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Ferula vesceritensis

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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 UUID64401c42c731f132958264
Scientific name Ferula vesceritensis
Authority Coss. & Durieu ex Trab.
First published in Fl. Algérie Tunisie 149. 1905

Description Top

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Synonyms Top

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Common names Top

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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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000686872
Tropicos 100336953
KEW urn:lsid:ipni.org:names:77221709-1
The Plant List kew-2808709
Open Tree Of Life 5801581
NCBI Taxonomy 1514058

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
Success stories of natural product-derived compounds from plants as multidrug resistance modulators in microorganisms Zhai X, Wu G, Tao X, Yang S, Lv L, Zhu Y, Dong D, Xiang H RSC Adv 08-Mar-2023
PMCID:PMC9994607
doi:10.1039/d3ra00184a
PMID:36909750
Ethnobotanical survey of the traditional antiparasitic use of medicinal plants in humans and animals in Laghouat (Southern Algeria) Benlarbi F, Mimoune N, Chaachouay N, Souttou K, Saidi R, Mokhtar MR, Kaidi R, Benaissa MH Vet World 24-Feb-2023
PMCID:PMC10082715
doi:10.14202/vetworld.2023.357-368
PMID:37041995
Variable Secondary Metabolite Profiles Across Cultivars of Curcuma longa L. and C. aromatica Salisb. Kulyal P, Acharya S, Ankari AB, Kokkiripati PK, Tetali SD, Raghavendra AS Front Pharmacol 30-Jun-2021
PMCID:PMC8278146
doi:10.3389/fphar.2021.659546
PMID:34276362
Volatiles and Antifungal-Antibacterial-Antiviral Activity of South African Salvia spp. Essential Oils Cultivated in Uniform Conditions Najar B, Mecacci G, Nardi V, Cervelli C, Nardoni S, Mancianti F, Ebani VV, Giannecchini S, Pistelli L Molecules 10-May-2021
PMCID:PMC8126244
doi:10.3390/molecules26092826
PMID:34068756
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
Ethnopharmacological study of natural products used for traditional cancer therapy in Algeria Taïbi K, Abderrahim LA, Ferhat K, Betta S, Taïbi F, Bouraada F, Boussaid M Saudi Pharm J 21-Sep-2020
PMCID:PMC7679473
doi:10.1016/j.jsps.2020.09.011
PMID:33250653
Carotane sesquiterpenes from Ferula vesceritensis: in silico analysis as SARS-CoV-2 binding inhibitors Mohamed TA, Elshamy AI, Ibrahim MA, Zellagui A, Moustafa MF, Abdelrahman AH, Ohta S, Pare PW, Hegazy ME RSC Adv 18-Sep-2020
PMCID:PMC9056801
doi:10.1039/d0ra06901a
PMID:35514418
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
The Chemistry and Biological Activities of Natural Products from Northern African Plant Families: From Taccaceae to Zygophyllaceae Ntie-Kang F, Njume LE, Malange YI, Günther S, Sippl W, Yong JN Nat Prod Bioprospect 01-Mar-2016
PMCID:PMC4805656
doi:10.1007/s13659-016-0091-9
PMID:26931529
Phytochemical investigation and antimicrobial activity of crude extract of the roots of Ferula vesceritensis A. Zellagui, N. Gherraf, M. E. F. Hegazy, S. Akkal, S. Rhouati, H. Dendougui, and A. A. Ahmed Springer Science and Business Media LLC 16-Nov-2012
doi:10.1007/S10600-012-0414-Y
Chemical composition and antibacterial activity of the essential oils of Ferula vesceritensis Coss et Dur. leaves, endemic in Algeria Zellagui A, Gherraf N, Rhouati S Org Med Chem Lett 03-Sep-2012
PMCID:PMC3517384
doi:10.1186/2191-2858-2-31
PMID:22937773
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
A crystal lapiferin derived from Ferula vesceritensis induces apoptosis pathway in MCF-7 breast cancer cells. Gamal-Eldeen AM, Hegazy ME Nat Prod Res 01-Feb-2010
doi:10.1080/14786410802685398
PMID:20140803
Sesquiterpenes from aerial parts of Ferula vesceritensis. Oughlissi-Dehak K, Lawton P, Michalet S, Bayet C, Darbour N, Hadj-Mahammed M, Badjah-Hadj-Ahmed YA, Dijoux-Franca MG, Guilet D Phytochemistry 01-Jun-2008
doi:10.1016/J.PHYTOCHEM.2008.03.010
PMID:18485426
Ferulsinaic acid, a sesquiterpene coumarin with a rare carbon skeleton from Ferula species. Ahmed AA, Hegazy ME, Zellagui A, Rhouati S, Mohamed TA, Sayed AA, Abdella MA, Ohta S, Hirata T Phytochemistry 01-Mar-2007
doi:10.1016/J.PHYTOCHEM.2006.12.011
PMID:17258243

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
[(1aS,2R,2aS,3R,5R,5aS,6S,7aR)-3-acetyloxy-2,5-dihydroxy-2a,7a-dimethyl-5-propan-2-yl-2,3,4,5a,6,7-hexahydro-1aH-azuleno[6,7-b]oxiren-6-yl] 4-methoxybenzoate 102408130 Click to see CC(C)C1(CC(C2(C1C(CC3(C(C2O)O3)C)OC(=O)C4=CC=C(C=C4)OC)C)OC(=O)C)O 462.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.010
[(1R,3aS,9S,9aS)-1-hydroxy-3a,6-dimethyl-4-oxo-1-propan-2-yl-2,3,7,8,9,9a-hexahydrocyclopenta[8]annulen-9-yl] 4-methoxybenzoate 162870632 Click to see CC1=CC(=O)C2(CCC(C2C(CC1)OC(=O)C3=CC=C(C=C3)OC)(C(C)C)O)C 400.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.010
[(1R,3S,3aR,9S,9aS)-3-acetyloxy-1-hydroxy-3a,6-dimethyl-1-propan-2-yl-3,4,7,8,9,9a-hexahydro-2H-cyclopenta[8]annulen-9-yl] 4-methoxybenzoate 162817011 Click to see CC1=CCC2(C(CC(C2C(CC1)OC(=O)C3=CC=C(C=C3)OC)(C(C)C)O)OC(=O)C)C 444.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.010
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
(2-acetyloxy-5-hydroxy-2a,7a-dimethyl-5-propan-2-yl-2,3,4,5a,6,7-hexahydro-1aH-azuleno[6,7-b]oxiren-6-yl) 2-methylbut-2-enoate 3831821 Click to see CC=C(C)C(=O)OC1CC2(C(O2)C(C3(C1C(CC3)(C(C)C)O)C)OC(=O)C)C 394.50 unknown https://doi.org/10.1080/14786410802685398
[(1aS,2S,2aS,5R,5aS,6S,7aR)-2-acetyloxy-5-hydroxy-2a,7a-dimethyl-5-propan-2-yl-2,3,4,5a,6,7-hexahydro-1aH-azuleno[6,7-b]oxiren-6-yl] (Z)-2-methylbut-2-enoate 40565714 Click to see CC=C(C)C(=O)OC1CC2(C(O2)C(C3(C1C(CC3)(C(C)C)O)C)OC(=O)C)C 394.50 unknown https://doi.org/10.1080/14786410802685398
[(2aS,5R,7aR)-2-acetyloxy-5-hydroxy-2a,7a-dimethyl-5-propan-2-yl-2,3,4,5a,6,7-hexahydro-1aH-azuleno[6,7-b]oxiren-6-yl] 2-methylbut-2-enoate 11969644 Click to see CC=C(C)C(=O)OC1CC2(C(O2)C(C3(C1C(CC3)(C(C)C)O)C)OC(=O)C)C 394.50 unknown https://doi.org/10.1007/S10600-012-0414-Y
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,3aS,8S,8aS)-1,8-dihydroxy-3a,6-dimethyl-1-propan-2-yl-3,7,8,8a-tetrahydro-2H-azulen-4-one 14239512 Click to see CC1=CC(=O)C2(CCC(C2C(C1)O)(C(C)C)O)C 252.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.010
[(1R,3aR,4S,8aS)-8a-hydroxy-3a,6-dimethyl-1-propan-2-yl-1,2,3,4,7,8-hexahydroazulen-4-yl] 4-methoxybenzoate 162891810 Click to see CC1=CC(C2(CCC(C2(CC1)O)C(C)C)C)OC(=O)C3=CC=C(C=C3)OC 372.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.010
[(1R,3R,3aS,4S,6R,8aR)-1-acetyloxy-3,6-dihydroxy-6,8a-dimethyl-8-oxo-3-propan-2-yl-1,2,3a,4,5,7-hexahydroazulen-4-yl] 4-methoxybenzoate 162875433 Click to see CC(C)C1(CC(C2(C1C(CC(CC2=O)(C)O)OC(=O)C3=CC=C(C=C3)OC)C)OC(=O)C)O 462.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.010
[(1R,3R,3aS,4S,6R,8aR)-1,8-diacetyloxy-3,6-dihydroxy-6,8a-dimethyl-3-propan-2-yl-2,3a,4,5-tetrahydro-1H-azulen-4-yl] 4-methoxybenzoate 163020808 Click to see CC(C)C1(CC(C2(C1C(CC(C=C2OC(=O)C)(C)O)OC(=O)C3=CC=C(C=C3)OC)C)OC(=O)C)O 504.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.010
[(3R,3aS,4S,8R,8aS)-3,8-dihydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl] benzoate 162817017 Click to see CC1=CC(C2(CCC(C2C(C1)OC(=O)C3=CC=CC=C3)(C(C)C)O)C)O 358.50 unknown https://doi.org/10.1007/S10600-012-0414-Y
[(3R,3aS,4S,8R,8aS)-3,8-dihydroxy-6,8a-dimethyl-7-oxo-3-propan-2-yl-2,3a,4,8-tetrahydro-1H-azulen-4-yl] 4-methoxybenzoate 102408129 Click to see CC1=CC(C2C(CCC2(C(C)C)O)(C(C1=O)O)C)OC(=O)C3=CC=C(C=C3)OC 402.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.010
[(3R,3aS,4S,8R,8aS)-8-acetyloxy-3-hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl] 4-hydroxybenzoate 162817019 Click to see CC1=CC(C2(CCC(C2C(C1)OC(=O)C3=CC=C(C=C3)O)(C(C)C)O)C)OC(=O)C 416.50 unknown https://doi.org/10.1007/S10600-012-0414-Y
[(3R,3aS,4S,8R,8aS)-8-acetyloxy-3-hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl] 4-methoxybenzoate 162984538 Click to see CC1=CC(C2(CCC(C2C(C1)OC(=O)C3=CC=C(C=C3)OC)(C(C)C)O)C)OC(=O)C 430.50 unknown https://doi.org/10.1007/S10600-012-0414-Y
6Alpha,10Alpha-Diangeloyl-Jaeschkeanadiol 54597865 Click to see CC=C(C)C(=O)OC1CC(=CC(C2(C1C(CC2)(C(C)C)O)C)OC(=O)C(=CC)C)C 418.60 unknown https://doi.org/10.1007/S10600-012-0414-Y
Benzoic acid (3R)-3alpha,8alpha-dihydroxy-3-isopropyl-6,8aalpha-dimethyl-7-oxo-1,2,3,3abeta,4,7,8,8a-octahydroazulene-4beta-yl ester 102408127 Click to see CC1=CC(C2C(CCC2(C(C)C)O)(C(C1=O)O)C)OC(=O)C3=CC=CC=C3 372.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.010
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/10.1007/S10600-012-0414-Y
Lancerodiol P-Methoxybenzoate 56662345 Click to see CC1=CC(C2C(CCC2(C(C)C)O)(CC1=O)C)OC(=O)C3=CC=C(C=C3)OC 386.50 unknown https://doi.org/10.1007/S10600-012-0414-Y
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(1R,3aS,9S)-1,9-dihydroxy-3a,6-dimethyl-1-propan-2-yl-2,3,7,8,9,9a-hexahydrocyclopenta[8]annulen-4-one 162817009 Click to see CC1=CC(=O)C2(CCC(C2C(CC1)O)(C(C)C)O)C 266.38 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.010
> Phenylpropanoids and polyketides / Coumarins and derivatives
[(1S,2S,4aS,5S,8aR)-2-acetyloxy-1,4a,6-trimethyl-5-[(2-oxochromen-7-yl)oxymethyl]-2,3,4,5,8,8a-hexahydronaphthalen-1-yl]methyl acetate 102469380 Click to see CC1=CCC2C(C1COC3=CC4=C(C=C3)C=CC(=O)O4)(CCC(C2(C)COC(=O)C)OC(=O)C)C 482.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.12.011
[(2S,4aR,5S,8aR)-1,1,4a,8a-tetramethyl-6-methylidene-5-[(2-oxochromen-7-yl)oxymethyl]-2,3,4,5,7,8-hexahydronaphthalen-2-yl] (Z)-2-methylbut-2-enoate 102469381 Click to see CC=C(C)C(=O)OC1CCC2(C(C(=C)CCC2(C1(C)C)C)COC3=CC4=C(C=C3)C=CC(=O)O4)C 478.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.12.011
7-[[(1R,4aS,6R,8aS)-6-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one 7002461 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/10.1016/J.PHYTOCHEM.2008.03.010
7-[[(1S,4aR,5S,6S,8aS)-6-hydroxy-5-(hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methoxy]chromen-2-one 102469379 Click to see CC1=CCC2C(C1COC3=CC4=C(C=C3)C=CC(=O)O4)(CCC(C2(C)CO)O)C 398.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.12.011
7-[[(1S,4aS,6R,8aS)-6-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one 28966206 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/10.1016/J.PHYTOCHEM.2008.03.010
7-[[(1S,4aS)-6-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one 5317322 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/10.1016/J.PHYTOCHEM.2008.03.010
Farnesiferol A 7067262 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/10.1016/J.PHYTOCHEM.2008.03.010
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/10.1016/J.PHYTOCHEM.2008.03.010

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