Skip to content
2000
Volume 3, Issue 3
  • ISSN: 1570-1808
  • E-ISSN: 1875-628X

Abstract

The odds of drug hit identification in screening are closely related to the diversity of libraries or the availability of focused libraries. There are no truly diverse libraries and it is difficult to design focused libraries without sufficient information. Hence alternative approaches need to be explored for enhancing the odds of hit discovery from existing libraries. Protein homologs have been used collectively targeted in inhibitor design and other discovery applications by exploiting the correlation between protein homologs and their ligands from specific compound classes. A receptor-homolog-based screening scheme may be derived as a strategy to potentially increase the odds of hit identification.

Loading

Article metrics loading...

/content/journals/lddd/10.2174/157018006776286970
2006-04-01
2025-10-16
Loading full text...

Full text loading...

/content/journals/lddd/10.2174/157018006776286970
Loading

  • Article Type:
    Research Article
Keyword(s): Drug design; drug discovery; high throughput screening; homologs; virtual screening
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test