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RATIONAL DESIGN OF BUTABINDIDE, THE FIRST INHIBITOR OF THE CHOLECYSTOKININ (CCK-8) INACTIVATING PEPTIDASE
Authors: GANELLIN CR ROSE C VARGAS F FACCHINETTI P BOURGEAT P BAMBAL R BISHOP PB CHAN SMT MOORE ANJ SCHWARTZ JC
Citation: Cr. Ganellin et al., RATIONAL DESIGN OF BUTABINDIDE, THE FIRST INHIBITOR OF THE CHOLECYSTOKININ (CCK-8) INACTIVATING PEPTIDASE, British Journal of Pharmacology, 122, 1997, pp. 189-189
SYNTHESIS OF N-EPSILON-(P-BROMOPHENYL)-L-LYSINE AND N-TAU-(P-BROMOPHENYL)-L-HISTIDINE AS MODELS FOR ADDUCTS OF BROMOBENZENE 3,4-OXIDE TO PROTEIN - OBSERVATION OF AN UNUSUAL PD-CATALYZED N-TAU-ARYL TO N-PI-ARYLSUBSTITUENT MIGRATION
Authors: BAMBAL R HANZLIK RP
Citation: R. Bambal et Rp. Hanzlik, SYNTHESIS OF N-EPSILON-(P-BROMOPHENYL)-L-LYSINE AND N-TAU-(P-BROMOPHENYL)-L-HISTIDINE AS MODELS FOR ADDUCTS OF BROMOBENZENE 3,4-OXIDE TO PROTEIN - OBSERVATION OF AN UNUSUAL PD-CATALYZED N-TAU-ARYL TO N-PI-ARYLSUBSTITUENT MIGRATION, Journal of organic chemistry, 59(4), 1994, pp. 729-732
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