Molecular diversity in drug design / edited by Philip M. Dean and Richard A. Lewis.

Includes bibliographical references and index.

Issues in molecular diversity and the role of ligand binding sites / James Smith, Philip M. Dean and Richard A. Lewis -- Molecular diversity in drug design : application to high-speed synthesis and high-throughput screening / Christopher G. Newton -- Background theory of molecular diversity / Valerie J. Gillet -- Absolute vs relative similarity and diversity / Jonathan S. Mason -- Diversity in very large libraries / Lutz Weber and Michael Almstetter -- Subset-selection methods for chemical databases / P. Willett -- Molecular diversity in site-focused libraries / Diana C. Roe -- Managing combinatorial chemistry information / Keith Davies and Catherine White -- Design of small libraries for lead exploration / Per M. Andersson [and others] -- The design of small- and medium-sized focused combinatorial libraries / Richard A. Lewis.

This book focuses on the theoretical problems associated with molecular diversity as it is being applied in the pharmaceutical industry. Therefore, this book deals with algorithms that are involved in understanding chemical space and selection of diverse sets of structures. The algorithms also deal with the problem of focused diversity where chemical libraries are being created within a structured physical volume. Diversity is necessarily connected to combinational chemistry, although this book is limited to the application of diversity methods to combinational chemistry and does not deal with synthetic methods. It is this focus on algorithms and strategies for exploiting molecular diversity that makes it different from books on combinational chemistry. The intended readership of the book falls into two categories: those actively engaged in applying molecular diversity in the chemical industry and those in academia who are developing strategies to embrace, understand and accept the many problems thrown up by this new research field of molecular diversity.

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