药效团
天然产物
生物信息学
数量结构-活动关系
组合化学
计算生物学
虚拟筛选
金黄色葡萄球菌
抗生素
化学
耐甲氧西林金黄色葡萄球菌
化学空间
立体化学
计算机科学
药物发现
细菌
生物
生物化学
遗传学
基因
作者
Philipp Peslalz,Andreas Vorbach,Anton Bleisch,Elisa Liberini,Frank Kraus,Flavia Izzo,Heike Brötz‐Oesterhelt,Friedrich Götz,Bernd Plietker
标识
DOI:10.1002/chem.202401955
摘要
In response to the pressing global challenge of antibiotic resistance, time efficient design and synthesis of novel antibiotics are of immense need. Polycyclic polyprenylated acylphloroglucinols (PPAP) were previously reported to effectively combat a range of gram-positive bacteria. Although the exact mode of action is still not clear, we conceptualized a late-stage divergent synthesis approach to expand our natural product-based PPAP library by 30 additional entities to perform SAR studies against methicillin-resistant Staphylococcus aureus (MRSA). Although at this point only data from cellular assays are available and understanding of molecular drug-target interactions are lacking, the experimental data were used to generate 3D-QSAR models via an artificial intelligence training and to identify a common pharmacophore model. The experimentally validated QSAR model enabled the estimation of anti-MRSA activities of a virtual compound library consisting of more than 100,000 in-silico generated B PPAPs, out of which the 20 most promising candidates were synthesized. These novel PPAPs revealed significantly improved cellular activities against MRSA with growth inhibition down to concentrations less than 1 μm.
科研通智能强力驱动
Strongly Powered by AbleSci AI