Colchicum soboliferum - Unknown
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Internal ID UUID644025a93c858416114889
Scientific name Colchicum soboliferum
Authority Stef.
First published in Sborn. B'lghar. Akad. Nauk 22: 44 (1926)

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Synonyms Top

Scientific name Authority First published in
Merendera sobolifera Fisch. & C.A.Mey. Index Seminum [St.Petersburg (Petropolitanus)] i. 34.
Merendera hastulata Baker J. Linn. Soc., Bot. 17: 439 (1879)
Bulbocodium hastulatum Friwald. Flora 19: 434 (1836)
Bulbocodium soboliferum Heynh. Alph. Aufz. Gew. : 81 (1846)

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Language Common/alternative name
Arabic لحلاح أشطائي
Azerbaijani budaqlı danaqıran
Czech merendera výběžkatá
German sprossende zeitlose

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • Middle Asia
      • Tadzhikistan
      • Turkmenistan
    • Western Asia
      • Afghanistan
      • East Aegean Islands
      • Iran
      • Lebanon-Syria
      • Turkey
  • Europe
    • Southeastern Europe
      • Bulgaria
      • Greece
      • Romania
      • Turkey-in-Europe
      • Yugoslavia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000764017
Tropicos 100170738
KEW urn:lsid:ipni.org:names:533388-1
The Plant List kew-302949
Open Tree Of Life 111352
NCBI Taxonomy 1094118
IPNI 533388-1
iNaturalist 482893
GBIF 2739852
EOL 1003731
CMAUP NPO18273

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
Alkaloids and phenolics of three Merendera species A. Husek, N. Sütlüpinar, H. Potěšilová, S. Dvořáčková, V. Hanuš, P. Sedmera, P. Maloň, V. Šimánek Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80310-3

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1016/0031-9422(89)80310-3
> Hydrocarbon derivatives / Tropones
3-Desmethylcolchicine 299664 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)O 385.40 unknown https://doi.org/10.1016/0031-9422(89)80310-3
Colchicine 6167 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC 399.40 unknown https://doi.org/10.1016/0031-9422(89)80310-3
Demecolcine 220401 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC 371.40 unknown https://doi.org/10.1016/0031-9422(89)80310-3
N-(1,2,3,10-Tetramethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-7-yl)acetamide 2833 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC 399.40 unknown https://doi.org/10.1016/0031-9422(89)80310-3
O(sup 2)-Demethylcolchicine 541033 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)O)OC 385.40 unknown https://doi.org/10.1016/0031-9422(89)80310-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3S,3aR,4S,6aR,8S,9S,9aR,9bR)-3-(chloromethyl)-3,4,8-trihydroxy-9-methyl-6-methylidene-4,5,6a,7,8,9,9a,9b-octahydro-3aH-azuleno[4,5-b]furan-2-one 11197890 Click to see CC1C(CC2C1C3C(C(CC2=C)O)C(C(=O)O3)(CCl)O)O 316.77 unknown via CMAUP database
[(3aR,4S,6aR,8S,9aR,9bR)-8-hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl] 2-methylpropanoate 13996677 Click to see CC(C)C(=O)OC1CC(=C)C2CC(C(=C)C2C3C1C(=C)C(=O)O3)O 332.40 unknown via CMAUP database
11beta,13-Dihydroxydesacylcynaropicrin 8-O-beta-D-gucoside 14138152 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)O)OC4C(C(C(C(O4)CO)O)O)O 426.50 unknown via CMAUP database
Aguerin B 155102 Click to see CC(=C)C(=O)OC1CC(=C)C2CC(C(=C)C2C3C1C(=C)C(=O)O3)O 330.40 unknown via CMAUP database
CID 12149911 12149911 Click to see CC1C(CC2C1C3C(CCC2=C)C(C(=O)O3)(CO)O)O 282.33 unknown via CMAUP database
Cynarascoloside A 44144276 Click to see CC1C(CC2C1C3C(C(C(=O)O3)C)C(CC2=C)OC4C(C(C(C(O4)CO)O)O)O)O 428.50 unknown via CMAUP database
Cynarascoloside B 44144277 Click to see CC1C(CC2C1C3C(C(C(=O)O3)C)C(CC2=C)OC4C(C(C(C(O4)CO)O)O)O)O 428.50 unknown via CMAUP database
Cynarascoloside C 101156886 Click to see CC1C2C(CC1=O)C(=C)CC(C3C2OC(=O)C3C)OC4C(C(C(C(O4)CO)O)O)O 426.50 unknown via CMAUP database
Cynarinin A 11289450 Click to see CC1C2C(CC1=O)C(=C)CC(C3C2OC(=O)C3(CO)O)O 296.31 unknown via CMAUP database
Cynaropicrin 119093 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)OC(=O)C(=C)CO 346.40 unknown via CMAUP database
Grosheimin 442256 Click to see CC1C2C(CC1=O)C(=C)CC(C3C2OC(=O)C3=C)O 262.30 unknown via CMAUP database
Maximolide 12047616 Click to see CC1C2C(CC1=O)C(=C)CC(C3C2OC(=O)C3C)O 264.32 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
[1S-(1alpha,3beta,4beta,5alpha)]-3-[[3-(3,4-dihydroxyphenyl)-1-oxoallyl]oxy]-1,4,5-trihydroxycyclohexanecarboxylic acid 6436237 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
4,5-Dicaffeoylquinic acid 5281780 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
Cynarine 5281769 Click to see C1C(C(C(CC1(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O 516.40 unknown via CMAUP database
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
N-[(9R)-5,19-dimethoxy-6-oxo-15,17-dioxatetracyclo[10.7.0.02,8.014,18]nonadeca-1(19),2,4,7,12,14(18)-hexaen-9-yl]acetamide 163028593 Click to see CC(=O)NC1CCC2=CC3=C(C(=C2C4=CC=C(C(=O)C=C14)OC)OC)OCO3 383.40 unknown https://doi.org/10.1016/0031-9422(89)80310-3
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
Isorhoifolin 9851181 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O 578.50 unknown via CMAUP database
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
Luteolin 7-rutinoside 10461109 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O 594.50 unknown via CMAUP database
Narirutin 442431 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)O)O)O)O)O)O 580.50 unknown via CMAUP database

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