|
Volumn 127, Issue 50, 2005, Pages 17667-17671
|
Hybrids of the hemiasterlin analogue taltobulin and the dolastatins are potent antimicrotubule agents
|
Author keywords
[No Author keywords available]
|
Indexed keywords
CHEMOTHERAPY;
DIMERS;
ONCOLOGY;
POLYMERIZATION;
SYNTHESIS (CHEMICAL);
ANTIMICROTUBULE AGENTS;
CANCER CHEMOTHERAPY;
CLINICAL TRIALS;
TRIPEPTIDE HEMIASTERLIN;
PROTEINS;
AURISTATIN PE;
CEMADOTIN;
DOLASTATIN;
GLYCOPROTEIN P;
ILX 651;
SYNTHADOTIN;
TALTOBULIN;
TRIPEPTIDE;
TUBULIN;
UNCLASSIFIED DRUG;
AMINO TERMINAL SEQUENCE;
ARTICLE;
CANCER CHEMOTHERAPY;
CARBOXY TERMINAL SEQUENCE;
DRUG ACTIVITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
MICROTUBULE;
MICROTUBULE ASSEMBLY;
STRUCTURE ACTIVITY RELATION;
ANTINEOPLASTIC AGENTS;
CELL LINE, TUMOR;
DEPSIPEPTIDES;
DRUG SCREENING ASSAYS, ANTITUMOR;
HUMANS;
KB CELLS;
MODELS, MOLECULAR;
OLIGOPEPTIDES;
PROTEIN CONFORMATION;
STRUCTURE-ACTIVITY RELATIONSHIP;
THERMODYNAMICS;
TUBULIN MODULATORS;
|
EID: 29344454439
PISSN: 00027863
EISSN: None
Source Type: Journal
DOI: 10.1021/ja053663v Document Type: Article |
Times cited : (31)
|
References (19)
|