| Literature DB >> 10230640 |
A J Cocuzza1, F W Hobbs, C R Arnold, D R Chidester, J A Yarem, S Culp, L Fitzgerald, P J Gilligan.
Abstract
A series of 4-aryl-2-(N-ethylanilino)pyrimidines has been synthesized as corticotropin-releasing hormone (CRH) inhibitors. The effect of substitution on each aromatic ring on receptor binding was investigated.Entities:
Mesh:
Substances:
Year: 1999 PMID: 10230640 DOI: 10.1016/s0960-894x(99)00132-8
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823