INHIBITORS OF a-HEMOL YSIN OF STAPHYLOCOCCUS AUREUS

A compound of formula (I):

• wherein
• R2 is hydrogen, halogen, OH, NO2, CN or NH2;
• or a C1-4 alkyl group, a C2-4 alkenyl group, a C2-4 alkynyl group, a C3-5 cycloalkyl group, an —O—C3-5 cycloalkyl group, a C4-8 alkylcycloalkyl group, or a C1-4 heteroalkyl group;
• and
• R1 is an optionally substituted phenyl group;
• an optionally substituted naphthyl group;
• an optionally substituted heteroaryl group containing 1 or 2 rings and 5 to 10 ring atoms selected from O, S, N and C;
• an optionally substituted cycloalkyl aryl group comprising a phenyl group and a cycloalkyl group containing 5 or 6 ring atoms;
• an optionally substituted heterocycloalkyl aryl group comprising a phenyl group and a heterocycloalkyl group containing 5 or 6 ring atoms selected from O, S, B, N and C;
• an optionally substituted cycloalkyl heteroaryl group comprising a heteroaryl group comprising 5 or 6 ring atoms selected from O, S, N and C and a cycloalkyl group containing 5 or 6 ring atoms;
• or an optionally substituted heterocycloalkyl heteroaryl group comprising a heteroaryl group comprising 5 or 6 ring atoms selected from O, S, N and C and a heterocycloalkyl group containing 5 or 6 ring atoms selected from O, S, N and C;
• or an optionally substituted cycloalkyl group containing 1 or 2 rings and 3 to 10 ring atoms;
• or a solvate, a hydrate or a salt thereof.