Peucedanum zenkeri

Details Top

Internal ID UUID643ff767c5eba790364720
Scientific name Peucedanum zenkeri
Authority Engl.
First published in Bot. Jahrb. Syst. 57(2): 231. 1921 [6 May 1921]

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Dried leaf, whole or ground; also sold as a whole herb and occasionally as crushed leaf/seed for culinary and flavor applications.
- Essential oil (obtained by steam distillation), used in flavor–fragrance compositions.

Food and beverages (non-medicinal):
- Leaf and seed are used as a condiment and aromatic herb in soups, stews, and other dishes in parts of West Africa; examples are recorded in the Lake Chad Basin. Commercially, the herb is sold as a food seasoning.
- In the same region, the leaf (and sometimes seed) is used in the preparation of traditional fermented beverages (for example, burukuto and pito), functioning as an aromatic and flavoring component; use is as an ingredient rather than a fermentative substrate.

Fragrance and cosmetics:
- Essential oil is a natural flavor and fragrance material, typically employed at low concentrations as a flavorant and scent component; applications are documented in food flavors and selected fragrance applications.
- Volatile profile is characterized by monoterpenes, notably α- and β-phellandrene and limonene, which underpin the aromatic properties.

Properties relevant to use:
- The monoterpene-rich essential oil (α- and β-phellandrene; limonene) provides characteristic citrus–herbal aroma notes suitable for flavor–fragrance use.
- The herb’s essential oil fraction is utilized as a flavoring extract in food and beverage formulations.

Standards and regulation:
- No specific ISO/ASTM/EN standards are identified for this species’ leaf or oil; where used in food or flavor applications, general national food and flavor regulations apply.

Synonyms Top

No known synonyms.

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000391110
Tropicos 1701944
KEW urn:lsid:ipni.org:names:2402707-4
The Plant List kew-2402707
Open Tree Of Life 462529
NCBI Taxonomy 408992
IPNI 846538-1
GBIF 3640193
EPPO PCDZE

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
Phytochemical screening and antibacterial activity of Skimmia anquetilia N.P. Taylor and Airy Shaw: A first study from Kashmir Himalaya Nabi M, Tabassum N, Ganai BA Front Plant Sci 12-Aug-2022
PMCID:PMC9412939
doi:10.3389/fpls.2022.937946
PMID:36035710
Deverra tortuosa (Desf.) DC from Saudi Arabia as a new source of marmin and furanocoumarins derivatives with α-glucosidase, antibacterial and cytotoxic activities Oueslati MH, Guetat A, Bouajila J, Alzahrani AK, Basha J Heliyon 05-Apr-2021
PMCID:PMC8056227
doi:10.1016/j.heliyon.2021.e06656
PMID:33898812
Aromatic Plants of Tropical Central Africa. XVIII. Essential Oils of Leaf and Rhizome of<i>Peucedanum zenkeri</i>Engl. from Cameroon Chantal Menut, Celestin Eyele Mve-Mba, G. Lamaty, Paul-H. Amvam Zollo, Francois Tchoumbougnang, Jean-Marie Bessiere Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1995.9698468
Effects of Naturally Occurring Coumarins on Hepatic Drug Metabolizing Enzymes in Mice Kleiner HE, Xia X, Sonoda J, Zhang J, Pontius E, Abey J, Evans RM, Moore DD, DiGiovanni. J Toxicol Appl Pharmacol 15-Jul-2008
PMCID:PMC2585982
doi:10.1016/j.taap.2008.07.004
PMID:18692084

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 / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698468
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698468
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698468
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1080/10412905.1995.9698468
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698468
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1995.9698468
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698468
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698468
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1995.9698468
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1995.9698468
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1995.9698468
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1995.9698468
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698468
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698468
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698468
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698468
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698468
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698468
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698468
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
7-epi-alpha-Selinene 10123 Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698468
alpha-Selinene 10856614 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698468
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698468
Germacrene B 5281519 Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698468
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698468
> Organoheterocyclic compounds / Benzodioxoles
Dillapiol 10231 Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC 222.24 unknown https://doi.org/10.1080/10412905.1995.9698468
Myristicin 4276 Click to see 192.21 unknown https://doi.org/10.1080/10412905.1995.9698468

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