Journal
JOURNAL OF CHEMICAL INFORMATION AND MODELING
Volume 52, Issue 12, Pages 3308-3324Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ci3004094
Keywords
-
Categories
Funding
- Netherlands Organization for Scientific Research (NWO) [700.59.408]
- TI-Pharma [D1-105]
- Molecular Discovery Ltd.
Ask authors/readers for more resources
Virtual fragment screening (VFS) is a promising new method that uses computer models to identify small, fragment-like biologically active molecules as useful starting points for fragment-based drug discovery (FBDD). Training sets of true active and inactive fragment-like molecules to construct and validate target customized VFS methods are however lacking. We have for the first time explored the possibilities and challenges of VFS using molecular fingerprints derived from a unique set of fragment affinity data for the histamine H-3 receptor (H3R), a pharmaceutically relevant G protein-coupled receptor (GPCR). Optimized FLAP (Fingerprints of Ligands and Proteins) models containing essential molecular interaction fields that discriminate known H3R binders from inactive molecules were successfully used for the identification of new H3R ligands. Prospective virtual screening of 156 090 molecules yielded a high hit rate of 62% (18 of the 29 tested) experimentally confirmed novel fragment-like H3R ligands that offer new potential starting points for the design of H3R targeting drugs. The first construction and application of customized FLAP models for the discovery of fragment-like biologically active molecules demonstrates that VFS is an efficient way to explore protein-fragment interaction space in silico.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available