Prodrugs of dynemicin analogs for selective chemotherapy mediated by an aldolase catalytic Ab

Proceedings of the National Academy of Sciences of the United States of America

Volumn 101, Issue 9, 2004, Pages 3095-3099

  Sinha, Subhash C ^a   Li, Lian Sheng ^a   Miller, Gregory P ^a   Dutta, Shantanu ^a   Rader, Christoph ^a   Lerner, Richard A ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE REDUCTASE; ALDOLASE ANTIBODY; ALKENYLDIALKYNE DERIVATIVE; CAMPTOTHECIN; DOXORUBICIN; DYNEMICIN A; DYNEMICIN DERIVATIVE; ENZYME ANTIBODY; ETOPOSIDE; MONOCLONAL ANTIBODY; MONOCLONAL ANTIBODY 38C2; PRODRUG; UNCLASSIFIED DRUG;

ANTIGEN BINDING; ARTICLE; CANCER CHEMOTHERAPY; CANCER INHIBITION; CONJUGATION; CONTROLLED STUDY; CROSS COUPLING REACTION; DNA CLEAVAGE; DRUG DESIGN; DRUG SYNTHESIS; HUMAN; HUMAN CELL; PRIORITY JOURNAL; TUMOR GROWTH;

ANTHRAQUINONES; ANTIBIOTICS, ANTINEOPLASTIC; ANTIBODIES, CATALYTIC; CELL DIVISION; CELL LINE, TUMOR; COLONIC NEOPLASMS; DRUG DESIGN; FRUCTOSE-BISPHOSPHATE ALDOLASE; HUMANS; INDICATORS AND REAGENTS; MASS SPECTROMETRY; PRODRUGS;

EID: 1542267801     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0307319101     Document Type: Article

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