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Volumn 67, Issue , 2013, Pages 75-80

Synthesis and biological evaluations of a monomethylauristatin E glucuronide prodrug for selective cancer chemotherapy

(9) Legigan, Thibaut a Clarhaut, Jonathan b Renoux, Brigitte a Tranoy Opalinski, Isabelle a Monvoisin, Arnaud a Jayle, Christophe b Alsarraf, Jérôme a Thomas, Mikaël a Papot, Sébastien a

a UNIVERSITÉ DE POITIERS (France)

b POITIERS UNIVERSITY HOSPITAL (France)

Author keywords

Cancer; Chemotherapy; Glucuronide; Prodrug; Tumor targeting

Indexed keywords

ANTINEOPLASTIC AGENT; BRENTUXIMAB VEDOTIN; GLUCURONIDE; MONOMETHYLAURISTATIN E; PRODRUG; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTINEOPLASTIC ACTIVITY; ANTIPROLIFERATIVE ACTIVITY; ARTICLE; CANCER CELL CULTURE; CANCER CHEMOTHERAPY; CANCER GROWTH; CELL VIABILITY; CONTROLLED STUDY; CYTOTOXICITY; DRUG RELEASE; DRUG STABILITY; DRUG SYNTHESIS; HUMAN; HUMAN CELL; HUMAN TISSUE; HYDROLYSIS; IN VITRO STUDY; IN VIVO STUDY; MOUSE; NONHUMAN; NUCLEOPHILICITY;

CANCER; CHEMOTHERAPY; GLUCURONIDE; PRODRUG; TUMOR TARGETING;

ANIMALS; ANTINEOPLASTIC AGENTS; CARCINOMA, LEWIS LUNG; CELL PROLIFERATION; CELL SURVIVAL; DOSE-RESPONSE RELATIONSHIP, DRUG; GLUCURONIDES; HUMANS; KB CELLS; MICE; MICE, INBRED C57BL; MOLECULAR STRUCTURE; OLIGOPEPTIDES; PRODRUGS; STRUCTURE-ACTIVITY RELATIONSHIP; TUMOR CELLS, CULTURED;

EID: 84880181729 PISSN: 02235234 EISSN: 17683254 Source Type: Journal
DOI: 10.1016/j.ejmech.2013.06.037 Document Type: Article

Times cited : (25)

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