SELECTIVE LIGANDS FOR CHOLECYSTOKININ RECEPTOR SUBTYPES CCK-A AND CCK-B WITHIN A SINGLE STRUCTURAL CLASS

被引：19

作者：

HIGGINBOTTOM, M ^{[1
]}

HORWELL, DC ^{[1
]}

ROBERTS, E ^{[1
]}

机构：

[1] PARKE DAVIS & CO,NEUROSCI RES CTR,ADDENBROOKES HOSP SITE,HILLS RD,CAMBRIDGE CB2 2QB,ENGLAND

来源：

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS | 1993年 / 3卷 / 05期

关键词：

D O I：

10.1016/S0960-894X(00)80685-X

中图分类号：

R914 [药物化学];

学科分类号：

100701 ;

摘要：

[No abstract available]

引用

页码：881 / 884

页数：4

共 6 条

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[4] DESIGN OF POTENT, ORALLY EFFECTIVE, NONPEPTIDAL ANTAGONISTS OF THE PEPTIDE-HORMONE CHOLECYSTOKININ [J].

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[5] RATIONALLY DESIGNED DIPEPTOID ANALOGS OF CCK - ALPHA-METHYLTRYPTOPHAN DERIVATIVES AS HIGHLY SELECTIVE AND ORALLY ACTIVE GASTRIN AND CCK-B ANTAGONISTS WITH POTENT ANXIOLYTIC PROPERTIES [J].

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[6]

WOODRUFF GN, 1991, ANNU REV PHARMACOL, V31, P469

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