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The Chemical Basis of Pharmacology

[Image: see text] Molecular biology now dominates pharmacology so thoroughly that it is difficult to recall that only a generation ago the field was very different. To understand drug action today, we characterize the targets through which they act and new drug leads are discovered on the basis of t...

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Detalles Bibliográficos
Autores principales: Keiser, Michael J., Irwin, John J., Shoichet, Brian K.
Formato: Texto
Lenguaje:English
Publicado: American Chemical Society 2010
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2994275/
https://www.ncbi.nlm.nih.gov/pubmed/21058655
http://dx.doi.org/10.1021/bi101540g
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author Keiser, Michael J.
Irwin, John J.
Shoichet, Brian K.
author_facet Keiser, Michael J.
Irwin, John J.
Shoichet, Brian K.
author_sort Keiser, Michael J.
collection PubMed
description [Image: see text] Molecular biology now dominates pharmacology so thoroughly that it is difficult to recall that only a generation ago the field was very different. To understand drug action today, we characterize the targets through which they act and new drug leads are discovered on the basis of target structure and function. Until the mid-1980s the information often flowed in reverse: investigators began with organic molecules and sought targets, relating receptors not by sequence or structure but by their ligands. Recently, investigators have returned to this chemical view of biology, bringing to it systematic and quantitative methods of relating targets by their ligands. This has allowed the discovery of new targets for established drugs, suggested the bases for their side effects, and predicted the molecular targets underlying phenotypic screens. The bases for these new methods, some of their successes and liabilities, and new opportunities for their use are described.
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spelling pubmed-29942752010-11-30 The Chemical Basis of Pharmacology Keiser, Michael J. Irwin, John J. Shoichet, Brian K. Biochemistry [Image: see text] Molecular biology now dominates pharmacology so thoroughly that it is difficult to recall that only a generation ago the field was very different. To understand drug action today, we characterize the targets through which they act and new drug leads are discovered on the basis of target structure and function. Until the mid-1980s the information often flowed in reverse: investigators began with organic molecules and sought targets, relating receptors not by sequence or structure but by their ligands. Recently, investigators have returned to this chemical view of biology, bringing to it systematic and quantitative methods of relating targets by their ligands. This has allowed the discovery of new targets for established drugs, suggested the bases for their side effects, and predicted the molecular targets underlying phenotypic screens. The bases for these new methods, some of their successes and liabilities, and new opportunities for their use are described. American Chemical Society 2010-11-08 2010-12-07 /pmc/articles/PMC2994275/ /pubmed/21058655 http://dx.doi.org/10.1021/bi101540g Text en Copyright © 2010 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org.
spellingShingle Keiser, Michael J.
Irwin, John J.
Shoichet, Brian K.
The Chemical Basis of Pharmacology
title The Chemical Basis of Pharmacology
title_full The Chemical Basis of Pharmacology
title_fullStr The Chemical Basis of Pharmacology
title_full_unstemmed The Chemical Basis of Pharmacology
title_short The Chemical Basis of Pharmacology
title_sort chemical basis of pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2994275/
https://www.ncbi.nlm.nih.gov/pubmed/21058655
http://dx.doi.org/10.1021/bi101540g
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