Can we accelerate medicinal chemistry by augmenting the chemist with Big Data and artificial intelligence?

被引:33
作者
Griffen, Edward J. [1 ]
Dossetter, Alexander G. [1 ]
Leach, Andrew G. [2 ]
Montague, Shane [1 ]
机构
[1] MedChem Ltd, Biohub, Alderley Pk, Macclesfield SK10 4TG, Cheshire, England
[2] Liverpool John Moores Univ, Sch Pharm & Biomol Sci, Byrom St, Liverpool L3 3AF, Merseyside, England
关键词
MATCHED MOLECULAR PAIRS; QUANTITATIVE STRUCTURE-ACTIVITY; DEVELOPMENT PRODUCTIVITY; DESIGN; OPTIMIZATION; SOLUBILITY; IMPACT; METABOLISM; GENERATION; PREDICTION;
D O I
10.1016/j.drudis.2018.03.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
It is both the best of times and the worst of times to be a medicinal chemist. Massive amounts of data combined with machine-learning and/or artificial intelligence (AI) tools to analyze it can increase our capabilities. However, drug discovery faces severe economic pressure and a high level of societal need set against challenging targets. Here, we show how improving medicinal chemistry by better curating and exchanging knowledge can contribute to improving drug hunting in all disease areas. Although securing intellectual property (IP) is a critical task for medicinal chemists, it impedes the sharing of generic medicinal chemistry knowledge. Recent developments enable the sharing of knowledge both within and between organizations while securing IP. We also explore the effects of the structure of the corporate ecosystem within drug discovery on knowledge sharing.
引用
收藏
页码:1373 / 1384
页数:12
相关论文
共 81 条
[1]   Where will we get the next generation of medicinal chemists? [J].
Allen, Dave .
DRUG DISCOVERY TODAY, 2016, 21 (05) :704-706
[2]   Small-Molecule Inhibitors of Protein-Protein Interactions: Progressing toward the Reality [J].
Arkin, Michelle R. ;
Tang, Yinyan ;
Wells, James A. .
CHEMISTRY & BIOLOGY, 2014, 21 (09) :1102-1114
[3]   New Substructure Filters for Removal of Pan Assay Interference Compounds (PAINS) from Screening Libraries and for Their Exclusion in Bioassays [J].
Baell, Jonathan B. ;
Holloway, Georgina A. .
JOURNAL OF MEDICINAL CHEMISTRY, 2010, 53 (07) :2719-2740
[4]   A Survey of the Role of Noncovalent Sulfur Interactions in Drug Design [J].
Beno, Brett R. ;
Yeung, Kap-Sun ;
Bartberger, Michael D. ;
Pennington, Lewis D. ;
Meanwell, Nicholas A. .
JOURNAL OF MEDICINAL CHEMISTRY, 2015, 58 (11) :4383-4438
[5]   Automated design of ligands to polypharmacological profiles [J].
Besnard, Jeremy ;
Ruda, Gian Filippo ;
Setola, Vincent ;
Abecassis, Keren ;
Rodriguiz, Ramona M. ;
Huang, Xi-Ping ;
Norval, Suzanne ;
Sassano, Maria F. ;
Shin, Antony I. ;
Webster, Lauren A. ;
Simeons, Frederick R. C. ;
Stojanovski, Laste ;
Prat, Annik ;
Seidah, Nabil G. ;
Constam, Daniel B. ;
Bickerton, G. Richard ;
Read, Kevin D. ;
Wetsel, William C. ;
Gilbert, Ian H. ;
Roth, Bryan L. ;
Hopkins, Andrew L. .
NATURE, 2012, 492 (7428) :215-+
[6]   Rationally Designing Safer Anilines: The Challenging Case of 4-Aminobiphenyls [J].
Birch, Alan M. ;
Groombridge, Sam ;
Law, Robert ;
Leach, Andrew G. ;
Mee, Christine D. ;
Schramm, Carolin .
JOURNAL OF MEDICINAL CHEMISTRY, 2012, 55 (08) :3923-3933
[7]  
BRIMBLECOMBE RW, 1978, GASTROENTEROLOGY, V74, P339
[8]  
Brown D. G., 2015, J MED CHEM, V59, P443
[9]  
Brynjolfsson E, 2017, HARV BUS REV
[10]  
Castelvecchi D, 2016, NATURE, V538, P21, DOI [10.1038/nature.2016.20491, 10.1038/538020a]