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27. Pharmacological profile of (R)-1-[2,3-dihydro-1-(2'-methylphenacyl)-2-oxo- 5-phenyl-1H-1,4-benzodiazepin-3-yl]-3-(3-methylphenyl)urea (YM022), a new potent and selective gastrin/cholecystokinin-B receptor antagonist, in vitro and in vivo. Nishida A, Miyata K, Tsutsumi R, Yuki H, Akuzawa S, Kobayashi A, Kamato T, Ito H, Yamano M, Katuyama Y. J Pharmacol Exp Ther; 1994 May; 269(2):725-31. PubMed ID: 7910212 [Abstract] [Full Text] [Related]
28. Pharmacological characterization of rebamipide: its cholecystokinin CCK1 receptor binding profile and effects on Ca2+ mobilization and amylase release in rat pancreatic acinar cells. Moon SJ, An JM, Kim J, Lee SI, Ahn W, Kim KH, Seo JT. Eur J Pharmacol; 2004 Nov 28; 505(1-3):61-6. PubMed ID: 15556137 [Abstract] [Full Text] [Related]
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32. Distinct requirements for activation at CCK-A and CCK-B/gastrin receptors: studies with a C-terminal hydrazide analogue of cholecystokinin tetrapeptide (30-33). Lin CW, Holladay MW, Barrett RW, Wolfram CA, Miller TR, Witte D, Kerwin JF, Wagenaar F, Nadzan AM. Mol Pharmacol; 1989 Dec 21; 36(6):881-6. PubMed ID: 2601685 [Abstract] [Full Text] [Related]
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