Details Top

Internal ID UUID643ffd6643831519437917
Scientific name Lophira lanceolata
Authority Tiegh. ex Keay
First published in Kew Bull. 8: 488 (1954)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Among the Yoruba of southwestern Nigeria, a thick stem‑bark decoction has long been taken as a hemolytic remedy for sickle‑cell disease (Okoli et al., 2009). The Tiv of Nigeria boil the same stem‑bark decoction for diarrhea and other gut complaints (Burkill, 1985). In northern Ghana, Fula healers prepare a leaf decoction and wash it over painful arthritic joints to ease swelling (Adjou, 2015). Across the savanna belt from Burkina Faso to Cameroon, healers have reported leaf infusions used as a mild internal tea for fever and stomach upset, and topical washes of leaf maceration for sores and skin infections (Burkill, 1985; Bruni et al., 2021). In rural Cameroon and Central African Republic communities, women crush fresh leaves into a paste and apply the macerated poultice to wounds and ulcerated skin lesions (Adjanohoun and Goudote, 1996; Bruni et al., 2021).

For practical use, a simple 1:5 (w/v) ethanol tincture is prepared with 50 g of air‑dried stem‑bark chopped into small pieces. Combine with 250 mL of 45% ethanol and macerate in a dark glass jar for 14 days, shaking daily. Strain through a fine cloth and keep in the refrigerator. Adults may take 2–3 mL in water up to three times a day for short periods; avoid use in pregnancy and liver disease, and discontinue if nausea or abdominal pain occurs (Bruni et al., 2021). These preparations are supported by documented ethnomedicinal applications of stem‑bark decoctions and leaf macerations in West and Central Africa.

The bark and leaves contain high levels of hydrolyzable tannins, proanthocyanidins, and flavonoids such as quercetin and kaempferol; these astringent polyphenols plausibly explain the recorded wound‑care and antidiarrheal actions (Burkill, 1985; Agyare et al., 2013). Today's scientific interest continues in the astringent and antimicrobial profiles of leaf extracts, while markets still carry dried bark and herbal teas in local communities across the savanna.

General Uses Top

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Common products:
- Heavy structural timber (sawn wood, sleepers, poles).
- Vegetable seed oil (edible grade after refining; also suitable for soap).
- Tanning extract (bark).
- Heartwood resin/oleoresin used as a craft varnish and as an adhesive additive.
- Potash-rich bark ash for mordanting vegetable fibers.
- Pulpwood for kraft pulp and paper.
- Charcoal.

Industrial and craft applications:
- Heartwood: a dark, hard, oily timber used where durability is critical—construction, railway sleepers, heavy-duty flooring, marine decking and pilings. Resistance to abrasion and insect attack is reported.
- Resin/oleoresin: harvested as a dark, sticky substance from the heartwood; employed as a varnish/lacquer (natural resinous coating) and as an additive to strengthen adhesive bonds in woodwork and basketry.
- Bark: a tannin source (15–20% condensed tannins reported) for leather tanning; also processed as a vegetable dye to produce brown-black shades on protein fibers.
- Bark ash: used to mordant cotton and other plant fibers; provides potassium ions that improve dye uptake and fastness.
- Pulpwood: suitable for kraft pulping due to favorable lignin/cellulose ratios.
- Fuelwood and charcoal: utilized locally.

Food and beverages (non-medicinal):
- Seed oil: edible after neutralization/refining; characterized by high linoleic acid and moderate polyunsaturated content. Oil is also processed into soap.

Colorants and tanning:
- Bark: yields brown/black tannins; used as a vegetable dye for wool, silk, and other protein fibers. High condensed-tannin content and low pH support mordanting-free dyeing and tanning of hides.

Wood and fiber:
- Sawn timber: used in heavy construction, sleepers, poles, and marine structures; fiber/lignin characteristics confer strength, density, and durability.
- Bast fiber: sometimes prepared locally for cordage and basketry; not a major industrial fiber.
- Pulp for paper: kraft pulp produced from the wood, leveraging lignocellulose composition.

Fragrance and cosmetics:
- Heartwood resin: contributes fixed oil/resin and a characteristic odor used in perfumery bases and to scent or set cosmetics (resin-based fixatives).

Properties relevant to use:
- Timbers: very high density, high strength, and durability in ground contact; oil-rich heartwood resists moisture and decay.
- Bark: condensed tannin content suitable for vegetable tanning and dyeing; acidity supports mordanting of natural fibers.
- Seed oil: high linoleic acid with moderate polyunsaturated fatty acids; iodine value ~110–130 and saponification value ~190–200 mg KOH/g reported for related Lophira species, used to estimate soap performance and oxidation stability.

Standards and regulation:
- Timber classifications: EN 13556 (nomenclature and commercial timbers in Europe) includes Lophira lanceolata under the trade name Azobe.
- Seed oil: processed as a food oil only when refined to meet national food laws (e.g., Codex Alimentarius, EU Regulation 1924/2006 on nutrition and health claims).
- Leather: tanning and dyeing practices follow national regulations and best-practice guides for vegetable tanning (e.g., Leather Working Group sustainability standards).

Sustainability and sourcing:
- Species typically regenerated naturally in savanna–forest mosaics; harvesting of bark and heartwood should be managed to avoid over-extraction. Forest certification (e.g., FSC/PEFC) applies where established, and regional timber trade follows national forestry regulations (e.g., CITES listing for Lophira lanceolata—Appendix II).
- Seed oil production is seasonal and localized, with processing limited by seed size and free fatty acid levels of the pressed oil.
- Tanning extracts may be produced via sustainable collection of bark under controlled cutting cycles; resin harvesting should target dead or selected trees to minimize impact.

Synonyms Top

Scientific name Authority First published in
Lophira spathulata Tiegh. J. Bot. (Morot) 15: 187. 1901

Common names Top

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Language Common/alternative name
English dwarf red ironwood
Bambara màkan
Bambara màna
Czech lofira kopinatá
Fulah kareehi gori
kcg nansham
mul dwarf red ironwood

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Sudan
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Mali
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000443230
Tropicos 22800594
KEW urn:lsid:ipni.org:names:606368-1
The Plant List kew-2493772
Open Tree Of Life 148603
Observations.org 521661
NCBI Taxonomy 670087
IUCN Red List 156106640
IPNI 606368-1
iNaturalist 186083
GBIF 3695585
EPPO LOHLA
Elurikkus 397343
USDA GRIN 401744
Wikipedia Lophira_lanceolata

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
Susceptibility of Mangifera indica (Sapindales: Anacardiaceae) cultivars to fruit flies (Diptera: Tephritidae) in 2 agroecological zones of Cameroon Mokam DG, Atougour N, Tadu Z, Aléné DC, Awono E, Lontsi Tapeo S, Ngamo Tinkeu LS, Djieto-Lordon C J Insect Sci 16-Mar-2024
PMCID:PMC10943628
doi:10.1093/jisesa/ieae027
PMID:38491950
How do plant demographic and ecological traits combined with social dynamics and human traits affect woody plant selection for medicinal uses in Benin (West Africa)? Ahoyo CC, Houéhanou TD, Yaoitcha AS, Akpi BP, Natta A, Houinato MR J Ethnobiol Ethnomed 09-Feb-2024
PMCID:PMC10854095
doi:10.1186/s13002-024-00655-2
PMID:38336725
New Insights Into The Evolution of Chloroplast Genomes in Ochna Species (Ochnaceae, Malpighiales) Nhat Nam N, Hoang Danh N, Minh Thiet V, Do HD Evol Bioinform Online 15-Nov-2023
PMCID:PMC10655658
doi:10.1177/11769343231210756
PMID:38020533
Searching for Natural Plants with Antimelanogenesis and Antityrosinase Properties for Cosmeceutical or Nutricosmetics Applications: A Systematic Review Tung XY, Yip JQ, Gew LT ACS Omega 06-Sep-2023
PMCID:PMC10515176
doi:10.1021/acsomega.3c02994
PMID:37744793
Antimalarial Efficacy and Antioxidant Activity of Lophira lanceolata Stem Bark Ethanol Extract Using Plasmodium berghei Induced-Malaria in Swiss Albino's Mice Azizi MA, Nadia NA, Cedric Y, Sidiki NN, Guy-Armand GN, Esther DD, Sandra TN, Kevin TD, Payne VK J Parasitol Res 18-Aug-2023
PMCID:PMC10457170
doi:10.1155/2023/9400650
PMID:37637978
Ethnoveterinary survey of trypanocidal medicinal plants of the beninese pharmacopoeia in the management of bovine trypanosomosis in North Benin (West Africa) Iwaka C, Azando EV, Houehanou TD, Kora S, Idrissou Y, Olounlade PA, Hounzangbe-Adote SM Heliyon 01-Jul-2023
PMCID:PMC10366400
doi:10.1016/j.heliyon.2023.e17697
PMID:37496927
Isoliensinine from Cissampelos pariera rhizomes exhibits potential gametocytocidal and anti-malarial activities against Plasmodium falciparum clinical isolates Muema JM, Mutunga JM, Obonyo MA, Getahun MN, Mwakubambanya RS, Akala HM, Cheruiyot AC, Yeda RA, Juma DW, Andagalu B, Johnson JL, Roth AL, Bargul JL Malar J 20-May-2023
PMCID:PMC10199507
doi:10.1186/s12936-023-04590-7
PMID:37208735
In vitro nematocidal potential of hydro-ethanolic and aqueous extracts of Calotropis procera (Aiton) W.T. Aiton, 1811 (Apocynaceae) and Faidherbia albida (Delile) A. Chev., 1934 (Fabacae) against Onchocerca ochengi and Caenorhabditiselegans Mamat A, Lame Y, Sabine Adeline FY, Yvette N, Ndode Herman ON, Arnold Roger BN, Dieudonné N Heliyon 18-May-2023
PMCID:PMC10209015
doi:10.1016/j.heliyon.2023.e16379
PMID:37251817
Antiplasmodial, Antioxidant and Cytotoxicity Activity of Ethanol and Aqueous Extracts of Khaya grandifoliola Stem Bark Guy-Armand GN, Cedric Y, Christelle Nadia NA, Azizi MA, Aboubakar Sidiki NN, Jemimah Sandra TN, Alex Kevin TD, Payne VK J Trop Med 28-Mar-2023
PMCID:PMC10072966
doi:10.1155/2023/8062453
PMID:37025605
In Vitro Antiplasmodial, Cytotoxicity, and Antioxidant Activities of Lophira lanceolata (Ochnaceae): A Cameroonian Plant Commonly Used to Treat Malaria Abdel Azizi M, Christelle Nadia NA, Cedric Y, Guy-Armand GN, Aboubakar Sidiki NN, Jemimah Sandra TN, Alex Kevin TD, Payne VK J Trop Med 11-Feb-2023
PMCID:PMC9938790
doi:10.1155/2023/4061592
PMID:36820149
Antihelminthic Activity of Lophira Lanceolata on Heligmosomoides polygyrus Using an Automated High-Throughput Method Cédric Y, Christelle Nadia NA, Sylvain Raoul SN, Berinyuy S, Azizi MA, Jemimah Sandra TN, Aboubakar Sidiki NN, Payne VK J Trop Med 20-Jan-2023
PMCID:PMC9883098
doi:10.1155/2023/9504296
PMID:36713298
Insecticidal and Detoxification Enzyme Inhibition Activities of Essential Oils for the Control of Pulse Beetle, Callosobruchus maculatus (F.) and Callosobruchus chinensis (L.) (Coleoptera: Bruchidae) Gupta H, Deeksha, Urvashi, Reddy SG Molecules 04-Jan-2023
PMCID:PMC9863611
doi:10.3390/molecules28020492
PMID:36677552
Anthelmintic Agents from African Medicinal Plants: Review and Prospects Jato J, Orman E, Duah Boakye Y, Oppong Bekoe E, Oppong Bekoe S, Asare-Nkansah S, Spiegler V, Hensel A, Liebau E, Agyare C Evid Based Complement Alternat Med 31-Dec-2022
PMCID:PMC9825222
doi:10.1155/2022/8023866
PMID:36624864
Suppressive, Curative, and Prophylactic Effects of Maesa lanceolata Forssk. against Rodent Malaria Parasite Plasmodium berghei Tekalign E, Tadege G, Fisseha N, Nureye D Biomed Res Int 12-Nov-2022
PMCID:PMC9675603
doi:10.1155/2022/8901555
PMID:36411769
Antileishmanial Activities of Medicinal Herbs and Phytochemicals In Vitro and In Vivo: An Update for the Years 2015 to 2021 Hassan AA, Khalid HE, Abdalla AH, Mukhtar MM, Osman WJ, Efferth T Molecules 04-Nov-2022
PMCID:PMC9656935
doi:10.3390/molecules27217579
PMID:36364404

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 / Benzophenones
Arugosin H 11844239 Click to see 356.40 unknown https://doi.org/10.1021/NP050169W
https://doi.org/10.1021/NP50062A011
https://doi.org/10.1016/S0031-9422(00)97794-X
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans
(2,4-dihydroxyphenyl)-[(2S,3R,4S,5R)-5-(2,4-dihydroxyphenyl)-2-(4-hydroxyphenyl)-4-[(4-hydroxyphenyl)methyl]oxolan-3-yl]methanone 162912725 Click to see C1=CC(=CC=C1CC2C(C(OC2C3=C(C=C(C=C3)O)O)C4=CC=C(C=C4)O)C(=O)C5=C(C=C(C=C5)O)O)O 514.50 unknown https://doi.org/10.1016/S0040-4039(00)99585-6
[(2R,3S,4S,5S)-4-(2,4-dihydroxybenzoyl)-2,5-bis(4-hydroxyphenyl)oxolan-3-yl]-(2,4-dihydroxyphenyl)methanone 102056152 Click to see 528.50 unknown https://doi.org/10.1016/0031-9422(90)83054-5
[(2S,3S,4S,5S)-4-(2,4-dihydroxybenzoyl)-2,5-bis(4-hydroxyphenyl)oxolan-3-yl]-(2,4-dihydroxyphenyl)methanone 102056153 Click to see 528.50 unknown https://doi.org/10.1016/0031-9422(90)83054-5
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
[(1S,2R,3S,4Z,5R)-4-(cyanomethylidene)-2,3-dihydroxy-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexyl] benzoate 101670835 Click to see 451.40 unknown https://doi.org/10.1021/NP50109A014
[(1S,2Z,3R,5S,6S)-2-(cyanomethylidene)-5,6-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexyl] benzoate 101670834 Click to see 451.40 unknown https://doi.org/10.1021/NP50109A014
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Breynioside A 11176815 Click to see 392.40 unknown https://doi.org/10.1021/NP970370+
Lanceoloside A 133556315 Click to see C1=CC(=CC=C1C(=O)OCC2C(C(C(C(O2)OC3=CC=C(C=C3)O)O)O)O)O 392.40 unknown https://doi.org/10.1021/NP970370+
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R)-7-hydroxy-2-[2-(4-hydroxyphenyl)-1-benzofuran-5-yl]-2,3-dihydrochromen-4-one 162990740 Click to see 372.40 unknown https://doi.org/10.1021/NP50103A021
(E)-3-[(2R,3R)-3-[(R)-[5-[(2R,3S,4R,5S)-4-(2,4-dihydroxybenzoyl)-5-(4-hydroxyphenyl)-3-[(4-hydroxyphenyl)methyl]oxolan-2-yl]-2,4-dihydroxyphenyl]-(2,4-dihydroxyphenyl)methyl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]-1-(2,4-dihydroxyphenyl)prop-2-en-1-one 162954354 Click to see 1009.00 unknown https://doi.org/10.1016/S0040-4039(00)99585-6
(E)-3-[3-[[5-[4-(2,4-dihydroxybenzoyl)-5-(4-hydroxyphenyl)-3-[(4-hydroxyphenyl)methyl]oxolan-2-yl]-2,4-dihydroxyphenyl]-(2,4-dihydroxyphenyl)methyl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]-1-(2,4-dihydroxyphenyl)prop-2-en-1-one 16168529 Click to see 1009.00 unknown https://doi.org/10.1016/S0040-4039(00)99585-6
Lophirachalcone 16131338 Click to see C1=CC(=CC=C1CC2C(C(OC2C3=CC(=C(C=C3O)O)C(C4C(OC5=C4C=C(C=C5)C=CC(=O)C6=C(C=C(C=C6)O)O)C7=CC=C(C=C7)O)C8=C(C=C(C=C8)O)O)C9=CC=C(C=C9)O)C(=O)C1=C(C=C(C=C1)O)O)O 1009.00 unknown https://doi.org/10.1271/BBB.56.769
Lophirone D 14376455 Click to see 400.40 unknown https://doi.org/10.1021/NP50062A011
Lophirone E 14376454 Click to see 372.40 unknown https://doi.org/10.1021/NP50062A011
https://doi.org/10.1021/NP50103A021
Lophirone I 42607815 Click to see 372.40 unknown https://doi.org/10.1021/NP50103A021
Lophirone J 42607816 Click to see 400.40 unknown https://doi.org/10.1021/NP50103A021
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1021/NP050169W
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
2-(3-((2R,3S)-5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochroman-3-yl)-4-hydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one 101673330 Click to see 540.50 unknown https://doi.org/10.1021/NP50111A015
3-[5-[(E)-3-(2,4-dihydroxyphenyl)-3-oxoprop-1-enyl]-2-hydroxyphenyl]-7-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 14311191 Click to see 510.50 unknown https://doi.org/10.1016/S0031-9422(00)97794-X
https://doi.org/10.1021/NP50062A011
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/S0305-1978(02)00187-4
> Phenylpropanoids and polyketides / Flavonoids / Furanoflavonoids and dihydrofuranoflavonoids
[(2S,3S,3aS,4S,9bR)-7-methoxy-2,4-bis(4-methoxyphenyl)-3,3a,4,9b-tetrahydro-2H-furo[3,2-c]chromen-3-yl]-(2,4-dimethoxyphenyl)methanone 102056154 Click to see 582.60 unknown https://doi.org/10.1016/0031-9422(90)83054-5
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Irilone 5281779 Click to see 298.25 unknown https://doi.org/10.1021/NP050169W
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
3-(4-Hydroxyphenyl)-5-methoxy-8,8-dimethylpyrano[2,3-h]chromen-4-one 10545788 Click to see 350.40 unknown https://doi.org/10.1021/NP970370+
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
3-[(1R)-1-[bis(4-hydroxyphenyl)methyl]-2-(2,4-dihydroxyphenyl)-2-oxo-ethyl]-7-hydroxy-chromen-4-one 11577090 Click to see 510.50 unknown https://doi.org/10.1016/S0040-4039(00)96256-7
Lophirone A 5488805 Click to see C1=CC(=CC=C1C(C2=CC=C(C=C2)O)C(C3=COC4=C(C3=O)C=CC(=C4)O)C(=O)C5=C(C=C(C=C5)O)O)O 510.50 unknown https://doi.org/10.1016/S0031-9422(00)97794-X
https://doi.org/10.1021/NP050169W
https://doi.org/10.1021/NP50062A011
https://doi.org/10.1021/NP50070A029
https://doi.org/10.1016/S0040-4039(00)96256-7
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
Alatachalcone 16131034 Click to see 1009.00 unknown https://doi.org/10.1271/BBB.56.769

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