Patent Number: 8,796,247

Title: Indole derivative, and pharmacologically acceptable salt thereof

Abstract: The present invention provides a compound represented by the general formula (I) of the present invention, which has EP.sub.1 receptor antagonism: ##STR00001## wherein A represents a pyridine ring, a furan ring, or the like; Y.sup.1 represents a C.sub.1-6 alkylene group; Y.sup.2 represents a single bond or the like; R.sup.1 represents --C(.dbd.O)--NH--SO.sub.2R.sup.6, an acidic 5-membered hetero ring group, or the like; R.sup.2 represents an optionally substituted phenyl group, an optionally substituted 5-membered aromatic heterocyclic group, or the like; R.sup.3 represents a halogen atom, a C.sub.1-6 alkoxy group, or the like; R.sup.4 represents a hydrogen atom, a halogen atom, or the like; R.sup.5 represents a hydrogen atom or the like; and R.sup.6 represents a C.sub.1-6 alkyl group or the like], and a pharmaceutically acceptable salt thereof. Furthermore, the compound (I) of the present invention can be used as an agent for treating or preventing LUTS, in particular, various symptoms of OABs.

Inventors: Tatani; Kazuya (Nagano, JP), Kondo; Atsushi (Nagano, JP), Kondo; Tatsuhiro (Niigata, JP), Kawamura; Naohiro (Nagano, JP), Seto; Shigeki (Nogi, JP), Kohno; Yasushi (Nogi, JP)

Assignee: Kissei Pharmaceutical Co., Ltd.

International Classification: C07D 209/08 (20060101); A61K 31/444 (20060101); A61K 31/4439 (20060101); A61K 31/443 (20060101); A61K 31/4025 (20060101); A61K 31/40 (20060101); A61K 45/06 (20060101); C07D 401/06 (20060101); C07D 401/14 (20060101); C07D 405/06 (20060101); C07D 405/14 (20060101); C07D 409/14 (20060101); C07D 413/14 (20060101); C07D 417/14 (20060101)

Expiration Date: 8/05/12018