Tellew John E, Luo Zhiyong
Department of Medicinal Chemistry, Neurocrine Biosciences, San Diego, California, USA.
Curr Top Med Chem. 2008;8(6):506-20. doi: 10.2174/156802608783955665.
Antagonists of the corticotropin releasing factor (CRF or CRH) receptor have shown promise for the treatment of anxiety, depression, and irritable bowel syndrome. In the present article, medicinal chemistry developments surrounding small molecule CRF receptor antagonists are reviewed, focusing on publications and patents from mid-2004 through the first quarter of 2006. While the CRF type 2 receptor remains an intractable target, incremental progress has been made in the search for drug-like antagonists of the CRF type 1 receptor. Most recent work has not ventured far from previously-established pharmacophoric topologies. A common theme in recent patent disclosures is the addition of novel polar substituents to known heterocyclic core structures to reduce overall lipophilicity. New disclosures of pharmacokinetic (PK) data for several series of antagonists reveal that achieving appropriate PK remains a challenge for the field. The recent publication of selection patents and patents relating to salt and crystal forms of particular compounds suggests that several second generation compounds are nearing or have entered clinical development.
促肾上腺皮质激素释放因子(CRF 或 CRH)受体拮抗剂已显示出在治疗焦虑症、抑郁症和肠易激综合征方面的潜力。在本文中,对围绕小分子 CRF 受体拮抗剂的药物化学进展进行了综述,重点关注 2004 年年中至 2006 年第一季度的出版物和专利。虽然 CRF 2 型受体仍然是一个难以攻克的靶点,但在寻找 CRF 1 型受体的类药物拮抗剂方面已取得了渐进式进展。最近的工作与先前确立的药效团拓扑结构相差不大。近期专利披露中的一个共同主题是在已知的杂环核心结构上添加新型极性取代基以降低整体亲脂性。几个系列拮抗剂的药代动力学(PK)数据的新披露表明,实现合适的药代动力学对该领域来说仍然是一项挑战。近期关于特定化合物的选择专利以及盐和晶体形式的专利的公布表明,几种第二代化合物已接近或已进入临床开发阶段。