发明名称 Antiproliferative 1,2,3-thiadiazole compounds
摘要 This invention is directed to methods of using compounds having the structure: and including stereoisomers, solvates, and pharmaceutically acceptable salts thereof, wherein each of R<SUP>1</SUP>, R<SUP>2</SUP>, R<SUP>3 </SUP>and R<SUP>4 </SUP>is independently selected from hydrogen, R<SUP>5</SUP>, R<SUP>6</SUP>, and R<SUP>7</SUP>; R<SUP>5 </SUP>is selected from alkyl, heteroalkyl, aryl and heteroaryl; R<SUP>6 </SUP>is selected from (R<SUP>5</SUP>)<SUB>n</SUB>-alkylene, (R<SUP>5</SUP>)<SUB>n</SUB>-heteroalkylene, (R<SUP>5</SUP>)<SUB>n</SUB>-arylene and (R<SUP>5</SUP>)<SUB>n</SUB>-heteroarylene; R<SUP>7 </SUP>is selected from (R<SUP>6</SUP>)<SUB>n</SUB>-alkylene, (R<SUP>6</SUP>)<SUB>n</SUB>-heteroalkylene, (R<SUP>6</SUP>)<SUB>n</SUB>-arylene, and (R<SUP>6</SUP>)<SUB>n</SUB>-heteroarylene; and n is selected from 0, 1, 2, 3, 4 and 5, where R<SUP>1 </SUP>and R<SUP>2 </SUP>may together form a heterocyclic structure including the nitrogen to which they are both attached, and R<SUP>3 </SUP>and R<SUP>4 </SUP>may together form a heterocyclic structure including the nitrogen to which they are both attached; and each of L<SUP>1 </SUP>and L<SUP>2 </SUP>is independently selected from -A1-A2-A3- where each of A1, A2, and A3 is independently selected from a direct bond, alkylene, heteroalkylene, arylene and heteroarylene. These compounds are useful in treating hyperproliferative disorders and inducing apoptosis.
申请公布号 US2006009500(A1) 申请公布日期 2006.01.12
申请号 US20050218969 申请日期 2005.09.02
申请人 QLT INC. 发明人 ZHANG ZALHUI;CHOPIUK GREGORY B.;DAYNARD TIMOTHY S.;WANG SHISEN
分类号 A61K31/433;C07D285/06 主分类号 A61K31/433
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