| Literature DB >> 16236513 |
Kelly McClure1, Michael Hack, Liming Huang, Clark Sehon, Magda Morton, Lina Li, Terrance D Barrett, Nigel Shankley, J Guy Breitenbucher.
Abstract
High throughput screening revealed compound 1 as a potent antagonist of the CCK(1) receptor. Evaluation of the CCK(1) SAR in a series of these diarylpyrazole antagonists was conducted in a matrix synthesis format revealing additive (Free-Wilson) and non-additive SAR. This use of additive QSAR modeling in conjunction with combinatorial libraries represents a unique approach to the evaluation of SAR interactions between the variables of any combinatorial matrix.Entities:
Mesh:
Substances:
Year: 2005 PMID: 16236513 DOI: 10.1016/j.bmcl.2005.09.048
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823