Natural product derived promising anti-MRSA drug leads: A review

被引:30
|
作者
Gatadi, Srikanth [1 ]
Gour, Jitendra [1 ]
Nanduri, Srinivas [1 ]
机构
[1] NIPER, Dept Med Chem, Hyderabad 500037, Andhra Pradesh, India
关键词
Methicillin resistant Staphylococcus aureus (MRSA); Natural products; Antibacterial agents; Structure Activity Relationships; RESISTANT STAPHYLOCOCCUS-AUREUS; ANTIBACTERIAL ACTIVITY; IN-VIVO; PLEUROMUTILIN DERIVATIVES; ANTIMICROBIAL RESISTANCE; BIOLOGICAL EVALUATION; XANTHONE DERIVATIVES; CARBAZOLE ALKALOIDS; DESIGN; VANCOMYCIN;
D O I
10.1016/j.bmc.2019.07.023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Multi-drug resistant Staphylococcus aureus infections have created a critical need for the development of new classes of antibacterials. Discovery of new naturally derived antibacterial agents with new mechanism of action remains a high priority globally. Several of the available antibacterial agents like beta-lactams, polyketides, phenylpropanoids, aminoglycosides, macrolides, glycopeptides, streptogramins and lipopeptides are natural products or their semisynthetic variations. In the current scenario of alarming rise in antibacterial resistance, revisiting natural products with modern chemistry and biology tools has fascinated many medicinal chemists for discovery and development of natural products or derived semisynthetic derivatives as effective antibacterial agents. This review underlines the structures and anti-MRSA activity of various natural product derivatives covering recent reports, in vivo activities and brief Structure Activity Relationships (SARs).
引用
收藏
页码:3760 / 3774
页数:15
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