Literature DB >> 17703586

High-throughput lead finding and optimisation for GPCR targets.

A Sewing1, D Cawkill.   

Abstract

Driven by past successes and the detailed knowledge of signalling cascades and physiological processes, G-protein-coupled receptors are taking a prominent place in the portfolios of many pharmaceutical companies. To successfully address this target class, scientists need not only a good understanding of the specific receptor under investigation, but also the right tools from assay technology, reagent production to a hit-to-lead process that acknowledges the importance of parameters beyond potency and embraces the gain in knowledge of the last decade. This manuscripts attempts to summarise some of the changes and progress made across the pharmaceutical industry to design an efficient and effective strategy for finding and optimising small molecules modulating the activity of GPCRs.

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Year:  2006        PMID: 17703586     DOI: 10.1007/2789_2006_012

Source DB:  PubMed          Journal:  Ernst Schering Found Symp Proc


  2 in total

1.  Improvement in the handling of drug-drug interactions.

Authors:  Uwe Fuhr
Journal:  Eur J Clin Pharmacol       Date:  2008-01-03       Impact factor: 2.953

2.  Comparative docking study of anibamine as the first natural product CCR5 antagonist in CCR5 homology models.

Authors:  Guo Li; Kendra M Haney; Glen E Kellogg; Yan Zhang
Journal:  J Chem Inf Model       Date:  2009-01       Impact factor: 4.956

  2 in total

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