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Title: Structural modification of H/sub 2/-receptor antagonists provide post-H/sub 2/-receptor gastric antisecretory activity

Conference · · Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
OSTI ID:5498275

In the course of investigations into the gastric antisecretory activity of potential H/sub 2/-receptor antagonists, examples were discovered in which structural modification of the molecule altered a) antisecretory activity in the pylorus-ligated rat and b) the response to various stimulants of (/sup 14/C)aminopyrine (AP) uptake in isolated rat gastric mucosal cell preparations. Wy-45,662 (N-(3-(3-(1-piperidinylmethyl)phenoxy)propyl)thieno(3,4-d) isothiazol-3-amine 1, 1-dioxide)), a very potent histamine H/sub 2/-antagonist and antisecretory agent in the rat (ED/sub 50/ (approx.) 0.3 mg/kg), had no effect in vitro at 1 ..mu..M on forskolin-induced (/sup 14/C)AP uptake while 10 nM Wy-45,662 completely suppressed histamine-stimulated (/sup 14/C)AP uptake. In contrast, the N-benzylated form of Wy-45,662, Wy-46,499 dose-dependently (10/sup -7/-10/sup -6/M) suppressed forskolin-stimulated (/sup 14/C)AP uptake while retaining modest antisecretory activity (ED/sub 50/approx.8 mg/kg) in vivo. Wy-46,499's modest antisecretory activity was thus attributable to inhibition via a post-histamine H/sub 2/-receptor mechanism.

Research Organization:
Wyeth Labs., Inc., Philadelphia, PA
OSTI ID:
5498275
Report Number(s):
CONF-8604222-; TRN: 86-026536
Journal Information:
Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States), Vol. 45:3; Conference: 70. annual meeting of the Federation of American Society for Experimental Biology, St. Louis, MO, USA, 13 Apr 1986
Country of Publication:
United States
Language:
English