摘要:
The present invention is directed to certain 3, 5 substituted, 4, 5-dihydroisoxazoles, and methods for their use. These compounds are transglutaminase inhibitors, and are particularly effective in the inhibition of epidermal transglutaminase and the treatment of acne.
摘要:
The present invention is directed to certain 3, 5 substituted, 4, 5-dihydroisoxazoles, and methods for their use. These compounds are transglutaminase inhibitors, and are particularly effective in the inhibition of epidermal transglutaminase and the treatment of acne.
摘要:
Novel 2-amino-4H-3,1-benzoxazin-4-ones represented by the formula and the pharmaceutically acceptable esters and salts thereof wherein R' is hydrogen or lower alkyl; R 2 and R 3 are each independently hydrogen, halo, lower alkyl, hydroxy, lower alkoxy, lower thioalkyl, -N0 2 , -N(R') 2 , -NR'COR', -NHCON(R') 2 or -NHCOOR', with the proviso that at least one of R 1 , R 2 and R 3 is not hydrogen when X is NHR or NR'COR"; and X is a radical chosen trom in which: R is lower alkyl, lower alkenyl, lower alkynyl, optionally substituted lower cycloalkyl or optionally substituted phenyl lower alkyl; each R' is independently hydrogen or lower alkyl, or lower alkenyl or lower alkynyl where the unsaturated bond is at least one carbon removed from the O or N atom; each R" is independently R, lower alkoxy, NHR' or AOR'; and A is an amino acid residue, or a peptide of 2 to 3 amino acid residues, are useful as enzyme inhibitors in animals.
摘要:
Novel 2-amino-4H-3,1-benzoxazin-4-ones represented by the formula and the pharmaceutically acceptable esters and salts thereof wherein R' is hydrogen or lower alkyl;
R 2 and R 3 are each independently hydrogen, halo, lower alkyl, hydroxy, lower alkoxy, lower thioalkyl, -N0 2 , -N(R') 2 , -NR'COR', -NHCON(R') 2 or -NHCOOR', with the proviso that at least one of R 1 , R 2 and R 3 is not hydrogen when X is NHR or NR'COR"; and X is a radical chosen trom in which: R is lower alkyl, lower alkenyl, lower alkynyl, optionally substituted lower cycloalkyl or optionally substituted phenyl lower alkyl; each R' is independently hydrogen or lower alkyl, or lower alkenyl or lower alkynyl where the unsaturated bond is at least one carbon removed from the O or N atom; each R" is independently R, lower alkoxy, NHR' or AOR'; and A is an amino acid residue, or a peptide of 2 to 3 amino acid residues, are useful as enzyme inhibitors in animals.