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Bioorganic and Medicinal Chemistry

Volumn 21, Issue 11, 2013, Pages 3240-3244

The discovery of colchicine-SAHA hybrids as a new class of antitumor agents

(9) Zhang, Xuan a Zhang, Jie b Tong, Linjiang b Luo, Yu a Su, Mingbo b Zang, Yi b Li, Jia b Lu, Wei a Chen, Yi b

a EAST CHINA NORMAL UNIVERSITY (China)

b SHANGHAI INSTITUTE OF MATERIA MEDICA (China)

Author keywords

Colchicine; HDAC; Hybrid; SAHA; Tubulin

Indexed keywords

ANTINEOPLASTIC AGENT; COLCHICINE DERIVATIVE; HISTONE DEACETYLASE 1; HISTONE DEACETYLASE 3; HISTONE DEACETYLASE 6; TUBULIN; VORINOSTAT;

ARTICLE; CANCER CELL CULTURE; CELL CYCLE; CELL CYCLE G2 PHASE; CELL CYCLE M PHASE; CELL PROLIFERATION; CONTROLLED STUDY; DRUG CYTOTOXICITY; DRUG DESIGN; DRUG STRUCTURE; DRUG SYNTHESIS; ENZYME INHIBITION; HUMAN; HUMAN CELL; IN VITRO STUDY; INHIBITION KINETICS; MICROTUBULE ASSEMBLY;

ANTINEOPLASTIC AGENTS; CELL CYCLE; CELL LINE, TUMOR; CELL SURVIVAL; DRUG DISCOVERY; HISTONE DEACETYLASE INHIBITORS; HISTONE DEACETYLASES; HUMANS; HYDROXAMIC ACIDS; INHIBITORY CONCENTRATION 50; ISOENZYMES; RECOMBINANT PROTEINS; TUBULIN MODULATORS;

EID: 84877794404 PISSN: 09680896 EISSN: 14643391 Source Type: Journal
DOI: 10.1016/j.bmc.2013.03.049 Document Type: Article

Times cited : (69)

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