Synthesis and receptor-binding affinity of dipeptoid cholecystokinin ligands
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Pharmacology,General Medicine
Reference26 articles.
1. Rationally designed "dipeptoid" analogs of CCK. .alpha.-Methyltryptophan derivatives as highly selective and orally active gastrin and CCK-B antagonists with potent anxiolytic properties
2. The behavioural properties of CI-988, a selective cholecystokininB receptor antagonist
3. Synthesis of an α-CH2CO2H functionalized tryptophan and its incorporation into an analogue of cholecystokinin.
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. ChemInform Abstract: Synthesis and Receptor-Binding Affinity of Dipeptoid Cholecystokinin Ligands.;ChemInform;2010-08-05
2. “Dipeptoids”: From the Chemical Structure of the Endogenous Peptide to the Design of Peptidomimetics;Mini-Reviews in Medicinal Chemistry;2004-08-01
3. Synthesis and Evaluation of 1,5-Benzodiazepines with Bridged Cycloalkyl Substituents at the N-1 Position as Potent and Selective CCK-B Ligands;Archiv der Pharmazie;1998-01
4. CCKB/gastrin receptor antagonists as potential drugs for peptic ulcer therapy;Drug Discovery Today;1997-07
5. Novel 1,5-Benzodiazepines as CCK-B Ligands. Effect of Aryl-Carbamic Substituents at the C-3 Position Together with Halogen Substitution on the Benzo-Fused Ring;Archiv der Pharmazie;1997
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