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Antimicrobial activity of bitespiramycin, a new genetically engineered macrolide
Bioorganic & Medicinal Chemistry Letters ( IF 2.7 ) Pub Date : 2017-08-24 , DOI: 10.1016/j.bmcl.2017.08.046
Weiqing He , Chunping Yang , Xiaofeng Zhao , Yiguang Wang

The antimicrobial activity of bitespiramycin (BT) against Chlamydia trachomatis (Ct), Chlamydia pneumoniae (Cp), Ureaplasma urealyticum (Uu), and Mycoplasma pneumoniae (Mp), was compared with those of azithromycin (AZM) and acetylspiramycin (AT-SP) in vitro. Furthermore, the anti-Mp activities of BT and AZM were evaluated in a hamster model. The activities of BT in vitro were similar to those of AZM but were more effective than those of AT-SP. BT effectively inhibited Mp infection at a dose of 200 mg/kg in a hamster model.



中文翻译:

新型基因工程大环内酯类比螺旋霉素的抗菌活性

将比特螺旋霉素(BT)对沙眼衣原体(Ct),肺炎衣原体(Cp),解脲脲原体(Uu)和肺炎支原体(Mp)的抗菌活性与阿奇霉素(AZM)和乙酰螺旋霉素(AT-SP)的抗菌活性进行了比较体外。此外,在仓鼠模型中评估了BT和AZM的抗Mp活性。BT的体外活性与AZM相似,但比AT-SP更有效。在仓鼠模型中,BT以200 mg / kg的剂量有效抑制Mp感染。

更新日期:2017-08-24
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