Annedi S C, Kotra L P
Faculty of Pharmacy, University of Toronto, ON, Canada.
Curr Opin Investig Drugs. 2001 Jun;2(6):752-4.
Aventis Pharma AG is investigating a series of novel coumarin DNA gyrase B inhibitors, including RU-79115, as potential treatments for bacterial infections. These inhibitors have displayed potent inhibitory activity in vitro against DNA supercoiling by DNA gyrase B and have antibacterial activity. Good antibacterial activity against vancomycin- and teicoplanin-resistant enterococci was observed with most analogs (where the 3-acylamino residue was replaced with reversed isosteres). Amide derivatives were also active against novobiocin-resistant strains [335149]. RU-79115 has shown activity against Gram-positive bacteria, particularly staphylococci and enterococci, and its activity compares favorably to vancomycin. Against oxacillin- and ofloxacin-resistant staphylococci, RU-79115 had MIC50 values 7.5-fold lower than eperezolid and significantly lower than vancomycin. In vivo data suggest that the compound is safe and carries a satisfactory pharmacokinetic profile [216256], [340969], [376199]. The compound is the most potent in the series which also includes RU-78535 and RU-64135 [340969], [341039].
安万特制药公司正在研究一系列新型香豆素DNA促旋酶B抑制剂,包括RU - 79115,作为细菌感染的潜在治疗药物。这些抑制剂在体外对DNA促旋酶B介导的DNA超螺旋显示出强效抑制活性,并具有抗菌活性。大多数类似物(其中3 - 酰基氨基残基被反向电子等排体取代)对万古霉素和替考拉宁耐药的肠球菌具有良好的抗菌活性。酰胺衍生物对新生霉素耐药菌株也有活性[335149]。RU - 79115已显示出对革兰氏阳性菌,特别是葡萄球菌和肠球菌的活性,其活性与万古霉素相当。对于对苯唑西林和氧氟沙星耐药的葡萄球菌,RU - 79115的MIC50值比依哌唑胺低7.5倍,且显著低于万古霉素。体内数据表明该化合物是安全的,并且具有令人满意的药代动力学特征[216256],[340969],[376199]。该化合物是该系列中最有效的,该系列还包括RU - 78535和RU - 64135[340969],[341039]。