Two analogues of the C-terminal heptapeptide of cholecystokinin have been synthesized, in
which the C-terminal phenylalanine residue has been replaced by a phenylethylester (JMV …

Analogues of the C-terminal octapeptide of cholecystokinin (CCK) modified in the Met 28-
Gly 29 region, were tested for their ability to interact with peripheral cholecystokinin …

JMV 236, a new cholecystokinin-octapeptide-sulfate (CCK 8 S) derivative (Boc-Tyr (SO 3)-
Nle-Gly-Trp-Nle-Asp-Phe-NH 2) has been synthesized in the Centre de Pharmacologie …

Cholecystokinin octapeptide, administered into the third cerebral ventricle (icv), suppresses
feeding in sheep, pigs, chicken, rats, and dogs. Because of the species differences in the …

Maletínská, L., J. Pírková, J. Hlaváček and J. Slaninová. Cholecystokinin analogs with
suppressed central activities. Peptides 19 (2) 301–308, 1998.—Several analogs of Boc …

In the present study, hepta-and octapeptide analogues of the C-terminal part of
cholecystokinin, modified on the C-terminal phenylalanine residue, were synthesized. CCK …

Structural determinants of cholecystokinin octapeptide (CCK-8) binding to central nervous
system receptors have been studied to assess the relative importance of the amino and the …

New glutaramic acid derivatives with cholecystokinin antagonistic activity were evaluated for
their capacity to inhibit the satiety effect induced in the rat by intraperitoneal (ip) injection of …

Cholecystokinin (CCK) is found in high concentrations in the brain, mainly as the C-terminal
octapeptide. CCK meets most of the criteria of a CNS neurotransmitter and has an excitatory …

We reported earlier on the synthesis and biological activities of synthetic analogs of
cholecystokinin (CCK) in whichthe C-terminal primary amide group was deleted. Compound …