Theravance, Inc., 901 Gateway Blvd, South San Francisco, CA 94080, United States.
Bioorg Med Chem Lett. 2012 Oct 1;22(19):6048-52. doi: 10.1016/j.bmcl.2012.08.051. Epub 2012 Aug 21.
Utilization of Theravance's multivalent approach to drug discovery towards 5-HT(4) receptor agonists with a focus on identification of neutral (non-charged at physiological pH) secondary binding groups is described. Optimization of a quinolone-tropane primary binding group with a chiral 2-propanol linker to a range of neutral secondary binding group motifs, for binding affinity and functional potency at the 5-HT(4) receptor, selectivity over the 5-HT(3) receptor, oral pharmacokinetics, and in vivo efficacy in models of GI motility, afforded velusetrag (TD-5108). Velusetrag has achieved proof-of-concept in patients with chronic idiopathic constipation.
利用 Theravance 的多价药物发现方法开发 5-HT(4) 受体激动剂,重点是鉴定中性(生理 pH 下不带电荷)的次级结合基团。优化喹诺酮-托烷的主要结合基团,使用手性 2-丙醇连接子与一系列中性次级结合基团模式,以获得对 5-HT(4)受体的结合亲和力和功能效力、对 5-HT(3)受体的选择性、口服药代动力学以及在胃肠道运动模型中的体内疗效,得到了 velusetrag(TD-5108)。Velusetrag 在慢性特发性便秘患者中已证明具有概念验证。