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Steroidal C-21 heteroaryl thioethers. Part 3: Pregn-4-eno-[3,2-c]pyrazole fused A ring modified steroids as selective glucocorticoid receptor modulators (dissociated steroids)

  作者 Biju, P; Wang, HW; Anthes, J; McCormick, K; Aslanian, R; Berlin, M; Bitar, R; Lim, YH; Lee, YJ; Prelusky, D; Mcleod, R; Jia, YL; Fernandez, X; Lieber, G; Jimenez, J; Eckel, S; House, A; Chapman, R; Phillips, J  
  选自 期刊  Bioorganic & Medicinal Chemistry Letters;  卷期  2012年22-9;  页码  3291-3295  
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[摘要]The introduction of A ring pyrazole modification to the hydrocortisone C-21 heteroaryl thioethers generated compounds with excellent transrepression potency (IL-8 inhibition) compared to their hydrocortisone analogs. However, the transcriptional transactivation activity of these compounds were considerably higher than the corresponding hydrocortisone analogs. Among all the compounds evaluated, a quinoxaline thioether modification demonstrated the best overall in vitro separation. (C) 2012 Elsevier Ltd. All rights reserved.

 
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