Lewis Ian, Bauer Wilfried, Albert Rainer, Chandramouli Nagarajan, Pless Janos, Weckbecker Gisbert, Bruns Christian
Transplantation Research Department, Novartis Pharma, CH-4002 Basel, Switzerland.
J Med Chem. 2003 Jun 5;46(12):2334-44. doi: 10.1021/jm021093t.
A rational drug design approach, capitalizing on structure-activity relationships and involving transposition of functional groups from somatotropin release inhibitory factor (SRIF) into a reduced size cyclohexapeptide template, has led to the discovery of SOM230 (25), a novel, stable cyclohexapeptide somatostatin mimic that exhibits unique high-affinity binding to human somatostatin receptors (subtypes sst1-sst5). SOM230 has potent, long-lasting inhibitory effects on growth hormone and insulin-like growth factor-1 release and is a promising development candidate currently under evaluation in phase I clinical trials.
一种基于构效关系的合理药物设计方法,即将生长抑素释放抑制因子(SRIF)的官能团转接到一个更小的环己肽模板上,从而发现了SOM230(25),一种新型的、稳定的环己肽类生长抑素模拟物,它对人类生长抑素受体(亚型sst1-sst5)具有独特的高亲和力结合能力。SOM230对生长激素和胰岛素样生长因子-1的释放具有强效、持久的抑制作用,是一种很有前景的开发候选药物,目前正处于I期临床试验评估阶段。