Zobrazeno 1 - 9
of 9
pro vyhledávání: '"B S, Barbaz"'
Autor:
W. D. Cash, Albert Braunwalder, P.S. Bernard, G. C. Mazzenga, R. A. Lovell, B. S. Barbaz, Francis John E, J. L. Hyun, Debra A. Bennett, R. C. Friedmann, P. S. Loo
Publikováno v:
ChemInform. 22
Autor:
R. A. Lovell, J. L. Hyun, R. C. Friedmann, Francis John E, P. S. Loo, P.S. Bernard, G. C. Mazzenga, B. S. Barbaz, W. D. Cash, Albert Braunwalder
Publikováno v:
Journal of medicinal chemistry. 34(1)
Investigation of tricyclic heterocycles related to the 2-arylpyrazolo[4,3-c]quinolin-3(5H)-ones, structures with high affinity for the benzodiazepine (BZ) receptor, led to the synthesis of 2-phenyl-[1,2,4]triazolo[1,5-c]quinazolin-5(6H)-one, a compou
Publikováno v:
Molecular pharmacology. 28(6)
The proteolytic degradation of the enkephalin-containing heptapeptide Tyr-Gly-Gly-Phe-Met-Arg-Phe (YGGFMRF) was investigated by incubating the peptide with synaptic membranes from mouse whole brain and characterizing the formed products. The degradat
Publikováno v:
Neuropharmacology. 25(8)
The antinociceptive activity of sulfated cholecystokinin octapeptide (CCK-8-S) was characterized by comparison with two other endogenous forms, unsulfated CCK-8 (CCK-8-U) and the carboxyl tetrapeptide fragment (CCK-4) and two other peptides present i
Publikováno v:
Peptides. 10(1)
Previous studies have shown that unsulfated cholecystokinin octapeptide (CCK-8-U) shares with the sulfated octapeptide (CCK-8-S) and the carboxyl-terminal tetrapeptide (CCK-4) the ability to block abdominal irritant-induced stretching when administer
Publikováno v:
Chemischer Informationsdienst. 4
Publikováno v:
Archives internationales de pharmacodynamie et de therapie. 191(1)
Publikováno v:
Archives internationales de pharmacodynamie et de therapie. 195(2)
Publikováno v:
Annals of the New York Academy of Sciences. 448:573-574