Hazard Information | Back Directory | [Description]
CS1 is a potent inhibitor of microtubule polymerization via interaction with the colchicine-binding pocket of tubulin, inducing unique histone phosphorylation patterns distinct from those induced by colchicine. CS1 is an antimitotic. | [Uses]
CS1 is a potent DNA Topo II α inhibitor. CS1 displays broad-spectrum in vitro antitumor effects, low toxicity in vivo and potential anti-multidrug resistance capabilities. CS1 leads to DNA damage, cell cycle arrest at G2/M phase and apoptosis[1]. | [in vivo]
CS1 (20 mg/kg; i.v.; every other day for two weeks) shows antitumor effects[1]. Animal Model: | Five-week-old female athymic nude mice (BALB/c-nu)[1] | Dosage: | 20 mg/kg | Administration: | i.v., every other day for two weeks | Result: | Showed antitumor effects. |
| [IC 50]
topoisomerase II alpha | [References]
[1] Shen Y, et al. CS1 is a novel topoisomerase IIα inhibitor with favorable drug resistance profiles. Biochem Biophys Res Commun. 2014; 453(3):302-8. DOI:10.1016/j.bbrc.2014.09.042 |
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BOC Sciences
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https://www.bocsci.com |
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Energy Chemical
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021-58432009 400-005-6266 |
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http://www.energy-chemical.com |
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