Title of article
Both 5-arylidene-2-thioxodihydropyrimidine-4,6(1H,5H)-diones and 3-thioxo-2,3-dihydro-1H-imidazo[1,5-a]indol-1-ones are light-Dependent tumor necrosis factor-α antagonists
Author/Authors
Matthew E. Voss، نويسنده , , Percy H. Carter، نويسنده , , Andrew J. Tebben، نويسنده , , Peggy A. Scherle، نويسنده , , Gregory D. Brown، نويسنده , , Lorin A. Thompson، نويسنده , , Meizhong Xu، نويسنده , , Yvonne C. Lo، نويسنده , , Gengjie Yang، نويسنده , , Ruiqin Liu، نويسنده , , Paul Strzemienski، نويسنده , , J. Gerry Everlof، نويسنده , , James M. Trzaskos، نويسنده , , Carl P. Decicco، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2003
Pages
6
From page
533
To page
538
Abstract
Based on the realization that N-alkyl 5-arylidene-2-thioxo-1,3-thiazolidin-4-ones are tumor necrosis factor-α 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.
Journal title
Bioorganic & Medicinal Chemistry Letters
Serial Year
2003
Journal title
Bioorganic & Medicinal Chemistry Letters
Record number
792960
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