| Literature DB >> 12565966 |
Matthew E Voss1, Percy H Carter, Andrew J Tebben, Peggy A Scherle, Gregory D Brown, Lorin A Thompson, Meizhong Xu, Yvonne C Lo, Gengjie Yang, Rui-Qin Liu, Paul Strzemienski, J Gerry Everlof, James M Trzaskos, Carl P Decicco.
Abstract
Based on the realization that N-alkyl 5-arylidene-2-thioxo-1,3-thiazolidin-4-ones are tumor necrosis factor-alpha antagonists, we discovered two additional classes of antagonists: 3-thioxo-2,3-dihydro-1H-imidazo[1,5-a]indol-1-ones (via rational design) and 5-arylidene-2-thioxodihydropyrimidine-4,6(1H,5H)-diones (via computer-guided screening). Chemical modification of the lead structures showed that the structure-activity relationship profiles for both of these series were dependent on the electronic properties of the molecules. Subsequent studies showed that they were light-dependent inhibitors.Entities:
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Year: 2003 PMID: 12565966 DOI: 10.1016/s0960-894x(02)00941-1
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823