tert-butyl (4-(2-(2-aminopyridin-3-yl)-3H-imidazo[4,5-b]-pyridin-3-yl)benzyl)carbamate | 1313878-21-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: tert-butyl (4-(2-(2-aminopyridin-3-yl)-3H-imidazo[4,5-b]-pyridin-3-yl)benzyl)carbamate
• 英文别名: tert-butyl N-[[4-[2-(2-aminopyridin-3-yl)imidazo[4,5-b]pyridin-3-yl]phenyl]methyl]carbamate
• CAS: 1313878-21-5
• 化学式: C₂₃H₂₄N₆O₂
• 分子量: 416.483
• InChiKey: UJDBIWOTZJFYQT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  31
• 可旋转键数：
  6
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  108
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  tert-butyl (4-(2-(2-aminopyridin-3-yl)-3H-imidazo[4,5-b]-pyridin-3-yl)benzyl)carbamate 在 盐酸 、 N,N'-羰基二咪唑 作用下， 以 1,4-二氧六环 、 甲醇 、 二甲胺 为溶剂， 反应 4.0h， 生成 N-(4-(2-(2-aminopyridin-3-yl)-3H-imidazo[4,5-b]pyridin-3-yl)benzyl)-2-phenylacetamide
  参考文献：
  名称：

  Discovery and Optimization of a Series of 3-(3-Phenyl-3H-imidazo[4,5-b]pyridin-2-yl)pyridin-2-amines: Orally Bioavailable, Selective, and Potent ATP-Independent Akt Inhibitors

  摘要：

  This paper describes the implementation of a biochemical and biophysical screening strategy to identify and optimize small molecule Akt1 inhibitors that act through a mechanism distinct from that observed for kinase domain ATP-competitive inhibitors. With the aid of an unphosphorylated Akt1 cocrystal structure of 12j solved at 2.25 A, it was possible to confirm that as a consequence of binding these novel inhibitors, the ATP binding cleft contained a number of hydrophobic residues that occlude ATP binding as expected. These Akt inhibitors potently inhibit intracellular Akt activation and its downstream target (PRAS40) in vitro. In vivo pharmacodynamic and pharmacokinetic studies with two examples, 12e and 12j, showed the series to be similarly effective at inhibiting the activation of Akt and and additional downstream effector (p70S6) following oral dosing in mice.

  DOI：

  10.1021/jm300276x
• 作为产物：
  描述：

  2-氯-3-硝基吡啶 在 sodium dithionite 、 N,N-二异丙基乙胺 作用下， 以 1,4-二氧六环 、 甲醇 、 二甲基亚砜 为溶剂， 反应 42.0h， 生成 tert-butyl (4-(2-(2-aminopyridin-3-yl)-3H-imidazo[4,5-b]-pyridin-3-yl)benzyl)carbamate
  参考文献：
  名称：

  发现3-（3-（4-（1-氨基环丁基）苯基）-5-苯基-3 H-咪唑并[4,5 - b ]吡啶-2-基）吡啶-2-胺（ARQ 092）口服生物利用性，选择性和强效变构性AKT抑制剂

  摘要：

  本文的工作描述了3-（3-苯基-3 H-咪唑并[4,5 - b ]吡啶-2-基）吡啶-2-胺化学系列的优化，作为AKT激酶的有效，选择性变构抑制剂，导致发现了ARQ 092（21a）。与全长AKT1结合的化合物21a的共晶体结构证实了该化学类别的变构抑制模式以及环丁胺部分的作用。化合物21a对AKT1，AKT2和AKT3具有很高的酶促效力，并且对AKT活化和下游靶标PRAS40的磷酸化具有强大的细胞抑制作用。化合物21a 它还在人子宫内膜腺癌异种移植小鼠模型中用作AKT1-E17K突变蛋白的有效抑制剂，并抑制肿瘤生长。

  DOI：

  10.1021/acs.jmedchem.6b00619

文献信息

• Substituted Imidazopyridinyl-Aminopyridine Compounds
  申请人：Ashwell Mark A.

  公开号：US20110172203A1

  公开（公告）日：2011-07-14

  The present invention relates to substituted imidazopyridinyl-aminopyridine compounds and methods of synthesizing these compounds. The present invention also relates to pharmaceutical compositions containing substituted imidazopyridinyl-aminopyridine compounds and methods of treating cell proliferative disorders, such as cancer, by administering these compounds and pharmaceutical compositions to subjects in need thereof.

  本发明涉及取代咪唑吡啶基-氨基吡啶化合物及合成这些化合物的方法。本发明还涉及含有取代咪唑吡啶基-氨基吡啶化合物的药物组合物，以及通过向需要的受试者施用这些化合物和药物组合物来治疗细胞增殖性疾病，如癌症的方法。
• [EN] COVALENT MODIFIERS OF AKT1 AND USES THEREOF<br/>[FR] MODIFICATEURS COVALENTS DE AKT1 ET LEURS UTILISATIONS
  申请人：TERREMOTO BIOSCIENCES INC

  公开号：WO2023168291A1

  公开（公告）日：2023-09-07

  Described herein are compounds and methods for the modulation of AKT1 proteins, such as AKT1 E17K. In some aspects, the present disclosure provides an AKT1 protein, wherein a compound is bound to a lysine residue of the AKT1 protein. In another aspect, the present disclosure provides compounds of Formula (I) and (II), useful for the modulation of AKT1 proteins. In another aspect, the instant disclosure provides a method of attenuating AKT1 activity using the compounds described herein.

  本文描述了调节 AKT1 蛋白（如 AKT1 E17K）的化合物和方法。在某些方面，本公开提供了一种 AKT1 蛋白，其中化合物与 AKT1 蛋白的赖氨酸残基结合。在另一个方面，本公开提供了式(I)和(II)化合物，用于调节AKT1蛋白。在另一方面，本公开提供了一种使用本文所述化合物减弱 AKT1 活性的方法。
• SUBSTITUTED IMIDAZOPYRIDINYL-AMINOPYRIDINE COMPOUNDS
  申请人：ArQule, Inc.

  公开号：EP2519522A2

  公开（公告）日：2012-11-07
• US8501770B2
  申请人：——

  公开号：US8501770B2

  公开（公告）日：2013-08-06
• [EN] SUBSTITUTED IMIDAZOPYRIDINYL-AMINOPYRIDINE COMPOUNDS<br/>[FR] COMPOSÉS IMIDAZOPYRIDINYL-AMINOPYRIDINE SUBSTITUÉS
  申请人：ARQULE INC

  公开号：WO2011082270A2

  公开（公告）日：2011-07-07

  The present invention relates to substituted imidazopyridinyl-aminopyridine compounds and methods of synthesizing these compounds. The present invention also relates to pharmaceutical compositions containing substituted imidazopyridinyl- aminopyridine compounds and methods of treating cell proliferative disorders, such as cancer, by administering these compounds and pharmaceutical compositions to subjects in need thereof.