An appraisal of anti-mycobacterial activity with structure-activity relationship of piperazine and its analogues: A review

被引:40
作者
Girase, Pankaj S. [1 ]
Dhawan, Sanjeev [1 ]
Kumar, Vishal [1 ]
Shinde, Suraj R. [1 ]
Palkar, Mahesh B. [1 ,2 ]
Karpoormath, Rajshekhar [1 ]
机构
[1] Univ KwaZulu Natal Westville, Coll Hlth Sci, Dept Pharmaceut Chem, Discipline Pharmaceut Sci, ZA-4000 Durban, South Africa
[2] KLE Coll Pharm, Dept Pharmaceut Chem, Hubballi 580031, Karnataka, India
基金
新加坡国家研究基金会;
关键词
Piperazine; Mycobacterium tuberculosis; Structure-activity relationship; Anti-mycobacterial agent; CARRIER PROTEIN REDUCTASE; MICROTITER ASSAY PLATE; MYCOBACTERIUM-TUBERCULOSIS; MULTIDRUG-RESISTANT; ANTITUBERCULAR EVALUATION; IN-VITRO; POTENT INHIBITORS; DERIVATIVES; DESIGN; ANTIBACTERIAL;
D O I
10.1016/j.ejmech.2020.112967
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Piperazine, is privileged six membered nitrogen containing heterocyclic ring also known as 1,4-Diazacyclohexane. Consequently, piperazine is a versatile medicinally important scaffold and is an essential core in numerous marketed drugs with diverse pharmacological activities. In recent years several potent molecules containing piperazine as an essential subunit of the structural frame have been reported, especially against Mycobacterium tuberculosis (MTB). Remarkably, a good number of these reported molecules also displayed potential activity against multidrug-resistant (MDR), and extremely drug-resistant (XDR) strains of MTB. In this review, we have made a concerted effort to retrace anti-mycobacterial compounds for the past five decades (1971-2019) specifically where piperazine has been used as a vital building block. This review will benefit medicinal chemists as it elaborates on the design, rationale and structure-activity relationship (SAR) of the reported potent piperazine based anti-TB molecules, which in turn will assist them in addressing the gaps, exploiting the reported strategies and developing safer, selective, and cost-effective anti-mycobacterial agents. (C) 2020 Elsevier Masson SAS. All rights reserved.
引用
收藏
页数:39
相关论文
共 110 条
  • [1] Design, synthesis and evaluation against Mycobacterium tuberculosis of azole piperazine derivatives as dicyclotyrosine (cYY) mimics
    Abd El-Wahab, Hend A. A.
    Accietto, Mauro
    Marino, Leonardo B.
    McLean, Kirsty J.
    Levy, Colin W.
    Abdel-Rahman, Hamdy M.
    El-Gendy, Mahmoud A.
    Munro, Andrew W.
    Aboraia, Ahmed S.
    Simons, Claire
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2018, 26 (01) : 161 - 176
  • [2] Synthesis and antibacterial, antimycobacterial and docking studies of novel N-piperazinyl fluoroquinolones
    Agrawal, Kapil M.
    Talele, Gokul S.
    [J]. MEDICINAL CHEMISTRY RESEARCH, 2013, 22 (02) : 818 - 831
  • [3] Mechanism of Quinolone Action and Resistance
    Aldred, Katie J.
    Kerns, Robert J.
    Osheroff, Neil
    [J]. BIOCHEMISTRY, 2014, 53 (10) : 1565 - 1574
  • [4] [Anonymous], [No title captured]
  • [5] [Anonymous], [No title captured], Patent No. [WO2006109323A1, 2006109323]
  • [6] [Anonymous], [No title captured], Patent No. [WO2012066518A1, 2012066518]
  • [7] [Anonymous], [No title captured], Patent No. [WO2019243971A1, 201924397]
  • [8] [Anonymous], [No title captured], Patent No. [WO2013072903A1, 2013072903]
  • [9] [Anonymous], [No title captured], Patent No. [WO2005007625A2, 2005007625]
  • [10] [Anonymous], 2015, Research Journal of Pharmacy and Technology, DOI [10.5958/0974-360X.2015.00100.6, DOI 10.5958/0974-360X.2015.00100.6]