Novel compounds of the structural formula I, and the pharmaceutically acceptable salts thereof, are inhibitors of TarO and may be useful in the prevention, treatment and suppression of diseases mediated by TarO, such as bacterial infections, including gram negative bacterial infections and gram positive bacterial infections such as MRSA and MRSE, alone or in combination with a β-lactam antibiotic.
                            化学结构式I的新型化合物及其药学上可接受的盐,是TarO的
抑制剂,可用于预防、治疗和抑制由TarO介导的疾病,如细菌感染,包括革兰氏阴性细菌感染和革兰氏阳性细菌感染,例如耐
甲氧西林金黄色葡萄球菌和耐
甲氧西林表皮葡萄球菌,单独或与β-内酰胺类抗生素联合使用。