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Novel Phenotypic Outcomes Identified for a Public Collection of Approved Drugs from a Publicly Accessible Panel of Assays.
Lee, Jonathan A; Shinn, Paul; Jaken, Susan; Oliver, Sarah; Willard, Francis S; Heidler, Steven; Peery, Robert B; Oler, Jennifer; Chu, Shaoyou; Southall, Noel; Dexheimer, Thomas S; Smallwood, Jeffrey; Huang, Ruili; Guha, Rajarshi; Jadhav, Ajit; Cox, Karen; Austin, Christopher P; Simeonov, Anton; Sittampalam, G Sitta; Husain, Saba; Franklin, Natalie; Wild, David J; Yang, Jeremy J; Sutherland, Jeffrey J; Thomas, Craig J.
Afiliação
  • Lee JA; Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, United States of America.
  • Shinn P; Division of Preclinical Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Jaken S; Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, United States of America.
  • Oliver S; Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, United States of America.
  • Willard FS; Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, United States of America.
  • Heidler S; Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, United States of America.
  • Peery RB; Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, United States of America.
  • Oler J; Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, United States of America.
  • Chu S; Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, United States of America.
  • Southall N; Division of Preclinical Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Dexheimer TS; Division of Preclinical Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Smallwood J; Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, United States of America.
  • Huang R; Division of Preclinical Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Guha R; Division of Preclinical Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Jadhav A; Division of Preclinical Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Cox K; Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, United States of America.
  • Austin CP; Division of Preclinical Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Simeonov A; Division of Preclinical Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Sittampalam GS; Division of Preclinical Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Husain S; Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, United States of America.
  • Franklin N; Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, United States of America.
  • Wild DJ; Indiana University School of Informatics and Computing, Bloomington, Indiana, United States of America.
  • Yang JJ; Indiana University School of Informatics and Computing, Bloomington, Indiana, United States of America.
  • Sutherland JJ; Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, United States of America.
  • Thomas CJ; Division of Preclinical Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland, United States of America.
PLoS One ; 10(7): e0130796, 2015.
Article em En | MEDLINE | ID: mdl-26177200
Phenotypic assays have a proven track record for generating leads that become first-in-class therapies. Whole cell assays that inform on a phenotype or mechanism also possess great potential in drug repositioning studies by illuminating new activities for the existing pharmacopeia. The National Center for Advancing Translational Sciences (NCATS) pharmaceutical collection (NPC) is the largest reported collection of approved small molecule therapeutics that is available for screening in a high-throughput setting. Via a wide-ranging collaborative effort, this library was analyzed in the Open Innovation Drug Discovery (OIDD) phenotypic assay modules publicly offered by Lilly. The results of these tests are publically available online at www.ncats.nih.gov/expertise/preclinical/pd2 and via the PubChem Database (https://pubchem.ncbi.nlm.nih.gov/) (AID 1117321). Phenotypic outcomes for numerous drugs were confirmed, including sulfonylureas as insulin secretagogues and the anti-angiogenesis actions of multikinase inhibitors sorafenib, axitinib and pazopanib. Several novel outcomes were also noted including the Wnt potentiating activities of rotenone and the antifolate class of drugs, and the anti-angiogenic activity of cetaben.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Reposicionamento de Medicamentos Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Reposicionamento de Medicamentos Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article