Silene chalcedonica
Table of Contents
Details Top
Internal ID | UUID643ffcfd108a4366237574 |
Scientific name | Silene chalcedonica |
Authority | E.H.L.Krause |
First published in | Deutschl. Fl. Abbild. , ed. 2, 5: 96 (1901) |
Description Top
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No description added yet. Help us by writing one.
Synonyms Top
Scientific name | Authority | First published in |
---|---|---|
Lychnis chalcedonica | L. | Sp. Pl. : 436 (1753) |
Agrostemma chalcedonica | (L.) Doell. |
Common names Top
Add a new one! Suggest a correction!Language | Common/alternative name |
---|---|
English | scarlet lychnis |
English | maltese-cross |
English | london-pride |
Czech | kohoutek plamenný |
Welsh | croes malta |
German | brennende liebe |
Estonian | loitev tulinelk |
Finnish | palavarakkaus |
Finnish | palava rakkaus |
Upper Sorbian | Čerwjena kukelička |
Lithuanian | goštautinė gaisrena |
Latvian | sarkanā guntiņa |
Malayalam | ലിച്ച്നിസ് ചാൽസെഡോണിക്ക |
Norwegian Bokmål | ildkjærlighet |
Dutch | brandende liefde |
Norwegian Nynorsk | eldkjærleik |
Polish | firletka chalcedońska |
Russian | Зорька обыкновенная |
Samogitian | guoštauts |
Slovak | kukučka hustokvetá |
tt | Сабын чәчәге |
Chinese | 皺葉剪秋羅 |
Chinese | 皱叶蝇子草 |
Chinese | 皱叶剪秋罗 |
Germination/Propagation Top
Suggest a correction or add new data!Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment. |
Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium. |
Germination Improved by GA3: Gibberellic Acid(GA3) is a plant growth hormone that can break dormancy and improve germination rates for seeds that are otherwise difficult to sprout. |
Distribution (via POWO/KEW) Top
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
-
Asia-temperate click to expand
-
China
- China North-central
- Xinjiang
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Eastern Asia
- Japan
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Middle Asia
- Kazakhstan
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Mongolia
- Mongolia
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Russian Far East
- Khabarovsk
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Siberia
- Altay
- Irkutsk
- Krasnoyarsk
- West Siberia
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China
-
Asia-tropical click to expand
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Indo-China
- Vietnam
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Indo-China
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Australasia click to expand
-
Australia
- New South Wales
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Australia
-
Europe click to expand
-
Eastern Europe
- Central European Russia
- East European Russia
- North European Russia
- South European Russia
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Middle Europe
- Czechoslovakia
- Germany
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Northern Europe
- Denmark
- Finland
- Norway
- Sweden
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Southeastern Europe
- Bulgaria
- Romania
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Eastern Europe
-
Northern America click to expand
-
Eastern Canada
- New Brunswick
- Nova Scotia
- Ontario
- Prince Edward Island
- Québec
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North-central U.S.A.
- Illinois
- Iowa
- Minnesota
- Wisconsin
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Northeastern U.S.A.
- Connecticut
- Indiana
- Maine
- Massachusetts
- Michigan
- New Hampshire
- New Jersey
- New York
- Pennsylvania
- Vermont
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Northwestern U.S.A.
- Idaho
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Western Canada
- Alberta
- British Columbia
- Manitoba
- Saskatchewan
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Eastern Canada
Links to other databases Top
Suggest others/fix!Database | ID/link to page |
---|---|
World Flora Online | wfo-0000438581 |
Canadensys | 4370 |
Tropicos | 6303615 |
KEW | urn:lsid:ipni.org:names:157059-1 |
The Plant List | kew-2485408 |
Open Tree Of Life | 115695 |
Observations.org | 20264 |
NCBI Taxonomy | 39855 |
NBN Atlas | NHMSYS0021008313 |
IPNI | 157059-1 |
iNaturalist | 406034 |
GBIF | 5584611 |
Freebase | /m/04m7cp |
WisFlora | 13320 |
EPPO | LYHCH |
EOL | 587272 |
Elurikkus | 549946 |
USDA GRIN | 429989 |
Wikipedia | Silene_chalcedonica |
Plantarium | 53302 |
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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Phytochemical Profile Top
Add a new one!
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 | |||||
(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3R)-2,3,6-trihydroxy-6-methyl-5-methylideneheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one | 13889301 | Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CC(=C)C(C)(C)O)O)O)O | 492.60 | unknown | https://doi.org/10.1007/BF00636589 |
(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3S)-2,3,6-trihydroxy-6-methyl-5-methylideneheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one | 162969801 | Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CC(=C)C(C)(C)O)O)O)O | 492.60 | unknown |
https://doi.org/10.1007/BF00636589 https://doi.org/10.1007/BF00579144 |
(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,5,14-tetrahydroxy-10,13-dimethyl-17-[(2R,3S)-2,3,6-trihydroxy-6-methylheptan-2-yl]-1,2,3,4,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-6-one | 162981122 | 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/BF00579144 https://doi.org/10.1007/BF00636589 |
2,3,14-trihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methyl-5-methylideneheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one | 13889300 | Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CC(=C)C(C)(C)O)O)O)O | 492.60 | unknown |
https://doi.org/10.1007/BF00636589 https://doi.org/10.1007/BF00579144 |
2,3,14-trihydroxy-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 | 271605 | Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O | 480.60 | unknown |
https://doi.org/10.1007/BF00579144 https://doi.org/10.1007/BF00636589 |
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/BF00636589 https://doi.org/10.1007/BF00579144 |
20-Hydroxyecdysone | 5459840 | Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O | 480.60 | unknown | https://doi.org/10.1007/BF00636589 |
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/BF00636589 |
Integristerone A | 16038795 | 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/BF00636589 |
> 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 | |||||
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/BF00636590 |
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/BF00636590 |
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives | |||||
5beta,20xi-Cholest-7-en-6-one, 22,25-epoxy-2beta,3beta,14,20-tetrahydroxy- | 91745162 | Click to see CC1(CCC(O1)C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)C | 462.60 | unknown | https://doi.org/10.1007/BF00636590 |
Collections Top
In private collections | 0 |
In public collections | 0 |