Designing the molecular future

作者：Schneider Gi**ert^*

来源：Journal of Computer-Aided Molecular Design, 2012, 26(1): 115-120.

DOI：10.1007/s10822-011-9485-2

• Drug design
• Computational chemistry
• Fragment-based design
• De novo design

Approximately 25 years ago the first computer applications were conceived for the purpose of automated 'de novo' drug design, prominent pioneering tools being ALADDIN, CAVEAT, GENOA, and DYLOMMS. Many of these early concepts were enabled by innovative techniques for ligand-receptor interaction modeling like GRID, MCSS, DOCK, and CoMFA, which still provide the theoretical framework for several more recently developed molecular design algorithms. After a first wave of software tools and groundbreaking applications in the 1990s-expressly GROW, GrowMol, LEGEND, and LUDI representing some of the key players-we are currently witnessing a renewed strong interest in this field. Innovative ideas for both receptor and ligand-based drug design have recently been published. We here provide a personal perspective on the evolution of de novo design, highlighting some of the historic achievements as well as possible future developments of this exciting field of research, which combines multiple scientific disciplines and is, like few other areas in chemistry, subject to continuous enthusiastic discussion and compassionate dispute.

• 出版日期2012-1