Literature DB >> 10856911

Diversity screening versus focussed screening in drug discovery.

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Abstract

Which strategy is best for hit identification? Making the right choices in the capital-intensive world of modern drug discovery can make the difference between success and expensive failure. Keeping an open mind to all the options is essential. Two well-established strategies are diversity-based and focussed screening. This review will provide contrasting viewpoints highlighting the strengths and deficiencies of each approach, as well as some insights into why both strategies are likely to have a place in the research armoury of a successful drug company.

Entities:  

Year:  2000        PMID: 10856911     DOI: 10.1016/s1359-6446(00)01517-8

Source DB:  PubMed          Journal:  Drug Discov Today        ISSN: 1359-6446            Impact factor:   7.851


  13 in total

1.  Combinatorial chemistry and high-throughput screening in drug discovery: different strategies and formats.

Authors:  P Seneci; S Miertus
Journal:  Mol Divers       Date:  2000       Impact factor: 2.943

2.  Reactant- and product-based approaches to the design of combinatorial libraries.

Authors:  Valerie J Gillet
Journal:  J Comput Aided Mol Des       Date:  2002 May-Jun       Impact factor: 3.686

Review 3.  Identifying ligands at orphan GPCRs: current status using structure-based approaches.

Authors:  Tony Ngo; Irina Kufareva; James Lj Coleman; Robert M Graham; Ruben Abagyan; Nicola J Smith
Journal:  Br J Pharmacol       Date:  2016-03-05       Impact factor: 8.739

Review 4.  High throughput screening in drug discovery.

Authors:  A Carnero
Journal:  Clin Transl Oncol       Date:  2006-07       Impact factor: 3.405

Review 5.  Origin and evolution of high throughput screening.

Authors:  D A Pereira; J A Williams
Journal:  Br J Pharmacol       Date:  2007-07-02       Impact factor: 8.739

6.  Estimation of the size of drug-like chemical space based on GDB-17 data.

Authors:  P G Polishchuk; T I Madzhidov; A Varnek
Journal:  J Comput Aided Mol Des       Date:  2013-08-21       Impact factor: 3.686

7.  GSA: a GPU-accelerated structure similarity algorithm and its application in progressive virtual screening.

Authors:  Xin Yan; Qiong Gu; Feng Lu; Jiabo Li; Jun Xu
Journal:  Mol Divers       Date:  2012-10-19       Impact factor: 2.943

8.  An ultra-specific avian antibody to phosphorylated tau protein reveals a unique mechanism for phosphoepitope recognition.

Authors:  Heather H Shih; Chao Tu; Wei Cao; Anne Klein; Renee Ramsey; Brian J Fennell; Matthew Lambert; Deirdre Ní Shúilleabháin; Bénédicte Autin; Eugenia Kouranova; Sri Laxmanan; Steven Braithwaite; Leeying Wu; Mostafa Ait-Zahra; Anthony J Milici; Jo Ann Dumin; Edward R LaVallie; Maya Arai; Christopher Corcoran; Janet E Paulsen; Davinder Gill; Orla Cunningham; Joel Bard; Lydia Mosyak; William J J Finlay
Journal:  J Biol Chem       Date:  2012-11-12       Impact factor: 5.157

9.  Symmetric kv1.5 blockers discovered by focused screening.

Authors:  Jonas Boström
Journal:  ACS Med Chem Lett       Date:  2012-08-16       Impact factor: 4.345

Review 10.  Perspectives on NMR in drug discovery: a technique comes of age.

Authors:  Maurizio Pellecchia; Ivano Bertini; David Cowburn; Claudio Dalvit; Ernest Giralt; Wolfgang Jahnke; Thomas L James; Steve W Homans; Horst Kessler; Claudio Luchinat; Bernd Meyer; Hartmut Oschkinat; Jeff Peng; Harald Schwalbe; Gregg Siegal
Journal:  Nat Rev Drug Discov       Date:  2008-09       Impact factor: 84.694

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