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Ferula tingitana

Ferula tingitana - 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 UUID64401c4194b7e884331833
Scientific name Ferula tingitana
Authority L.
First published in Sp. Pl. : 247 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Agasulis tingitana (L.) Raf. Good Book : 58 (1840)
Ferula bolivari Pau Mem. Real Soc. Esp. Hist. Nat. 12: 332 (1924)
Ferula sancta Boiss. Diagn. Pl. Orient. 10: 39 (1849)

Common names Top

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Language Common/alternative name
Arabic كلخ بوليفاري
Arabic كلخ طنجي
French férule de tanger

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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Start at 4°C for 3 months, then warm to 20°C for another 3 months.
plant in deep pot

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Western Asia
      • East Aegean Islands
      • Lebanon-Syria
      • Palestine
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000686851
Tropicos 50194534
INPN 610575
KEW urn:lsid:ipni.org:names:842533-1
The Plant List kew-2808690
PFAF Ferula tingitana
Open Tree Of Life 122474
Observations.org 147874
NCBI Taxonomy 99503
IPNI 842533-1
iNaturalist 82617
GBIF 3636208
Freebase /m/0gg6zbl
EPPO FERTI
USDA GRIN 405561
Wikipedia Ferula_tingitana

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
Essential Oils in Cervical Cancer: Narrative Review on Current Insights and Future Prospects Abd Rashid N, Mohamad Najib NH, Abdul Jalil NA, Teoh SL Antioxidants (Basel) 13-Dec-2023
PMCID:PMC10740549
doi:10.3390/antiox12122109
PMID:38136228
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
Phylogeny and Historical Biogeography of Veronica Subgenus Pentasepalae (Plantaginaceae): Evidence for Its Origin and Subsequent Dispersal Doostmohammadi M, Bordbar F, Albach DC, Mirtadzadini M Biology (Basel) 21-Apr-2022
PMCID:PMC9138021
doi:10.3390/biology11050639
PMID:35625367
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
Chemical Composition, Antimicrobial and Antitumor Potentiality of Essential Oil of Ferula tingitana L. Apiaceae Grow in Libya Elghwaji W, El-Sayed AM, El-Deeb KS, ElSayed AM Pharmacogn Mag 11-Oct-2017
PMCID:PMC5669080
doi:10.4103/pm.pm_323_15
PMID:29142397
When foods become remedies in ancient Greece: The curious case of garlic and other substances Totelin L J Ethnopharmacol 05-Jun-2015
PMCID:PMC4469375
doi:10.1016/j.jep.2014.08.018
PMID:25173971
A Unified Approach to the Daucane and Sphenolobane Bicyclo[5.3.0]decane Core: Enantioselective Total Syntheses of Daucene, Daucenal, Epoxydaucenal B, and 14-p-Anisoyloxydauc-4,8-diene Bennett NB, Stoltz BM Chemistry 02-Dec-2013
PMCID:PMC3927641
doi:10.1002/chem.201302353
PMID:24302464
European Materia Medica in Historical Texts: Longevity of a Tradition and Implications for Future Use De Vos P J Ethnopharmacol 16-Jun-2010
PMCID:PMC2956839
doi:10.1016/j.jep.2010.05.035
PMID:20561577
Crystal and molecular structure of lancerodiol–p–hydroxybenzoate Abd El–Razek MH, Hegazy MF, Mohamed AE Pharmacognosy Res 01-Mar-2010
PMCID:PMC3140109
doi:10.4103/0974-8490.62950
PMID:21808543
A New sesquiterpene ester from ferula tingitana Mahmut Miski, Ayhan Ulubelen, Tom J. Mabry, William H. Watson, Ivan Vickovic, Miroslav Holub Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(01)91270-0
New daucane esters from Ferula tingitana. Miski M, Mabry TJ J Nat Prod 01-Jul-1986
doi:10.1021/NP50046A016
PMID:3783161
Sesquiterpene-coumarin ethers of Ferula tingitana. Miski M, Ulubelen A J Nat Prod 01-Mar-1985
doi:10.1021/NP50038A024
PMID:4009187

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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Acetyltingitanol 5825382 Click to see CC=C(C)C(=O)OC1CC(=CC(C2(C1C(CC2OC(=O)C)(C(C)C)O)C)OC(=O)C(=CC)C)C 476.60 unknown https://doi.org/10.1021/NP50046A016
Fercomin 14486243 Click to see CC1=CC(C2(C(=O)CC(C2(CC1)O)C(C)C)C)OC(=O)C3=CC=C(C=C3)OC 386.50 unknown https://doi.org/10.1021/NP50046A016
Tingitanol 54612525 Click to see CC=C(C)C(=O)OC1CC(=CC(C2(C1C(CC2O)(C(C)C)O)C)OC(=O)C(=CC)C)C 434.60 unknown https://doi.org/10.1016/S0040-4020(01)91270-0
> Organoheterocyclic compounds / Benzodioxoles
1-Propanone, 1-(7-methoxy-1,3-benzodioxol-5-yl)- 177099 Click to see CCC(=O)C1=CC2=C(C(=C1)OC)OCO2 208.21 unknown https://doi.org/10.1021/NP50038A024
Laserine 102571636 Click to see CC=C(C)C(=O)OC(C)C(C1=CC2=C(C(=C1)OC)OCO2)OC(=O)C(=CC)C 390.40 unknown https://doi.org/10.1021/NP50046A016
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-[[(1S,4aR,6S,8aS)-6-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one 21627903 Click to see CC1(C2CCC(=C)C(C2(CCC1O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)C 382.50 unknown https://doi.org/10.1021/NP50038A024
Colladonin 375430 Click to see CC1(C2CCC(=C)C(C2(CCC1O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)C 382.50 unknown https://doi.org/10.1021/NP50038A024
Feselol 179577 Click to see CC1=CCC2C(C(CCC2(C1COC3=CC4=C(C=C3)C=CC(=O)O4)C)O)(C)C 382.50 unknown https://doi.org/10.1021/NP50038A024

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Collections Top

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