Thomas M G, Lang S D
J Antimicrob Chemother. 1986 Aug;18(2):171-5. doi: 10.1093/jac/18.2.171.
The in-vitro activity of coumermycin was compared with that of vancomycin, rifampicin, fusidic acid, trimethoprim-sulphamethoxazole, norfloxacin and cefamandole against seven isolates of methicillin-resistant Staphylococcus aureus and 97 isolates of methicillin-resistant coagulase negative staphylococci. Apart from one strain of methicillin-resistant S. aureus all isolates were inhibited by less than or equal to 0.06 mg/l of coumermycin. Cefamandole was more active against strains of S. epidermidis than against other coagulase negative staphylococci.
将香豆霉素的体外活性与万古霉素、利福平、夫西地酸、甲氧苄啶-磺胺甲恶唑、诺氟沙星和头孢孟多针对7株耐甲氧西林金黄色葡萄球菌和97株耐甲氧西林凝固酶阴性葡萄球菌的活性进行了比较。除1株耐甲氧西林金黄色葡萄球菌外，所有分离株均被浓度小于或等于0.06mg/L的香豆霉素抑制。头孢孟多对表皮葡萄球菌菌株的活性比对其他凝固酶阴性葡萄球菌的活性更强。
