Check nearby libraries
Buy this book
Recent progress in high-throughput screening, combinatorial chemistry and molecular biology has radically changed the approach to drug discovery in the pharmaceutical industry. New challenges in synthesis result in new analytical methods. At present, typically 100,000 to one million molecules have to be tested within a short period and, therefore, highly effective screening methods are necessary for today's researchers - preparing and characterizing one compound after another belongs to the past. Intelligent, computer-based search agents are needed and "virtual screening" provides so.
Check nearby libraries
Buy this book
Previews available in: English
Subjects
Structure-Activity Relationship, MEDICAL, Drug Design, Factual Databases, Screening, Molekulbibliothek, Computerunterstutztes Verfahren, Chemistry, Nursing, Computer simulation, Bioaktive Verbindungen, Drug Guides, Organic Chemicals, Pharmacology, Drugs, Testing, Decision Making, Computer-Assisted, Design, Pharmacy, Molekulardesign, Drugs, design, Drugs, testingShowing 1 featured edition. View all 1 editions?
Edition | Availability |
---|---|
1 |
aaaa
Libraries near you:
WorldCat
|
Book Details
Edition Notes
Includes bibliographical references and index.
Classifications
External Links
The Physical Object
ID Numbers
Source records
Community Reviews (0)
Feedback?History
- Created April 1, 2008
- 8 revisions
Wikipedia citation
×CloseCopy and paste this code into your Wikipedia page. Need help?
November 14, 2023 | Edited by MARC Bot | import existing book |
October 17, 2022 | Edited by ImportBot | import existing book |
December 4, 2020 | Edited by MARC Bot | import existing book |
May 24, 2020 | Edited by ImportBot | import existing book |
April 1, 2008 | Created by an anonymous user | Imported from Scriblio MARC record |