Compounds having therapeutic utility are of formula (I) B--X--(CH.sub.2).sub.n --CR.sup.2 R.sup.3 --CR.sup.4 R.sup.5 --COY (I) wherein n=0-1; X is S(O).sub.0-2 ; Y is OR.sup.1 or NHOH; R.sup.2 and R.sup.4 are independently H or a group (optionally substituted with R.sup.10) selected from C.sub.1-6 alkyl, C.sub.2-6 alkenyl, aryl, C.sub.1-6 alkyl-aryl, heteroaryl, C.sub.1-6 alkyl-heteroaryl, heterocycloalkyl, C.sub.1-6 alkyl-heterocycloalkyl, cycloalkyl and C.sub.1-6 alkyl-cycloalkyl; and R.sup.1, R.sup.3 and R.sup.5 are independently H or C.sub.1-6 alkyl, provided that not more than two of R.sup.2, R.sup.3, R.sup.4 and R.sup.5 are H; or any of CR.sup.2 R.sup.3, CR.sup.4 R.sup.5 and CR.sup.2 --CR.sup.4 is a cycloalkyl or heterocycloalkyl ring optionally substituted with R.sup.10 or a group (optionally substituted with R.sup.10) selected from C.sub.1-6 alkyl, aryl, C.sub.1-6 alkyl-aryl, heteroaryl and C.sub.1-6 alkyl-heteroaryl; B is heterocycloalkyl (optionally substituted by R.sup.6 or R.sup.7) bonded through carbon to X, or C.sub.1-6 alkyl-heterocycloalkyl (optionally substituted with R.sup.6 or R.sup.7), or a group (substituted with R.sup.6) selected from C.sub.1-8 alkyl, C.sub.2-6 alkenyl and C.sub.2-6 alkynyl; R.sup.6 is N(R.sup.7).sub.2, OR.sup.7, COR.sup.7, C(.dbd.NOR.sup.9)R.sup.7, NR.sup.7 R.sup.8, S(O).sub.0-2 R.sup.9 or SO.sub.2 N(R.sup.7).sub.2 ; R.sup.7 is H or a group selected from C.sub.1-6 alkyl, aryl, C.sub.1-6 alkyl-aryl, heteroaryl, C.sub.1-6 alkyl-heteroaryl, cycloalkyl, C.sub.1-6 alkyl-cycloalkyl, heterocycloalkyl and C.sub.1-6 alkyl-heterocycloalkyl, wherein said group is optionally substituted with R.sup.9, COR.sup.9, SO.sub.0-2 R.sup.9, CO.sub.2 R.sup.9, OR.sup.9, CONR.sup.1 R.sup.9, NR.sup.1 R.sup.9, halogen, CN, SO.sub.2 NR.sup.1 R.sup.9 or NO.sub.2, and for each case of N(R.sup.7).sub.2 the R.sup.7 groups are the same or different or N(R.sup.7).sub.2 is heterocycloalkyl optionally substituted with R.sup.9, COR.sup.9, SO.sub.0-2 R.sup.9, CO.sub.2 R.sup.9, OR.sup.9, CONR.sup.1 R.sup.9, NR.sup.1 R.sup.9, NR.sup.1 R.sup.9 halogen, CN, SO.sub.2 NR.sup.1 R.sup.9 or NO.sub.2, R.sup.8 is COR.sup.7, CON(R.sup.7).sub.2, CO.sub.2 R.sup.9 or SO.sub.2 R.sup.9 ; R.sup.9 is C.sub.1-6 alkyl, aryl, C.sub.1-6 alkyl-aryl, heteroaryl or C.sub.1-6 alkyl-heteroaryl; and R.sup.10 is OR.sup.7, COR.sup.7, CO.sub.2 R.sup.1, CON(R.sup.7).sub.2, NR.sup.7 R.sup.8, S(O).sub.0-2 R.sup.9, SO.sub.2 N(R.sup.7).sub.2, CN, halogen or cycloimidyl (optionally substituted with R.sup.1); and the salts, solvates, hydrates, N-oxides, protected amino, protected carboxy and protected hydroxamic acid derivatives thereof.

 
Web www.patentalert.com

< Electro-medical device for use with biologics

< Process of preparing 3S-3-amino-3-aryl proprionic acid and derivatives thereof

> Methods for spectral analysis and their applications: spectral replacement

> N-(4-carbamimidoyl-phenyl)-glycine derivatives

~ 00096