Odyendea klaineana
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
Suggest a correction!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
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| dag | gahaŋ gwolugu |
| Fulah | bummere baaɗi |
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
Suggest others/fix!| 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)!
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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 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |