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Ferula elaeochytris

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Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
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Details Top

Internal ID UUID64401c31068ee798883349
Scientific name Ferula elaeochytris
Authority Korovin
First published in Ill. Monogr. Ferula 61. 1947

Description Top

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Synonyms Top

Scientific name Authority First published in
Peucedanum meifolium Boiss. Diagn. Pl. Orient. 10: 34 (1849)
Dorema meifolium Fenzl Pug. Pl. Nov. Syr. : 18 (1842)
Ferula amani Zohary & P.H.Davis Kew Bull. 2: 90 (1947)
Ferula cassii Zohary & P.H.Davis Kew Bull. 2: 90 (1947)
Ferula meifolia (Fenzl) Boiss. Fl. Orient. [Boissier] 2: 986. [Dec 1872 or Jan 1873]

Common names Top

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Language Common/alternative name
Arabic كلخ لؤلؤي
diq helız

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

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-0000686539
Tropicos 100336815
KEW urn:lsid:ipni.org:names:77203034-1
The Plant List kew-2808401
Open Tree Of Life 1047222
NCBI Taxonomy 662809
IPNI 77203034-1
GBIF 5831957

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
Review of potential spermatogenic and aphrodisiac effects of the Ferula genus Bagheri SM, Shieh A, Ghalenoei JA, Yadegari M, Alborzi N Clin Exp Reprod Med 28-Jul-2023
PMCID:PMC10477414
doi:10.5653/cerm.2023.05995
PMID:37643827
Effect of In Vitro Digestion on the Phenolic Content of Herbs Collected from Eastern Anatolia Ozkan G, Sakarya FB, Tas D, Yurt B, Ercisli S, Capanoglu E ACS Omega 28-Mar-2023
PMCID:PMC10099410
doi:10.1021/acsomega.2c07881
PMID:37065041
Influence of Direct-fed Microbial Blend and Ferula Elaeochytris on in Vitro Rumen Fermentation Pattern and Degradability During Simulated Ruminal Acidosis Sizmaz O, Mickdam E, Eren Gultepe E J Vet Res 30-Sep-2022
PMCID:PMC9597934
doi:10.2478/jvetres-2022-0052
PMID:36349133
Metabolic Profile, Bioactivities, and Variations in the Chemical Constituents of Essential Oils of the Ferula Genus (Apiaceae) Sonigra P, Meena M Front Pharmacol 12-Mar-2021
PMCID:PMC7994278
doi:10.3389/fphar.2020.608649
PMID:33776754
Ferula asafoetida: chemical composition, thermal behavior, antioxidant and antimicrobial activities of leaf and gum hydroalcoholic extracts Niazmand R, Razavizadeh BM J Food Sci Technol 17-Aug-2020
PMCID:PMC8076422
doi:10.1007/s13197-020-04724-8
PMID:33967312
A New Ferula (Apiaceae) Species from Southwest Anatolia: Ferula pisidica Akalın & Miski Akalın E, Tuncay HO, Olcay B, Miski M Plants (Basel) 12-Jun-2020
PMCID:PMC7355485
doi:10.3390/plants9060740
PMID:32545501
In Vitro Screening of Tumoricidal Properties of International Medicinal Herbs: Part II Mazzio EA, Soliman KF Phytother Res 01-Dec-2010
PMCID:PMC2957567
doi:10.1002/ptr.3191
PMID:20564497
Activity of elaeochytrin A from Ferula elaeochytris on leukemia cell lines. Alkhatib R, Hennebelle T, Joha S, Idziorek T, Preudhomme C, Quesnel B, Sahpaz S, Bailleul F Phytochemistry 01-Dec-2008
doi:10.1016/J.PHYTOCHEM.2008.09.019
PMID:18992904
Six sesquiterpene alcohol esters from ferula elaeochytris Mahmut Miski, Ayhan Ulubelen, Tom J. Mabry Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80153-3

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
(5-hydroxy-2a,7a-dimethyl-5-propan-2-yl-2,3,4,5a,6,7-hexahydro-1aH-azuleno[6,7-b]oxiren-6-yl) 4-hydroxybenzoate 4545936 Click to see CC(C)C1(CCC2(C1C(CC3(C(C2)O3)C)OC(=O)C4=CC=C(C=C4)O)C)O 374.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
[(1aS,2aR,5R,5aS,6S,7aR)-5-hydroxy-2a,7a-dimethyl-5-propan-2-yl-2,3,4,5a,6,7-hexahydro-1aH-azuleno[6,7-b]oxiren-6-yl] 4-hydroxybenzoate 10237282 Click to see CC(C)C1(CCC2(C1C(CC3(C(C2)O3)C)OC(=O)C4=CC=C(C=C4)O)C)O 374.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3-Hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl) 4-hydroxy-3-methoxy-benzoate 496288 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC(=C(C=C3)O)OC)(C(C)C)O)C 388.50 unknown https://doi.org/10.1016/S0031-9422(00)80153-3
(3-Hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl) benzoate 496287 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC=CC=C3)(C(C)C)O)C 342.50 unknown https://doi.org/10.1016/S0031-9422(00)80153-3
https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
(3-Hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,6-hexahydroazulen-4-yl) 4-hydroxybenzoate 74400478 Click to see CC1CC(C2C(CCC2(C(C)C)O)(C=C1)C)OC(=O)C3=CC=C(C=C3)O 358.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
(3-Hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl) 2-aminobenzoate 162888285 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC=CC=C3N)(C(C)C)O)C 357.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
(3-Hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl) 2-hydroxybenzoate 14466054 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC=CC=C3O)(C(C)C)O)C 358.50 unknown https://doi.org/10.1016/S0031-9422(00)80153-3
(3-Hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl) 2-methylbut-2-enoate 162970430 Click to see CC=C(C)C(=O)OC1CC(=CCC2(C1C(CC2)(C(C)C)O)C)C 320.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
https://doi.org/10.1016/S0031-9422(00)80153-3
(3-Hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl) 4-hydroxybenzoate 496289 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC=C(C=C3)O)(C(C)C)O)C 358.50 unknown https://doi.org/10.1016/S0031-9422(00)80153-3
https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
(3-Hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl) 4-methoxybenzoate 14039831 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC=C(C=C3)OC)(C(C)C)O)C 372.50 unknown https://doi.org/10.1016/S0031-9422(00)80153-3
(3,7-Dihydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,7,8-hexahydroazulen-4-yl) 4-hydroxybenzoate 162877926 Click to see CC1=CC(C2C(CCC2(C(C)C)O)(CC1O)C)OC(=O)C3=CC=C(C=C3)O 374.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
[(3R,3aS,4R,7S,8aR)-3,7-dihydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,7,8-hexahydroazulen-4-yl] 4-hydroxybenzoate 162877930 Click to see CC1=CC(C2C(CCC2(C(C)C)O)(CC1O)C)OC(=O)C3=CC=C(C=C3)O 374.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
[(3R,3aS,4S,6S,8aR)-3-hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,6-hexahydroazulen-4-yl] 4-hydroxybenzoate 25180955 Click to see CC1CC(C2C(CCC2(C(C)C)O)(C=C1)C)OC(=O)C3=CC=C(C=C3)O 358.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
[(3R,3aS,4S,6S,8aS)-3-hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,6-hexahydroazulen-4-yl] 4-hydroxybenzoate 162929625 Click to see CC1CC(C2C(CCC2(C(C)C)O)(C=C1)C)OC(=O)C3=CC=C(C=C3)O 358.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
[(3R,3aS,4S,7S,8aR)-3,7-dihydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,7,8-hexahydroazulen-4-yl] 4-hydroxybenzoate 162877927 Click to see CC1=CC(C2C(CCC2(C(C)C)O)(CC1O)C)OC(=O)C3=CC=C(C=C3)O 374.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
[(3R,3aS,4S,8aR)-3-hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl] (Z)-2-methylbut-2-enoate 14138876 Click to see CC=C(C)C(=O)OC1CC(=CCC2(C1C(CC2)(C(C)C)O)C)C 320.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
https://doi.org/10.1016/S0031-9422(00)80153-3
[(3R,3aS,4S,8aR)-3-hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl] 2-hydroxybenzoate 14466055 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC=CC=C3O)(C(C)C)O)C 358.50 unknown https://doi.org/10.1016/S0031-9422(00)80153-3
[(3R,3aS,4S,8aS)-3-hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl] 4-hydroxybenzoate 91747167 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC=C(C=C3)O)(C(C)C)O)C 358.50 unknown https://doi.org/10.1016/S0031-9422(00)80153-3
[(3S,8aR)-3-hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl] 4-hydroxy-3-methoxybenzoate 389016 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC(=C(C=C3)O)OC)(C(C)C)O)C 388.50 unknown https://doi.org/10.1016/S0031-9422(00)80153-3
Elaeochytrin A 25154876 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC=CC=C3N)(C(C)C)O)C 357.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
Ferutidin 10172562 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC=C(C=C3)OC)(C(C)C)O)C 372.50 unknown https://doi.org/10.1016/S0031-9422(00)80153-3
Ferutinine 354654 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC=C(C=C3)O)(C(C)C)O)C 358.50 unknown https://doi.org/10.1016/S0031-9422(00)80153-3
https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
Teferdin 10125942 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC=CC=C3)(C(C)C)O)C 342.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
https://doi.org/10.1016/S0031-9422(00)80153-3
Teferidine 91747169 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC=CC=C3)(C(C)C)O)C 342.50 unknown https://doi.org/10.1016/S0031-9422(00)80153-3
Teferin 10271607 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC(=C(C=C3)O)OC)(C(C)C)O)C 388.50 unknown https://doi.org/10.1016/S0031-9422(00)80153-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
6-[[4,4,6a,6b,11,11,14b-Heptamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[4,5-dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 85203639 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C2C1)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O)C 1119.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
Sandrosaponin IX 10606202 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C2C1)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O)C 1119.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 348159 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
Chlorogensaure 12310830 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.019
> Organoheterocyclic compounds / Benzodioxoles
4-Hydroxy-5,6-methylenedioxy-2-(1-oxopropyl)benzene 23261099 Click to see CCC(=O)C1=CC(=C2C(=C1)OCO2)O 194.18 unknown https://doi.org/10.1016/S0031-9422(00)80153-3

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