Department of Pharmaceutical Sciences, College of Pharmacy, University of Tennessee Health Science Center, 881 Madison Avenue, Memphis, TN 38163-0001, United States.
Institute for Tuberculosis Research, College of Pharmacy, University of Illinois at Chicago, 833 S. Wood Street, Chicago, IL 60612, United States.
Bioorg Med Chem. 2018 Sep 15;26(17):4787-4796. doi: 10.1016/j.bmc.2018.07.034. Epub 2018 Aug 18.
Pleuromutilin is a promising pharmacophore to design new antibacterial agents for Gram-positive bacteria. However, there are limited studies on the development of pleuromutilin analogues that inhibit growth of Mycobacterium tuberculosis (Mtb). In screening of our library of pleuromutilin derivatives, UT-800 (1) was identified to kill replicating- and non-replicating Mtb with the MIC values of 0.83 and 1.20 μg/mL, respectively. UT-800 also kills intracellular Mtb faster than rifampicin at 2× MIC concentrations. Pharmacokinetic studies indicate that 1 has an oral bioavailability with an average F-value of 27.6%. Pleuromutilin may have the potential to be developed into an orally administered anti-TB drug.
截短侧耳素是设计用于治疗革兰氏阳性菌的新型抗菌药物的有前途的药效团。然而,关于抑制结核分枝杆菌(Mtb)生长的截短侧耳素类似物的开发研究有限。在筛选我们的截短侧耳素衍生物文库时,鉴定出 UT-800(1)能够以分别为 0.83 和 1.20μg/mL 的 MIC 值杀灭复制期和非复制期的 Mtb。与 2×MIC 浓度的利福平相比,UT-800 还能更快地杀死细胞内的 Mtb。药代动力学研究表明,1 具有口服生物利用度,平均 F 值为 27.6%。截短侧耳素有可能被开发成一种口服抗结核药物。