Non-specificity of drug-Target interactions - Consequences for drug discovery

Gerald Maggiora, Vijay Gokhale

Research output: Chapter in Book/Report/Conference proceedingChapter

2 Scopus citations

Abstract

Dealing with the complexity of the human biosystem in drug discovery is a daunting task. At best we have an imperfect picture of its underlying physiology and pharmacology, which raises the question of how to identify potential drug compounds from the vast sea of xenobiotics that populate chemical space. The dominant approach is still based on the single-Target paradigm, which has a number of inherent problems not the least of which is the difficulty of altering disease phenotypes by intervening at single targets embedded within complex, interconnected biological pathways. While newer multi-Target approaches address some of the problems, they are not entirely without problems of their own. Superimposed on all of these difficulties is a surprising lack of compound and target specificity that the growing amount of data clearly shows is a more pervasive problem than has generally been assumed. And although sophisticated phenotypic screening methods are being developed in an effort to deal with some of these issues, many remain refractory.

Original languageEnglish (US)
Title of host publicationFrontiers in Molecular Design and Chemical Information Science - Herman Skolnik Award Symposium 2015: Jurgen Bajorath
PublisherAmerican Chemical Society
Pages91-142
Number of pages52
Volume1222
ISBN (Electronic)9780841231412
Publication statusPublished - 2016

Publication series

NameACS Symposium Series
Volume1222
ISSN (Print)00976156
ISSN (Electronic)19475918

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ASJC Scopus subject areas

  • Chemistry(all)
  • Chemical Engineering(all)

Cite this

Maggiora, G., & Gokhale, V. (2016). Non-specificity of drug-Target interactions - Consequences for drug discovery. In Frontiers in Molecular Design and Chemical Information Science - Herman Skolnik Award Symposium 2015: Jurgen Bajorath (Vol. 1222, pp. 91-142). (ACS Symposium Series; Vol. 1222). American Chemical Society.