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Colchicoside is a bioactive tropolone alkaloid with anti-leishmanial and anti-leishmanial activities [1]. Uses: Scientific research. Group: Natural products. CAS No. 477-29-2. Pack Sizes: 5 mg; 10 mg. Product ID: HY-131300.
Hexa-O-benzoyl 10-Demethyl Colchicoside
Hexa-O-benzoyl 10-Demethyl Colchicoside is an intermediate in synthesizing Isothiocolcicoside, which is an impurity of Thiocolchicoside, a GABA receptor antagonist which is prescribed as a muscle relaxant having analgesic effects. Synonyms: (2S,3R,4S,5R,6R)-2-(((S)-10-(Benzoyloxy)-1,2-dimethoxy-9-oxo-7-(3-oxo-3-phenylpropanamido)-5,6,7,9-tetrahydrobenzo[a]heptalen-3-yl)oxy)-6-((benzoyloxy)methyl)tetrahydro-2H-pyran-3,4,5-triyl Tribenzoate. Molecular formula: C68H55NO17. Mole weight: 1158.16.
Penta-O-benzoyl 10-Demethyl Colchicoside
Penta-O-benzoyl 10-Demethyl Colchicoside, an intermediate in the synthesis of Isothiocolcicoside, is an impurity of Thiocolchicoside, a GABA receptor antagonist that is prescribed as a muscle relaxant having analgesic effects. Synonyms: (2S,3R,4S,5R,6R)-2-(((S)-7-Acetamido-10-(benzoyloxy)-1,2-dimethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-3-yl)oxy)-6-((benzoyloxy)methyl)tetrahydro-2H-pyran-3,4,5-triyl Tribenzoate. Molecular formula: C61H51NO16. Mole weight: 1054.05.
Potent competitive gamma-aminobutyric acid type A (GABAA) receptor antagonist and glycine receptor agonist. Weak nicotinic acetylcholine receptor agonist. Muscle relaxant. Anti-inflammatory. Has analgesic properties. Shows strong epileptogenic and convulsant activity. Anticancer compound through inhibition of NF-kappaB and NF-kappaB-regulated gene products. Apoptosis inducer.Suppressed osteoclastogenesis induced by RANKL and tumor cells via the NF-kappaB signaling pathway. Therapeutic option for the management of bone metastatic disease. Group: Biochemicals. Alternative Names: BRN 0072205, NSC 147755, Coltramyl, 10-thio-Colchicoside, 2-Demethoxy-2-glucosidoxythiocolchic ine. Grades: Highly Purified. CAS No. 602-41-5. Pack Sizes: 1mg, 5mg, 25mg. Molecular Formula: C27H33NO10S. US Biological Life Sciences.
Worldwide
Thiocolchicoside
Thiocolchicoside is a competitive γ-aminobutyric acid type A (GAB A A) receptor antagonist and glycine receptor agonist in the central nervous system. Thiocolchicoside is a semisynthetic sulfur derivative of colchicoside. Thiocolchicoside is a muscle relaxant and has anti-inflammatory, and analgesic properties [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 602-41-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 20 mg; 50 mg; 100 mg. Product ID: HY-N0301.
Colchicine EP impurity D
Colchicoside is a significantly toxic Colchicine analog with no anti-inflammatory properties. Synonyms: (S)-N-[3-(b-D-Glucopyranosyloxy)-5,6,7,9-tetrahydro-1,2,10-trimethoxy-9-oxobenzo[a]heptalen-7-yl]acetamide; N-[(7S)-3-(b-D-Glucopyranosyloxy)-5,6,7,9-tetrahydro-1,2,10-trimethoxy-9-oxobenzo[a]heptalen-7-yl]acetamide; 3-Demethylcolchicine glucoside. Grades: > 95%. CAS No. 477-29-2. Molecular formula: C27H33NO11. Mole weight: 547.55.
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