化学
抗菌活性
枯草芽孢杆菌
抗菌剂
立体化学
结构-活动关系
化学合成
酶抑制剂
粪肠球菌
酶
生物化学
细菌
体外
抗生素
大肠杆菌
生物
基因
遗传学
作者
A. Gilbert,Matthew Kirisits,P.L. Toy,David S. Nunn,A. FAILLI,Elizabeth G. Dushin,Елена Новикова,Peter J. Petersen,Diane Joseph‐McCarthy,Iain J. McFadyen,Christian Fritz
标识
DOI:10.1016/j.bmcl.2003.10.032
摘要
D-optimal design and Projection to Latent Structures (PLS) analysis were used to optimize screening hit 5 (B. subtilis AcpS IC(50): 15 microM, B. subtilis MIC: >200 microM) into a series of 4H-oxazol-5-one, small molecule, antibacterial, AcpS inhibitors. Specifically, 15, 16 and 18 show microM or sub-microM AcpS inhibition (IC(50)s: 15: 1.1 microM, 16: 1.5 microM, 18: 0.27 microM) and moderate antibacterial activity (MICs: 12.5-50 microM) against B. subtilis, E. faecalis ATCC, E. faecalis VRE and S. pneumo+.
科研通智能强力驱动
Strongly Powered by AbleSci AI