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
[41]   From Fragment Screening to Potent Binders: Strategies for Fragment-to-Lead Evolution [J].
Eitner, Krystian ;
Koch, Uwe .
MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2009, 9 (08) :956-961
[42]   From carbohydrate leads to glycomimetic drugs [J].
Ernst, Beat ;
Magnani, John L. .
NATURE REVIEWS DRUG DISCOVERY, 2009, 8 (08) :661-677
[43]   Natural product-likeness score and its application for prioritization of compound libraries [J].
Ertl, Peter ;
Roggo, Silvio ;
Schuffenhauer, Ansgar .
JOURNAL OF CHEMICAL INFORMATION AND MODELING, 2008, 48 (01) :68-74
[44]   Property distributions: Differences between drugs, natural products, and molecules from combinatorial chemistry [J].
Feher, M ;
Schmidt, JM .
JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 2003, 43 (01) :218-227
[45]   A high-throughput screen for aggregation-based inhibition in a large compound library [J].
Feng, Brian Y. ;
Simeonov, Anton ;
Jadhav, Ajit ;
Babaoglu, Kerim ;
Inglese, James ;
Shoichet, Brian K. ;
Austin, Christopher P. .
JOURNAL OF MEDICINAL CHEMISTRY, 2007, 50 (10) :2385-2390
[46]   Drug-like inhibitors of protein-protein interactions: A structural examination of effective protein mimicry [J].
Fry, D. C. .
CURRENT PROTEIN & PEPTIDE SCIENCE, 2008, 9 (03) :240-247
[47]   Protein-protein interactions as targets for small molecule drug discovery [J].
Fry, David C. .
BIOPOLYMERS, 2006, 84 (06) :535-552
[48]   Predicting druggable binding sites at the protein-protein interface [J].
Fuller, Jonathan C. ;
Burgoyne, Nicholas J. ;
Jackson, Richard M. .
DRUG DISCOVERY TODAY, 2009, 14 (3-4) :155-161
[49]   The discovery of antibacterial agents using diversity-oriented synthesis [J].
Galloway, Warren R. J. D. ;
Bender, Andreas ;
Welch, Martin ;
Spring, David R. .
CHEMICAL COMMUNICATIONS, 2009, (18) :2446-2462
[50]   The impact of natural products upon modern drug discovery [J].
Ganesan, A. .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2008, 12 (03) :306-317