl-2,3-dihydrofuro[3,2-c]chromen-4-one 162882795 Click to see 242.27 unknown https://doi.org/10.1016/S0031-9422(97)00783-8
2-Acetyl-9-methylfuro[3,2-c]chromen-4-one 15838083 Click to see 242.23 unknown https://doi.org/10.1016/S0031-9422(97)00783-8
3-Hydroxy-9-methyl-2-prop-1-en-2-yl-2,3-dihydrofuro[3,2-c]chromen-4-one 15838084 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(C3O)C(=C)C 258.27 unknown https://doi.org/10.1016/S0031-9422(97)00783-8
9-Methyl-2-prop-1-en-2-yl-2,3-dihydrofuro[3,2-c]chromen-4-one 15838081 Click to see 242.27 unknown https://doi.org/10.1016/S0031-9422(97)00783-8
Pterophyllin 2 10977554 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(=C3)C(=C)C 240.25 unknown https://doi.org/10.1016/S0031-9422(97)00783-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Iwrbspvhsctefr-uhfffaoysa- 15838082 Click to see 244.28 unknown https://doi.org/10.1016/S0031-9422(97)00783-8

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