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Seseli transcaucasicum

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 UUID6440471902ea5137242895
Scientific name Seseli transcaucasicum
Authority (Schischk.) Pimenov & Sdobnina
First published in Bot. Zhurn. (Moscow & Leningrad) 60: 1119 (1975)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Balinotella transcaucasica (Schischk.) Soják Zprávy Krajsk. Vlastiv. Muz. Olomouci 215: 4 (1982)
Libanotis transcaucasica Schischk. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 13: 161 (1950)
Libanotis montana var. lasiopetala Bornm. Verh. K. K. Zool.-Bot. Ges. Wien 60: 120 (1910)

Common names Top

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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
    • Western Asia
      • Iran
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001068823
Tropicos 1703239
KEW urn:lsid:ipni.org:names:848747-1
The Plant List tro-1703239
Open Tree Of Life 3890414
Observations.org 148121
NCBI Taxonomy 2502083
IPNI 848747-1
iNaturalist 896562
GBIF 3629086

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
Unity in diversity—food plants and fungi of Sakartvelo (Republic of Georgia), Caucasus Bussmann RW, Paniagua Zambrana NY, Ur Rahman I, Kikvidze Z, Sikharulidze S, Kikodze D, Tchelidze D, Khutsishvili M, Batsatsashvili K J Ethnobiol Ethnomed 31-Dec-2021
PMCID:PMC8719402
doi:10.1186/s13002-021-00490-9
PMID:34972527
Unpalatable plants induce a species-specific associational effect on neighboring communities Erfanian MB, Memariani F, Atashgahi Z, Mesdaghi M, Saeedi M, Darrudi M, Hamedian M, Hosseini S, Ejtehadi H Sci Rep 13-Jul-2021
PMCID:PMC8277879
doi:10.1038/s41598-021-93698-4
PMID:34257345
Natural Products and Synthetic Analogs as a Source of Antitumor Drugs Sharifi-Rad J, Ozleyen A, Boyunegmez Tumer T, Oluwaseun Adetunji C, El Omari N, Balahbib A, Taheri Y, Bouyahya A, Martorell M, Martins N, C. Cho W Biomolecules 01-Nov-2019
PMCID:PMC6920853
doi:10.3390/biom9110679
PMID:31683894
Essential Oils and Their Constituents as Anticancer Agents: A Mechanistic View Gautam N, Mantha AK, Mittal S Biomed Res Int 09-Jun-2014
PMCID:PMC4070586
doi:10.1155/2014/154106
PMID:25003106
Oxygen-containing fractions of the essential oil ofLibanotis transcaucasica. II G. V. Pigulevskii, L. A. Bakina Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00568028
Coumarins of the roots of Libanotis transcaucasica D. G. Turabelidze, G. K. Nikonov, É. P. Kemertelidze Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00563911

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 / Sesquiterpenoids
alpha,4-Dimethyl-alpha-(4-methyl-3-penten-1-yl)-3-cyclohexene-1-methanol 10586 Click to see 222.37 unknown https://doi.org/10.1007/BF00568028
Bisabolol 1549992 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1007/BF00568028
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(1S,4R,5S)-1,8-dimethyl-4-propan-2-ylspiro[4.5]dec-7-en-9-one 101194428 Click to see CC1CCC(C12CC=C(C(=O)C2)C)C(C)C 220.35 unknown https://doi.org/10.1007/BF00568028
Spiro[4.5]dec-6-en-8-one, 1,7-dimethyl-4-(1-methylethyl)- 573024 Click to see CC1CCC(C12CC=C(C(=O)C2)C)C(C)C 220.35 unknown https://doi.org/10.1007/BF00568028
> Phenylpropanoids and polyketides / Coumarins and derivatives
Osthol 10228 Click to see 244.28 unknown https://doi.org/10.1007/BF00563911
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins
2-(9-Acetyloxy-2-oxo-6a,8,9,9a-tetrahydrofuro[2,3-h]chromen-8-yl)propan-2-yl 2-methylbutanoate 163024827 Click to see 390.40 unknown https://doi.org/10.1007/BF00563911
2-[(6aR,8R,9R,9aS)-9-acetyloxy-2-oxo-6a,8,9,9a-tetrahydrofuro[2,3-h]chromen-8-yl]propan-2-yl (2R)-2-methylbutanoate 163186714 Click to see 390.40 unknown https://doi.org/10.1007/BF00563911
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Libanotin 91698393 Click to see 386.40 unknown https://doi.org/10.1007/BF00563911
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
2-(7-oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl)propan-2-yl (E)-3-(4-hydroxyphenyl)prop-2-enoate 101311663 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)OC(=O)C=CC4=CC=C(C=C4)O 392.40 unknown https://doi.org/10.1007/BF00563911

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