Tanitame Akihiko, Oyamada Yoshihiro, Ofuji Keiko, Terauchi Hideo, Kawasaki Motoji, Wachi Masaaki, Yamagishi Jun-ichi
Chemistry Research Laboratories, Dainippon Pharmaceutical Co., Ltd, 33-94, Enoki, Suita, Osaka 564-0053, Japan.
Bioorg Med Chem Lett. 2005 Oct 1;15(19):4299-303. doi: 10.1016/j.bmcl.2005.06.103.
The 2-arylvinyl moiety in 1-(3-chlorophenyl)-3-(4-piperidyl)-5-[(E)-2-(5-chloro-1H-indol-3-yl)vinyl]pyrazole 2, which has previously shown improved DNA gyrase inhibition and target-related antibacterial activity, was transformed to other groups and the in vitro antibacterial activity of the synthesized compounds was evaluated. Many of the 5-[(E)-2-arylvinyl]pyrazoles synthesized in this study exhibited potent antibacterial activity against quinolone-resistant clinical isolates of gram-positive bacteria with minimal inhibitory concentration values equivalent to those against susceptible strains.
1-(3-氯苯基)-3-(4-哌啶基)-5-[(E)-2-(5-氯-1H-吲哚-3-基)乙烯基]吡唑2中的2-芳基乙烯基部分先前已显示出改善的DNA促旋酶抑制作用和与靶点相关的抗菌活性,现将其转化为其他基团,并对合成化合物的体外抗菌活性进行评估。本研究中合成的许多5-[(E)-2-芳基乙烯基]吡唑对喹诺酮耐药的革兰氏阳性菌临床分离株表现出强效抗菌活性,其最低抑菌浓度值与对敏感菌株的相当。