Piperazine skeleton in the structural modification of natural products: a review
Piperazine moiety is a cyclic molecule containing two nitrogen atoms in positions 1 and 4, as well as four carbon atoms. Piperazine is one of the most sought heterocyclics for the development of new drug candidates with a wide range of applications. Over 100 molecules with a broad range of bioactivi...
Gespeichert in:
Veröffentlicht in: | Journal of enzyme inhibition and medicinal chemistry 2021-01, Vol.36 (1), p.1165-1197 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1197 |
---|---|
container_issue | 1 |
container_start_page | 1165 |
container_title | Journal of enzyme inhibition and medicinal chemistry |
container_volume | 36 |
creator | Zhang, Run-Hui Guo, Hong-Yan Deng, Hao Li, Jinzi Quan, Zhe-Shan |
description | Piperazine moiety is a cyclic molecule containing two nitrogen atoms in positions 1 and 4, as well as four carbon atoms. Piperazine is one of the most sought heterocyclics for the development of new drug candidates with a wide range of applications. Over 100 molecules with a broad range of bioactivities, including antitumor, antibacterial, anti-inflammatory, antioxidant, and other activities, were reviewed. This article reviewed investigations regarding piperazine groups for the modification of natural product derivatives in the last decade, highlighting parameters that affect their biological activity. |
doi_str_mv | 10.1080/14756366.2021.1931861 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8183565</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_00ae8632a7f441969f95c82cbc9fde1b</doaj_id><sourcerecordid>2536796857</sourcerecordid><originalsourceid>FETCH-LOGICAL-c577t-674b35d72ca0b6686a1a5988974a3c873b6493c53876e788bc6f7eb03870683f3</originalsourceid><addsrcrecordid>eNp9kU9v1DAQxS0Eon_gIyDlyGUXO47HDgcEqoBWqkQPcLYmjt26JPZiO63Kp8dLlkq9cJqZN29-lvUIecPollFF37FOCuAA25a2bMt6zhSwZ-R4r2-Ay-75Yw9wRE5yvqXV2bLuJTniXUUIRo_J1ZXf2YS_fbBN_mknW2JofGjKTZ1LWkxZEk7NHEfvvMHi6zq6JuCq71Icqye_b7BJ9s7b-1fkhcMp29eHekp-fPn8_ex8c_nt68XZp8uNEVKWDchu4GKUrUE6AChAhqJXqpcdcqMkH6DruRFcSbBSqcGAk3agdaaguOOn5GLljhFv9S75GdODjuj1XyGma42peDNZTSlaBbxF6bqO9dC7XhjVmsH0brRsqKwPK2u3DLMdjQ2lfu4J9Okm-Bt9He-0YooLEBXw9gBI8ddic9Gzz8ZOEwYbl6xbwUH2oISsVrFaTYo5J-sen2FU75PV_5LV-2T1Idl693G988HFNON9TNOoCz5MMbmEwfis-f8RfwCCvamH</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2536796857</pqid></control><display><type>article</type><title>Piperazine skeleton in the structural modification of natural products: a review</title><source>Taylor & Francis Open Access</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Zhang, Run-Hui ; Guo, Hong-Yan ; Deng, Hao ; Li, Jinzi ; Quan, Zhe-Shan</creator><creatorcontrib>Zhang, Run-Hui ; Guo, Hong-Yan ; Deng, Hao ; Li, Jinzi ; Quan, Zhe-Shan</creatorcontrib><description>Piperazine moiety is a cyclic molecule containing two nitrogen atoms in positions 1 and 4, as well as four carbon atoms. Piperazine is one of the most sought heterocyclics for the development of new drug candidates with a wide range of applications. Over 100 molecules with a broad range of bioactivities, including antitumor, antibacterial, anti-inflammatory, antioxidant, and other activities, were reviewed. This article reviewed investigations regarding piperazine groups for the modification of natural product derivatives in the last decade, highlighting parameters that affect their biological activity.</description><identifier>ISSN: 1475-6366</identifier><identifier>EISSN: 1475-6374</identifier><identifier>DOI: 10.1080/14756366.2021.1931861</identifier><identifier>PMID: 34080510</identifier><language>eng</language><publisher>Taylor & Francis</publisher><subject>natural product ; pharmacological activity ; Piperazine ; Review ; structure-activity relationship</subject><ispartof>Journal of enzyme inhibition and medicinal chemistry, 2021-01, Vol.36 (1), p.1165-1197</ispartof><rights>2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2021</rights><rights>2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2021 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c577t-674b35d72ca0b6686a1a5988974a3c873b6493c53876e788bc6f7eb03870683f3</citedby><cites>FETCH-LOGICAL-c577t-674b35d72ca0b6686a1a5988974a3c873b6493c53876e788bc6f7eb03870683f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8183565/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8183565/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2095,27482,27904,27905,53771,53773,59121,59122</link.rule.ids></links><search><creatorcontrib>Zhang, Run-Hui</creatorcontrib><creatorcontrib>Guo, Hong-Yan</creatorcontrib><creatorcontrib>Deng, Hao</creatorcontrib><creatorcontrib>Li, Jinzi</creatorcontrib><creatorcontrib>Quan, Zhe-Shan</creatorcontrib><title>Piperazine skeleton in the structural modification of natural products: a review</title><title>Journal of enzyme inhibition and medicinal chemistry</title><description>Piperazine moiety is a cyclic molecule containing two nitrogen atoms in positions 1 and 4, as well as four carbon atoms. Piperazine is one of the most sought heterocyclics for the development of new drug candidates with a wide range of applications. Over 100 molecules with a broad range of bioactivities, including antitumor, antibacterial, anti-inflammatory, antioxidant, and other activities, were reviewed. This article reviewed investigations regarding piperazine groups for the modification of natural product derivatives in the last decade, highlighting parameters that affect their biological activity.</description><subject>natural product</subject><subject>pharmacological activity</subject><subject>Piperazine</subject><subject>Review</subject><subject>structure-activity relationship</subject><issn>1475-6366</issn><issn>1475-6374</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><sourceid>DOA</sourceid><recordid>eNp9kU9v1DAQxS0Eon_gIyDlyGUXO47HDgcEqoBWqkQPcLYmjt26JPZiO63Kp8dLlkq9cJqZN29-lvUIecPollFF37FOCuAA25a2bMt6zhSwZ-R4r2-Ay-75Yw9wRE5yvqXV2bLuJTniXUUIRo_J1ZXf2YS_fbBN_mknW2JofGjKTZ1LWkxZEk7NHEfvvMHi6zq6JuCq71Icqye_b7BJ9s7b-1fkhcMp29eHekp-fPn8_ex8c_nt68XZp8uNEVKWDchu4GKUrUE6AChAhqJXqpcdcqMkH6DruRFcSbBSqcGAk3agdaaguOOn5GLljhFv9S75GdODjuj1XyGma42peDNZTSlaBbxF6bqO9dC7XhjVmsH0brRsqKwPK2u3DLMdjQ2lfu4J9Okm-Bt9He-0YooLEBXw9gBI8ddic9Gzz8ZOEwYbl6xbwUH2oISsVrFaTYo5J-sen2FU75PV_5LV-2T1Idl693G988HFNON9TNOoCz5MMbmEwfis-f8RfwCCvamH</recordid><startdate>20210101</startdate><enddate>20210101</enddate><creator>Zhang, Run-Hui</creator><creator>Guo, Hong-Yan</creator><creator>Deng, Hao</creator><creator>Li, Jinzi</creator><creator>Quan, Zhe-Shan</creator><general>Taylor & Francis</general><general>Taylor & Francis Group</general><scope>0YH</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20210101</creationdate><title>Piperazine skeleton in the structural modification of natural products: a review</title><author>Zhang, Run-Hui ; Guo, Hong-Yan ; Deng, Hao ; Li, Jinzi ; Quan, Zhe-Shan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c577t-674b35d72ca0b6686a1a5988974a3c873b6493c53876e788bc6f7eb03870683f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>natural product</topic><topic>pharmacological activity</topic><topic>Piperazine</topic><topic>Review</topic><topic>structure-activity relationship</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Run-Hui</creatorcontrib><creatorcontrib>Guo, Hong-Yan</creatorcontrib><creatorcontrib>Deng, Hao</creatorcontrib><creatorcontrib>Li, Jinzi</creatorcontrib><creatorcontrib>Quan, Zhe-Shan</creatorcontrib><collection>Taylor & Francis Open Access</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of enzyme inhibition and medicinal chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Run-Hui</au><au>Guo, Hong-Yan</au><au>Deng, Hao</au><au>Li, Jinzi</au><au>Quan, Zhe-Shan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Piperazine skeleton in the structural modification of natural products: a review</atitle><jtitle>Journal of enzyme inhibition and medicinal chemistry</jtitle><date>2021-01-01</date><risdate>2021</risdate><volume>36</volume><issue>1</issue><spage>1165</spage><epage>1197</epage><pages>1165-1197</pages><issn>1475-6366</issn><eissn>1475-6374</eissn><abstract>Piperazine moiety is a cyclic molecule containing two nitrogen atoms in positions 1 and 4, as well as four carbon atoms. Piperazine is one of the most sought heterocyclics for the development of new drug candidates with a wide range of applications. Over 100 molecules with a broad range of bioactivities, including antitumor, antibacterial, anti-inflammatory, antioxidant, and other activities, were reviewed. This article reviewed investigations regarding piperazine groups for the modification of natural product derivatives in the last decade, highlighting parameters that affect their biological activity.</abstract><pub>Taylor & Francis</pub><pmid>34080510</pmid><doi>10.1080/14756366.2021.1931861</doi><tpages>33</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1475-6366 |
ispartof | Journal of enzyme inhibition and medicinal chemistry, 2021-01, Vol.36 (1), p.1165-1197 |
issn | 1475-6366 1475-6374 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8183565 |
source | Taylor & Francis Open Access; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | natural product pharmacological activity Piperazine Review structure-activity relationship |
title | Piperazine skeleton in the structural modification of natural products: a review |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-21T09%3A44%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Piperazine%20skeleton%20in%20the%20structural%20modification%20of%20natural%20products:%20a%20review&rft.jtitle=Journal%20of%20enzyme%20inhibition%20and%20medicinal%20chemistry&rft.au=Zhang,%20Run-Hui&rft.date=2021-01-01&rft.volume=36&rft.issue=1&rft.spage=1165&rft.epage=1197&rft.pages=1165-1197&rft.issn=1475-6366&rft.eissn=1475-6374&rft_id=info:doi/10.1080/14756366.2021.1931861&rft_dat=%3Cproquest_pubme%3E2536796857%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2536796857&rft_id=info:pmid/34080510&rft_doaj_id=oai_doaj_org_article_00ae8632a7f441969f95c82cbc9fde1b&rfr_iscdi=true |