Optimization in Drug Discovery

Name: Optimization in Drug Discovery
Brand: Humana Press Inc.
SKU: 9781617374999
Price: 61807 HUF
Availability: InStock

Szerző: Zhengyin Yan, Gary W. Caldwell

Nyelv:

Kötés: Puha kötésű

Kiadó: Humana Press Inc.

Elérhetőség: Beszállítói készleten alacsony példányszámban

Küldés 13-18 napon belül

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Although parallel synthesis combined with high-throughput screening has made it easier to generate h...

Információk a könyvről

Szerző

Zhengyin Yan, Gary W. Caldwell

Nyelv

Angol

Kötés

Könyv - Puha kötésű

Kiadva

2010

oldal

420

EAN

9781617374999

ISBN

1617374997

Enbook ID

01432119

Kiadó

Humana Press Inc.

Súly

637

Méretek

152 x 23 x 25

Teljes leírás

Although parallel synthesis combined with high-throughput screening has made it easier to generate highly potent drug candidates, many of these compounds never make the grade because they either prove to be unsafe or lack the necessary physicochemical and pharmacokinetic properties. In Optimization in Drug Discovery: In Vitro Methods, a panel of researchers and experts from leading universities and major pharmaceutical companies from all over the world provide proven solutions to this expensive problem with a collection of cutting-edge experimental protocols for early in vitro evaluation of new chemical entities (NCE). These readily reproducible assays measure such critical parameters as physicochemical properties, adsorption, plasma binding, metabolism, drug interactions, and toxicity. All protocols follow the successful Methods in Molecular Biology series format, each one offering step-by-step laboratory instructions, an introduction outlining the principle behind the technique, lists of equipment and reagents, and tips on troubleshooting and avoiding known pitfalls. §Comprehensive and highly practical, Optimization in Drug Discovery: In Vitro Methods systematically collects and describes the key methods for uncovering-as early in the discovery stage as possible-those defects that can eliminate candidate drugs from preclinical and clinical development.A panel of researchers and experts from leading universities and major pharmaceutical companies from all over the world systematically describe cutting-edge experimental protocols for the early in vitro evaluation of new chemical entities (NCE). These readily reproducible assays measure such critical parameters as physicochemical properties, adsorption, plasma binding, metabolism, drug interactions, and toxicity. By uncovering early in the discovery stage the defects that can eliminate candidate drugs from preclinical and clinical development, these techniques can save millions of dollars in time and effort.

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Optimization in Drug Discovery

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