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2000
Volume 14, Issue 6
  • ISSN: 1386-2073
  • E-ISSN: 1875-5402

Abstract

A pharmacophore is a model which represents the key physico-chemical interactions that mediate biological activity. There is a long history of using pharmacophore modeling methods to select subsets of compounds, focused towards a specific target of interest. This paper will review existing computational methods for deriving and comparing pharmacophore models. We outline a new classification of pharmacophore methods based on the abstraction of the underlying chemical interactions which embody a pharmacophore, and the methods available to quantitatively compare them. Within the context of this classification, example studies, using specific pharmacophore modeling methods for focused library selection, will be discussed.

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/content/journals/cchts/10.2174/138620711795767820
2011-07-01
2024-11-26
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/content/journals/cchts/10.2174/138620711795767820
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