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Internal ID UUID64401c3906cd5167442251
Scientific name Ferula litwinowiana
Authority Koso-Pol.
First published in Spisok Rast. Gerb. Russk. Fl. Bot. Muz. Rossiisk. Akad. Nauk 8: 111 (1922)

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Synonyms Top

Scientific name Authority First published in
Ferula androssowii (B.Fedtsch.) M.Hiroe Umbell. World : 1522 (1979)
Merwia androssowi B.Fedtsch. Bot. Mater. Gerb. Glavn. Bot. Sada R.S.F.S.R. 5: 49 (1924)

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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-0000686660
Tropicos 1702758
KEW urn:lsid:ipni.org:names:842360-1
The Plant List kew-2808514
Open Tree Of Life 214834
Observations.org 132274
NCBI Taxonomy 371364
IPNI 842360-1
GBIF 3637695
Elurikkus 388403
USDA GRIN 16615

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 CentralĀ®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Endangered Uyghur Medicinal Plant Ferula Identification through the Second Internal Transcribed Spacer Fan C, Li X, Zhu J, Song J, Yao H Evid Based Complement Alternat Med 15-Jun-2015
PMCID:PMC4451158
doi:10.1155/2015/479879
PMID:26120347
Terpenoids ofFerula litwinowiana A. U. Babekov, A. I. Saidkhodzhaev, B. M. Keneshov Springer Science and Business Media LLC 21-Oct-2005
doi:10.1007/BF02234866
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
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[3,6,9-trimethyl-4-(2-methylpropanoyloxy)-2,7-dioxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-3-yl] 2-methylbut-2-enoate 71437703 Click to see CC=C(C)C(=O)OC1(C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)OC(=O)C(C)C)C 430.50 unknown https://doi.org/10.1007/BF02234866
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-[[(2S,4aS,6S)-2,6-dihydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one 5459231 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/BF02234866
Conferol 11892267 Click to see CC1=CCC2C(C(CCC2(C1COC3=CC4=C(C=C3)C=CC(=O)O4)C)O)(C)C 382.50 unknown https://doi.org/10.1007/BF02234866
Conferone 3108117 Click to see CC1=CCC2C(C(=O)CCC2(C1COC3=CC4=C(C=C3)C=CC(=O)O4)C)(C)C 380.50 unknown https://doi.org/10.1007/BF02234866
Diversin 13800313 Click to see CC(=C)CC(=O)C=C(C)CCOC1=CC2=C(C=C1)C=CC(=O)O2 312.40 unknown https://doi.org/10.1007/BF00574600
Feselol 179577 Click to see CC1=CCC2C(C(CCC2(C1COC3=CC4=C(C=C3)C=CC(=O)O4)C)O)(C)C 382.50 unknown https://doi.org/10.1007/BF02234866
Samarcandin 71587098 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/BF02234866
> 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/BF00574600

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