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(12) PATENT APPLICATION PUBLICATION<br />

(19) INDIA (21) Application No.: 01041/KOLNP/2005 A<br />

(22) Date <strong>of</strong> filing <strong>of</strong> Application: 01/06/2005 (43) Publication Date: 09/06/2006<br />

(54) Title <strong>of</strong> <strong>the</strong> invention: AGENT FOR PREVENTING OR TREATING NEUROPATHY<br />

(51) International classification : A61K 31/381,<br />

31/4155, 31/4174,<br />

31/4178, 31/4184,<br />

31/427, 31/402,<br />

31/4439, 31/5377,<br />

C07D 417/10,<br />

417/12, 403/10,<br />

403/12, 417/04,<br />

(31) Priority Document No<br />

231/12, C07F 9/40<br />

: 2002-320153<br />

(32) Priority Date : 01/11/2002<br />

(33) Name <strong>of</strong> priority country : JAPAN<br />

(86) International Application No and : PCT/JP03/013901<br />

Filing Date<br />

: & 30/10/2003<br />

(87) International Publication No : WO 04/039365<br />

(61) Patent <strong>of</strong> addition to Application No : NA<br />

Filed on : NA<br />

(62) Divisional to Application No : NA<br />

Filed on : NA<br />

(71) Name <strong>of</strong> Applicant:<br />

TAKEDA PHARMECEUTICAL COMPANY<br />

LIMITED<br />

Address <strong>of</strong> <strong>the</strong> Applicant:<br />

1-1, DOSHOMACHI 4-CHOME, CHUO-KU,<br />

OSAKA-SHI, OSAKA 541-0045, JAPAN.<br />

(72) Name <strong>of</strong> <strong>the</strong> Inventor:<br />

1. MOMOSE, YU<br />

2. SAKAI, NOZOMU<br />

3. MAEKAWA, TSUYOSHI<br />

4. HAZAMA, MASATOSHI<br />

5. KAWAMURA, TORU<br />

6. SERA, MISAYO<br />

Filed U/S 5(2) before The <strong>Patents</strong> (Amendment)<br />

Act, 2005: NO<br />

(57) Abstract:<br />

The present invention provides an agent for preventing or treating neuropathy having superior action and low toxicity. This agent<br />

comprises a compound represented by <strong>the</strong> formula:wherein ring A is a 5-membered aromatic heterocycle containing 2 or more nitrogen<br />

atoms, which may fur<strong>the</strong>r have substituent(s);B is an optionally substituted hydrocarbon group or an optionally substituted heterocyclic<br />

group;X is a divalent acyclic hydrocarbon group;Z is -O-, -S-, -NR2-, -CONR2- or -NR2CO- (R2 is a hydrogen atom or an optionally<br />

substituted alkyl group);Y is a bond or a divalent acyclic hydrocarbon group;R1 is an optionally substituted cyclic group, an optionally<br />

substituted amino group or an optionally substituted acyl group, provided that when <strong>the</strong> 5-membered aromatic heterocycle represented by<br />

ring A is imidazole, <strong>the</strong>n Z should not be -O-, or a salt <strong>the</strong>re<strong>of</strong>.<br />

(FIG). nil<br />

The Patent Office Journal 09/06/2006 11067

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