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Design, synthesis and antitumor activity of sorafenib analogues containing 2-picolinylhydrazide moiety / 药学学报
Acta Pharmaceutica Sinica ; (12): 1623-1629, 2012.
Article in Chinese | WPRIM | ID: wpr-274612
ABSTRACT
A novel series of sorafenib analogs containing 2-picolinyl hydrazide moiety were designed and synthesized. In vitro, most of synthesized compounds have antiproliferation activity on MDA-MB-231, ACHN, HepG2, Mia-PaCa-2 and SW1990 cell lines tested by MTT assay. It is worth noting that the antitumor activities of compounds 2c, 2d and 2f are more potent than that of sorafenib on pancreatic cancer cells Mia-PaCa-2 and SW1990, and the activities of compounds 3f and 3g are 2-3 times than that of sorafenib on human hepatocellular carcinoma HepG2 cell line.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pharmacology / Phenylurea Compounds / Structure-Activity Relationship / Drug Screening Assays, Antitumor / Drug Design / Molecular Structure / Chemistry / Niacinamide / Cell Line, Tumor / Cell Proliferation Limits: Humans Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2012 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pharmacology / Phenylurea Compounds / Structure-Activity Relationship / Drug Screening Assays, Antitumor / Drug Design / Molecular Structure / Chemistry / Niacinamide / Cell Line, Tumor / Cell Proliferation Limits: Humans Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2012 Type: Article