POLYSUBSTITUTED IMIDAZOPYRIDINES AS GASTRIC SECRETION INHIBITORS
申请人:——
公开号:US20040106642A1
公开(公告)日:2004-06-03
The invention relates to imidazopyridines of a certain formula 1, in which the substituents and symbols have the meanings indicated in the description. The compounds have gastric secretion-inhibiting properties.
Compounds of formula (1), in which the substituents have the meanings mentioned in the description are suitable for the prevention and treatment of gastrointestinal diseases.
1
式(1)化合物,其中取代基具有描述中提到的含义,适用于预防和治疗胃肠疾病。
Pyridinium salts and their use for the control of helicobacter bacteria
申请人:BYK Gulden Lomberg Chemische Fabrik GmbH
公开号:US05824687A1
公开(公告)日:1998-10-20
8-phenalkoxyimidazo\x9b1,2-a!pyridinium salts are useful for controlling Helicobacter bacteria. Medicament compositions based on such compounds are prepared and used for the noted purpose.
Antiulcer agents. 1. Gastric antisecretory and cytoprotective properties of substituted imidazo[1,2-a]pyridines
作者:James J. Kaminski、James A. Bristol、Chester Puchalski、Raymond G. Lovey、Arthur J. Elliott、Henry Guzik、Daniel M. Solomon、David J. Conn、Martin S. Domalski
DOI:10.1021/jm00145a006
日期:1985.7
A novel class of antiulcer agents, the substituted imidazo[1,2-a]pyridines, is described. The present compounds are not histamine (H2) receptor antagonists nor are they prostaglandin analogues, yet they exhibit both gastricantisecretory and cytoprotective properties. The mechanism of gastricantisecretory activity may involve inhibition of the H+/K+-ATPase enzyme. Structure-activity studies led to
描述了新型的抗溃疡剂,取代的咪唑并[1,2-a]吡啶。本发明的化合物既不是组胺(H 2)受体拮抗剂,也不是前列腺素类似物,但它们既具有胃分泌作用又具有细胞保护作用。胃抗分泌活性的机制可能涉及抑制H + / K + -ATPase酶。结构活性研究导致鉴定出3-(氰基甲基)-2-甲基-8-(苯甲氧基)咪唑并[1,2-a]吡啶,SCH 28080(27),已被选择用于进一步开发和临床评价。
Skin Lightening Compositions
申请人:Niki Yoko
公开号:US20110171149A1
公开(公告)日:2011-07-14
Compositions and methods for lightening and/or depigmenting skin are provided, the compositions comprising compounds having the structure:
or having the structure:
as defined herein.