Enhancements of screening collections to address areas of unmet medical need: an industry perspective

被引:107
作者
Drewry, David H. [1 ]
Macarron, Ricardo [2 ]
机构
[1] GlaxoSmithKline, Mol Discovery Res, Res Triangle Pk, NC 27709 USA
[2] GlaxoSmithKline, Mol Discovery Res, Collegeville, PA 19426 USA
关键词
PROTEIN-PROTEIN INTERACTIONS; DIVERSITY-ORIENTED SYNTHESIS; ALPHA-HELIX MIMETICS; NATURAL-PRODUCT STRUCTURE; DRUG DISCOVERY; CHEMICAL SPACE; COMBINATORIAL LIBRARIES; MOLECULAR COMPLEXITY; COMPOUND COLLECTION; GUIDING PRINCIPLES;
D O I
10.1016/j.cbpa.2010.03.024
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The past 20 years have witnessed an impressive expansion of the 'drug space'; defined as the intersection of the Medicinal Chemistry space and the Biologically Active space relevant in the quest for new treatments for disease. Despite the success of known lead discovery tactics, areas of unmet medical need are often linked to challenging or novel targets and are poorly served by current screening collections. A successful strategy to fill the gaps is to diversify the approaches taken in the enhancement of screening collections. Possible strategies include investments through proven methods, exploring areas of chemical space previously neglected (e.g. hydrophilic compounds, natural product mimics), and applying tactics to the lead discovery process that are complementary to HTS (e.g. fragment based screening or multidisciplinary team efforts to tackle new target classes).
引用
收藏
页码:289 / 298
页数:10
相关论文
共 149 条
[1]   Genomic-scale prioritization of drug targets: the TDR Targets database [J].
Agueero, Fernan ;
Al-Lazikani, Bissan ;
Aslett, Martin ;
Berriman, Matthew ;
Buckner, Frederick S. ;
Campbell, Robert K. ;
Carmona, Santiago ;
Carruthers, Ian M. ;
Chan, A. W. Edith ;
Chen, Feng ;
Crowther, Gregory J. ;
Doyle, Maria A. ;
Hertz-Fowler, Christiane ;
Hopkins, Andrew L. ;
McAllister, Gregg ;
Nwaka, Solomon ;
Overington, John P. ;
Pain, Arnab ;
Paolini, Gala V. ;
Pieper, Ursula ;
Ralph, Stuart A. ;
Riechers, Aaron ;
Roos, David S. ;
Sali, Andrej ;
Shanmugam, Dhanasekaran ;
Suzuki, Takashi ;
Van Voorhis, Wesley C. ;
Verlinde, Christophe L. M. J. .
NATURE REVIEWS DRUG DISCOVERY, 2008, 7 (11) :900-907
[2]   Kinase-targeted libraries: The design and synthesis of novel, potent, and selective kinase inhibitors [J].
Akritopoulou-Zanze, Irini ;
Hajduk, Philip J. .
DRUG DISCOVERY TODAY, 2009, 14 (5-6) :291-297
[3]   An integrated approach to fragment-based lead generation: Philosophy, strategy and case studies from AstraZeneca's drug discovery programmes [J].
Albert, Jeffrey S. ;
Blomberg, Niklas ;
Breeze, Alexander L. ;
Brown, Alastair J. H. ;
Burrows, Jeremy N. ;
Edwards, Philip D. ;
Folmer, Rutger H. A. ;
Geschwindner, Stefan ;
Griffen, Ed J. ;
Kenny, Peter W. ;
Nowak, Thorsten ;
Olsson, Lise-Lotte ;
Sanganee, Hitesh ;
Shapiro, Adam B. .
CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2007, 7 (16) :1600-1629
[4]   Fragment-based drug discovery: What has it achieved so fair? [J].
Alex, Alexander A. ;
Flocco, Maria M. .
CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2007, 7 (16) :1544-1567
[5]   The road less traveled: modulating signal transduction enzymes by inhibiting their protein-protein interactions [J].
Arkin, Michelle R. ;
Whitty, Adrian .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2009, 13 (03) :284-290
[6]   Kinase-likeness and kinase-privileged fragments: Toward virtual polypharmacology [J].
Aronov, Alex M. ;
McClain, Brian ;
Moody, Cameron Stuver ;
Murcko, Mark A. .
JOURNAL OF MEDICINAL CHEMISTRY, 2008, 51 (05) :1214-1222
[7]   Charting biological and chemical space: PSSC and SCONP as guiding principles for the development of compound collections based on natural product scaffolds [J].
Arve, Lars ;
Voigt, Tobias ;
Waldmann, Herbert .
QSAR & COMBINATORIAL SCIENCE, 2006, 25 (5-6) :449-456
[8]   Investigation of the incidence of "undesirable" molecular moieties for high-throughput screening compound libraries in marketed drug compounds [J].
Axerio-Cilies, Peter ;
Castaneda, Ivan P. ;
Mirza, Amin ;
Reynisson, Johannes .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2009, 44 (03) :1128-1134
[9]   Properties and identification of human protein drug targets [J].
Bakheet, Tala M. ;
Doig, Andrew J. .
BIOINFORMATICS, 2009, 25 (04) :451-457
[10]   Design of compound libraries based on natural product scaffolds and protein structure similarity clustering (PSSC) [J].
Balamurugan, R ;
Dekker, FJ ;
Waldmann, H .
MOLECULAR BIOSYSTEMS, 2005, 1 (01) :36-45