Literature DB >> 20601095

Drug profiling: knowing where it hits.

Alejandro Merino1, Agnieszka K Bronowska, David B Jackson, Dolores J Cahill.   

Abstract

Off-target hits of drugs can lead to serious adverse effects or, conversely, to unforeseen alternative medical utility. Selectivity profiling against large panels of potential targets is essential for the drug discovery process to minimize attrition and maximize therapeutic utility. Lately, it has become apparent that drug promiscuity (polypharmacology) goes well beyond target families; therefore, lowering the profiling costs and expanding the coverage of targets is an industry-wide challenge to improve predictions. Here, we review current and promising drug profiling alternatives and commercial solutions in these exciting emerging fields.
Copyright © 2010 Elsevier Ltd. All rights reserved.

Mesh:

Year:  2010        PMID: 20601095     DOI: 10.1016/j.drudis.2010.06.006

Source DB:  PubMed          Journal:  Drug Discov Today        ISSN: 1359-6446            Impact factor:   7.851


  21 in total

Review 1.  The new toxicology of sophisticated materials: nanotoxicology and beyond.

Authors:  Andrew D Maynard; David B Warheit; Martin A Philbert
Journal:  Toxicol Sci       Date:  2010-12-22       Impact factor: 4.849

2.  A quantum mechanics-based halogen bonding scoring function for protein-ligand interactions.

Authors:  Zhuo Yang; Yingtao Liu; Zhaoqiang Chen; Zhijian Xu; Jiye Shi; Kaixian Chen; Weiliang Zhu
Journal:  J Mol Model       Date:  2015-05-10       Impact factor: 1.810

3.  How promiscuous are pharmaceutically relevant compounds? A data-driven assessment.

Authors:  Ye Hu; Jürgen Bajorath
Journal:  AAPS J       Date:  2012-10-23       Impact factor: 4.009

Review 4.  Shifting from the single to the multitarget paradigm in drug discovery.

Authors:  José L Medina-Franco; Marc A Giulianotti; Gregory S Welmaker; Richard A Houghten
Journal:  Drug Discov Today       Date:  2013-01-20       Impact factor: 7.851

5.  What is the likelihood of an active compound to be promiscuous? Systematic assessment of compound promiscuity on the basis of PubChem confirmatory bioassay data.

Authors:  Ye Hu; Jürgen Bajorath
Journal:  AAPS J       Date:  2013-04-19       Impact factor: 4.009

6.  A new fingerprint to predict nonribosomal peptides activity.

Authors:  Ammar Abdo; Ségolène Caboche; Valérie Leclère; Philippe Jacques; Maude Pupin
Journal:  J Comput Aided Mol Des       Date:  2012-09-29       Impact factor: 3.686

7.  Deducing the mechanism of action of compounds identified in phenotypic screens by integrating their multiparametric profiles with a reference genetic screen.

Authors:  Varadharajan Sundaramurthy; Rico Barsacchi; Mikhail Chernykh; Martin Stöter; Nadine Tomschke; Marc Bickle; Yannis Kalaidzidis; Marino Zerial
Journal:  Nat Protoc       Date:  2014-01-30       Impact factor: 13.491

8.  Efficient modeling and active learning discovery of biological responses.

Authors:  Armaghan W Naik; Joshua D Kangas; Christopher J Langmead; Robert F Murphy
Journal:  PLoS One       Date:  2013-12-17       Impact factor: 3.240

9.  Molecular modeling and structure-based drug discovery approach reveals protein kinases as off-targets for novel anticancer drug RH1.

Authors:  Pramodkumar P Gupta; Virupaksha A Bastikar; Dalius Kuciauskas; Shanker Lal Kothari; Jonas Cicenas; Mindaugas Valius
Journal:  Med Oncol       Date:  2017-09-06       Impact factor: 3.064

10.  Effects of the nicotinic agonist varenicline on the performance of tasks of cognition in aged and middle-aged rhesus and pigtail monkeys.

Authors:  Alvin V Terry; Marc Plagenhoef; Patrick M Callahan
Journal:  Psychopharmacology (Berl)       Date:  2015-11-27       Impact factor: 4.530

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