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Ferula karatavica

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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 UUID64401c35296f5117640961
Scientific name Ferula karatavica
Authority Regel & Schmalh.
First published in Trudy Imp. S.-Peterburgsk. Bot. Sada 5: 594 (1877)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ferula aitchisonii Koso-Pol. Bot. Mater. Gerb. Glavn. Bot. Sada R.S.F.S.R. 2: 61 (1921)
Ferula eremophila Korovin Monogr. Ferula : 68 (1947)
Ferula sassyr Koso-Pol. Izv. Glavn. Bot. Sada R.S.F.S.R. 16: 224 (1916)

Common names Top

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Language Common/alternative name
Kazakh Қаратау сасыры

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
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Uzbekistan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000686615
Tropicos 1702740
KEW urn:lsid:ipni.org:names:842320-1
The Plant List kew-2808473
Open Tree Of Life 687054
Observations.org 130054
NCBI Taxonomy 371352
IPNI 842320-1
iNaturalist 991988
GBIF 3638090
EOL 5045715
Elurikkus 388478
USDA GRIN 16613

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
Esters from the roots of Ferula kyzylkumica and F. karategina A. I. Saidkhodzhaev, V. M. Malikov, M. G. Pimenov, S. Melibaev Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630134
Terpenoid coumarins ofFerula aitchisonii N. V. Veselovskaya, Yu. E. Sklyar, M. G. Pimenov Springer Science and Business Media LLC 22-Nov-2004
doi:10.1007/BF00580473
Sesquiterpene lactones ofJurinea suffruticosa S. Kh. Zakirov, Sh. Z. Kasymov, G. P. Sidyakin Springer Science and Business Media LLC 22-Nov-2004
doi:10.1007/BF00580475
The structures of feroside and of reoselin a — New glycosides from the roots ofFerula korshinskyi A. Sh. Kadyrov, A. I. Saidkhodzhaev, G. K. Nikonov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00567694
An aromatic aldehyde fromFerula equisetacea V. Yu. Bagirov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00567157
A sesquiterpene alcohol fromFerula karatavica V. Yu. Bagirov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00567163

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 / M-methoxybenzoic acids and derivatives
(1S,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 4-hydroxy-3-methoxybenzoate 1294694 Click to see CC1(C2CCC1(C(C2)OC(=O)C3=CC(=C(C=C3)O)OC)C)C 304.40 unknown https://doi.org/10.1007/BF00630134
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(3aS,4S,7S,8aR)-1,4-dimethyl-7-propan-2-yl-3a,5,6,7,8,8a-hexahydro-3H-azulen-4-ol 163083802 Click to see CC1=CCC2C1CC(CCC2(C)O)C(C)C 222.37 unknown https://doi.org/10.1007/BF00567157
1,4-dimethyl-7-propan-2-yl-3a,5,6,7,8,8a-hexahydro-3H-azulen-4-ol 23264999 Click to see CC1=CCC2C1CC(CCC2(C)O)C(C)C 222.37 unknown https://doi.org/10.1007/BF00567163
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
5-Cycloundecene-1-carboxylic acid, 1,5-dimethyl-9-methylene-2-((2-oxo-2H-1-benzopyran-7-yl)oxy)- 6433797 Click to see CC1=CCCC(=C)CCC(C(CC1)OC2=CC3=C(C=C2)C=CC(=O)O3)(C)C(=O)O 396.50 unknown https://doi.org/10.1007/BF00580473
Karatavicinol 44386968 Click to see CC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)CCC(C(C)(C)O)O 400.50 unknown https://doi.org/10.1007/BF00580473
Karatavikin 1799234 Click to see CC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)CCC(=O)C(C)(C)O 398.50 unknown https://doi.org/10.1007/BF00567694
Umbelliprenin 1781413 Click to see CC(=CCCC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C)C 366.50 unknown https://doi.org/10.1007/BF00580475
https://doi.org/10.1007/BF00580473
> Phenylpropanoids and polyketides / Coumarins and derivatives
Tavicone 3694933 Click to see CC1=CCC2C(C(=O)CC2(C1COC3=CC4=C(C=C3)C=CC(=O)O4)C)(C)C 366.40 unknown https://doi.org/10.1007/BF00580473

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