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Colchicum schimperi

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644025a8a3dfc720042244
Scientific name Colchicum schimperi
Authority Janka
First published in Sborn. B'lghar. Akad. Nauk 22: 31 (1926)

Description Top

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Synonyms Top

Scientific name Authority First published in
Colchicum ritchii var. guessfeldtianum (Asch. & Schweinf.) Stef. Sborn. B'lghar. Akad. Nauk 22: 100. 1926
Colchicum cornigerum (Sickenb.) Täckh. & Drar Publ. Cairo Univ. Herb. 5: 79 (1972 publ. 1974)
Colchicum deserti-syriaci Feinbrun Palestine J. Bot., Jerusalem Ser. 6: 81 (1953)
Colchicum guessfeldtianum Asch. & Schweinf. Ill. Fl. Égypte , Suppl. 2: 774 (1889)
Colchicum jesdianum Czerniakotoska Izv. Glavn. Bot. Sada S.S.S.R. 29: 356 (1930)
Colchicum palmetorum Czerniak. Izv. Glavn. Bot. Sada S.S.S.R. 29: 356 (1930)
Colchicum szovitsii var. cornigerum Schweinf. Mém. Inst. Égypt. 4: 294 1901
Colchicum velutinum Bornm. & Kneuck. Allg. Bot. Z. Syst. 9: 63 (1903)

Common names Top

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Language Common/alternative name
Arabic لحلاح شمبر

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
    • Arabian Peninsula
      • Saudi Arabia
    • Western Asia
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Sinai

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000764012
Tropicos 100170733
KEW urn:lsid:ipni.org:names:533384-1
The Plant List kew-302944
Open Tree Of Life 111333
NCBI Taxonomy 1094115
IPNI 533384-1
iNaturalist 884872
GBIF 2740005
EOL 1086987

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
Ethnobotany of the medicinal plants used by the ethnic communities of Kerman province, Southeast Iran Hosseini SH, Bibak H, Ghara AR, Sahebkar A, Shakeri A J Ethnobiol Ethnomed 28-Apr-2021
PMCID:PMC8082778
doi:10.1186/s13002-021-00438-z
PMID:33910616
Ethnopharmacological study of native medicinal plants and the impact of pastoralism on their loss in arid to semiarid ecosystems of southeastern Iran Sharafatmandrad M, Khosravi Mashizi A Sci Rep 23-Sep-2020
PMCID:PMC7511295
doi:10.1038/s41598-020-72536-z
PMID:32968162
Substances from the plants of the subfamily Wurmbaeoideae and their derivatives. LIII. Chemical investigation of Colchicum cornigerum (SWEINF.) TÄCKH. et DRAR. A. El-Hamidi, F. Šantavý Institute of Organic Chemistry & Biochemistry 02-Sep-2013
doi:10.1135/CCCC19622111
Substances from the plants of the subfamily Wurmbaeoideae and their derivatives. LXXII. Further chemical investigation of the plant Colchicum cornigerum (SCHWEINF.)TÄCKH. et DRAR. H. Potěšilová, J. Šantavý, A. El-Hamidi, F. Šantavý Institute of Organic Chemistry & Biochemistry 18-Dec-2012
doi:10.1135/CCCC19693540
Cornigerine, a potent antimitotic Colchicum alkaloid of unusual structure. Interactions with tubulin. Hamel E, Ho HH, Kang GJ, Lin CM Biochem Pharmacol 15-Jun-1988
doi:10.1016/0006-2952(88)90372-3
PMID:3390207

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
> Alkaloids and derivatives / Androcymbine alkaloids
O-methylandrocymbine 15286666 Click to see CN1CCC23C=C(C(=O)C=C2C1CCC4=CC(=C(C(=C34)OC)OC)OC)OC 385.50 unknown https://doi.org/10.1135/CCCC19693540
> Alkaloids and derivatives / Homoaporphines
Kreysigine 15560400 Click to see CN1CCC2=CC(=C(C3=C2C1CCC4=CC(=C(C(=C43)OC)OC)OC)O)OC 385.50 unknown https://doi.org/10.1135/CCCC19693540
> Alkaloids and derivatives / Phenethylisoquinoline alkaloids
(S)-autumnaline 13878324 Click to see CN1CCC2=CC(=C(C=C2C1CCC3=CC(=C(C(=C3)OC)OC)O)O)OC 373.40 unknown https://doi.org/10.1135/CCCC19693540
> Hydrocarbon derivatives / Tropones
(7R)-1,2,3,10-tetramethoxy-7-(methylamino)-6,7-dihydro-5H-benzo[a]heptalen-9-one 638269 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC 371.40 unknown https://doi.org/10.1135/CCCC19622111
1,2,3,10-tetramethoxy-7-(methylamino)-6,7-dihydro-5H-benzo[a]heptalen-9-one 2832 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC 371.40 unknown https://doi.org/10.1135/CCCC19622111
https://doi.org/10.1135/CCCC19693540
2-Demethylcolchicine 23757 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/10.1135/CCCC19693540
2-Demthyldemecolcine 146030 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)O)OC 357.40 unknown https://doi.org/10.1135/CCCC19693540
3-Demethyldemecolcine 14413737 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)O 357.40 unknown https://doi.org/10.1135/CCCC19693540
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/10.1135/CCCC19693540
https://doi.org/10.1135/CCCC19622111
Methylademecolcine, N- 23759 Click to see CN(C)C1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC 385.50 unknown https://doi.org/10.1135/CCCC19622111
https://doi.org/10.1135/CCCC19693540
N-(3-hydroxy-1,2,10-trimethoxy-9-oxo-6,7-dihydro-5H-benzo[a]heptalen-7-yl)acetamide 494161 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/10.1135/CCCC19622111
N-[(7R)-3-hydroxy-1,2,10-trimethoxy-9-oxo-6,7-dihydro-5H-benzo[a]heptalen-7-yl]acetamide 92142360 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/10.1135/CCCC19622111
N-Formyldemecolcine 26819 Click to see CN(C=O)C1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC 399.40 unknown https://doi.org/10.1135/CCCC19693540
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1135/CCCC19622111
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-(-)-Fructose 5984 Click to see C(C(C(C(C(=O)CO)O)O)O)O 180.16 unknown https://doi.org/10.1135/CCCC19622111
D-Fructose 2723872 Click to see C1C(C(C(C(O1)(CO)O)O)O)O 180.16 unknown https://doi.org/10.1135/CCCC19622111
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1135/CCCC19622111
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1135/CCCC19622111
> Organoheterocyclic compounds / Benzodioxoles
Cornigerine 100188 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/10.1135/CCCC19622111
https://doi.org/10.1135/CCCC19693540
https://doi.org/10.1016/0006-2952(88)90372-3
N-(5,19-dimethoxy-6-oxo-15,17-dioxapentacyclo[10.7.0.02,8.03,7.014,18]nonadeca-1(19),2(8),4,12,14(18)-pentaen-9-yl)acetamide 162955104 Click to see CC(=O)NC1CCC2=CC3=C(C(=C2C4=C1C5C4C=C(C5=O)OC)OC)OCO3 383.40 unknown https://doi.org/10.1135/CCCC19693540
N-[(9R)-5,14-dimethoxy-6-oxo-16,18-dioxatetracyclo[10.7.0.02,8.015,19]nonadeca-1(19),2,4,7,12,14-hexaen-9-yl]acetamide 162848277 Click to see CC(=O)NC1CCC2=CC(=C3C(=C2C4=CC=C(C(=O)C=C14)OC)OCO3)OC 383.40 unknown https://doi.org/10.1135/CCCC19622111
> Organoheterocyclic compounds / Coumarans
(1R,4S,5S,6S,15R)-5,9,10-trimethoxy-16-methyl-7-oxa-16-azapentacyclo[10.6.1.01,6.02,15.08,19]nonadeca-2,8(19),9,11-tetraen-4-ol 101289845 Click to see CN1CCC23C4C(C(C=C2C1CCC5=CC(=C(C(=C35)O4)OC)OC)O)OC 373.40 unknown https://doi.org/10.1135/CCCC19693540
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(8R,9R,10R,11S)-11-acetyloxy-3-hydroxy-4,5,14,15,16-pentamethoxy-9,10-dimethyl-8-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl] (E)-2-methylbut-2-enoate 162965547 Click to see CC=C(C)C(=O)OC1C(C(C(C2=CC(=C(C(=C2C3=C(C(=C(C=C13)OC)OC)O)OC)OC)OC)OC(=O)C)C)C 558.60 unknown https://doi.org/10.1135/CCCC19622111

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