POTENT, SELECTIVE, WATER-SOLUBLE BENZODIAZEPINE-BASED CCKB RECEPTOR ANTAGONISTS THAT CONTAIN LIPOPHILIC CARBOXYLATE SURROGATES

被引:23
作者
CHAMBERS, MS
HOBBS, SC
GRAHAM, MI
WATT, AP
FLETCHER, SR
BAKER, R
FREEDMAN, SB
PATEL, S
SMITH, AJ
MATASSA, VG
机构
[1] Merck, Sharp and Dohme Research Laboratories, Neuroscience Research Centre, Harlow, Essex CM20 2QR, Terlings Park, Eastwick Road
关键词
D O I
10.1016/0960-894X(95)00399-E
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Acylsulphonamide analogues of the meta-tolylurea L-708,474 have been synthesised and evaluated as CCKB receptor antagonists. Such derivatives retain very high affinity and subtype selectivity for the CCKB receptor, and have good aqueous solubility. The ortho-tolyl acylsulphonamide L-736,309 is orally bioavailable and brain penetrant in rat.
引用
收藏
页码:2303 / 2308
页数:6
相关论文
共 13 条
[11]  
PINNOCK R D, 1992, Molecular Neuropharmacology, V1, P211
[12]   PEPTIDE LEUKOTRIENES - CURRENT STATUS OF RESEARCH [J].
SHAW, A ;
KRELL, RD .
JOURNAL OF MEDICINAL CHEMISTRY, 1991, 34 (04) :1235-1242
[13]   HIGH-AFFINITY AND POTENT, WATER-SOLUBLE 5-AMINO-1,4-BENZODIAZEPINE CCK(B) GASTRIN RECEPTOR ANTAGONISTS CONTAINING A CATIONIC SOLUBILIZING GROUP [J].
SHOWELL, GA ;
BOURRAIN, S ;
NEDUVELIL, JG ;
FLETCHER, SR ;
BAKER, R ;
WATT, AP ;
FLETCHER, AE ;
FREEDMAN, SB ;
KEMP, JA ;
MARSHALL, GR ;
PATEL, S ;
SMITH, AJ ;
MATASSA, VG .
JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (06) :719-721