An appraisal of anti-mycobacterial activity with structure-activity relationship of piperazine and its analogues: A review
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...
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Veröffentlicht in: | European journal of medicinal chemistry 2021-01, Vol.210, p.112967-112967, Article 112967 |
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container_title | European journal of medicinal chemistry |
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creator | Girase, Pankaj S. Dhawan, Sanjeev Kumar, Vishal Shinde, Suraj R. Palkar, Mahesh B. Karpoormath, Rajshekhar |
description | 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.
[Display omitted]
•Tuberculosis is an extremely contagious bacterial infection caused by Mycobacterium Tuberculosis.•The recent advances in the invention of anti-mycobacterial drugs have outlined.•This review-article is focusing on the previously reported piperazine based anti-mycobacterial agents. |
doi_str_mv | 10.1016/j.ejmech.2020.112967 |
format | Article |
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[Display omitted]
•Tuberculosis is an extremely contagious bacterial infection caused by Mycobacterium Tuberculosis.•The recent advances in the invention of anti-mycobacterial drugs have outlined.•This review-article is focusing on the previously reported piperazine based anti-mycobacterial agents.</description><identifier>ISSN: 0223-5234</identifier><identifier>EISSN: 1768-3254</identifier><identifier>DOI: 10.1016/j.ejmech.2020.112967</identifier><identifier>PMID: 33190957</identifier><language>eng</language><publisher>France: Elsevier Masson SAS</publisher><subject>Animals ; Anti-mycobacterial agent ; Antitubercular Agents - chemistry ; Antitubercular Agents - pharmacology ; Drug Design ; Drug Discovery ; Humans ; Mycobacterium tuberculosis ; Mycobacterium tuberculosis - drug effects ; Piperazine ; Piperazine - chemistry ; Piperazine - pharmacology ; Structure-Activity Relationship ; Tuberculosis - drug therapy</subject><ispartof>European journal of medicinal chemistry, 2021-01, Vol.210, p.112967-112967, Article 112967</ispartof><rights>2020 Elsevier Masson SAS</rights><rights>Copyright © 2020 Elsevier Masson SAS. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-34e7a249d2d1e0b367c659683e3e61a2efd307986d2a1934c830be88e2492a5c3</citedby><cites>FETCH-LOGICAL-c362t-34e7a249d2d1e0b367c659683e3e61a2efd307986d2a1934c830be88e2492a5c3</cites><orcidid>0000-0001-7486-5275</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ejmech.2020.112967$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33190957$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Girase, Pankaj S.</creatorcontrib><creatorcontrib>Dhawan, Sanjeev</creatorcontrib><creatorcontrib>Kumar, Vishal</creatorcontrib><creatorcontrib>Shinde, Suraj R.</creatorcontrib><creatorcontrib>Palkar, Mahesh B.</creatorcontrib><creatorcontrib>Karpoormath, Rajshekhar</creatorcontrib><title>An appraisal of anti-mycobacterial activity with structure-activity relationship of piperazine and its analogues: A review</title><title>European journal of medicinal chemistry</title><addtitle>Eur J Med Chem</addtitle><description>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.
[Display omitted]
•Tuberculosis is an extremely contagious bacterial infection caused by Mycobacterium Tuberculosis.•The recent advances in the invention of anti-mycobacterial drugs have outlined.•This review-article is focusing on the previously reported piperazine based anti-mycobacterial agents.</description><subject>Animals</subject><subject>Anti-mycobacterial agent</subject><subject>Antitubercular Agents - chemistry</subject><subject>Antitubercular Agents - pharmacology</subject><subject>Drug Design</subject><subject>Drug Discovery</subject><subject>Humans</subject><subject>Mycobacterium tuberculosis</subject><subject>Mycobacterium tuberculosis - drug effects</subject><subject>Piperazine</subject><subject>Piperazine - chemistry</subject><subject>Piperazine - pharmacology</subject><subject>Structure-Activity Relationship</subject><subject>Tuberculosis - drug therapy</subject><issn>0223-5234</issn><issn>1768-3254</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtPwzAQhC0EoqXwDxDKkUuKH4mTcECqKl4SEhc4W46zpVvlhe0UlV-Pq0CPnNYazcx6P0IuGZ0zyuTNZg6bBsx6zikPEuOFzI7IlGUyjwVPk2MypZyLOOUimZAz5zaU0lRSekomQrCCFmk2Jd-LNtJ9bzU6XUfdKtKtx7jZma7UxoPFoIYHbtHvoi_068h5Oxg_WIgPuoVae-xat8Z-39FjD1Z_YwuhrorQuzB13X0M4G6jRfBvEb7OyclK1w4ufueMvD_cvy2f4pfXx-fl4iU2QnIfiwQyzZOi4hUDWgqZGZkWMhcgQDLNYVUJmhW5rLhmhUhMLmgJeQ4hw3VqxIxcj7297T7DD7xq0Bmoa91CNzjFE8koFYmUwZqMVmM75yysVG-x0XanGFV76mqjRupqT12N1EPs6nfDUDZQHUJ_mIPhbjRAuDPcbpUzCK2BCi0Yr6oO_9_wA_Xqlq8</recordid><startdate>20210115</startdate><enddate>20210115</enddate><creator>Girase, Pankaj S.</creator><creator>Dhawan, Sanjeev</creator><creator>Kumar, Vishal</creator><creator>Shinde, Suraj R.</creator><creator>Palkar, Mahesh B.</creator><creator>Karpoormath, Rajshekhar</creator><general>Elsevier Masson SAS</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7486-5275</orcidid></search><sort><creationdate>20210115</creationdate><title>An appraisal of anti-mycobacterial activity with structure-activity relationship of piperazine and its analogues: A review</title><author>Girase, Pankaj S. ; Dhawan, Sanjeev ; Kumar, Vishal ; Shinde, Suraj R. ; Palkar, Mahesh B. ; Karpoormath, Rajshekhar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-34e7a249d2d1e0b367c659683e3e61a2efd307986d2a1934c830be88e2492a5c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Anti-mycobacterial agent</topic><topic>Antitubercular Agents - chemistry</topic><topic>Antitubercular Agents - pharmacology</topic><topic>Drug Design</topic><topic>Drug Discovery</topic><topic>Humans</topic><topic>Mycobacterium tuberculosis</topic><topic>Mycobacterium tuberculosis - drug effects</topic><topic>Piperazine</topic><topic>Piperazine - chemistry</topic><topic>Piperazine - pharmacology</topic><topic>Structure-Activity Relationship</topic><topic>Tuberculosis - drug therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Girase, Pankaj S.</creatorcontrib><creatorcontrib>Dhawan, Sanjeev</creatorcontrib><creatorcontrib>Kumar, Vishal</creatorcontrib><creatorcontrib>Shinde, Suraj R.</creatorcontrib><creatorcontrib>Palkar, Mahesh B.</creatorcontrib><creatorcontrib>Karpoormath, Rajshekhar</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of medicinal chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Girase, Pankaj S.</au><au>Dhawan, Sanjeev</au><au>Kumar, Vishal</au><au>Shinde, Suraj R.</au><au>Palkar, Mahesh B.</au><au>Karpoormath, Rajshekhar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An appraisal of anti-mycobacterial activity with structure-activity relationship of piperazine and its analogues: A review</atitle><jtitle>European journal of medicinal chemistry</jtitle><addtitle>Eur J Med Chem</addtitle><date>2021-01-15</date><risdate>2021</risdate><volume>210</volume><spage>112967</spage><epage>112967</epage><pages>112967-112967</pages><artnum>112967</artnum><issn>0223-5234</issn><eissn>1768-3254</eissn><abstract>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.
[Display omitted]
•Tuberculosis is an extremely contagious bacterial infection caused by Mycobacterium Tuberculosis.•The recent advances in the invention of anti-mycobacterial drugs have outlined.•This review-article is focusing on the previously reported piperazine based anti-mycobacterial agents.</abstract><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>33190957</pmid><doi>10.1016/j.ejmech.2020.112967</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-7486-5275</orcidid></addata></record> |
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subjects | Animals Anti-mycobacterial agent Antitubercular Agents - chemistry Antitubercular Agents - pharmacology Drug Design Drug Discovery Humans Mycobacterium tuberculosis Mycobacterium tuberculosis - drug effects Piperazine Piperazine - chemistry Piperazine - pharmacology Structure-Activity Relationship Tuberculosis - drug therapy |
title | An appraisal of anti-mycobacterial activity with structure-activity relationship of piperazine and its analogues: A review |
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