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Silene linicola

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 UUID643ffd31ec933941890598
Scientific name Silene linicola
Authority C.C.Gmel.
First published in Fl. Bad. 4: 304 (1826)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
German flachs-leimkraut
Swedish linglim

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
  • Europe
    • Middle Europe
      • Germany
    • Southeastern Europe
      • Italy
      • Yugoslavia
    • Southwestern Europe
      • France

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000440879
Tropicos 6300477
INPN 123526
Flora of Italy 865
KEW urn:lsid:ipni.org:names:157683-1
The Plant List kew-2488731
Open Tree Of Life 418327
Observations.org 132116
NCBI Taxonomy 39891
IPNI 157683-1
iNaturalist 482183
GBIF 5586656
EPPO SILLI
EOL 5200205
Elurikkus 550610

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
Biotic Elicitors in Adventitious and Hairy Root Cultures: A Review from 2010 to 2022 Alcalde MA, Perez-Matas E, Escrich A, Cusido RM, Palazon J, Bonfill M Molecules 17-Aug-2022
PMCID:PMC9416168
doi:10.3390/molecules27165253
PMID:36014492
Phytoecdysteroids from Silene jenisseensis D. N. Olennikov, N. I. Kashchenko Springer Science and Business Media LLC 21-Nov-2017
doi:10.1007/S10600-017-2239-1
The impact of agricultural intensification and land-use change on the European arable flora Storkey J, Meyer S, Still KS, Leuschner C Proc Biol Sci 12-Oct-2011
PMCID:PMC3282365
doi:10.1098/rspb.2011.1686
PMID:21993499
16th International Ecdysone Workshop: July 10–14, 2006, Ghent University, Belgium Bellés X, Billas I, Cherbas P, Delbecque JP, Dhadialla T, Fujiwara H, Hill R, Hiruma K, Hermann R, Iatrou K, Koolman J, Lafont R, Lepesant JA, Nakagawa Y, Palli R, Raikhel A, Riddiford L, Rees H, Sehnal F, Slama K, Smagghe G, Spindler KD, Steel C, Swevers L, Thummel C J Insect Sci 08-Mar-2007
PMCID:PMC2999422
doi:10.1673/031.007.1301
Phytoecdysteroids from the Silene genus N. Z. Mamadalieva, L. N. Zibareva, R. Lafont, L. Dainan, Z. Saatov Springer Science and Business Media LLC 01-Apr-2005
doi:10.1007/S10600-005-0040-Z

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 / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
1,2,3,14-tetrahydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 13799577 Click to see CC12CCC3C(=CC(=O)C4C3(C(C(C(C4)O)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 496.60 unknown https://doi.org/10.1007/S10600-005-0040-Z
2,3,11,14-tetrahydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 4254739 Click to see 496.60 unknown https://doi.org/10.1007/S10600-005-0040-Z
2,3,14,20,22,25-Hexahydroxycholest-7-en-6-one 271605 Click to see 480.60 unknown https://doi.org/10.1007/S10600-005-0040-Z
2,3,5,14-Tetrahydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-1,2,3,4,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-6-one 271604 Click to see CC12CCC3C(=CC(=O)C4(C3(CC(C(C4)O)O)C)O)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 496.60 unknown https://doi.org/10.1007/S10600-005-0040-Z
20-Hydroxyecdysone 5459840 Click to see 480.60 unknown https://doi.org/10.1007/S10600-017-2239-1
2beta,3beta,5beta,14,20,22R,25-Heptahydroxycholest-7-en-6-one 441833 Click to see CC12CCC3C(=CC(=O)C4(C3(CC(C(C4)O)O)C)O)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 496.60 unknown https://doi.org/10.1007/S10600-017-2239-1
Integristerone A 16038795 Click to see 496.60 unknown https://doi.org/10.1007/S10600-017-2239-1
Turkesterone 14376672 Click to see 496.60 unknown https://doi.org/10.1007/S10600-017-2239-1
https://doi.org/10.1007/S10600-005-0040-Z
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
[5,6-dihydroxy-2-methyl-6-(2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)heptan-2-yl] acetate 538673 Click to see 522.70 unknown https://doi.org/10.1007/S10600-005-0040-Z
2-Deoxy-20-hydroxyecdysone 9912297 Click to see CC12CCC(CC1C(=O)C=C3C2CCC4(C3(CCC4C(C)(C(CCC(C)(C)O)O)O)O)C)O 464.60 unknown https://doi.org/10.1007/S10600-005-0040-Z
2,3,14,22,25-Pentahydroxycholest-7-en-6-one 4233007 Click to see 464.60 unknown https://doi.org/10.1007/S10600-005-0040-Z
3,14-dihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 628409 Click to see CC12CCC(CC1C(=O)C=C3C2CCC4(C3(CCC4C(C)(C(CCC(C)(C)O)O)O)O)C)O 464.60 unknown https://doi.org/10.1007/S10600-005-0040-Z
Ecdysone 19212 Click to see CC(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)C(CCC(C)(C)O)O 464.60 unknown https://doi.org/10.1007/S10600-005-0040-Z
https://doi.org/10.1007/S10600-017-2239-1
Viticosterone E 11226211 Click to see CC(=O)OC(C)(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O 522.70 unknown https://doi.org/10.1007/S10600-005-0040-Z
https://doi.org/10.1007/S10600-017-2239-1

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