A new potential approach to block HIV-1 replication via protein-protein interaction and strand-transfer inhibition
Therapeutic treatment of AIDS is recently characterized by a crescent effort towards the identification of multiple ligands able to target different steps of HIV-1 life cycle. Taking into consideration our previously obtained SAR information and combining some important chemical structural features...
Gespeichert in:
Veröffentlicht in: | Bioorganic & Medicinal Chemistry 2014-02, Vol.22 (7), p.2269-2279 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 2279 |
---|---|
container_issue | 7 |
container_start_page | 2269 |
container_title | Bioorganic & Medicinal Chemistry |
container_volume | 22 |
creator | Ferro, Stefania De Luca, Laura Lo Surdo, Giuseppa Morreale, Francesca Christ, Frauke Debyser, Zeger Gitto, Rosaria Chimirri, Alba |
description | Therapeutic treatment of AIDS is recently characterized by a crescent effort towards the identification of multiple ligands able to target different steps of HIV-1 life cycle. Taking into consideration our previously obtained SAR information and combining some important chemical structural features we report herein the synthesis of novel benzyl-indole derivatives as anti-HIV agents. Through this work we identified new dual target small molecules able to inhibit both IN-LEDGF/p75 interaction and the IN strand-transfer step considered as two crucial phases of viral life cycle. |
format | Article |
fullrecord | <record><control><sourceid>kuleuven</sourceid><recordid>TN_cdi_kuleuven_dspace_123456789_447796</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>123456789_447796</sourcerecordid><originalsourceid>FETCH-kuleuven_dspace_123456789_4477963</originalsourceid><addsrcrecordid>eNqNjLuOwjAQRV2wEs9_mI5iZckhIYlLhEBsv9o2GswgDJZt2QPL5xMQH0BzT3GO7kCMlK5bqVpdD8U457NSalHpYiTSCjz9QwxMni06wBhTQHMCDrB3wVxg9_MnC0gUnTXINni4WYS-YrJevgnWMyU0L4_-AJlTD_ncfKTU-5Pd26eeiq8jukyzNydivt38rnfycnV0vZHvDjmioa5YlNWyblrdVVXT6LqciO_Pyo7vXH7--wA8kFoT</addsrcrecordid><sourcetype>Institutional Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>A new potential approach to block HIV-1 replication via protein-protein interaction and strand-transfer inhibition</title><source>Lirias (KU Leuven Association)</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Ferro, Stefania ; De Luca, Laura ; Lo Surdo, Giuseppa ; Morreale, Francesca ; Christ, Frauke ; Debyser, Zeger ; Gitto, Rosaria ; Chimirri, Alba</creator><creatorcontrib>Ferro, Stefania ; De Luca, Laura ; Lo Surdo, Giuseppa ; Morreale, Francesca ; Christ, Frauke ; Debyser, Zeger ; Gitto, Rosaria ; Chimirri, Alba</creatorcontrib><description>Therapeutic treatment of AIDS is recently characterized by a crescent effort towards the identification of multiple ligands able to target different steps of HIV-1 life cycle. Taking into consideration our previously obtained SAR information and combining some important chemical structural features we report herein the synthesis of novel benzyl-indole derivatives as anti-HIV agents. Through this work we identified new dual target small molecules able to inhibit both IN-LEDGF/p75 interaction and the IN strand-transfer step considered as two crucial phases of viral life cycle.</description><identifier>ISSN: 0968-0896</identifier><language>eng</language><publisher>Pergamon</publisher><ispartof>Bioorganic & Medicinal Chemistry, 2014-02, Vol.22 (7), p.2269-2279</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,315,780,784,27860</link.rule.ids></links><search><creatorcontrib>Ferro, Stefania</creatorcontrib><creatorcontrib>De Luca, Laura</creatorcontrib><creatorcontrib>Lo Surdo, Giuseppa</creatorcontrib><creatorcontrib>Morreale, Francesca</creatorcontrib><creatorcontrib>Christ, Frauke</creatorcontrib><creatorcontrib>Debyser, Zeger</creatorcontrib><creatorcontrib>Gitto, Rosaria</creatorcontrib><creatorcontrib>Chimirri, Alba</creatorcontrib><title>A new potential approach to block HIV-1 replication via protein-protein interaction and strand-transfer inhibition</title><title>Bioorganic & Medicinal Chemistry</title><description>Therapeutic treatment of AIDS is recently characterized by a crescent effort towards the identification of multiple ligands able to target different steps of HIV-1 life cycle. Taking into consideration our previously obtained SAR information and combining some important chemical structural features we report herein the synthesis of novel benzyl-indole derivatives as anti-HIV agents. Through this work we identified new dual target small molecules able to inhibit both IN-LEDGF/p75 interaction and the IN strand-transfer step considered as two crucial phases of viral life cycle.</description><issn>0968-0896</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>FZOIL</sourceid><recordid>eNqNjLuOwjAQRV2wEs9_mI5iZckhIYlLhEBsv9o2GswgDJZt2QPL5xMQH0BzT3GO7kCMlK5bqVpdD8U457NSalHpYiTSCjz9QwxMni06wBhTQHMCDrB3wVxg9_MnC0gUnTXINni4WYS-YrJevgnWMyU0L4_-AJlTD_ncfKTU-5Pd26eeiq8jukyzNydivt38rnfycnV0vZHvDjmioa5YlNWyblrdVVXT6LqciO_Pyo7vXH7--wA8kFoT</recordid><startdate>201402</startdate><enddate>201402</enddate><creator>Ferro, Stefania</creator><creator>De Luca, Laura</creator><creator>Lo Surdo, Giuseppa</creator><creator>Morreale, Francesca</creator><creator>Christ, Frauke</creator><creator>Debyser, Zeger</creator><creator>Gitto, Rosaria</creator><creator>Chimirri, Alba</creator><general>Pergamon</general><scope>FZOIL</scope></search><sort><creationdate>201402</creationdate><title>A new potential approach to block HIV-1 replication via protein-protein interaction and strand-transfer inhibition</title><author>Ferro, Stefania ; De Luca, Laura ; Lo Surdo, Giuseppa ; Morreale, Francesca ; Christ, Frauke ; Debyser, Zeger ; Gitto, Rosaria ; Chimirri, Alba</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kuleuven_dspace_123456789_4477963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ferro, Stefania</creatorcontrib><creatorcontrib>De Luca, Laura</creatorcontrib><creatorcontrib>Lo Surdo, Giuseppa</creatorcontrib><creatorcontrib>Morreale, Francesca</creatorcontrib><creatorcontrib>Christ, Frauke</creatorcontrib><creatorcontrib>Debyser, Zeger</creatorcontrib><creatorcontrib>Gitto, Rosaria</creatorcontrib><creatorcontrib>Chimirri, Alba</creatorcontrib><collection>Lirias (KU Leuven Association)</collection><jtitle>Bioorganic & Medicinal Chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ferro, Stefania</au><au>De Luca, Laura</au><au>Lo Surdo, Giuseppa</au><au>Morreale, Francesca</au><au>Christ, Frauke</au><au>Debyser, Zeger</au><au>Gitto, Rosaria</au><au>Chimirri, Alba</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A new potential approach to block HIV-1 replication via protein-protein interaction and strand-transfer inhibition</atitle><jtitle>Bioorganic & Medicinal Chemistry</jtitle><date>2014-02</date><risdate>2014</risdate><volume>22</volume><issue>7</issue><spage>2269</spage><epage>2279</epage><pages>2269-2279</pages><issn>0968-0896</issn><abstract>Therapeutic treatment of AIDS is recently characterized by a crescent effort towards the identification of multiple ligands able to target different steps of HIV-1 life cycle. Taking into consideration our previously obtained SAR information and combining some important chemical structural features we report herein the synthesis of novel benzyl-indole derivatives as anti-HIV agents. Through this work we identified new dual target small molecules able to inhibit both IN-LEDGF/p75 interaction and the IN strand-transfer step considered as two crucial phases of viral life cycle.</abstract><pub>Pergamon</pub><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0968-0896 |
ispartof | Bioorganic & Medicinal Chemistry, 2014-02, Vol.22 (7), p.2269-2279 |
issn | 0968-0896 |
language | eng |
recordid | cdi_kuleuven_dspace_123456789_447796 |
source | Lirias (KU Leuven Association); Elsevier ScienceDirect Journals Complete |
title | A new potential approach to block HIV-1 replication via protein-protein interaction and strand-transfer inhibition |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-24T11%3A50%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-kuleuven&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20new%20potential%20approach%20to%20block%20HIV-1%20replication%20via%20protein-protein%20interaction%20and%20strand-transfer%20inhibition&rft.jtitle=Bioorganic%20&%20Medicinal%20Chemistry&rft.au=Ferro,%20Stefania&rft.date=2014-02&rft.volume=22&rft.issue=7&rft.spage=2269&rft.epage=2279&rft.pages=2269-2279&rft.issn=0968-0896&rft_id=info:doi/&rft_dat=%3Ckuleuven%3E123456789_447796%3C/kuleuven%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |