Details Top

Internal ID UUID64400e7c3b1bf332518230
Scientific name Cachrys sicula
Authority L.
First published in Sp. Pl. ed. 2 : 355 (1762)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Cachrys sicula is not reported in reliable sources to be used for commercial timber, fiber, gums/resins, seed oils, starch/flour, dyes, fragrances, or beverages.

Industrial and craft applications:
No documented industrial or craft applications are found in the literature.

Food and beverages (non-medicinal):
No non-medicinal food or beverage uses are reported.

Colorants and tanning:
No documented use as a dye or tannin source is reported.

Wood and fiber:
No timber, wood products, or bast/leaf fiber uses are documented.

Fragrance and cosmetics:
No use in fragrance or cosmetic formulations is reported.

Properties relevant to use:
No species-specific properties relevant to use (e.g., fiber morphology, oil profile, tannin content) are documented in the consulted sources.

Standards and regulation:
No relevant standards or regulatory frameworks are applicable due to lack of reported uses.

Sustainability and sourcing:
No documented commercial cultivation, harvesting, or supply chain is reported.

Synonyms Top

Scientific name Authority First published in
Ulospermum siculum Link Handbuch 1: 343 (1829)
Smyrnium hispidum Crantz Cl. Umbell. Emend. : 73 (1767)
Seseli brachylobum (Batt.) M.Hiroe Umbell. World : 1126 (1979)
Cachrys crispata Pomel Nouv. Mat. Fl. Atl. 1: 151 (1874)
Cachrys pterochlaena DC. Prodr. 4: 237 (1830)
Hippomarathrum brachylobum (Batt.) Sennen & Mauricio Cat. Fl. Rif Orient. : 49 (1933)
Hippomarathrum crispatum Pomel Nouv. Mat. Fl. Atl. 1: 151 (1874)
Hippomarathrum pterochlaenum Boiss. Ann. Sci. Nat., Bot. sér. 3, 2: 74. 1844
Hippomarathrum siculum Hoffmanns. & Link Enum. Hort. Berol. Alt. 1: 271 (1821)
Hippomarathrum bocconei var. brachylobum Batt. Fl. Algérie Dicot.: 358 1889
Hippomarathrum bocconei subsp. crispatum (Pomel) Batt. Fl. Algérie Dicot.: 358 1889
Hippomarathrum libanotis var. crispatum (Pomel) Maire Bull. Soc. Hist. Nat. Afrique N. 25: 302 1934
Hippomarathrum libanotis var. crispulum Maire Bull. Soc. Hist. Nat. Afrique N. 25: 302 1934
Hippomarathrum libanotis subsp. pterochlaenum (Boiss.) Maire Bull. Soc. Hist. Nat. Afrique N. 25: 302 1934
Hippomarathrum libanotis var. siculum (L.) Fiori Fl. Italia 2: 206 1900
Hippomarathrum tineoi Lojac. Malpighia 20: 296 (1906)
Hippomarathrum pterochlaenum (DC.) Boiss. Ann. Sci. Nat., Bot. , sér. 3, 2: 74 (1844)

Common names Top

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Language Common/alternative name
Arabic كاشريس صقلي

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
  • Europe
    • Southeastern Europe
      • Italy
      • Sicilia
    • Southwestern Europe
      • Portugal
      • Sardegna
      • Spain

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000577591
Tropicos 100302913
Flora of Italy 3537
KEW urn:lsid:ipni.org:names:839577-1
The Plant List kew-2688939
Open Tree Of Life 5386
Observations.org 144760
NCBI Taxonomy 489421
IPNI 839577-1
iNaturalist 341573
GBIF 3634425
EPPO CJYSI
EOL 31021534

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
Cachrys L. Genus: A Comprehensive Review on Botany, Phytochemistry and Biological Properties Musolino V, Perri MR, Conforti F, Gliozzi M, Marrelli M, Mollace V Plants (Basel) 26-Jan-2023
PMCID:PMC9921173
doi:10.3390/plants12030565
PMID:36771650
Analysis of Primary Liquid Chromatography Mass Spectrometry Data by Neural Networks for Plant Samples Classification Turova P, Stavrianidi A, Svekolkin V, Lyskov D, Podolskiy I, Rodin I, Shpigun O, Buryak A Metabolites 19-Oct-2022
PMCID:PMC9611620
doi:10.3390/metabo12100993
PMID:36295895
Floristic and Vegetation Changes on a Small Mediterranean Island over the Last Century Sciandrello S, Cambria S, Giusso del Galdo G, Guarino R, Minissale P, Pasta S, Tavilla G, Cristaudo A Plants (Basel) 01-Apr-2021
PMCID:PMC8065674
doi:10.3390/plants10040680
PMID:33916121
Assessment of Photo-Induced Cytotoxic Activity of Cachrys sicula and Cachrys libanotis Enriched-Coumarin Extracts against Human Melanoma Cells Marrelli M, Perri MR, Amodeo V, Giordano F, Statti GA, Panno ML, Conforti F Plants (Basel) 08-Jan-2021
PMCID:PMC7826759
doi:10.3390/plants10010123
PMID:33435579
Coumarins and ferulol esters from Cachrys sicula Manuel Grande, María T. Aguado, Balbino Mancheño, Francisco Piera Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)85511-9

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 / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see 228.37 unknown https://doi.org/10.1016/S0031-9422(00)85511-9
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.1016/S0031-9422(00)85511-9
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1016/S0031-9422(00)85511-9
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown https://doi.org/10.1016/S0031-9422(00)85511-9
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1016/S0031-9422(00)85511-9
> Phenylpropanoids and polyketides / Coumarins and derivatives
Ulopterol 176475 Click to see 278.30 unknown https://doi.org/10.1016/S0031-9422(00)85511-9
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(-)-Deltoin 906525 Click to see 328.40 unknown https://doi.org/10.1016/S0031-9422(00)85511-9
(+)-Oxypeucedanin 928465 Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C 286.28 unknown https://doi.org/10.1016/S0031-9422(00)85511-9
Gosferol 511358 Click to see 286.28 unknown https://doi.org/10.1016/S0031-9422(00)85511-9
Imperatorin 10212 Click to see 270.28 unknown https://doi.org/10.1016/S0031-9422(00)85511-9
Isoimperatorin 68081 Click to see 270.28 unknown https://doi.org/10.1016/S0031-9422(00)85511-9
Pabulenol 3009225 Click to see CC(=C)C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O 286.28 unknown https://doi.org/10.1016/S0031-9422(00)85511-9
Pranchimgin 908164 Click to see 328.40 unknown https://doi.org/10.1016/S0031-9422(00)85511-9
Saxalin 182277 Click to see 322.74 unknown https://doi.org/10.1016/S0031-9422(00)85511-9
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1016/S0031-9422(00)85511-9
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1016/S0031-9422(00)85511-9
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown https://doi.org/10.1016/S0031-9422(00)85511-9

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