摘要 |
The present invention relates to compounds of the general formula(Ig) or pharmaceutically acceptable salts thereof with an acid or a base, or pharmaceutically acceptable prodrugs or a stereoisomer thereof, wherein R<SUP>1 </SUP>independently represents H, alkyl, cycloalkyl, hydroxyalkyl, haloalkyl, haloalkyloxy, aryl, or heteroaryl; R<SUP>2 </SUP>independently represents NR<SUP>3</SUP>R<SUP>5</SUP>, R<SUP>3 </SUP>independently represents H, COR<SUP>6</SUP>, CO<SUB>2</SUB>R<SUP>6</SUP>, SOR<SUP>6</SUP>, SO<SUB>2</SUB>R<SUP>6</SUP>, SO<SUB>3</SUB>R<SUP>6</SUP>, alkyl, cycloalkyl, alkoxy, -NH<SUB>2</SUB>, alkylamine, -NR<SUP>7</SUP>COR<SUP>6</SUP>, halogen, -OH, -SH, alkylthio, hydroxyalkyl, haloalkyl, haloalkyloxy, aryl or heteroaryl; R<SUP>5 </SUP>independently represents H, COR<SUP>6</SUP>, CO<SUB>2</SUB>R<SUP>6</SUP>, SOR<SUP>6</SUP>, SO<SUB>2</SUB>R<SUP>6</SUP>, SO<SUB>3</SUB>R<SUP>6</SUP>, alkyl, cycloalkyl alkoxy, -NH<SUB>2</SUB>, alkylamine, -NR<SUP>7</SUP>COR<SUP>6</SUP>, halogen, -OH, -SH, alkylthio, hydroxyalkyl, haloalkyl, haloalkyloxy, aryl or heteroaryl; R<SUP>6 </SUP>independently represents H, alkyl, cycloalkyl, -NH<SUB>2</SUB>, alkylamine, aryl or heteroaryl; R<SUP>7 </SUP>independently represents H, alkyl, cycloalkyl, alkoxy, -OH, -SH, alkylthio, hydroxyalkyl, aryl, or heteroaryl; p is 0, or 1; q is 0, or 1; X is CO, CS, or SO<SUB>2</SUB>.
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