发明名称 Benzimidazole derivatives and medical uses thereof
摘要 The present invention provides benzimidazole derivatives represented by the following formula (I) or pharmaceutically acceptable salts thereof, or prodrugs thereof, which exert an inhibitory activity on sodium-dependent nucleoside transporter 2 and are useful for a disease associated with an abnormality of plasma uric acid level. The compounds of the present invention are useful for the prevention or treatment of gout, hyperuricemia, urinary lithiasis, hyperuricemic nephropathy or the like. In the formula, n is 1 or 2; R<SUP>1 </SUP>and R<SUP>2 </SUP>are H, a halogen atom, cyano group, optionally substituted alkyl group, optionally substituted aryl group or the like; R<SUP>3 </SUP>is H, a halogen atom, optionally substituted alkyl group or the like; R<SUP>4 </SUP>and R<SUP>5 </SUP>are H, a halogen atom, OH or the like; and R<SUP>6 </SUP>and R<SUP>X </SUP>are H or OH: R<SUP>Y </SUP>is F or OH.
申请公布号 US2008038242(A1) 申请公布日期 2008.02.14
申请号 US20060473957 申请日期 2006.06.23
申请人 KIKUCHI NORHIKO;NONAKA YOSHINORI;TATANI KAZUYA;HIRATOCHI MASAHIRO;KURAMOCHI YU;ISAJI MASAYUKI;SHIMIZU KAZUO;MIYAGI TAKASHI 发明人 KIKUCHI NORHIKO;NONAKA YOSHINORI;TATANI KAZUYA;HIRATOCHI MASAHIRO;KURAMOCHI YU;ISAJI MASAYUKI;SHIMIZU KAZUO;MIYAGI TAKASHI
分类号 A61K38/44;A61K31/4184;A61K31/421;A61K31/426;A61K31/44;A61K31/4427;A61K31/4523;A61K31/496;A61K31/519;A61K31/5377;A61K31/7056;A61K33/00;A61P7/00;A61P13/12;A61P19/02;A61P19/06;A61P29/00;A61P43/00;C07D213/02;C07D221/00;C07D235/04;C07D295/00;C07H19/052 主分类号 A61K38/44
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