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A review: Structure-activity relationship and antibacterial activities of Quinoline based hybrids
被引:46
作者:

Patel, Kajalben B.
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机构:
Sardar Vallabhbhai Natl Inst Technol, Dept Chem, Surat 395007, Gujarat, India Sardar Vallabhbhai Natl Inst Technol, Dept Chem, Surat 395007, Gujarat, India

Kumari, Premlata
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机构:
Sardar Vallabhbhai Natl Inst Technol, Dept Chem, Surat 395007, Gujarat, India Sardar Vallabhbhai Natl Inst Technol, Dept Chem, Surat 395007, Gujarat, India
机构:
[1] Sardar Vallabhbhai Natl Inst Technol, Dept Chem, Surat 395007, Gujarat, India
关键词:
Quinoline;
Drug resistance;
Antibacterial;
SAR;
STAPHYLOCOCCUS-AUREUS;
BIOLOGICAL EVALUATION;
ANTIMICROBIAL ACTIVITY;
HYDRAZONE DERIVATIVES;
MOLECULAR DOCKING;
RESISTANCE;
INHIBITORS;
DESIGN;
PYRIMIDINE;
QUINOLONES;
D O I:
10.1016/j.molstruc.2022.133634
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
The drug resistance problem is most acute in the case of bacteria. There is always a need to develop novel antibacterial drugs with better mechanisms of action. Most of the quinoline-based antibiotics developed are potential antibacterial drug candidates. This review represents quinoline-based hybrids with antibacterial activity and their structure-activity relationship (SAR), which provide further insight into the improvement of quinoline-based antibiotics especially against multidrug-resistant bacterial strains. (C) 2022 Elsevier B.V. All rights reserved.
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