1-(3-cyano-benzyl)-4-(5-amino-pyridin-2-yl)-piperazine | 381706-53-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪烷类
• 英文名称: 1-(3-cyano-benzyl)-4-(5-amino-pyridin-2-yl)-piperazine
• 英文别名: 1-(3-Cyano-benzyl)-4-(5-amino-piridin-2-yl)-piperazine；3-[[4-(5-aminopyridin-2-yl)piperazin-1-yl]methyl]benzonitrile
• CAS: 381706-53-2
• 化学式: C₁₇H₁₉N₅
• 分子量: 293.371
• InChiKey: OGKJYHQVHLLGEI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  22
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  69.2
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  4'-isopropyl-6-methoxy-biphenyl-2-carboxylic acid 、 1-(3-cyano-benzyl)-4-(5-amino-pyridin-2-yl)-piperazine 在 1-羟基苯并三唑 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 生成 4'-isopropyl-6-methoxy-biphenyl-2-carboxylic acid [2-(4-(3-cyano-benzyl)-piperazin-1-yl)-pyridin-5-yl)-amide
  参考文献：
  名称：

  Bioisosteric bensamide derivatives and their use as apob-100 secretion inhibitors

  摘要：

  本发明涉及一种化合物，其化学式为（I），其中A、U、V、X、Z、R1、Y、R2和R3在说明中有定义，或其生理上可接受的盐、溶剂或衍生物，以及制备所述化合物的组合物和方法，以及它们在治疗由apoB-100和/或MTP抑制剂改善的状况中的应用。

  公开号：

  US20040009988A1

文献信息

• BIPHENYLCARBOXAMIDE DERIVATIVES AS HEDGEHOD PATHWAY MODULATORS
  申请人：Dierks Christine

  公开号：US20100197659A1

  公开（公告）日：2010-08-05

  The invention provides a method for modulating the activity of the hedgehog signaling pathway. In particular, the invention provides a method for inhibiting aberrant growth states resulting from phenotypes such as Ptc loss-of-function, hedgehog gain-of-function, smoothened gain-of-function or Gli gain-of-function, comprising contacting a cell with a sufficient amount of a compound of Formula I.

  该发明提供了一种调节刺猬信号通路活性的方法。具体来说，该发明提供了一种抑制由于Ptc功能丧失、刺猬功能增强、smoothened功能增强或Gli功能增强等表型引起的异常生长状态的方法，包括将细胞与化合物I式的足够量接触。
• COMPOUNDS AND COMPOSITIONS AS HEDGEHOG PATHWAY MODULATORS
  申请人：Gao Wenqi

  公开号：US20090203666A1

  公开（公告）日：2009-08-13

  The invention provides a method for modulating the activity of the hedgehog signaling pathway. In particular, the invention provides a method for inhibiting aberrant growth states resulting from phenotypes such as Ptc loss-of-function, hedgehog gain-of-function, smoothened gain-of-function or Gli gain-of-function, comprising contacting a cell with a sufficient amount of a compound of Formula I.

  本发明提供了一种调节刺猬信号通路活性的方法。具体而言，本发明提供了一种通过接触细胞与化合物I的足够量来抑制由于Ptc功能缺失、刺猬功能增强、平滑蛋白功能增强或Gli功能增强等表型引起的异常生长状态的方法。
• Amide compounds
  申请人：FUJISAWA PHARMACEUTICAL CO., LTD.

  公开号：US20040133008A1

  公开（公告）日：2004-07-08

  A compound of the formula (I) 1 wherein R 1 is hydrogen, lower alkyl, lower alkenyl, halo(lower)alkyl, cyclo(lower)alkyl, lower alkoxy, lower alkylthio, acyl, optionally substituted aryl or NR 3 R 4 ; R 2 is hydrogen; or aryl or heteroaryl, each of which may be substituted; X is direct bond or bivalent residue derived from piperazine; Y is -(A 1 ) n -(A 2 ) m -, wherein n and m are independently 0 or 1); 2 is bivalent residue derived from arene or heteroarene; and 3 is bivalent residue derived from arene or heteroarene, or a salt thereof. The compound of the present invention and a salt thereof inhibit apolipoprotein B (Apo B) secretion and are useful as a medicament for prophylactic and treatment of diseases or conditions resulting from elevated circulating levels of Apo B.

  化合物的式子为（I）1，其中R1为氢、低级烷基、低级烯基、卤素（低）烷基、环（低）烷基、低级烷氧基、低级烷硫基、酰基、可选取代的芳基或NR3R4；R2为氢；或芳基或杂环芳基，每个可以被取代；X为直接键或由哌嗪衍生的二价残基；Y为-(A1)n-(A2)m-，其中n和m独立地为0或1）；2为由芳烃或杂芳烃衍生的二价残基；3为由芳烃或杂芳烃衍生的二价残基，或其盐。本发明的化合物及其盐抑制载脂蛋白B（Apo B）的分泌，并可用作预防和治疗由高循环Apo B水平引起的疾病或状况的药物。
• Smoothened antagonism for the treatment of hedgehog pathway-related disorders
  申请人：Novartis AG

  公开号：EP2617414A2

  公开（公告）日：2013-07-24

  The invention provides methods for modulating, e.g., antagonizing, the activity of the Hedgehog signaling pathway, and for treating Hedgehog related disorders such as cancers (e.g., medulloblastoma). In particular, the invention provides methods for inhibiting aberrant growth states resulting from phenotypes such as Ptch loss-of function, Hedgehog gain-of-function, smoothened gain-of-function or Gli gain-of-function by administering to a mammal combinations of Smoothened inhibitors (e.g., a compound of Formula I, Formula II, or Formula III, or any of the compounds listed herein or incorporated by reference) and Gli inhibitors, and/or Phosphatidylinositol 3-kinase (PI3K) inhibitors.

  本发明提供了调节（如拮抗）刺猬信号通路活性的方法，以及治疗刺猬相关疾病如癌症（如髓母细胞瘤）的方法。特别是，本发明提供了通过向哺乳动物施用 Smoothened 抑制剂（例如，式 I、式 II 或式 III 的化合物，或本文所列或通过参考文献并入的任何化合物）和 Gli 抑制剂和/或磷脂酰肌醇 3- 激酶（PI3K）抑制剂的组合，抑制表型（如 Ptch 功能缺失、刺猬蛋白功能增益、smoothened 功能增益或 Gli 功能增益）导致的异常生长状态的方法。
• SMOOTHENED ANTAGONISM FOR THE TREATMENT OF HEDGEHOG PATHWAY-RELATED DISORDERS
  申请人：Novartis AG

  公开号：EP3023097A1

  公开（公告）日：2016-05-25

  The invention provides methods for modulating, e.g., antagonizing, the activity of the Hedgehog signaling pathway, and for treating Hedgehog related disorders such as cancers (e.g., medulloblastoma). In particular, the invention provides methods for inhibiting aberrant growth states resulting from phenotypes such as Ptch loss-of-function, Hedgehog gain-of-function, smoothened gain-of-function or Gli gain-of-function by administering to a mammal combinations of Smoothened inhibitors (e.g., a compound of Formula I, Formula II, or Formula III, or any of the compounds listed herein or incorporated by reference) and Gli inhibitors, and/or Phosphatidylinositol 3-kinase (PI3K) inhibitors.

  本发明提供了调节（如拮抗）刺猬信号通路活性的方法，以及治疗刺猬相关疾病如癌症（如髓母细胞瘤）的方法。特别是，本发明提供了通过向哺乳动物施用 Smoothened 抑制剂（例如，式 I、式 II 或式 III 的化合物，或本文所列或通过参考文献并入的任何化合物）和 Gli 抑制剂和/或磷脂酰肌醇 3- 激酶（PI3K）抑制剂的组合，抑制表型如 Ptch 功能缺失、Hedgehog 功能增益、smoothened 功能增益或 Gli 功能增益所导致的异常生长状态的方法。