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Finding Promiscuous Old Drugs for New Uses
ABSTRACT From research published in the last six years we have identified 34 studies that have screened libraries of FDA-approved drugs against various whole cell or target assays. These studies have each identified one or more compounds with a suggested new bioactivity that had not been described p...
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Published in: | Pharmaceutical research 2011-08, Vol.28 (8), p.1785-1791 |
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container_title | Pharmaceutical research |
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creator | Ekins, Sean Williams, Antony J. |
description | ABSTRACT
From research published in the last six years we have identified 34 studies that have screened libraries of FDA-approved drugs against various whole cell or target assays. These studies have each identified one or more compounds with a suggested new bioactivity that had not been described previously. We now show that 13 of these drugs were active against more than one additional disease, thereby suggesting a degree of promiscuity. We also show that following compilation of all the studies, 109 molecules were identified by screening
in vitro.
These molecules appear to be statistically more hydrophobic with a higher molecular weight and AlogP than orphan-designated products with at least one marketing approval for a common disease indication or one marketing approval for a rare disease from the FDA’s rare disease research database. Capturing these
in vitro
data on old drugs for new uses will be important for potential reuse and analysis by others to repurpose or reposition these or other existing drugs. We have created databases which can be searched by the public and envisage that these can be updated as more studies are published. |
doi_str_mv | 10.1007/s11095-011-0486-6 |
format | article |
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From research published in the last six years we have identified 34 studies that have screened libraries of FDA-approved drugs against various whole cell or target assays. These studies have each identified one or more compounds with a suggested new bioactivity that had not been described previously. We now show that 13 of these drugs were active against more than one additional disease, thereby suggesting a degree of promiscuity. We also show that following compilation of all the studies, 109 molecules were identified by screening
in vitro.
These molecules appear to be statistically more hydrophobic with a higher molecular weight and AlogP than orphan-designated products with at least one marketing approval for a common disease indication or one marketing approval for a rare disease from the FDA’s rare disease research database. Capturing these
in vitro
data on old drugs for new uses will be important for potential reuse and analysis by others to repurpose or reposition these or other existing drugs. We have created databases which can be searched by the public and envisage that these can be updated as more studies are published.</description><identifier>ISSN: 0724-8741</identifier><identifier>EISSN: 1573-904X</identifier><identifier>DOI: 10.1007/s11095-011-0486-6</identifier><identifier>PMID: 21607776</identifier><identifier>CODEN: PHREEB</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Biochemistry ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedical Engineering and Bioengineering ; Biomedicine ; Data processing ; Databases, Factual ; Drug Discovery ; Drug Industry ; Drug Repositioning ; Drugs ; General pharmacology ; Hydrophobicity ; Medical Law ; Medical sciences ; Molecular biology ; Molecular weight ; Perspectives ; Pharmaceutical Preparations ; Pharmaceutical sciences ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Pharmacology/Toxicology ; Pharmacy ; Prescription drugs ; United States ; United States Food and Drug Administration</subject><ispartof>Pharmaceutical research, 2011-08, Vol.28 (8), p.1785-1791</ispartof><rights>Springer Science+Business Media, LLC 2011</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c476t-3cce60d0e8e400ccbc202c8b586a54f33ec56decf8d14144c5704e033f1272da3</citedby><cites>FETCH-LOGICAL-c476t-3cce60d0e8e400ccbc202c8b586a54f33ec56decf8d14144c5704e033f1272da3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24476037$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21607776$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ekins, Sean</creatorcontrib><creatorcontrib>Williams, Antony J.</creatorcontrib><title>Finding Promiscuous Old Drugs for New Uses</title><title>Pharmaceutical research</title><addtitle>Pharm Res</addtitle><addtitle>Pharm Res</addtitle><description>ABSTRACT
From research published in the last six years we have identified 34 studies that have screened libraries of FDA-approved drugs against various whole cell or target assays. These studies have each identified one or more compounds with a suggested new bioactivity that had not been described previously. We now show that 13 of these drugs were active against more than one additional disease, thereby suggesting a degree of promiscuity. We also show that following compilation of all the studies, 109 molecules were identified by screening
in vitro.
These molecules appear to be statistically more hydrophobic with a higher molecular weight and AlogP than orphan-designated products with at least one marketing approval for a common disease indication or one marketing approval for a rare disease from the FDA’s rare disease research database. Capturing these
in vitro
data on old drugs for new uses will be important for potential reuse and analysis by others to repurpose or reposition these or other existing drugs. We have created databases which can be searched by the public and envisage that these can be updated as more studies are published.</description><subject>Biochemistry</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedical Engineering and Bioengineering</subject><subject>Biomedicine</subject><subject>Data processing</subject><subject>Databases, Factual</subject><subject>Drug Discovery</subject><subject>Drug Industry</subject><subject>Drug Repositioning</subject><subject>Drugs</subject><subject>General pharmacology</subject><subject>Hydrophobicity</subject><subject>Medical Law</subject><subject>Medical sciences</subject><subject>Molecular biology</subject><subject>Molecular weight</subject><subject>Perspectives</subject><subject>Pharmaceutical Preparations</subject><subject>Pharmaceutical sciences</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacy</subject><subject>Prescription drugs</subject><subject>United States</subject><subject>United States Food and Drug Administration</subject><issn>0724-8741</issn><issn>1573-904X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp9kE1Lw0AQhhdRbK3-AC8SBFGE6Mx-5yjVqlCsBwveQrrZlJQ00d0G8d-7JdWCoKc57DPvvPsQcoxwhQDq2iNCImJAjIFrGcsd0kehWJwAf90lfVCUx1px7JED7xcAoDHh-6RHUYJSSvbJ5ais87KeR8-uWZbetE3ro0mVR7eunfuoaFz0ZD-iqbf-kOwVWeXt0WYOyHR09zJ8iMeT-8fhzTg2XMlVzIyxEnKw2nIAY2aGAjV6JrTMBC8Ys0bI3JpC58iRcyMUcAuMFUgVzTM2IOdd7ptr3lvrV-m6mK2qrLahXaqVUKg10kBe_EsiUCokCkwCevoLXTStq8M_1nkgZFATIOwg4xrvnS3SN1cuM_cZktK18bQzngbj6dp4KsPOySa4nS1t_rPxrTgAZxsg8yarCpfVpvRbjgdrwFTgaMf58FTPrds2_Pv6FzBYlUk</recordid><startdate>20110801</startdate><enddate>20110801</enddate><creator>Ekins, Sean</creator><creator>Williams, Antony J.</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</scope><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>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20110801</creationdate><title>Finding Promiscuous Old Drugs for New Uses</title><author>Ekins, Sean ; Williams, Antony J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c476t-3cce60d0e8e400ccbc202c8b586a54f33ec56decf8d14144c5704e033f1272da3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Biochemistry</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedical Engineering and Bioengineering</topic><topic>Biomedicine</topic><topic>Data processing</topic><topic>Databases, Factual</topic><topic>Drug Discovery</topic><topic>Drug Industry</topic><topic>Drug Repositioning</topic><topic>Drugs</topic><topic>General pharmacology</topic><topic>Hydrophobicity</topic><topic>Medical Law</topic><topic>Medical sciences</topic><topic>Molecular biology</topic><topic>Molecular weight</topic><topic>Perspectives</topic><topic>Pharmaceutical Preparations</topic><topic>Pharmaceutical sciences</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Pharmacology/Toxicology</topic><topic>Pharmacy</topic><topic>Prescription drugs</topic><topic>United States</topic><topic>United States Food and Drug Administration</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ekins, Sean</creatorcontrib><creatorcontrib>Williams, Antony J.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Pharmaceutical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ekins, Sean</au><au>Williams, Antony J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Finding Promiscuous Old Drugs for New Uses</atitle><jtitle>Pharmaceutical research</jtitle><stitle>Pharm Res</stitle><addtitle>Pharm Res</addtitle><date>2011-08-01</date><risdate>2011</risdate><volume>28</volume><issue>8</issue><spage>1785</spage><epage>1791</epage><pages>1785-1791</pages><issn>0724-8741</issn><eissn>1573-904X</eissn><coden>PHREEB</coden><abstract>ABSTRACT
From research published in the last six years we have identified 34 studies that have screened libraries of FDA-approved drugs against various whole cell or target assays. These studies have each identified one or more compounds with a suggested new bioactivity that had not been described previously. We now show that 13 of these drugs were active against more than one additional disease, thereby suggesting a degree of promiscuity. We also show that following compilation of all the studies, 109 molecules were identified by screening
in vitro.
These molecules appear to be statistically more hydrophobic with a higher molecular weight and AlogP than orphan-designated products with at least one marketing approval for a common disease indication or one marketing approval for a rare disease from the FDA’s rare disease research database. Capturing these
in vitro
data on old drugs for new uses will be important for potential reuse and analysis by others to repurpose or reposition these or other existing drugs. We have created databases which can be searched by the public and envisage that these can be updated as more studies are published.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>21607776</pmid><doi>10.1007/s11095-011-0486-6</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biochemistry Biological and medical sciences Biomedical and Life Sciences Biomedical Engineering and Bioengineering Biomedicine Data processing Databases, Factual Drug Discovery Drug Industry Drug Repositioning Drugs General pharmacology Hydrophobicity Medical Law Medical sciences Molecular biology Molecular weight Perspectives Pharmaceutical Preparations Pharmaceutical sciences Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Pharmacology/Toxicology Pharmacy Prescription drugs United States United States Food and Drug Administration |
title | Finding Promiscuous Old Drugs for New Uses |
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