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Ferula varia

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64401c42aebaf895232166
Scientific name Ferula varia
Authority Trautv.
First published in Bull. Soc. Imp. Naturalistes Moscou 39(I): 325 (1866)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Peucedanum shair Baill. Hist. Pl. 7: 186 (1879)
Ferula schair Borszcz. Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7 , 3(1): 37 (1860)
Peucedanum varium Schrenk Index Seminum (LE, Petropolitanus) 9(Suppl.): 15 (1844)

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

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-0000686870
Tropicos 1702804
KEW urn:lsid:ipni.org:names:842549-1
The Plant List kew-2808707
Open Tree Of Life 1085925
Observations.org 149451
NCBI Taxonomy 555417
IPNI 842549-1
iNaturalist 976724
GBIF 3636032
Elurikkus 388081
USDA GRIN 406711

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
Plants as Modulators of Melanogenesis: Role of Extracts, Pure Compounds and Patented Compositions in Therapy of Pigmentation Disorders Merecz-Sadowska A, Sitarek P, Stelmach J, Zajdel K, Kucharska E, Zajdel R Int J Mol Sci 26-Nov-2022
PMCID:PMC9736547
doi:10.3390/ijms232314787
PMID:36499134
Phytochemical studies on traditional herbal medicines based on the ethnopharmacological information obtained by field studies Tanaka N, Kashiwada Y J Nat Med 13-Jul-2021
PMCID:PMC8397699
doi:10.1007/s11418-021-01545-7
PMID:34255289
Physico-Chemical Parameters, Phenolic Profile, In Vitro Antioxidant Activity and Volatile Compounds of Ladastacho (Lavandula stoechas) from the Region of Saidona Karabagias IK, Karabagias VK, Riganakos KA Antioxidants (Basel) 28-Mar-2019
PMCID:PMC6523715
doi:10.3390/antiox8040080
PMID:30925770
Sesquiterpene lactones from the roots of Ferula varia and their cytotoxic activity. Suzuki K, Okasaka M, Kashiwada Y, Takaishi Y, Honda G, Ito M, Takeda Y, Kodzhimatov OK, Ashurmetov O, Sekiya M, Ikeshiro Y J Nat Prod 01-Dec-2007
doi:10.1021/NP0703996
PMID:18052129
Phylogenetic Variation in the Silicon Composition of Plants HODSON MJ, WHITE PJ, MEAD A, BROADLEY MR Ann Bot 21-Sep-2005
PMCID:PMC4247092
doi:10.1093/aob/mci255
PMID:16176944
Development of a method for the quantitative determination of neerotsizin (luteolin 7-O-?-D-glucopyranoside) in the leaves of Ferula varia N. S. Maksumova, G. L. Genkina Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630110
Luteolin glucosides fromFerula varia N. S. Maksumova, M. P. Yuldashev, É. Kh. Batirov Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00629880

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
[(1R,2S,5S,6R,9S,10S,11R,13R)-5-hydroxy-9-methyl-10-[(E)-2-methylbut-2-enoyl]oxy-14-methylidene-4-oxo-3,12-dioxatetracyclo[7.5.0.02,6.011,13]tetradecan-5-yl]methyl (Z)-2-methylbut-2-enoate 44445506 Click to see CC=C(C)C(=O)OCC1(C2CCC3(C(C2OC1=O)C(=C)C4C(C3OC(=O)C(=CC)C)O4)C)O 460.50 unknown https://doi.org/10.1021/NP0703996
[(3R,3aR,5aS,6R,9aR,9bS)-3-hydroxy-3,5a-dimethyl-9-methylidene-2-oxo-3a,4,5,6,9a,9b-hexahydrobenzo[g][1]benzofuran-6-yl] (E)-2-methylbut-2-enoate 44445436 Click to see CC=C(C)C(=O)OC1C=CC(=C)C2C1(CCC3C2OC(=O)C3(C)O)C 346.40 unknown https://doi.org/10.1021/NP0703996
[(3R,3aS,5aR,8S,9aS,9bR)-3,5a-dimethyl-9-methylidene-2-oxo-3a,4,5,8,9a,9b-hexahydro-3H-benzo[g][1]benzofuran-8-yl] 2-methylbutanoate 44445516 Click to see CCC(C)C(=O)OC1C=CC2(CCC3C(C(=O)OC3C2C1=C)C)C 332.40 unknown https://doi.org/10.1021/NP0703996
Dehydrooopodin 44445508 Click to see 328.40 unknown https://doi.org/10.1021/NP0703996
Oopodin 40530726 Click to see 330.40 unknown https://doi.org/10.1021/NP0703996
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
[(3R,3aR,4S,6S,9aS,9bS)-6-hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,6a,7,9a,9b-octahydroazuleno[4,5-b]furan-4-yl] (E)-2-methylbut-2-enoate 44445509 Click to see CC=C(C)C(=O)OC1CC(C2CC=C(C2C3C1C(C(=O)O3)C)C)(C)O 348.40 unknown https://doi.org/10.1021/NP0703996
> Organoheterocyclic compounds / Naphthofurans
[(1R,2S,5R,6R,9S,10S,11R,13R)-9-methyl-10-[(E)-2-methylbut-2-enoyl]oxy-14-methylidene-4-oxo-3,12-dioxatetracyclo[7.5.0.02,6.011,13]tetradecan-5-yl] (Z)-2-methylbut-2-enoate 44445507 Click to see 430.50 unknown https://doi.org/10.1021/NP0703996
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Luteolin 3'-glucoside 12309350 Click to see 448.40 unknown https://doi.org/10.1007/BF00629880
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00630110
https://doi.org/10.1007/BF00629880

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