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Identification and optimisation of novel sulfonamide, selective vasopressin V(1B) receptor antagonists

  作者 Baker, J; Bingham, M; Blackburn-Munro, R; Cai, JQ; Craighead, M; Gilfillan, R; Goan, K; Jaap, D; Milne, R; Morphy, JR; Napier, S; Presland, J; Spinks, G; Thomson, F  
  选自 期刊  Bioorganic & Medicinal Chemistry Letters;  卷期  2011年21-12;  页码  3603-3607  
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[摘要]The synthesis and preliminary structure-activity relationships (SAR) of a novel class of vasopressin V(1B) receptor antagonists are described. Hit compound 5, identified via high throughput screening of the corporate collection, showed good activity in a V(1B) binding assay (K(i) 63 nM) but did not possess the lead-like physicochemical properties typically required in a hit compound. A 'deletion approach' on the HTS hit 5 was performed, with the focus on improvement of physicochemical properties, yielding the selective V(1B) antagonist 9f (K(i) 190 nM), with improved druglike characteristics. (C) 2011 Elsevier Ltd. All rights reserved.

 
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