发明名称 Inhibitors of matrix metalloproteinase
摘要 Compounds of formula (I): wherein R<SUP>1 </SUP>represents optionally substituted C<SUB>4-12 </SUB>alkyl, optionally substituted C<SUB>2-6</SUB>alkylaryl, or optionally substituted 5- or 6-membered aryl or heteroaryl; Z represents a bond, CH<SUB>2</SUB>, O, S, SO, SO<SUB>2</SUB>, NR<SUP>4</SUP>, OCR<SUP>4</SUP>R<SUP>5</SUP>, CR<SUP>4</SUP>R<SUP>5</SUP>O, or Z, R<SUP>1 </SUP>and Q together form an optionally substituted fused tricyclic group; Q represents an optionally substituted 5- or 6-membered aryl or heteroaryl ring; X represents COR<SUP>3 </SUP>or N(OR<SUP>8</SUP>)COR<SUP>9</SUP>; R<SUP>2 </SUP>represents SO<SUB>2</SUB>R<SUP>10 </SUP>or SO<SUB>2</SUB>NR<SUP>10</SUP>R<SUP>11</SUP>; R<SUP>3 </SUP>represents OR<SUP>6</SUP>, NR<SUP>6</SUP>R<SUP>7 </SUP>or NR<SUP>6</SUP>OH; R<SUP>4 </SUP>and R<SUP>5 </SUP>each independently represents H, C<SUB>1-6 </SUB>alkyl or C<SUB>1-4 </SUB>alkylaryl; R<SUP>6 </SUP>and R<SUP>7 </SUP>each independently represents H, C<SUB>1-6 </SUB>alkyl, or C<SUB>1-6 </SUB>alkyl substituted with one or more heteroaryl groups, or R<SUP>6 </SUP>and R<SUP>7 </SUP>together with the nitrogen atom to which they are attached form a 5- or 6-membered ring which may optionally include 1 or more further heteroatoms selected from O, S and N; R<SUP>8 </SUP>and R<SUP>9 </SUP>each independently represents H or C<SUB>1-6 </SUB>alkyl; R<SUP>10 </SUP>and R<SUP>11 </SUP>each independently represents H or C<SUB>1-6 </SUB>alkyl; and and physiologically functional derivatives thereof, with the exception of N-(ethoxycarbonyl)-N-[4-(1H-tetrazol-1-yl)phenyl]glycine, processes for their preparation, pharmaceutical formulations containing them and their use as inhibitors of matrix metalloproteinase enzymes (MMPs) are described.
申请公布号 US2006142385(A1) 申请公布日期 2006.06.29
申请号 US20050561055 申请日期 2005.12.16
申请人 HOLMES IAN;WATSON STEPHEN P 发明人 HOLMES IAN;WATSON STEPHEN P.
分类号 A61K31/277;A61K31/195;A61P29/00;A61P37/00;C07C311/08;C07C311/30;C07D213/42 主分类号 A61K31/277
代理机构 代理人
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