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Virtual Screening: An Alternative or Complement to High Throughput Screening? - Proceedings of the Workshop 'New Approaches in Drug Design and Discovery', special topic 'Virtual Screening', Schloss Rauischholzhausen, Germany, March 15-18, 1999 (Hardcover, Reprinted from perspectives in drug discovery and design, 20, 2001) Loot Price: R4,275
Discovery Miles 42 750
Virtual Screening: An Alternative or Complement to High Throughput Screening? - Proceedings of the Workshop 'New...

Virtual Screening: An Alternative or Complement to High Throughput Screening? - Proceedings of the Workshop 'New Approaches in Drug Design and Discovery', special topic 'Virtual Screening', Schloss Rauischholzhausen, Germany, March 15-18, 1999 (Hardcover, Reprinted from perspectives in drug discovery and design, 20, 2001)

Gerhard Klebe

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Loot Price R4,275 Discovery Miles 42 750 | Repayment Terms: R401 pm x 12*

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In the next couple of years the human genome will be fully sequenced. This will provide us with the sequence and overall function of all human genes as well as the complete genome for many micro-organisms. Subsequently it is hoped, by means of powerful bioinformatic tools, to determine the gene variants that contribute to various multifactorial diseases and genes that exist in certain infectious agents but not humans. As a consequence, this will allow us to define the most appropriate levels for drug intervention. It can be expected that the number of potential drug targets will increase, possibly by a factor of 10 or more. Nevertheless, sequencing the human genome or, for that matter, the genome of other species will only be the starting point for the understanding of their biological function. Structural genomics is a likely follow-up, combined with new techniques to validate the therapeutic relevance of such newly discovered targets. Accordingly, it can be expected that in the near future we will witness a substantial increase in novel putative targets for drugs. To address these new targets effectively, we require new approaches and innovative tools. At present, two alternative, yet complementary, techniques are employed: experimental high-throughput screening (HTS) of large compound libraries, increasingly provided by combinatorial chemistry, and computational methods for virtual screening and de novo design. As kind of status report on the maturity of virtual screening as a technique in drug design, the first workshop on new approaches in drug design and discovery was held in March 1999, at Schloss Rauischholzhausen, near Marburg in Germany. More than 80 scientists gathered and discussed their experience with the different techniques. The speakers were invited to summarize their contributions together with their impressions on the present applicability of their approach. Several of the speakers followed this request which is summarized in this publication."

General

Imprint: Springer
Country of origin: Netherlands
Release date: November 2000
First published: 2002
Editors: Gerhard Klebe
Dimensions: 235 x 155 x 19mm (L x W x T)
Format: Hardcover
Pages: 295
Edition: Reprinted from perspectives in drug discovery and design, 20, 2001
ISBN-13: 978-0-7923-6633-1
Categories: Books > Medicine > Clinical & internal medicine > Medical diagnosis > General
Books > Medicine > Other branches of medicine > Pharmacology > General
Books > Professional & Technical > Industrial chemistry & manufacturing technologies > Industrial chemistry > Pharmaceutical technology
LSN: 0-7923-6633-6
Barcode: 9780792366331

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