METHODS FOR DRUG DISCOVERY - DEVELOPMENT OF POTENT, SELECTIVE, ORALLY EFFECTIVE CHOLECYSTOKININ ANTAGONISTS

被引:1325
作者
EVANS, BE [1 ]
RITTLE, KE [1 ]
BOCK, MG [1 ]
DIPARDO, RM [1 ]
FREIDINGER, RM [1 ]
WHITTER, WL [1 ]
LUNDELL, GF [1 ]
VEBER, DF [1 ]
ANDERSON, PS [1 ]
CHANG, RSL [1 ]
LOTTI, VJ [1 ]
CERINO, DJ [1 ]
CHEN, TB [1 ]
KLING, PJ [1 ]
KUNKEL, KA [1 ]
SPRINGER, JP [1 ]
HIRSHFIELD, J [1 ]
机构
[1] MERCK INST THERAPEUT RES,RAHWAY,NJ 07065
关键词
D O I
10.1021/jm00120a002
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
引用
收藏
页码:2235 / 2246
页数:12
相关论文
共 56 条
[1]   DIAZEPAM-BINDING INHIBITOR - A NEUROPEPTIDE LOCATED IN SELECTED NEURONAL POPULATIONS OF RAT-BRAIN [J].
ALHO, H ;
COSTA, E ;
FERRERO, P ;
FUJIMOTO, M ;
COSENZAMURPHY, D ;
GUIDOTTI, A .
SCIENCE, 1985, 229 (4709) :179-182
[2]   THE CHOLECYSTOKININ ANTAGONIST L-364,718 INHIBITS THE ACTION OF CHOLECYSTOKININ BUT NOT BOMBESIN ON RAT PANCREATIC-SECRETION INVIVO [J].
ANDERSON, L ;
DOCKRAY, GJ .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1988, 146 (2-3) :307-311
[3]  
ARIENS EJ, 1979, RECEPTORS COMPREHENS, V1, P33
[4]   A REARRANGEMENT OF 5-ARYL-1,3-DIHYDRO-2H-1,4-BENZODIAZEPINE-2-14-OXIDES [J].
BELL, SC ;
CHILDRESS, SJ .
JOURNAL OF ORGANIC CHEMISTRY, 1962, 27 (05) :1691-&
[5]  
BELL SC, 1964, J HETEROCYCL CHEM, V4, P647
[6]  
BELL SC, 1965, Patent No. 3198789
[7]  
BLOUNT JF, 1983, MOL PHARM, V24, P426
[8]   AN EXPEDIENT SYNTHESIS OF 3-AMINO-1,3-DIHYDRO-5-PHENYL-2H-1,4-BENZODIAZEPIN-2-ONE [J].
BOCK, MG ;
DIPARDO, RM ;
EVANS, BE ;
RITTLE, KE ;
VEBER, DF ;
FREIDINGER, RM .
TETRAHEDRON LETTERS, 1987, 28 (09) :939-942
[9]   SYNTHESIS AND RESOLUTION OF 3-AMINO-1,3-DIHYDRO-5-PHENYL-2H-1,4-BENZODIAZEPIN-2-ONES [J].
BOCK, MG ;
DIPARDO, RM ;
EVANS, BE ;
RITTLE, KE ;
VEBER, DF ;
FREIDINGER, RM ;
HIRSHFIELD, J ;
SPRINGER, JP .
JOURNAL OF ORGANIC CHEMISTRY, 1987, 52 (15) :3232-3239
[10]   BENZODIAZEPINES ANTAGONIZE CHOLECYSTOKININ-INDUCED ACTIVATION OF RAT HIPPOCAMPAL-NEURONS [J].
BRADWEJN, J ;
DEMONTIGNY, C .
NATURE, 1984, 312 (5992) :363-364