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Synthesis and biological evaluation of noscapine analogues as microtubule-interfering agents / 药学学报
Acta Pharmaceutica Sinica ; (12): 1347-1357, 2012.
Article in English | WPRIM | ID: wpr-274655
ABSTRACT
A series of noscapine analogues have been synthesized via 13-step reaction starting from 2-hydroxy-3-methoxybenzaldehyde. Anti-tumor activities of these compounds were evaluated against HL-60 cell lines in vitro by the standard MTT assay. It was found that most of these derivatives showed appreciable inhibitory activity against HL-60 and tubulin polymerization. The results also indicated that the potency of compound 31 is about three times more than that ofnoscapine against HL-60 cell line and tubulin polymerization. Moreover, it induced a massive accumulation of cells in G2/M phase. These results showed noscapine and its derivatives were worth to be intensively studied further.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pharmacology / Tubulin / Cell Cycle / HL-60 Cells / Tubulin Modulators / Polymerization / Metabolism / Antineoplastic Agents / Noscapine Limits: Humans Language: English Journal: Acta Pharmaceutica Sinica Year: 2012 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pharmacology / Tubulin / Cell Cycle / HL-60 Cells / Tubulin Modulators / Polymerization / Metabolism / Antineoplastic Agents / Noscapine Limits: Humans Language: English Journal: Acta Pharmaceutica Sinica Year: 2012 Type: Article