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Ferula ovina

Ferula ovina - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

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

Details Top

Internal ID UUID64401c3c2fc01495987717
Scientific name Ferula ovina
Authority Boiss.
First published in Fl. Orient. [Boissier] 2: 986. [Dec 1872 or Jan 1873] ; isonym

Description Top

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Synonyms Top

Scientific name Authority First published in
Ferula kopetdagensis Korovin Monogr. Ferula : 61 (1947)
Ferula microcarpa Korovin Monogr. Ferula : 58 (1947)
Ferula pachycarpa Korovin Trudy Sredne-Aziatsk. Gosud. Univ., Ser. 8b, Bot. 24: 11 (1935), in obs., nomen.
Ferula stewartiana var. affghanica O.E.Schulz Notizbl. Bot. Gart. Berlin-Dahlem 11: 877 1933
Ferula stylosa Korovin Monogr. Ferula : 58 (1947)
Peucedanum thomsonii C.B.Clarke Fl. Brit. India 2: 711 (1879)
Peucedanum ovinum (Boiss.) Boiss. Diagn. Pl. Orient. 6: 61 (1846)

Common names Top

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Language Common/alternative name
Arabic كلخ غنمي
Chinese 羊食阿魏

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

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-0000686728
Tropicos 1700113
KEW urn:lsid:ipni.org:names:77129493-1
The Plant List kew-2808577
Open Tree Of Life 131374
Observations.org 137044
NCBI Taxonomy 371376
IPNI 842427-1
iNaturalist 961936
GBIF 3637104
Elurikkus 388305
USDA GRIN 16618

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
Antitumor and Phytochemical Properties of Ferula assa-foetida L. Oleo-Gum–Resin against HT-29 Colorectal Cancer Cells In Vitro and in a Xenograft Mouse Model Elarabany N, Hamad A, Alzamel NM Molecules 08-Dec-2023
PMCID:PMC10746072
doi:10.3390/molecules28248012
PMID:38138502
Prevention and Control of Human Salmonella enterica Infections: An Implication in Food Safety Mkangara M Int J Food Sci 11-Sep-2023
PMCID:PMC10506869
doi:10.1155/2023/8899596
PMID:37727836
In Vitro Evaluation of Ferutinin Rich-Ferula communis L., ssp. glauca, Root Extract on Doxorubicin-Induced Cardiotoxicity: Antioxidant Properties and Cell Cycle Modulation Macrì R, Bava I, Scarano F, Mollace R, Musolino V, Gliozzi M, Greco M, Foti D, Tucci L, Maiuolo J, Carresi C, Tavernese A, Palma E, Muscoli C, Mollace V Int J Mol Sci 13-Aug-2023
PMCID:PMC10454821
doi:10.3390/ijms241612735
PMID:37628916
Current State of Knowledge Regarding WHO High Priority Pathogens—Resistance Mechanisms and Proposed Solutions through Candidates Such as Essential Oils: A Systematic Review Romanescu M, Oprean C, Lombrea A, Badescu B, Teodor A, Constantin GD, Andor M, Folescu R, Muntean D, Danciu C, Dalleur O, Batrina SL, Cretu O, Buda VO Int J Mol Sci 04-Jun-2023
PMCID:PMC10253476
doi:10.3390/ijms24119727
PMID:37298678
Natural Products as New Approaches for Treating Bladder Cancer: From Traditional Medicine to Novel Drug Discovery Kang Y, Park C, Lee H, Kang S, Cheon C, Kim B Pharmaceutics 31-Mar-2023
PMCID:PMC10145408
doi:10.3390/pharmaceutics15041117
PMID:37111603
The Role of Propolis as a Natural Product with Potential Gastric Cancer Treatment Properties: A Systematic Review Rivera-Yañez N, Ruiz-Hurtado PA, Rivera-Yañez CR, Arciniega-Martínez IM, Yepez-Ortega M, Mendoza-Arroyo B, Rebollar-Ruíz XA, Méndez-Cruz AR, Reséndiz-Albor AA, Nieto-Yañez O Foods 16-Jan-2023
PMCID:PMC9858610
doi:10.3390/foods12020415
PMID:36673507
Ferula communis L. (Apiaceae) Root Acetone-Water Extract: Phytochemical Analysis, Cytotoxicity and In Vitro Evaluation of Estrogenic Properties Maiuolo J, Musolino V, Guarnieri L, Macrì R, Coppoletta AR, Cardamone A, Serra M, Gliozzi M, Bava I, Lupia C, Tucci L, Bombardelli E, Mollace V Plants (Basel) 22-Jul-2022
PMCID:PMC9329896
doi:10.3390/plants11151905
PMID:35893609
Computational Study of Asian Propolis Compounds as Potential Anti-Type 2 Diabetes Mellitus Agents by Using Inverse Virtual Screening with the DIA-DB Web Server, Tanimoto Similarity Analysis, and Molecular Dynamic Simulation Syaifie PH, Harisna AH, Nasution MA, Arda AG, Nugroho DW, Jauhar MM, Mardliyati E, Maulana NN, Rochman NT, Noviyanto A, Banegas-Luna AJ, Pérez-Sánchez H Molecules 21-Jun-2022
PMCID:PMC9268573
doi:10.3390/molecules27133972
PMID:35807241
Natural Products-Based Metallic Nanoparticles as Antimicrobial Agents Susanti D, Haris MS, Taher M, Khotib J Front Pharmacol 02-Jun-2022
PMCID:PMC9205242
doi:10.3389/fphar.2022.895616
PMID:35721199
Endophytic Fungal Terpenoids: Natural Role and Bioactivities Galindo-Solís JM, Fernández FJ Microorganisms 01-Feb-2022
PMCID:PMC8875210
doi:10.3390/microorganisms10020339
PMID:35208794
Introduction to the potential of Ferula ovina in dental implant research due to estrogenic bioactive compounds and adhesive properties Zare Mirakabad H, Khorramizadeh MR PLoS One 18-Jan-2022
PMCID:PMC8765653
doi:10.1371/journal.pone.0262045
PMID:35041680
Natural Products Targeting Liver X Receptors or Farnesoid X Receptor She J, Gu T, Pang X, Liu Y, Tang L, Zhou X Front Pharmacol 05-Jan-2022
PMCID:PMC8766425
doi:10.3389/fphar.2021.772435
PMID:35069197
Ethnobotany of the medicinal plants used by the ethnic communities of Kerman province, Southeast Iran Hosseini SH, Bibak H, Ghara AR, Sahebkar A, Shakeri A J Ethnobiol Ethnomed 28-Apr-2021
PMCID:PMC8082778
doi:10.1186/s13002-021-00438-z
PMID:33910616
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
Next Chapter in the Legend of Silphion: Preliminary Morphological, Chemical, Biological and Pharmacological Evaluations, Initial Conservation Studies, and Reassessment of the Regional Extinction Event Miski M Plants (Basel) 06-Jan-2021
PMCID:PMC7825337
doi:10.3390/plants10010102
PMID:33418989

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 / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
(1S,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 4-hydroxy-3-methoxybenzoate 1294694 Click to see CC1(C2CCC1(C(C2)OC(=O)C3=CC(=C(C=C3)O)OC)C)C 304.40 unknown https://doi.org/10.1007/BF00569608
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
(2,3-diacetyloxy-5-hydroxy-2a,7a-dimethyl-5-propan-2-yl-2,3,4,5a,6,7-hexahydro-1aH-azuleno[6,7-b]oxiren-6-yl) 3,4-dimethoxybenzoate 4371509 Click to see CC(C)C1(CC(C2(C1C(CC3(C(C2OC(=O)C)O3)C)OC(=O)C4=CC(=C(C=C4)OC)OC)C)OC(=O)C)O 534.60 unknown https://doi.org/10.1007/BF00579449
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
1-Methyl-2-methylenecyclohexane 137725 Click to see CC1CCCCC1=C 110.20 unknown https://doi.org/10.1080/10412905.2005.9698829
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl isovalerate 5362830 Click to see CC(C)CC(=O)OCC=C(C)CCC=C(C)C 238.37 unknown https://doi.org/10.1080/10412905.2005.9698829
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-CITRONELLOL, (+/-)- 8842 Click to see CC(CCC=C(C)C)CCO 156.26 unknown https://doi.org/10.1080/10412905.2005.9698829
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.2005.9698829
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1080/10412905.2005.9698829
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.2005.9698829
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1080/10412905.2005.9698829
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1080/10412905.2005.9698829
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.2005.9698829
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.2005.9698829
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1080/10412905.2005.9698829
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1080/10412905.2005.9698829
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1080/10412905.2005.9698829
Fenchol 15406 Click to see CC1(C2CCC(C2)(C1O)C)C 154.25 unknown https://doi.org/10.1080/10412905.2005.9698829
Fenchone 14525 Click to see CC1(C2CCC(C2)(C1=O)C)C 152.23 unknown https://doi.org/10.1080/10412905.2005.9698829
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.2005.9698829
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.2005.9698829
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3-Hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl) 3-hydroxy-4-methoxybenzoate 4524229 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC(=C(C=C3)OC)O)(C(C)C)O)C 388.50 unknown https://doi.org/10.1007/BF00563840
[(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/10.1007/BF00563840
Alpha-Farnesene 5281516 Click to see CC(=CCCC(=CCC=C(C)C=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.2005.9698829
Carotol 442347 Click to see CC1=CCC2(CCC(C2(CC1)O)C(C)C)C 222.37 unknown https://doi.org/10.1080/10412905.2005.9698829
Jaeschkeanadiol 10125228 Click to see CC1=CCC2(CCC(C2C(C1)O)(C(C)C)O)C 238.37 unknown https://doi.org/10.1007/BF00563839
https://doi.org/10.1007/BF00563840
Lapidin 11872435 Click to see CC=C(C)C(=O)OC1CC(=CC(=O)C2(C1C(CC2)(C(C)C)O)C)C 334.40 unknown https://doi.org/10.1007/BF00629636
Lapidine 6440625 Click to see CC=C(C)C(=O)OC1CC(=CC(=O)C2(C1C(CC2)(C(C)C)O)C)C 334.40 unknown https://doi.org/10.1007/BF00629636
https://doi.org/10.1007/BF00568511

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