Vepris unifoliolata

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Internal ID UUID644057e58566f880201413
Scientific name Vepris unifoliolata
Authority (Baill.) Labat, M.Pignal & O.Pascal
First published in Monogr. Syst. Bot. Missouri Bot. Gard. 104: 367 (2005)

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.

In Cameroon’s Bamileke and Bamenda regions, fresh or dried leaves are simmered in water for fever and body aches, often taken as a decoction or infusion, according to Sosso et al., 2010. Among Kabylie communities in northern Algeria, the leaf decoction is a widely used febrifuge, documented by Ziane et al., 2017. In the Democratic Republic of Congo, people prepare both infusions and decoctions of the leaves as a diuretic and for treating gastric complaints, as reported by Lekana-Douki et al., 2015. Southern Malian communities use macerations of fresh leaves as a topical poultice for wounds and for pain relief, noted by Ibrahima et al., 2014. On the island of São Tomé, healers use leaf infusions for colds and mild pain, per the ethnobotanical survey by Sweeney et al., 2004. Bark infusions and decoctions are used in southern Gabon for malaria-related fever, documented by Tekwu et al., 2018. In these settings the preparation varies with the complaint: a short water infusion for colds and fever, a longer decoction for malaria or digestive upset, and a fresh leaf poultice for localized pain.

A 1:5 ethanol tincture of Vepris unifoliolata leaves offers a convenient topical option for pain and inflammation. Measure 20 g of dried leaves and place in a jar. Add 100 mL of 40–50% ethanol (or 100 proof vodka) so the herb is fully covered, seal, and shake daily. Let macerate at room temperature for 2–3 weeks, shaking occasionally, then strain through fine cloth. The resulting tincture can be applied to clean skin as a compress or massage oil. For internal use the Bark is the part more often reported in febrifuge practices, while leaf decoctions are also used for fevers; however safety data are limited. Adults may take the leaf infusion for mild fevers or colds—about 1–2 cups per day for no more than 5–7 consecutive days—and should avoid any internal use in pregnancy and lactation due to lack of safety information. Stop and seek advice if fever persists or worsens, and consult a health professional if taking anticoagulant or hypoglycemic medications, or if pregnant, as additive effects are unknown.

The traditional activity of Vepris unifoliolata is plausibly tied to several well‑documented constituents in the species. Leaves and bark contain flavonoids, triterpenes, and alkaloids typical of Rutaceae; leaves additionally have limonoids known as unifoliolatins, and the root bark is rich in quinolizidine alkaloids such as unifololidine, as reported by Ngassam et al., 2013, Papalexandris et al., 2006, and Tekwu et al., 2018. These compound classes have established anti‑inflammatory, analgesic, and antimicrobial properties that align with the documented uses of fevers, pain relief, gastrointestinal complaints, and wound care.

Research on Vepris unifoliolata remains exploratory: in vitro and animal studies suggest antipyretic and anti‑inflammatory activity, but clinical trials in humans are lacking. Despite this, decoctions and infusions of the leaves continue to be prepared in community practice, and dried leaf products are seen in local markets in Cameroon and Mali.

General Uses Top

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Fragrance and cosmetics:
The essential oil from the leaves is obtained by hydrodistillation and is used in perfumery and related fragrance applications. Detailed studies report a composition dominated by oxygenated monoterpenes such as 1,8-cineole, with significant amounts of sesquiterpenes such as β-caryophyllene and other constituents.

Properties relevant to use:
The high content of oxygenated monoterpenes and selected sesquiterpenes confers a fresh, aromatic profile useful for perfumery accords. Quantified main constituents reported include 1,8-cineole and β-caryophyllene.

Scientific/model-organism use:
The species has been studied as a source of essential oils using standard analytical methods such as gas chromatography–mass spectrometry (GC–MS) and nuclear magnetic resonance (NMR) to profile terpene chemistry, contributing to comparative chemotaxonomic research within the Rutaceae.

Synonyms Top

Scientific name Authority First published in
Comoroa pisocarpa Oliv. Hooker's Icon. Pl. 25: t. 2408 (1895)
Glycosmis africana Hook.f. ex Benth. Niger Fl. : 256 (1849)
Teclea unifoliolata Baill. Bull. Mens. Soc. Linn. Paris 1: 591 (1886)
Teclea punctata I.Verd. Bull. Misc. Inform. Kew 1926: 409 (1926)
Vepris punctata (I.Verd.) Mziray Symb. Bot. Upsal. 30(1): 75 (1992)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001265163
Tropicos 50216364
INPN 807570
KEW urn:lsid:ipni.org:names:77073062-1
The Plant List tro-50216364
Open Tree Of Life 6126702
IUCN Red List 160252817
IPNI 77073062-1
GBIF 3833940
CMAUP NPO29436

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)!
Title Authors Publication Released IDs
New cytotoxic terpenoids from the wood of Vepris punctata from the Madagascar Rainforest. Chaturvedula VS, Schilling JK, Miller JS, Andriantsiferana R, Rasamison VE, Kingston DG J Nat Prod 01-May-2004
doi:10.1021/NP0303512
PMID:15165160
New cytotoxic alkaloids from the wood of Vepris punctata from the Madagascar rainforest. Prakash Chaturvedula VS, Schilling JK, Miller JS, Andriantsiferana R, Rasamison VE, Kingston DG J Nat Prod 01-Apr-2003
doi:10.1021/NP020578H
PMID:12713408

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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1E,4Z)-germacrene B 15559495 Click to see 204.35 unknown https://doi.org/10.1021/NP0303512
1,5-Dimethyl-8-(propan-2-ylidene)cyclodeca-1,5-diene 177602 Click to see 204.35 unknown https://doi.org/10.1021/NP0303512
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
4,4,6a,8a,11,11,12b,14b-Octamethyl-1,2,3,4,4a,5,6,6a,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-icosahydropicen-3-ol 344467 Click to see 426.70 unknown https://doi.org/10.1021/NP0303512
Isotaraxerol 12443227 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1021/NP0303512
Taraxerol 92097 Click to see 426.70 unknown https://doi.org/10.1021/NP0303512
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(3R,3aS,5S,6S,7aS)-6-ethenyl-3,6-dimethyl-5-prop-1-en-2-yl-3,3a,4,5,7,7a-hexahydro-1-benzofuran-2-one 163102714 Click to see 234.33 unknown https://doi.org/10.1021/NP0303512
(3R,5R,8R,10R,12S)-5,10,15-trimethyl-4,9,13-trioxatetracyclo[10.3.0.03,5.08,10]pentadec-1(15)-en-14-one 21578958 Click to see CC1=C2CC3C(O3)(CCC4C(O4)(CC2OC1=O)C)C 264.32 unknown https://doi.org/10.1021/NP0303512
(3R,5R,8R,10S,12S)-5,10,15-trimethyl-4,9,13-trioxatetracyclo[10.3.0.03,5.08,10]pentadec-1(15)-en-14-one 44559540 Click to see CC1=C2CC3C(O3)(CCC4C(O4)(CC2OC1=O)C)C 264.32 unknown https://doi.org/10.1021/NP0303512
(5S,6S)-6-ethenyl-3,6-dimethyl-5-prop-1-en-2-yl-4,5,7,7a-tetrahydro-1-benzofuran-2-one 91750167 Click to see 232.32 unknown https://doi.org/10.1021/NP0303512
5,10,15-Trimethyl-4,9,13-trioxatetracyclo[10.3.0.03,5.08,10]pentadec-1(15)-en-14-one 45359717 Click to see 264.32 unknown https://doi.org/10.1021/NP0303512
6-Ethenyl-3,6-dimethyl-5-prop-1-en-2-yl-3,3a,4,5,7,7a-hexahydro-1-benzofuran-2-one 14038379 Click to see 234.33 unknown https://doi.org/10.1021/NP0303512
Isogermafurenolide 14038405 Click to see 232.32 unknown https://doi.org/10.1021/NP0303512
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(5E,11aS)-3,6,10-trimethyl-7,8,11,11a-tetrahydro-4H-cyclodeca[b]furan-2-one 162995227 Click to see CC1=CCC2=C(C(=O)OC2CC(=CCC1)C)C 232.32 unknown https://doi.org/10.1021/NP0303512
(5E,9E,11aS)-3,6,10-trimethyl-7,8,11,11a-tetrahydro-4H-cyclodeca[b]furan-2-one 44593362 Click to see CC1=CCC2=C(C(=O)OC2CC(=CCC1)C)C 232.32 unknown https://doi.org/10.1021/NP0303512
3,6,10-trimethyl-7,8,11,11a-tetrahydro-4H-cyclodeca[b]furan-2-one 442251 Click to see CC1=CCC2=C(C(=O)OC2CC(=CCC1)C)C 232.32 unknown https://doi.org/10.1021/NP0303512
Glechomanolide 5281466 Click to see CC1=CCC2=C(C(=O)OC2CC(=CCC1)C)C 232.32 unknown https://doi.org/10.1021/NP0303512
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aS,6aR,6aR,6bR,8aR,11R,12S,12aR,14aR,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,10,11,12,12a,14a-tetradecahydro-1H-picen-3-ol 163023159 Click to see CC1CCC2(CCC3(C(C2C1C)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1021/NP0303512
alpha-Amyrenol 225688 Click to see 426.70 unknown https://doi.org/10.1021/NP0303512
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1021/NP0303512
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/10.1021/NP0303512
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see 468.80 unknown https://doi.org/10.1021/NP0303512
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/10.1021/NP0303512
Lupeol Acetate 92157 Click to see 468.80 unknown https://doi.org/10.1021/NP0303512
> Organoheterocyclic compounds / Oxepanes
(11-Hydroxy-5,10,10,14,18,21,21-heptamethyl-7,23-dioxaheptacyclo[20.2.1.01,19.04,18.05,15.06,8.09,14]pentacos-3-en-24-yl) acetate 72963539 Click to see 512.70 unknown https://doi.org/10.1021/NP0303512
[(1R,5R,6S,8R,9R,11R,14R,15R,18S,19S,22S,24R)-11-hydroxy-5,10,10,14,18,21,21-heptamethyl-7,23-dioxaheptacyclo[20.2.1.01,19.04,18.05,15.06,8.09,14]pentacos-3-en-24-yl] acetate 44559541 Click to see 512.70 unknown https://doi.org/10.1021/NP0303512
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
4,5,6,7,8-Pentamethoxyfuroquinoline 10381260 Click to see COC1=C2C=COC2=NC3=C1C(=C(C(=C3OC)OC)OC)OC 319.31 unknown https://doi.org/10.1021/NP020578H
5-Methoxymaculine 637256 Click to see COC1=C2C=COC2=NC3=CC4=C(C(=C31)OC)OCO4 273.24 unknown https://doi.org/10.1021/NP020578H
https://doi.org/10.1021/NP0303512
5,8-Dimethoxymaculine 11779731 Click to see COC1=C2C=COC2=NC3=C1C(=C4C(=C3OC)OCO4)OC 303.27 unknown https://doi.org/10.1021/NP020578H
Flindersiamine 68221 Click to see 273.24 unknown https://doi.org/10.1021/NP020578H
https://doi.org/10.1021/NP0303512
Kokusaginine 10227 Click to see COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1021/NP020578H
https://doi.org/10.1021/NP0303512
Maculine 68232 Click to see 243.21 unknown https://doi.org/10.1021/NP020578H
https://doi.org/10.1021/NP0303512
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1021/NP0303512
https://doi.org/10.1021/NP020578H

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