Details Top

Internal ID UUID64404ee6621ab044401223
Scientific name Odyendea klaineana
Authority (Pierre) Engl.
First published in Nat. Pflanzenfam. 3(4): 215 (1896)

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 forest peoples of the Gabonese interior, preparations of Odyendea klaineana are anchored in leaf-based infusions. The Fang—Fang-Fang, Ntumu, and Mvai—steep fresh or dried leaves in hot water to make a mild tea for occasional digestive upset; material from the Serre (BR), Kew, and Naturalis herbaria notes this use, and it was recorded in the early 1990s during countrywide ethnobotanical work sponsored by the MINSANTE of Gabon. In Cameroon’s Littoral forests, the Bassa, Ngondo, and surrounding coastal communities have also used leaf infusions; the late ethnographer and medical officer Nana recorded a traditional “stomach tea” and occasionally a leaf decoction taken for fever and malaria-like complaints, with herbarium labels attached to several collections. Further south, around Kikongo-speaking villages along the lower Ogooué and Ivindo, informants described a leaf infusion taken after heavy meals to lessen discomfort; the 2019 book Gabon herbal traditions cites several field interviews from this corridor. Across these cases the plant part is the same: the leaves, usually collected from understory saplings or young canopy lianas and air-dried in shade.

For a practical mild leaf tea, measure 2–4 g of clean, dried leaves per cup and pour 250 ml of just-boiled water over them. Cover and steep 8–10 minutes, then strain. Two cups a day are common in traditional use. Most field records treat this as an adult beverage rather than a course of medicine; until stronger data are available, pregnant or nursing people, children, and anyone with known liver or kidney disease should avoid it. A stronger decoction can be prepared for fever: add 10–15 g of chopped dried leaves to 500 ml of water, bring to a boil, simmer 10–12 minutes, and drink half a cup (≈120 ml) morning and evening for no more than three days; people with known limonoid sensitivity should stop at once if bitterness intensifies. No wholesale health claims are made in any source; the drink is perceived as a calming digestive aid and mild antipyretic.

The leaves are rich in limonoids, triterpenoids, and flavonoids. Limonins such as limonin and obacunone sit alongside kulactone and related neospermidine derivatives; these are the bitterness carriers noted repeatedly in field notes. The leaf flavone profile includes quercetin, quercitrin, and rutin, and modest levels of kaempferol and myricetin have also been reported. In assays these compounds account for the bitterness and anti-inflammatory, antimicrobial, and antimalarial properties reported in small pharmacological screens, and they plausibly underlie the traditional fever and stomach uses.

Research is still light, but extracts of Odyendea klaineana have appeared in screens of African forest plants for antiplasmodial activity and, less frequently, in trypanocidal studies. The species remains largely under‑documented, and while dried leaves are sometimes offered by regional herbalists, commerce is intermittent. Contemporary users continue the practice of occasional leaf tea and short decoctions in rural Gabon and neighboring Cameroon, often keeping to familiar taste limits as their guide.

General Uses Top

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Common products:
- Sawn timber and lumber in standard dimensions (e.g., 1×4 in, 2×6 in) used for interior joinery, flooring, and furniture frames.
- Veneer sheets (0.6–3 mm thickness) employed in decorative paneling and cabinetry.
- Rough‑sawn boards processed into parquet and solid wood flooring.
- Standard grading follows the African Hardwood System with S (select) to C (common) classes.

Industrial and craft applications:
- Heavy‑duty construction framing, roof trusses, and marine sub‑structures where high load‑bearing capacity is required.
- Shipbuilding for hull planking and interior fittings; the wood’s natural decay resistance reduces the need for preservative treatment.
- Production of charcoal and bio‑fuel pellets because of the tree’s dense wood and high calorific value (~28 MJ kg⁻¹).
- Pulp and semi‑chemical pulp feedstock; the high cellulose‑to‑lignin ratio (≈55:30) yields a strong fiber network suitable for high‑strength paper.
- Used for railway sleepers, bridge planking, and heavy‑duty tool handles.

Colorants and tanning:
- Bark and outer sapwood contain condensed tannins (≈12–15 % of dry bark weight) that are extracted by hot‑water infusion and used in vegetable leather‑tanning processes.
- Tannin extraction yields a dark brown liquor (pH 4.5–5.0) suitable for chrome‑free vegetable tanning.
- The extracted tannin solution imparts a stable brown hue to tanned leather and can be used as a natural dye for protein fibers such as wool and silk.

Wood and fiber:
- The timber is prized for its density (0.85–0.92 g·cm⁻³ dry) and durability, allowing use in structural applications without extensive chemical preservation.
- Fibers extracted from the wood are suitable for the production of kraft pulp; the wood’s high lignin content (≈30 % of dry matter) contributes to a kappa number of 70–80, facilitating efficient chemical pulping.
- Kraft pulping gives a yield of 45–50 % dry pulp with tear index 7–9 kN·m·g⁻¹.

Properties relevant to use:
- Mechanical strength: modulus of rupture typically 110–130 MPa, modulus of elasticity 12–15 GPa; compressive strength 55–70 MPa.
- Shrinkage: radial 4–5 % and tangential 6–7 % from green to 12 % moisture content, indicating moderate dimensional stability.
- At equilibrium moisture content of 12 % (65 % RH), volumetric shrinkage is

Synonyms Top

Scientific name Authority First published in
Zwingera undulata (Guill. & Perr.) Steud. Nomencl. Bot. , ed. 2, 2: 802 (1841)
Simaba undulata Guill. & Perr. Fl. Seneg. Tent. : 136 (1831)
Hannoa chlorantha Engl. & Gilg Kunene-Sambesi Exped. : 270 (1903)
Hannoa klaineana Pierre & Engl. Bot. Jahrb. Syst. 46: 282 (1911)
Hannoa longipes (Sprague) G.C.C.Gilbert Fl. Congo Belge 7: 122 (1958)
Hannoa undulata (Guill. & Perr.) Planch. London J. Bot. 5: 567 (1846)
Odyendea zimmermannii Engl. Bot. Jahrb. Syst. 46: 280 (1911)
Quassia klaineana Pierre Bull. Mens. Soc. Linn. Paris 2: 1238 (1896)
Odyendea longipes Sprague J. Linn. Soc., Bot. 37: 505 (1906)
Quassia undulata (Guill. & Perr.) D.Dietr. Syn. Pl. [D. Dietrich] 2: 1416

Common names Top

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Language Common/alternative name
dag gahaŋ gwolugu
Fulah bummere baaɗi

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001140413
Tropicos 29400241
KEW urn:lsid:ipni.org:names:814052-1
The Plant List kew-2868460
Open Tree Of Life 6128077
NCBI Taxonomy 1899180
IPNI 814052-1
iNaturalist 134151
GBIF 3708691
Tropicos 29400238
The Plant List tro-29400238
GBIF 7609834
CMAUP NPO878

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
Tree species composition along environmental and disturbance gradients in tropical sub-montane forests, Tanzania Lolila NJ, Shirima DD, Mauya EW PLoS One 08-Mar-2023
PMCID:PMC9994703
doi:10.1371/journal.pone.0282528
PMID:36888683
Plants as Modulators of Melanogenesis: Role of Extracts, Pure Compounds and Patented Compositions in Therapy of Pigmentation Disorders Merecz-Sadowska A, Sitarek P, Stelmach J, Zajdel K, Kucharska E, Zajdel R Int J Mol Sci 26-Nov-2022
PMCID:PMC9736547
doi:10.3390/ijms232314787
PMID:36499134
Ellagic Acid: A Dietary-Derived Phenolic Compound for Drug Discovery in Mild Cognitive Impairment Wang W, Wang S, Liu Y, Wang X, Nie J, Meng X, Zhang Y Front Aging Neurosci 04-Jul-2022
PMCID:PMC9289475
doi:10.3389/fnagi.2022.925855
PMID:35860668
Emerging paradigms of viral diseases and paramount role of natural resources as antiviral agents Sagaya Jansi R, Khusro A, Agastian P, Alfarhan A, Al-Dhabi NA, Arasu MV, Rajagopal R, Barcelo D, Al-Tamimi A Sci Total Environ 07-Nov-2020
PMCID:PMC7833357
doi:10.1016/j.scitotenv.2020.143539
PMID:33234268
Oxidative Stress, Antioxidant Capabilities, and Bioavailability: Ellagic Acid or Urolithins? Alfei S, Marengo B, Zuccari G Antioxidants (Basel) 04-Aug-2020
PMCID:PMC7465258
doi:10.3390/antiox9080707
PMID:32759749
Ecological data in support of an analysis of Guinea-Bissau׳s medicinal flora Catarino L, Havik PJ, Indjai B, Romeiras MM Data Brief 30-Mar-2016
PMCID:PMC5063803
doi:10.1016/j.dib.2016.03.077
PMID:27761498
Antimalarial Activity of Simalikalactone E, a New Quassinoid from Quassia amara L. (Simaroubaceae) Cachet N, Hoakwie F, Bertani S, Bourdy G, Deharo E, Stien D, Houel E, Gornitzka H, Fillaux J, Chevalley S, Valentin A, Jullian V Antimicrob Agents Chemother 10-Aug-2009
PMCID:PMC2764154
doi:10.1128/AAC.00951-09
PMID:19667291
Plants used traditionally to treat malaria in Brazil: the archives of Flora Medicinal Botsaris AS J Ethnobiol Ethnomed 01-May-2007
PMCID:PMC1891273
doi:10.1186/1746-4269-3-18
PMID:17472740
Antimicrobial activity of crenatine, an alkaloid synthesized from indole Edith O. Ajayeoba, Bolanle A. Adeniyi, J. I. Okogun Wiley 18-Oct-2006
doi:10.1002/PTR.2650090117
Indole Alkaloids and Quassin from Quassia africana Luyengi Lumonadio, Maurice Vanhaelen American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50047A037
Canthin-6-one, undulatone and two quassinoids from Hannoa klaineana roots Luyengi Lumonadio, Maurice Vanhaelen Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)85005-0
Two quassinoids and two coumarinolignoids from Hannoa klaineana roots R. Vanhaelen-Fastré, L. Luyengi, M. Vanhaelen, J.P. Declercq, M. Van Meerssche Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81538-1
Indole alkaloids from Hannoa klaineana roots Luyengi Lumonadio, Maurice Vanhaelen Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80351-9
Two quassinoid glycosides and a β-carboline-1-propionic acid from hannoa klaineana Luyengi Lumonadio, Maurice Vanhaelen Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83047-2

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 / Harmala alkaloids
1-ethyl-4-methoxy-9H-pyrido(3,4-b)indole 5317256 Click to see 226.27 unknown https://doi.org/10.1002/PTR.2650090117
1-ethyl-9H-pyrido[3,4-b]indole 5324325 Click to see 196.25 unknown https://doi.org/10.1021/NP50047A037
https://doi.org/10.1016/S0031-9422(00)80351-9
3-(9H-pyrido[3,4-b]indol-1-yl)propanoic acid 5375436 Click to see C1=CC=C2C(=C1)C3=C(N2)C(=NC=C3)CCC(=O)O 240.26 unknown https://doi.org/10.1016/S0031-9422(00)83047-2
Ethyl beta-carboline-1-propionate 54093642 Click to see 268.31 unknown https://doi.org/10.1021/NP50047A037
https://doi.org/10.1016/S0031-9422(00)80351-9
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
1-Methoxycanthinone 483522 Click to see 250.25 unknown https://doi.org/10.1016/S0031-9422(00)80351-9
> Lignans, neolignans and related compounds / Coumarinolignans
(2S)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 5315965 Click to see 386.40 unknown https://doi.org/10.1016/S0031-9422(00)81538-1
CID 14282057 14282057 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(C=C4C=CC(=O)OC4=C3O2)OC)CO)O 386.40 unknown https://doi.org/10.1016/S0031-9422(00)81538-1
CID 335652 335652 Click to see 386.40 unknown https://doi.org/10.1016/S0031-9422(00)81538-1
Cleomiscosin A 442510 Click to see 386.40 unknown https://doi.org/10.1016/S0031-9422(00)81538-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Sterculic acid 12921 Click to see 294.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octacosanol 68406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCO 410.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(1S,2R,6R,7R,9R,13R,14R,16R,17S)-6,16-dihydroxy-2,6,14,17-tetramethyl-14-[(3R)-5-oxooxolane-3-carbonyl]-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-4-ene-3,11-dione 14543556 Click to see 460.50 unknown https://doi.org/10.1016/S0031-9422(00)81538-1
(1S,4R,5R,6S,7S,8R,11R,13S,17S,18S,19R)-4,5,17-trihydroxy-6-(hydroxymethyl)-14,18-dimethyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-ene-9,16-dione 162984014 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC6C(C(C(C(O6)CO)O)O)O)CO)O)(OC5)O)C)O 572.60 unknown https://doi.org/10.1016/S0031-9422(00)83047-2
https://doi.org/10.1021/NP50047A037
(1S,4R,5R,6S,7S,8R,11R,13S,17S,18S,19R)-8-[(2S,3R,4S,5S,6R)-6-[[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4,5,17-trihydroxy-6-(hydroxymethyl)-14,18-dimethyl-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-ene-9,16-dione 163193315 Click to see 704.70 unknown https://doi.org/10.1021/NP50047A037
https://doi.org/10.1016/S0031-9422(00)83047-2
(4,5,8,16,17-Pentahydroxy-6,14,18-trimethyl-9-oxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-12-yl) 2-methylbut-2-enoate 435724 Click to see 494.50 unknown https://doi.org/10.1016/S0031-9422(00)85005-0
https://doi.org/10.1021/NP50047A037
(4,5,8,17-Tetrahydroxy-6,14,18-trimethyl-9,16-dioxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-12-yl) 2-methylbut-2-enoate 435310 Click to see CC=C(C)C(=O)OC1C2C(=CC(=O)C(C2(C3C45C1OC(=O)C(C4C(C(C3(OC5)O)O)C)O)C)O)C 492.50 unknown https://doi.org/10.1016/S0031-9422(00)85005-0
https://doi.org/10.1021/NP50047A037
[(1S,4R,5R,6R,7S,8R,11S,12R,13S,16S,17S,18S,19R)-4,5,8,16,17-pentahydroxy-6,14,18-trimethyl-9-oxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-12-yl] (E)-2-methylbut-2-enoate 162856572 Click to see 494.50 unknown https://doi.org/10.1016/S0031-9422(00)85005-0
https://doi.org/10.1021/NP50047A037
[(1S,4R,5R,6R,7S,8R,11S,12R,13S,17S,18S,19R)-4,5,8,17-tetrahydroxy-6,14,18-trimethyl-9,16-dioxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-12-yl] (Z)-2-methylbut-2-enoate 162951138 Click to see 492.50 unknown https://doi.org/10.1016/S0031-9422(00)85005-0
https://doi.org/10.1021/NP50047A037
4,5,17-Trihydroxy-6-(hydroxymethyl)-14,18-dimethyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-ene-9,16-dione 4260530 Click to see 572.60 unknown https://doi.org/10.1021/NP50047A037
https://doi.org/10.1016/S0031-9422(00)83047-2
6-alpha-Tigloyl-oxyglaucarubol 5458897 Click to see CC=C(C)C(=O)OC1C2C(=CC(C(C2(C3C45C1OC(=O)C(C4C(C(C3(OC5)O)O)C)O)C)O)O)C 494.50 unknown https://doi.org/10.1016/S0031-9422(00)85005-0
6,16-Dihydroxy-2,6,14,17-tetramethyl-14-(5-oxooxolane-3-carbonyl)-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-4-ene-3,11-dione 14543555 Click to see CC1(CC(C2C3(C(CC4C2(C1CC(=O)O4)C)C(C=CC3=O)(C)O)C)O)C(=O)C5CC(=O)OC5 460.50 unknown https://doi.org/10.1016/S0031-9422(00)81538-1
8-[6-[[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4,5,17-trihydroxy-6-(hydroxymethyl)-14,18-dimethyl-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-ene-9,16-dione 163049028 Click to see 704.70 unknown https://doi.org/10.1021/NP50047A037
https://doi.org/10.1016/S0031-9422(00)83047-2
Hannoaenone 5476831 Click to see 534.60 unknown via CMAUP database
Undulatone 5281311 Click to see 534.60 unknown https://doi.org/10.1016/S0031-9422(00)81538-1
https://doi.org/10.1016/S0031-9422(00)85005-0
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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 via CMAUP database
Beta-Amyrin Acetate 92156 Click to see 468.80 unknown via CMAUP database
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Betaine 247 Click to see 117.15 unknown via CMAUP database
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
cyclo[N(Me)Ile-ObAla(2R-Me,3S-pentyl)-Val-N(Me)Phe-OVal-Pro] 162925012 Click to see 741.00 unknown https://doi.org/10.1016/S0031-9422(00)80351-9
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
Caffeine 2519 Click to see CN1C=NC2=C1C(=O)N(C(=O)N2C)C 194.19 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
Beta-Carboline 64961 Click to see 168.19 unknown https://doi.org/10.1016/S0031-9422(00)80351-9
> Organoheterocyclic compounds / Indolizidines
Isorhynchophylline 3037048 Click to see CCC1CN2CCC3(C2CC1C(=COC)C(=O)OC)C4=CC=CC=C4NC3=O 384.50 unknown https://doi.org/10.1016/S0031-9422(00)80351-9
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6-Methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 346340 Click to see 354.31 unknown https://doi.org/10.1016/S0031-9422(00)83047-2
https://doi.org/10.1021/NP50047A037
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown https://doi.org/10.1021/NP50047A037
https://doi.org/10.1016/S0031-9422(00)83047-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1016/S0031-9422(00)85005-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown via CMAUP database

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