摘要 |
The invention concerns compounds of general formula (1) wherein R<SUB>1 </SUB>represents H, alkyl,cycloalkyl or cycloalkylalkyl and R<SUB>2 </SUB>represents H or alkyl; R<SUB>3 </SUB>represents H, alkyl or aralkyl; X represents a bond or a linear or branched alkylene radical (II); Y represents H, cycloalkyl, OR<SUB>14</SUB>, SR<SUB>15</SUB>, NR<SUB>4</SUB>R<SUB>5 </SUB>or A represents a bond or phenyl; B and B' are independently selected among alkyl, NR<SUB>6</SUB>R<SUB>7</SUB>, SR<SUB>8 </SUB>and carbocyclic aryl orheterocyclic aryl radicals with five or six members optionally substituted; R<SUB>4 </SUB>represents H, alkyl, aryl, cycloalkyl, cycloalkylalkyl, aralkyl, C(O)R<SUB>9</SUB>, C(O)OR<SUB>9</SUB>, -C(O)NHR<SUB>9 </SUB>or -SO<SUB>2</SUB>R<SUB>9</SUB>, or further aryl or aralkyl whereof the aromatic ring is optionally substituted and R<SUB>5 </SUB>represents in particular H or alkyl, or further R, and R<SUB>5 </SUB>form with the nitrogen atom bearing them a non-aromatic hetcrocycle of five to seven members optionally substituted; R<SUB>6 </SUB>represents (in particular) II or alkyl and R<SUB>7 </SUB>represents (in particular) II or alkyl; R<SUB>8 </SUB>represents an alkyl radical optionally substituted; R<SUB>9 </SUB>represents alkyl, haloakyl, cycloalkyl or cycloalkylalkyl, or further one of the aralkyl or aryl or heteroaryl radicals optionally substituted; R<SUB>14 </SUB>and R<SUB>15 </SUB>independently represent (in particular) alkyl, phenyl or aralkyl. The compounds of general formula (I) can be used as NO synthase inhibitors and as modulators of sodium channels (for treating pains, multiple sclerosis, the central nervous system or the peripheral nervous system and the like).
|