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Internal ID UUID64401c2fe7489130874646
Scientific name Ferula conocaula
Authority Korovin
First published in Monogr. Ferula : 33 (1947)

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Language Common/alternative name
Chinese 圆锥茎阿魏

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Xinjiang
    • Middle Asia
      • Kirgizstan
      • Tadzhikistan
      • Uzbekistan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000686513
Tropicos 1702716
KEW urn:lsid:ipni.org:names:842239-1
The Plant List kew-2808378
PFAF Ferula conocaula
Open Tree Of Life 3888384
Observations.org 117860
IPNI 842239-1
GBIF 3639024
EOL 2890677
Elurikkus 388643

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)!
Title Authors Publication Released IDs
Structure and configuration of cauferinin Z. A. Kuliev, T. Kh. Khasanov, V. M. Malikov Springer Science and Business Media LLC 10-Jan-2005
doi:10.1007/BF00570778
Conferdione — A new coumarin from Ferula conocaula V. V. Vandyshev, Yu. E. Sklyar, M. E. Perel'son, M. D. Moroz Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00567873
The structures of ferocaulin, ferocaulinin, ferocaulidin, and ferocaulicin Z. A. Kuliev, T. Kh. Khasanov Springer Science and Business Media LLC 01-Dec-2004
doi:10.1007/BF00713313
Structures of cauferin and cauferidin Z. A. Kuliev, T. Kh. Khasanov Springer Science and Business Media LLC 01-Dec-2004
doi:10.1007/BF00713314
Coumarins of Ferula litwinowiana N. F. Mir-Babaev, S. V. Serkerov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00574600

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
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/BF00574600
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-[(2,4,6-trihydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)methoxy]chromen-2-one 74039795 Click to see CC1(C(CCC2(C1C(CC(C2COC3=CC4=C(C=C3)C=CC(=O)O4)(C)O)O)C)O)C 416.50 unknown https://doi.org/10.1007/BF00570778
7-[(4,6-dihydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)methoxy]chromen-2-one 85433038 Click to see CC1(C(CCC2(C1C(CC(=C)C2COC3=CC4=C(C=C3)C=CC(=O)O4)O)C)O)C 398.50 unknown https://doi.org/10.1007/BF00713314
Conferdione 5179580 Click to see CC1=CC(=O)C2C(C(=O)CCC2(C1COC3=CC4=C(C=C3)C=CC(=O)O4)C)(C)C 394.50 unknown https://doi.org/10.1007/BF00567873
Ferocaulicin 124356232 Click to see CC1=CC(=O)C2C(C(CCC2(C1COC3=CC4=C(C=C3)C=CC(=O)O4)C)OC(=O)C)(C)C 438.50 unknown https://doi.org/10.1007/BF00713313
Ferocaulidin 14865892 Click to see CC1=CC(=O)C2C(C(CCC2(C1COC3=CC4=C(C=C3)C=CC(=O)O4)C)O)(C)C 396.50 unknown https://doi.org/10.1007/BF00713313

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