Malm Johan, Gordon Sandra, Brandt Peter, Carlsson Bo, Agback Peter, Bäckbro Saeidi Anna, Sandberg Johnny
Karo Bio AB, Novum, Huddinge S-141 57, Sweden.
Bioorg Med Chem Lett. 2007 Apr 1;17(7):2018-21. doi: 10.1016/j.bmcl.2007.01.009. Epub 2007 Jan 13.
Based on the concept of 'indirect antagonism' of nuclear receptors, a series of thyroid hormone receptor (TR) antagonists were prepared with improved affinity compared with what was previously described. The results of a binding assay for the human TR and reporter cell assay revealed, within this series, that an m-bromobenzoyl substituent (11f) was optimal in terms of affinity and antagonist activity. Compared with already reported TR antagonists, their affinities are within the same range, thus potentially representing useful approach to novel and high-affinity TR-antagonists.
基于核受体“间接拮抗作用”的概念,制备了一系列甲状腺激素受体(TR)拮抗剂,与先前描述的相比,其亲和力有所提高。人TR结合试验和报告基因细胞试验的结果表明,在该系列中,间溴苯甲酰取代基(11f)在亲和力和拮抗活性方面是最佳的。与已报道的TR拮抗剂相比,它们的亲和力在同一范围内,因此可能是开发新型高亲和力TR拮抗剂的有用方法。