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Colchicum kesselringii

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 UUID644025a4c4a9e895944890
Scientific name Colchicum kesselringii
Authority Regel
First published in Trudy Imp. S.-Peterburgsk. Bot. Sada 8: 646 (1884)

Ethnobotanical Use Top

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General Uses Top

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Scientific and model-organism use:
Colchicum kesselringii is cited in phytochemical surveys of the genus as a source of colchicine-type alkaloids (e.g., colchicine and 3‑demethylcolchicine). These colchicine-type alkaloids from Colchicum species are widely used as anti-mitotic agents in plant cytogenetics and breeding to induce polyploidy by disrupting spindle formation during cell division, enabling polyploid induction in various crops and ornamentals. This use is documented in general plant cytogenetics literature and protocol repositories (e.g., colchicine treatments for seed or shoot meristems) rather than specifically for C. kesselringii. Laboratory handling must follow established chemical safety regulations and guidelines for the use of anti-mitotic toxicants (e.g., workplace safety standards and institutional chemical hygiene policies).

Synonyms Top

Scientific name Authority First published in
Synsiphon crociflorus Regel Trudy Imp. S.-Peterburgsk. Bot. Sada , prepr. 6: 491 (1879)
Colchicum luteum var. alberti (Regel) Priszter Bot. Közlem. 63: 48 (1976)
Colchicum regelii Stef. Sborn. B'lghar. Akad. Nauk 22: 22 (1926)
Colchicum crociflorum var. stenosepalum Regel Trudy Imp. S.-Peterburgsk. Bot. Sada 8: 646. 1884
Colchicum crociflorum (Regel) Regel Trudy Imp. S.-Peterburgsk. Bot. Sada 7: 385 (1880)

Common names Top

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Language Common/alternative name
German kesselring-zeitlose
Kazakh Кессельринг лапызы
Uzbek kesselring sarvinjoni

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
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Uzbekistan
    • Western Asia
      • Afghanistan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000763933
Tropicos 18404970
KEW urn:lsid:ipni.org:names:60454025-2
The Plant List kew-302872
Open Tree Of Life 355806
Observations.org 130274
NCBI Taxonomy 481257
IPNI 60454025-2
iNaturalist 868266
GBIF 2739911
EOL 1087012
Elurikkus 294027

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
The structure of regeline D. A. Abdullaeva, M. K. Yusupov, Kh. A. Aslanov Springer Science and Business Media LLC 09-Jul-2008
doi:10.1007/BF00564964
Structure of kesselridine A. K. Kasimov, M. K. Yusupov, É. Kh. Timbekov, Kh. A. Aslanov Springer Science and Business Media LLC 09-Jul-2008
doi:10.1007/BF00570668
Structure of regecoline A. M. Usmanov, B. Chommadov, M. K. Yusupov, Kh. A. Aslanov Springer Science and Business Media LLC 30-Nov-2004
doi:10.1007/BF00714919
Alkaloids ofColchicum luteum B. Chommadov, M. K. Yusupov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00576217
Speciosamine ? A new base fromColchicum speciosum B. Chommadov, M. K. Yusupov, Kh. A. Aslanov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00574233
Quaternary 7-oxo-4,5,6,6a-tetrahydrohomoproaporphine alkaloids ofCochicum kesselringii A. M. Usmanov, B. Chommadov, M. K. Yusupov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00574254
The structure of regelinone M. K. Yusupov, A. M. Usmanov, A. K. Kasimov, Kh. Turdikulov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00565544
The structure of kesselringine M. K. Yusupov, A. S. Sadykov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00567802
Flavonoids ofColchicum kesselringii Kh. S. Umarov, Z. P. Pakudina, M. K. Yusupov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00567047
Alkaloids of the corms of Colchicum kesselringii Kh. Turdikulov, M. K. Yusupov, A. S. Sadykov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00564779

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
> Hydrocarbon derivatives / Tropones
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/10.1007/BF00564779
3-Demethylcolchicine 299664 Click to see 385.40 unknown https://doi.org/10.1007/BF00564779
Colchicine 6167 Click to see 399.40 unknown https://doi.org/10.1007/BF00564779
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Regelin C 122391246 Click to see CC1C(CC(C2(C1C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C)O)C(=O)OC 484.70 unknown https://doi.org/10.1007/BF00564964
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromenopyridines
(1S,4S,5R)-4-hydroxy-5-methoxy-13-methyl-6-oxa-13-azapentacyclo[8.6.2.11,5.07,17.014,18]nonadeca-7(17),9,11,14(18)-tetraene-8,15-dione 163190122 Click to see 341.40 unknown https://doi.org/10.1007/BF00574233
(1S,4S,5S,14R)-5-methoxy-13-methyl-6-oxa-13-azapentacyclo[8.6.2.11,5.07,17.014,18]nonadeca-7,9,17-triene-4,8-diol 163012967 Click to see 331.40 unknown https://doi.org/10.1007/BF00574233
(1S,4S,5S)-4-hydroxy-5-methoxy-13-methyl-6-oxa-13-azapentacyclo[8.6.2.11,5.07,17.014,18]nonadeca-7(17),9,11,14(18)-tetraen-8-one 163195280 Click to see CN1C=CC2=CC(=O)C3=C4C2=C1CCC45CCC(C(C5)(O3)OC)O 327.40 unknown https://doi.org/10.1007/BF00576217
13-Methyl-6-oxa-13-azapentacyclo[8.6.2.11,5.07,17.014,18]nonadeca-7,9,17-triene-4,5,8-triol 102059821 Click to see 317.40 unknown https://doi.org/10.1007/BF00570668
4-Hydroxy-5-methoxy-13-methyl-6-oxa-13-azapentacyclo[8.6.2.11,5.07,17.014,18]nonadeca-7(17),9,11,14(18)-tetraen-8-one 163192442 Click to see CN1C=CC2=CC(=O)C3=C4C2=C1CCC45CCC(C(C5)(O3)OC)O 327.40 unknown https://doi.org/10.1007/BF00576217
4-Hydroxy-5-methoxy-13-methyl-6-oxa-13-azapentacyclo[8.6.2.11,5.07,17.014,18]nonadeca-7(17),9,11,14(18)-tetraene-8,15-dione 163192552 Click to see CN1C=CC2=CC(=O)C3=C4C2=C1C(=O)CC45CCC(C(C5)(O3)OC)O 341.40 unknown https://doi.org/10.1007/BF00574233
https://doi.org/10.1007/BF00565544
https://doi.org/10.1007/BF00574254
5-Methoxy-13-methyl-6-oxa-13-azapentacyclo[8.6.2.11,5.07,17.014,18]nonadeca-7,9,17-triene-4,8-diol 182351 Click to see 331.40 unknown https://doi.org/10.1007/BF00574233
7-Methoxy-1-methyl-1,2,3,7,8,9,10,11,12,12a-decahydro-7,10a-methano[1]benzoxocino[8,7,6-def]quinoline-5,8-diol 191332 Click to see 331.40 unknown https://doi.org/10.1007/BF00567802
https://doi.org/10.1007/BF00714919
Kesselringen 76967674 Click to see 317.40 unknown https://doi.org/10.1007/BF00714919
https://doi.org/10.1007/BF00567802
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
(1R,4S,5R)-4-hydroxy-5-methoxy-13-methyl-6-oxa-13-azapentacyclo[8.6.2.11,5.07,17.014,18]nonadeca-7(17),9,14(18)-trien-8-one 163189415 Click to see 329.40 unknown https://doi.org/10.1007/BF00574233
8-Hydroxy-7-methoxy-1-methyl-2,3,7,8,9,10,11,12-octahydro-7,10a-methano[1]benzoxocino[8,7,6-def]quinolin-1-ium-5-olate 4979409 Click to see CN1CCC2=CC(=O)C3=C4C2=C1CCC45CCC(C(C5)(O3)OC)O 329.40 unknown https://doi.org/10.1007/BF00574233
https://doi.org/10.1007/BF00714919
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[(2R,3S,4S,5S)-5-[(1R)-1,2-dihydroxyethyl]-3,4-dihydroxyoxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxychromen-4-one 162933659 Click to see 448.40 unknown https://doi.org/10.1007/BF00567047
7-[5-(1,2-Dihydroxyethyl)-3,4-dihydroxyoxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxychromen-4-one 162933657 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(O4)C(CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00567047

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