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Internal ID UUID643ffc8aaff68645038778
Scientific name Seseli grandivittatum
Authority Schischkin
First published in Izv. Kavkazsk. Muz. 11: 302 (1918)

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000434798
Tropicos 1700544
KEW urn:lsid:ipni.org:names:848568-1
Open Tree Of Life 3890591
Observations.org 127166
NCBI Taxonomy 2502070
IPNI 848568-1
iNaturalist 896522
GBIF 3631085
Elurikkus 387261

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)!
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Title Authors Publication Released IDs
Rutarin from the roots of Seseli grandivittatum A. Z. Abyshev, �. M. Agaev, M. A. Balabudkin Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630132
Coumarin composition of Seseli grandivittatum A. Z. Abyshev, P. P. Denisenko, D. Z. Abyshev, Yu. B. Kerumov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00569581
Coumarins of the roots ofSeseli grandivittatum D. G. Turabelidze, É. P. Kemertelidze Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00564817

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 / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00569581
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00569581
> Phenylpropanoids and polyketides / Coumarins and derivatives
Osthol 10228 Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)OC)C 244.28 unknown https://doi.org/10.1007/BF00564817
https://doi.org/10.1007/BF00569581
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
(2S)-2-(1-hydroxy-1-methyl-ethyl)-9-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-2,3-dihydrofuro[3,2-g]chromen-7-one 12315119 Click to see CC(C)(C1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)OC4C(C(C(C(O4)CO)O)O)O)O 424.40 unknown https://doi.org/10.1007/BF00630132
Rutarin 442149 Click to see CC(C)(C1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)OC4C(C(C(C(O4)CO)O)O)O)O 424.40 unknown https://doi.org/10.1007/BF00630132
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Edultin 5317013 Click to see CC=C(C)C(=O)OC1C(OC2=C1C3=C(C=C2)C=CC(=O)O3)C(C)(C)OC(=O)C 386.40 unknown https://doi.org/10.1007/BF00569581
Libanotin 91698393 Click to see CC=C(C)C(=O)OC1C(OC2=C1C3=C(C=C2)C=CC(=O)O3)C(C)(C)OC(=O)C 386.40 unknown https://doi.org/10.1007/BF00564817
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
(-)-Praeruptorin B 10251869 Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C(=CC)C 426.50 unknown https://doi.org/10.1007/BF00569581
https://doi.org/10.1007/BF00564817
Praeruptorin B 5319259 Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C(=CC)C 426.50 unknown https://doi.org/10.1007/BF00569581
https://doi.org/10.1007/BF00564817
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Decursinol, (-)- 1150962 Click to see CC1(C(CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O)C 246.26 unknown https://doi.org/10.1007/BF00569581

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