Chin N X, Neu H C
Antimicrob Agents Chemother. 1986 Apr;29(4):703-6. doi: 10.1128/AAC.29.4.703.
LY164846 is a semisynthetic arylglycyl cephalosporin which can be absorbed orally. It had in vitro activity comparable to that of cefaclor against beta-hemolytic streptococcal species and was two- to fourfold more active than cephalexin. Enterococci and Listeria species were resistant, and its activity against staphylococci was similar to that of other oral cephalosporins. Although some Bacteroides species were inhibited, the MICs for 25% were greater than or equal to 16 micrograms/ml. LY164846 was hydrolyzed by Staphylococcus aureus beta-lactamase and by cephalosporinases, but it was more stable than cefaclor.
LY164846是一种可口服吸收的半合成芳基甘氨酰头孢菌素。它在体外对β-溶血性链球菌的活性与头孢克洛相当,对头孢氨苄的活性高两至四倍。肠球菌和李斯特菌属耐药,其对葡萄球菌的活性与其他口服头孢菌素相似。虽然一些拟杆菌属受到抑制,但25%的菌株的最低抑菌浓度大于或等于16微克/毫升。LY164846可被金黄色葡萄球菌β-内酰胺酶和头孢菌素酶水解,但比头孢克洛更稳定。