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Seseli lehmannianum

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 UUID64404717a4f23591996230
Scientific name Seseli lehmannianum
Authority Boiss.
First published in Fl. Orient. 2: 967 (1872)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Seseli fedtschenkoanum Regel & Schmalh. Izv. Imp. Obshch. Lyubit. Estestv. Moskovsk. Univ. 34(2): 30 (1882)

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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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001068800
KEW urn:lsid:ipni.org:names:848600-1
Open Tree Of Life 3890109
iNaturalist 896666
GBIF 3630699

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
Coumarins of Libanotis lehmannae A. M. Aminov, K. B. Bizhanova, G. K. Nikonov Springer Science and Business Media LLC 09-Jul-2008
doi:10.1007/BF00570681
A chemical study of the roots of Libanotis lehmanniana G. K. Nikonov, A. M. Aminov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00563461
The coumarins of Seseli tenuisectum A. M. Aminov, G. K. Nikonov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00565359

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 / Diterpenoids / Aconitane-type diterpenoid alkaloids
(1S,2R,3R,4S,5S,6S,8S,9S,10R,13S,16S,17R)-11-ethyl-13-(hydroxymethyl)-6-methoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,16-triol 101457306 Click to see 393.50 unknown https://doi.org/10.1007/BF00570681
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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 11870456 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/BF00563461
https://doi.org/10.1007/BF00565359
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/BF00565359
https://doi.org/10.1007/BF00563461
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1007/BF00570681
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
((9R,10R)-8,8-Dimethyl-9-((Z)-2-Methylbut-2-Enoyl)Oxy-2-Oxo-9,10-Dihydropyrano(2,3-F)Chromen-10-Yl) (Z)-2-Methylbut-2-Enoate 10251869 Click to see 426.50 unknown https://doi.org/10.1007/BF00570681
Khellactone, cis-(+)- 455821 Click to see 262.26 unknown https://doi.org/10.1007/BF00570681
Praeruptorin B 5319259 Click to see 426.50 unknown https://doi.org/10.1007/BF00570681

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