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Ferula oopoda

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 UUID64401c3bca1d3957013821
Scientific name Ferula oopoda
Authority Boiss.
First published in Fl. Orient. 2: 984 (1872)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Peucedanum oopodum Boiss. & Buhse Nouv. Mém. Soc. Imp. Naturalistes Moscou 12: 100 (1860)
Ferula badghysi Korovin Monogr. Ferula : 67 (1947)

Common names Top

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Language Common/alternative name
Azerbaijani yumurtavari ilankölgəsi
tk okaraly çomuç

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • Middle Asia
      • Turkmenistan
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000686722
Tropicos 1700112
KEW urn:lsid:ipni.org:names:842421-1
The Plant List kew-2808571
Open Tree Of Life 27950
Observations.org 136616
NCBI Taxonomy 371375
IPNI 842421-1
iNaturalist 1106195
GBIF 3637152
EOL 2881603
Elurikkus 388316
USDA GRIN 410307

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
Crystal structure and Hirshfeld surface analysis of (5aS,8aR)-3,5a-dimethyl-8-methyl­idene-2-oxododeca­hydro­oxireno[2′,3′:6,7]naphtho­[1,2-b]furan-6-yl (Z)-2-methyl­but-2-enoate extracted from Ferula persica Karimli EG, Khrustalev VN, Kurasova MN, Akkurt M, Khalilov AN, Bhattarai A, Mamedov İG Acta Crystallogr E Crystallogr Commun 21-Apr-2023
PMCID:PMC10162084
doi:10.1107/S205698902300333X
PMID:37151821
Ethnoveterinary botanical survey of medicinal plants used in Pashto, Punjabi and Saraiki communities of Southwest Pakistan Abidin SZ, Munem A, Khan R, Batiha GE, Amhad M, Zafar M, Khalil AA, Hetta HF, Mahmoud MH, Sami A, Bhatti MZ Vet Med Sci 22-Jul-2021
PMCID:PMC8464251
doi:10.1002/vms3.582
PMID:34291882
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
Ethnopharmacological study of native medicinal plants and the impact of pastoralism on their loss in arid to semiarid ecosystems of southeastern Iran Sharafatmandrad M, Khosravi Mashizi A Sci Rep 23-Sep-2020
PMCID:PMC7511295
doi:10.1038/s41598-020-72536-z
PMID:32968162
Traditional medicinal plants used for respiratory disorders in Pakistan: a review of the ethno-medicinal and pharmacological evidence Alamgeer, Younis W, Asif H, Sharif A, Riaz H, Bukhari IA, Assiri AM Chin Med 18-Sep-2018
PMCID:PMC6145130
doi:10.1186/s13020-018-0204-y
PMID:30250499
Ethnobotanical knowledge of Apiaceae family in Iran: A review Amiri MS, Joharchi MR Avicenna J Phytomed 01-Nov-2016
PMCID:PMC5206921
PMID:28078243
Antioxidant effects of hydroalcoholic and polyphenolic extracts of Peucedanum pastinacifolium Boiss. & Hausskn. Movahedian A, Zolfaghari B, Mirshekari M Res Pharm Sci 01-Oct-2016
PMCID:PMC5122830
doi:10.4103/1735-5362.192492
PMID:27920823
Volatile oils: Potential agents for the treatment of respiratory infections Pasdaran A, Pasdaran A, Sheikhi D The Microbiology of Respiratory System Infections 05-Aug-2016
PMCID:PMC7149900
doi:10.1016/B978-0-12-804543-5.00016-6
Antimalarial natural products: a review Mojab F Avicenna J Phytomed 01-Mar-2012
PMCID:PMC4075661
PMID:25050231
Plant-Derived Antimalarial Agents: New Leads and Efficient Phytomedicines. Part II. Non-Alkaloidal Natural Products Batista R, de Jesus Silva Júnior A, de Oliveira AB Molecules 13-Aug-2009
PMCID:PMC6254980
doi:10.3390/molecules14083037
PMID:19701144
Screening the methanol extracts of some Iranian plants for acetylcholinesterase inhibitory activity Gholamhoseinian A, Moradi MN, Sharifi-far F Res Pharm Sci 01-Jul-2009
PMCID:PMC3093628
PMID:21589805
Lactones of Ferula badghysi S. V. Serkerov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00567821
The structure of semopodin and a hydroxylactone from Ferula oopoda S. V. Serkerov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00567820
Stereochemistry of the eudesmanolides ofFerula oopoda S. V. Serkerov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00568369
The structure of an ester from the fruit of Ferula oopoda S. V. Serkerov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00563688

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 / Fatty Acyls / Fatty acid esters
(3,6,9-Trimethyl-2,7-dioxo-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl) 2-methylbut-2-enoate 297958 Click to see 344.40 unknown https://doi.org/10.1007/BF00567821
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones
(1S,3aS,8aS,9R,9aS)-9-hydroxy-1,5,8-trimethyl-1,3a,4,8a,9,9a-hexahydroazuleno[6,5-b]furan-2,6-dione 163000057 Click to see CC1C2C(CC(=C3C(C2O)C(=CC3=O)C)C)OC1=O 262.30 unknown https://doi.org/10.1007/BF00564184
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3,5a,9-trimethyl-2,6-dioxo-3a,4,5,9b-tetrahydrobenzo[g][1]benzofuran-3-yl) (E)-2-methylbut-2-enoate 101967115 Click to see 344.40 unknown https://doi.org/10.1007/BF00567820
(3S,3aS,5aS,9aS,9bS)-3,5a,9-trimethyl-3,3a,4,5,9a,9b-hexahydrobenzo[g][1]benzofuran-2-one 11117930 Click to see 232.32 unknown https://doi.org/10.1007/BF00568369
[(1R,2R,5S,6S,9S,10S,11R,13R)-5,9-dimethyl-14-methylidene-4-oxo-3,12-dioxatetracyclo[7.5.0.02,6.011,13]tetradecan-10-yl] (E)-2-methylbut-2-enoate 162883832 Click to see CC=C(C)C(=O)OC1C2C(O2)C(=C)C3C1(CCC4C3OC(=O)C4C)C 346.40 unknown https://doi.org/10.1007/BF00563688
[(1S,2S,6R,9S,10R,11R,13R)-9-methyl-5,14-dimethylidene-4-oxo-3,12-dioxatetracyclo[7.5.0.02,6.011,13]tetradecan-10-yl] (E)-2-methylbut-2-enoate 162935601 Click to see 344.40 unknown https://doi.org/10.1007/BF00563688
[(1S,2S,6S,9R,10R,11S,13S)-9-methyl-5,14-dimethylidene-4-oxo-3,12-dioxatetracyclo[7.5.0.02,6.011,13]tetradecan-10-yl] (Z)-2-methylbut-2-enoate 101306928 Click to see 344.40 unknown https://doi.org/10.1007/BF00567821
[(3R,3aS,5aR,6S,9aS,9bS)-3,5a-dimethyl-9-methylidene-2-oxo-3a,4,5,6,9a,9b-hexahydro-3H-benzo[g][1]benzofuran-6-yl] (Z)-2-methylbut-2-enoate 101306868 Click to see 330.40 unknown https://doi.org/10.1007/BF00568369
[(3R,3aS,5aS,9bR)-3,5a,9-trimethyl-2,6-dioxo-3a,4,5,9b-tetrahydrobenzo[g][1]benzofuran-3-yl] (E)-2-methylbut-2-enoate 162950198 Click to see CC=C(C)C(=O)OC1(C2CCC3(C(=O)C=CC(=C3C2OC1=O)C)C)C 344.40 unknown https://doi.org/10.1007/BF00567821
Dehydrooopodin 44445508 Click to see 328.40 unknown https://doi.org/10.1007/BF00567821
https://doi.org/10.1007/BF00568369
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Ferulin 11896611 Click to see CC1C2C=C3C(=CC(=O)C3=C(CC2OC1=O)C)C 244.28 unknown https://doi.org/10.1007/BF00568369
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown https://doi.org/10.1007/BF00567821

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