PlantaeDB Logo
Login Sign-up

Ferula hermonis

We don't have an image yet. Upload an image!

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 UUID64401c3427adf700907083
Scientific name Ferula hermonis
Authority Boiss.
First published in Fl. Orient. 2: 985 (1872)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

No known synonyms.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English اليونانيه
Arabic كلخ حرموني
French férule du mont hermon
Dutch اليونانيه
Dutch zallouh

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000686593
Tropicos 50327755
KEW urn:lsid:ipni.org:names:842303-1
The Plant List kew-2808452
Open Tree Of Life 470672
NCBI Taxonomy 662815
IUCN Red List 80720954
IPNI 842303-1
iNaturalist 774286
GBIF 3638287
Freebase /m/05hlst
USDA GRIN 419852
Wikipedia Ferula_hermonis

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
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
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
Polysaccharides—Naturally Occurring Immune Modulators Murphy EJ, Fehrenbach GW, Abidin IZ, Buckley C, Montgomery T, Pogue R, Murray P, Major I, Rezoagli E Polymers (Basel) 19-May-2023
PMCID:PMC10222865
doi:10.3390/polym15102373
PMID:37242947
Phytochemicals: Alternative for Infertility Treatment and Associated Conditions Chorosho SH, Malik N, Panesar G, Kumari P, Jangra S, Kaur R, Al-Ghamdi MS, Albishi TS, Chopra H, Singh R, Murthy HC Oxid Med Cell Longev 11-May-2023
PMCID:PMC10195183
doi:10.1155/2023/1327562
PMID:37215366
Artificial neural network and response surface methodology for optimization of corrosion inhibition of mild steel in 1 M HCl by Musa paradisiaca peel extract Amodu OS, Odunlami MO, Akintola JT, Ojumu TV, Ayanda OS Heliyon 29-Nov-2022
PMCID:PMC9719004
doi:10.1016/j.heliyon.2022.e11955
PMID:36471832
Phytochemicals That Interfere With Drug Metabolism and Transport, Modifying Plasma Concentration in Humans and Animals Gómez-Garduño J, León-Rodríguez R, Alemón-Medina R, Pérez-Guillé BE, Soriano-Rosales RE, González-Ortiz A, Chávez-Pacheco JL, Solorio-López E, Fernandez-Pérez P, Rivera-Espinosa L Dose Response 21-Sep-2022
PMCID:PMC9500303
doi:10.1177/15593258221120485
PMID:36158743
Antibacterial and Antifungal Sesquiterpenoids: Chemistry, Resource, and Activity Li HY, Yang WQ, Zhou XZ, Shao F, Shen T, Guan HY, Zheng J, Zhang LM Biomolecules 09-Sep-2022
PMCID:PMC9496053
doi:10.3390/biom12091271
PMID:36139108
Bioactive Compounds, Antioxidant, Anti-Inflammatory, Anti-Cancer, and Toxicity Assessment of Tribulus terrestris—In Vitro and In Vivo Studies Abbas MW, Hussain M, Akhtar S, Ismail T, Qamar M, Shafiq Z, Esatbeyoglu T Antioxidants (Basel) 13-Jun-2022
PMCID:PMC9219970
doi:10.3390/antiox11061160
PMID:35740057
Phenanthrene-enriched extract from Eulophia macrobulbon using subcritical dimethyl ether for phosphodiesterase-5A1 inhibition Srivilai J, Boonnoun P, Saesong T, Pingyod C, Chaichamnong N, Engsuwan J, Temkitthawon P, Scholfield CN, Nuengchamnong N, Khorana N, Ingkaninan K Sci Rep 09-Apr-2022
PMCID:PMC8994770
doi:10.1038/s41598-022-08553-x
PMID:35397625
Health Benefits, Pharmacological Effects, Molecular Mechanisms, and Therapeutic Potential of α-Bisabolol Eddin LB, Jha NK, Goyal SN, Agrawal YO, Subramanya SB, Bastaki SM, Ojha S Nutrients 25-Mar-2022
PMCID:PMC9002489
doi:10.3390/nu14071370
PMID:35405982
Traditional Medicinal Plants as a Source of Antituberculosis Drugs: A System Review Xu Y, Liang B, Kong C, Sun Z Biomed Res Int 08-Sep-2021
PMCID:PMC8448615
doi:10.1155/2021/9910365
PMID:34541000
Antioxidant and Antisteatotic Activities of Fucoidan Fractions from Marine and Terrestrial Sources El Rashed Z, Lupidi G, Grasselli E, Canesi L, Khalifeh H, Demori I Molecules 24-Jul-2021
PMCID:PMC8347863
doi:10.3390/molecules26154467
PMID:34361619
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
Antioxidant and Antisteatotic Activities of a New Fucoidan Extracted from Ferula hermonis Roots Harvested on Lebanese Mountains El Rashed Z, Lupidi G, Kanaan H, Grasselli E, Canesi L, Khalifeh H, Demori I Molecules 22-Feb-2021
PMCID:PMC7926425
doi:10.3390/molecules26041161
PMID:33671715
The Pharmacological Action of Kaempferol in Central Nervous System Diseases: A Review Silva dos Santos J, Gonçalves Cirino JP, de Oliveira Carvalho P, Ortega MM Front Pharmacol 13-Jan-2021
PMCID:PMC7838523
doi:10.3389/fphar.2020.565700
PMID:33519431

Phytochemical Profile Top

Add a new one!
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 / Benzoic acid esters
[(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] benzoate 10309067 Click to see CC(C)C1(CCC2(C1C(CC3(C(C2)O3)C)OC(=O)C4=CC=CC=C4)C)O 358.50 unknown https://doi.org/10.1002/PTR.3609
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
[(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-hydroxy-3-methoxybenzoate 13992122 Click to see CC(C)C1(CCC2(C1C(CC3(C(C2)O3)C)OC(=O)C4=CC(=C(C=C4)O)OC)C)O 404.50 unknown https://doi.org/10.1002/PTR.3609
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2R)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol 6506009 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00250-1
(3R,3aR,8aR)-3-hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,8-tetrahydroazulene-4,7-dione 11207454 Click to see CC1=CC(=O)C2C(CCC2(C(C)C)O)(CC1=O)C 250.33 unknown https://doi.org/10.1021/NP049652H
[(3R,3aS,4S,6S,8aR)-3,6-dihydroxy-6,8a-dimethyl-3-propan-2-yl-2,3a,4,5-tetrahydro-1H-azulen-4-yl] 4-hydroxy-3-methoxybenzoate 14466072 Click to see CC(C)C1(CCC2(C1C(CC(C=C2)(C)O)OC(=O)C3=CC(=C(C=C3)O)OC)C)O 404.50 unknown https://doi.org/10.1002/PTR.3609
[(3R,3aS,4S,6S,8aR)-3,6-dihydroxy-6,8a-dimethyl-3-propan-2-yl-2,3a,4,5-tetrahydro-1H-azulen-4-yl] 4-hydroxybenzoate 13875698 Click to see CC(C)C1(CCC2(C1C(CC(C=C2)(C)O)OC(=O)C3=CC=C(C=C3)O)C)O 374.50 unknown https://doi.org/10.1002/PTR.3609
[(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(97)00250-1
https://doi.org/10.1055/S-2001-17354
https://doi.org/10.1021/NP800049Y
[(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/10.1055/S-2001-17354
[(8aS)-8a-methyl-3-propan-2-yl-2,4,5,8-tetrahydro-1H-azulen-6-yl]methyl 4-hydroxy-3-methoxybenzoate 163045137 Click to see CC(C)C1=C2CCC(=CCC2(CC1)C)COC(=O)C3=CC(=C(C=C3)O)OC 370.50 unknown https://doi.org/10.1021/NP000526X
[(8aS)-8a-methyl-3-propan-2-yl-2,4,5,8-tetrahydro-1H-azulen-6-yl]methyl 4-hydroxybenzoate 162866884 Click to see CC(C)C1=C2CCC(=CCC2(CC1)C)COC(=O)C3=CC=C(C=C3)O 340.50 unknown https://doi.org/10.1021/NP000526X
Bisabolol 1549992 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1021/NP50068A033
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/10.1021/NP800049Y
https://doi.org/10.1055/S-2001-17354
https://doi.org/10.1021/NP049652H
Jaeschkeanadiol 10125228 Click to see CC1=CCC2(CCC(C2C(C1)O)(C(C)C)O)C 238.37 unknown https://doi.org/10.1016/S0031-9422(97)00250-1
https://doi.org/10.1021/NP000526X
Levomenol 442343 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1021/NP049652H
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/10.1055/S-2001-17354
https://doi.org/10.1021/NP049652H
https://doi.org/10.1002/PTR.3609
https://doi.org/10.1016/S0031-9422(97)00250-1
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/10.1002/PTR.3609
https://doi.org/10.1002/PTR.3324
https://doi.org/10.1016/S0031-9422(97)00250-1
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/10.1055/S-2001-17354
Vaginatin 101289771 Click to see CC=C(C)C(=O)OC1C=C(CCC2(C1(C(=O)CC2C(C)C)C)O)C 334.40 unknown https://doi.org/10.1002/PTR.3609
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Epoxyjaeschkeanadiol 11345827 Click to see CC(C)C1(CCC2(C1C(CC3(C(C2)O3)C)O)C)O 254.36 unknown https://doi.org/10.1021/NP000526X

Biological Material Top ebay Auctions

Please wait .. loading items ..

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.