Literature DB >> 16677847

Obtaining and screening compound collections: a user's guide and a call to chemists.

Paul J Hergenrother1.   

Abstract

Advances in genetics, proteomics and cell biology over the past 20 years have unearthed a multitude of potential macromolecular targets for the selective treatment of disease. The challenge remains to find appropriate small molecule ligands for these proteins (or nucleic acids), and to use these ligands to validate novel disease targets. The advent of low-cost instrumentation has made industrial-style high-throughput screening possible in academic settings. Unfortunately for many, access to large collections of compounds is still limited and limiting. This article is aimed at the user who has an interest in compound screening but does not have ready access to large collections of small molecules. High-throughput screening need not be the exclusive domain of institutions and centers with vast resources and NIH Roadmap-funded compound repositories. As it turns out, many of the most interesting compounds are probably within arm's reach, in our laboratory freezers and in those of our colleagues.

Mesh:

Year:  2006        PMID: 16677847     DOI: 10.1016/j.cbpa.2006.04.005

Source DB:  PubMed          Journal:  Curr Opin Chem Biol        ISSN: 1367-5931            Impact factor:   8.822


  15 in total

1.  A continuous fluorometric assay for the assessment of MazF ribonuclease activity.

Authors:  Nora R Wang; Paul J Hergenrother
Journal:  Anal Biochem       Date:  2007-07-26       Impact factor: 3.365

2.  Chemical genetics: reshaping biology through chemistry.

Authors:  Stefan Florian; Stefan Hümmer; Mario Catarinella; Thomas U Mayer
Journal:  HFSP J       Date:  2007-07-12

3.  A general method for discovering inhibitors of protein-DNA interactions using photonic crystal biosensors.

Authors:  Leo L Chan; Maria Pineda; James T Heeres; Paul J Hergenrother; Brian T Cunningham
Journal:  ACS Chem Biol       Date:  2008-07-18       Impact factor: 5.100

Review 4.  Mitigating risk in academic preclinical drug discovery.

Authors:  Jayme L Dahlin; James Inglese; Michael A Walters
Journal:  Nat Rev Drug Discov       Date:  2015-04       Impact factor: 84.694

5.  Expanding the scope of drug repurposing in pediatrics: the Children's Pharmacy Collaborative.

Authors:  Julie Blatt; Sherif Farag; Seth J Corey; Zafeira Sarrimanolis; Eugene Muratov; Denis Fourches; Alexander Tropsha; William P Janzen
Journal:  Drug Discov Today       Date:  2014-08-19       Impact factor: 7.851

6.  Photonic Crystal Surfaces as a General Purpose Platform for Label-Free and Fluorescent Assays.

Authors:  Brian T Cunningham
Journal:  JALA Charlottesv Va       Date:  2010-04-01

7.  Differential requirements of Hsp90 and DNA for the formation of estrogen receptor homodimers and heterodimers.

Authors:  Emily Powell; Yidan Wang; David J Shapiro; Wei Xu
Journal:  J Biol Chem       Date:  2010-03-30       Impact factor: 5.157

8.  The identification, analysis and structure-based development of novel inhibitors of 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase.

Authors:  Mi-Kyung Yun; Daniel Hoagland; Gyanendra Kumar; M Brett Waddell; Charles O Rock; Richard E Lee; Stephen W White
Journal:  Bioorg Med Chem       Date:  2014-02-25       Impact factor: 3.641

9.  A new small molecule inhibitor of estrogen receptor alpha binding to estrogen response elements blocks estrogen-dependent growth of cancer cells.

Authors:  Chengjian Mao; Nicole M Patterson; Milu T Cherian; Irene O Aninye; Chen Zhang; Jamie Bonéy Montoya; Jingwei Cheng; Karson S Putt; Paul J Hergenrother; Elizabeth M Wilson; Ann M Nardulli; Steven K Nordeen; David J Shapiro
Journal:  J Biol Chem       Date:  2008-03-12       Impact factor: 5.157

10.  Structural studies of pterin-based inhibitors of dihydropteroate synthase.

Authors:  Kirk E Hevener; Mi-Kyung Yun; Jianjun Qi; Iain D Kerr; Kerim Babaoglu; Julian G Hurdle; Kanya Balakrishna; Stephen W White; Richard E Lee
Journal:  J Med Chem       Date:  2010-01-14       Impact factor: 7.446

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