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Ferula kokanica

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 UUID64401c36386d6428180011
Scientific name Ferula kokanica
Authority Regel & Schmalh.
First published in Trudy Imp. S.-Peterburgsk. Bot. Sada 5: 593 (1877)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Ferula schugnanica B.Fedtsch. Trudy Bot. Muz. Imp. Akad. Nauk 1: 136 (1902)

Common names Top

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Language Common/alternative name
French ferula schugnanica

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
  • Asia-temperate
    • Middle Asia
      • Kirgizstan
      • Tadzhikistan
      • Uzbekistan
    • Western Asia
      • Afghanistan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000686630
Tropicos 1700101
KEW urn:lsid:ipni.org:names:842333-1
The Plant List kew-2808487
Open Tree Of Life 695202
Observations.org 130432
NCBI Taxonomy 92052
IPNI 842333-1
GBIF 3637959
EOL 2881609
Elurikkus 388455

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
Terpenoid coumarins fromFerula kokanica A. U. Babekov, A. I. Saidkhodzhaev, B. M. Keneshov Springer Science and Business Media LLC 20-Oct-2005
doi:10.1007/BF02236438
Terpenoid coumarins ofFerula kokanica M. V. Sklyar, M. G. Pimenov, L. B. Drozhzhina Springer Science and Business Media LLC 22-Nov-2004
doi:10.1007/BF00579439

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
3-[(1R,2S,3S)-2,3-dimethyl-2-[(2-oxochromen-7-yl)oxymethyl]-6-propan-2-ylidenecyclohexyl]propanoic acid 3037129 Click to see 398.50 unknown https://doi.org/10.1007/BF02236438
5-Cycloundecene-1-carboxylic acid, 1,5-dimethyl-9-methylene-2-((2-oxo-2H-1-benzopyran-7-yl)oxy)- 6433797 Click to see 396.50 unknown https://doi.org/10.1007/BF02236438
Galbanic acid 7082474 Click to see CC1CCC(=C(C)C)C(C1(C)COC2=CC3=C(C=C2)C=CC(=O)O3)CCC(=O)O 398.50 unknown https://doi.org/10.1007/BF02236438
> Phenylpropanoids and polyketides / Coumarins and derivatives
2H-1-Benzopyran-2-one, 7-[[(1R,2S,4aS,6S,8aR)-decahydro-2,6-dihydroxy-2,5,5,8a-tetramethyl-1-naphthalenyl]methoxy]- 11873225 Click to see CC1(C2CCC(C(C2(CCC1O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)(C)O)C 400.50 unknown https://doi.org/10.1007/BF00579439
7-[[(1R,4aS,8aR)-5,5,8a-trimethyl-2-methylidene-6-oxo-1,3,4,4a,7,8-hexahydronaphthalen-1-yl]methoxy]chromen-2-one 14865891 Click to see CC1(C2CCC(=C)C(C2(CCC1=O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)C 380.50 unknown https://doi.org/10.1007/BF00579439
7-[[(1R,8aR)-5,5,8a-trimethyl-2-methylidene-6-oxo-1,3,4,4a,7,8-hexahydronaphthalen-1-yl]methoxy]chromen-2-one 101793077 Click to see 380.50 unknown https://doi.org/10.1007/BF00579439
7-[[(1S,2R,4aS,6S,8aR)-2,6-dihydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one 7091630 Click to see 400.50 unknown https://doi.org/10.1007/BF00579439
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 382.50 unknown https://doi.org/10.1007/BF00579439
https://doi.org/10.1007/BF02236438
Badrakemin acetate 1771505 Click to see 424.50 unknown https://doi.org/10.1007/BF00579439
Coumarin, 7-((decahydro-6-hydroxy-5,5,8a-trimethyl-2-methylene-1-naphthyl)methoxy)-, acetate 7002233 Click to see 424.50 unknown https://doi.org/10.1007/BF00579439
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/10.1007/BF02236438
https://doi.org/10.1007/BF00579439
Gummosin 7092581 Click to see 382.50 unknown https://doi.org/10.1007/BF00579439
Kellarin 40580807 Click to see 442.50 unknown https://doi.org/10.1007/BF00579439
Kokanidin 126961508 Click to see 442.50 unknown https://doi.org/10.1007/BF00579439
Polyanthin 1765141 Click to see 424.50 unknown https://doi.org/10.1007/BF02236438
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1007/BF00579439

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