...
首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Discovery of a series of 8-(2,3-dihydro-1,4-benzoxazin-4-ylmethyl)-2-morpholino-4-oxo-chromene-6-carboxamides as PI3K beta/delta inhibitors for the treatment of PTEN-deficient tumours
【24h】

Discovery of a series of 8-(2,3-dihydro-1,4-benzoxazin-4-ylmethyl)-2-morpholino-4-oxo-chromene-6-carboxamides as PI3K beta/delta inhibitors for the treatment of PTEN-deficient tumours

机译:发现了一系列用作PI3Kβ/δ抑制剂的8-(2,3-二氢-1,4-苯并恶嗪-4-基甲基)-2-吗啉代-4-氧代色烯-6-羧酰胺,用于治疗PTEN-肿瘤不足

获取原文
获取原文并翻译 | 示例
           

摘要

We report the discovery and optimisation of a series of 8-(2,3-dihydro-1,4-benzoxazin-4-ylmethyl)-2-morpholino-4-oxo-chromene-6-carboxamides, leading to compound 16 as a potent and selective PI3K beta/delta inhibitor: PI3K beta cell IC50 0.012 mu M (in PTEN null MDA-MB-468 cell) and PI3K delta cell IC50 0.047 mu M (in Jeko-1 B-cell), with good pharmacokinetics and physical properties. In vivo, 16 showed profound pharmacodynamic modulation of AKT phosphorylation in a mouse PTEN-deficient PC3 prostate tumour xenograft after a single oral dose and gave excellent tumour growth inhibition in the same model after chronic oral dosing. Compound 16 was selected as a preclinical candidate for the treatment of PTEN-deficient tumours. (C) 2016 Elsevier Ltd. All rights reserved.
机译:我们报告发现和优化一系列的8-(2,3-dihydro-1,4-benzoxazin-4-ylmethyl)-2-morpholino-4-oxo-chromene-6-boxamides,导致化合物16作为有效和选择性的PI3K beta / delta抑制剂:PI3K beta细胞IC50 0.012μM(在PTEN null MDA-MB-468细胞中)和PI3K delta细胞IC50 0.047μM(在Jeko-1 B细胞中),具有良好的药代动力学和物理属性。在体内,有16剂在单次口服剂量后在小鼠PTEN缺陷型PC3前列腺肿瘤异种移植物中显示出AKT磷酸化的深刻药效学调节作用,并且在长期口服后,在相同模型中,该药物对肿瘤的生长抑制作用极好。选择化合物16作为治疗PTEN缺陷型肿瘤的临床前候选药物。 (C)2016 Elsevier Ltd.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号