Synthesis and biological activity of 2-phenylethyl ester analogues of C-terminal heptapeptide of cholecystokinin modified in Trp 30 region
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3011.1991.tb01427.x/fullpdf
Reference27 articles.
1. 2-Phenylethyl ester and 2-phenylethyl amide derivative analogues of the C-terminal hepta- and octapeptide of cholecystokinin
2. CCK-JMV-180: a peptide that distinguishes high-affinity cholecystokinin receptors from low-affinity cholecystokinin receptors
Cited by 6 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. Structure activity studies of tryptophan30 modified analogs of Ac-CCK-7;International Journal of Peptide and Protein Research;2009-01-12
2. How a single inversion of configuration leads to a reversal of the binding mode: proposal of a novel arrangement of CCK2 ligands in their receptor, and contribution to the development of peptidomimetic or non-peptide CCK2 ligands;European Journal of Medicinal Chemistry;2003-07
3. Molecular Models for Cholecystokinin-A Receptor;Pharmacology & Toxicology;2002-12
4. Arginine 336 and Asparagine 333 of the Human Cholecystokinin-A Receptor Binding Site Interact with the Penultimate Aspartic Acid and the C-terminal Amide of Cholecystokinin;Journal of Biological Chemistry;1999-07
5. Biological Evaluation of JMV180 Cholecystokinin Analogs;Annals of the New York Academy of Sciences;1994-03
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