Literature DB >> 15742383

The target discovery process.

Ursula Egner1, Jörn Krätzschmar, Bertolt Kreft, Hans-Dieter Pohlenz, Martin Schneider.   

Abstract

In order to minimise attrition rates in drug development projects, a target discovery process is implemented to select and characterise the most suitable candidate kinase targets, before lead identification and lead optimisation are embarked upon. The process consists of 1) target selection, 2) target assessment, and 3) target validation. This rational approach to target discovery, as a prerequisite for lead discovery, ensures that new therapeutic targets fulfil a set of general criteria, as well as indication-specific, descriptive and functional ones. The approach should ultimately maximise the likelihood of achieving target-selective inhibition by small-molecule inhibitors with minimal in vivo side effects and a therapeutic effect based on a sound biological hypothesis.

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Year:  2005        PMID: 15742383     DOI: 10.1002/cbic.200400158

Source DB:  PubMed          Journal:  Chembiochem        ISSN: 1439-4227            Impact factor:   3.164


  9 in total

1.  Quantitative systems-level determinants of human genes targeted by successful drugs.

Authors:  Lixia Yao; Andrey Rzhetsky
Journal:  Genome Res       Date:  2007-12-14       Impact factor: 9.043

2.  A systematic study of the features critical for designing a high avidity multivalent aptamer.

Authors:  Xiaoching Zhao; John T Lis; Hua Shi
Journal:  Nucleic Acid Ther       Date:  2013-04-03       Impact factor: 5.486

Review 3.  Drug target identification in protozoan parasites.

Authors:  Joachim Müller; Andrew Hemphill
Journal:  Expert Opin Drug Discov       Date:  2016-06-16       Impact factor: 6.098

4.  Halogen bonding for the design of inhibitors by targeting the S1 pocket of serine proteases.

Authors:  Longguang Jiang; Xu Zhang; Yang Zhou; Yayu Chen; Zhipu Luo; Jinyu Li; Cai Yuan; Mingdong Huang
Journal:  RSC Adv       Date:  2018-08-06       Impact factor: 4.036

Review 5.  Halogen bonding (X-bonding): a biological perspective.

Authors:  Matthew R Scholfield; Crystal M Vander Zanden; Megan Carter; P Shing Ho
Journal:  Protein Sci       Date:  2012-12-29       Impact factor: 6.725

6.  5-alpha-reductase type I (SRD5A1) is up-regulated in non-small cell lung cancer but does not impact proliferation, cell cycle distribution or apoptosis.

Authors:  Friedrich G Kapp; Anette Sommer; Thomas Kiefer; Gottfried Dölken; Bernard Haendler
Journal:  Cancer Cell Int       Date:  2012-01-18       Impact factor: 5.722

7.  Drug discovery for primary amebic meningoencephalitis: from screen to identification of leads.

Authors:  Anjan Debnath
Journal:  Expert Rev Anti Infect Ther       Date:  2021-03-11       Impact factor: 5.854

8.  Advances in antisense oligonucleotide development for target identification, validation, and as novel therapeutics.

Authors:  Moizza Mansoor; Alirio J Melendez
Journal:  Gene Regul Syst Bio       Date:  2008-09-22

9.  Antiproliferative effects of DNA methyltransferase 3B depletion are not associated with DNA demethylation.

Authors:  Sabine Hagemann; Dirk Kuck; Carlo Stresemann; Florian Prinz; Bodo Brueckner; Cora Mund; Dominik Mumberg; Anette Sommer
Journal:  PLoS One       Date:  2012-05-01       Impact factor: 3.240

  9 in total

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