3-amino-N-3-pyridinyl-6-[4-[[[2-(1-pyrrolidinyl)ethyl]amino]carbonyl]phenyl]-2-pyrazinecarboxamide hydrochloride | 714237-31-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 3-amino-N-3-pyridinyl-6-[4-[[[2-(1-pyrrolidinyl)ethyl]amino]carbonyl]phenyl]-2-pyrazinecarboxamide hydrochloride
• 英文别名: 3-amino-N-pyridin-3-yl-6-[4-(2-pyrrolidin-1-ylethylcarbamoyl)phenyl]pyrazine-2-carboxamide;hydrochloride
• CAS: 714237-31-7
• 化学式: C₂₃H₂₅N₇O₂*ClH
• 分子量: 467.958
• InChiKey: JILYUBDKZZRGOU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.62
• 重原子数：
  33
• 可旋转键数：
  7
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.26
• 拓扑面积：
  126
• 氢给体数：
  4
• 氢受体数：
  7

文献信息

• [EN] NOBEL COMPOUNDS HAVING SELECTIVE INHIBITING EFFECT AT GSK3<br/>[FR] NOUVEAUX COMPOSES PRESENTANT UN EFFET INHIBITEUR SELECTIF DE LA GSK3
  申请人：ASTRAZENECA AB

  公开号：WO2004055006A1

  公开（公告）日：2004-07-01

  The present invention relates to new compounds, a process for their preparation and new intermediates used therein, pharmaceutical formulations containing said therapeutically active compounds and to the use of said active compounds in therapy, such as provide compounds having a selective inhibiting effect at GSK3.

  本发明涉及新化合物，其制备方法和其中使用的新中间体，包含上述治疗活性化合物的药物配方，以及该活性化合合物在治疗中的应用，例如提供具有对GSK3具有选择性抑制作用的化合物。
• Selective cellular targeting: multifunctional delivery vehicles, multifunctional prodrugs, use as antineoplastic drugs
  申请人：Drug Innovation & Design, Inc.

  公开号：US20030138432A1

  公开（公告）日：2003-07-24

  The present invention relates to the compositions, methods, and applications of a novel approach to selective cellular targeting. The purpose of this invention is to enable the selective delivery and/or selective activation of effector molecules to target cells for diagnostic or therapeutic purposes. The present invention relates to multi-functional prodrugs or targeting vehicles wherein each functionality is capable of enhancing targeting selectivity, affinity, intracellular transport, activation or detoxification. The present invention also relates to ultra-low dose, multiple target, multiple drug chemotherapy and targeted immunotherapy for cancer treatment.

  本发明涉及一种新的选择性细胞靶向的组合物、方法和应用。本发明的目的是为了实现对目标细胞的选择性输送和/或选择性激活效应分子，以进行诊断或治疗。本发明涉及多功能前药或靶向载体，其中每个功能都能增强靶向选择性、亲和力、细胞内转运、激活或解毒。本发明还涉及超低剂量、多靶点、多药物化疗和靶向免疫疗法，用于癌症治疗。
• Nobel compounds having selective inhibiting effect at gsk3
  申请人：Berg Stefan

  公开号：US20060173014A1

  公开（公告）日：2006-08-03

  The present invention relates to new compounds, a process for their preparation and new intermediates used therein, pharmaceutical formulations containing said therapeutically active compounds and to the use of said active compounds in therapy, such as provide compounds having a selective inhibiting effect at GSK3.

  本发明涉及新化合物、其制备方法和所使用的新中间体，包括含有上述治疗活性化合物的药物配方，以及上述活性化合物在治疗中的用途，提供具有选择性抑制GSK3作用的化合物。
• Novel Compounds Having Selective Inhibiting Effect at GSK3
  申请人：Berg Stefan

  公开号：US20100081660A1

  公开（公告）日：2010-04-01

  The present invention relates to new compounds, a process for their preparation and new intermediates used therein, pharmaceutical formulations containing said therapeutically active compounds and to the use of said active compounds in therapy, such as provide compounds having a selective inhibiting effect at GSK3.

  本发明涉及新化合物、其制备方法和其中使用的新中间体、含有所述治疗活性化合物的药物制剂以及所述活性化合物在治疗中的使用，例如提供具有选择性抑制GSK3效应的化合物。
• Process for determining inhibitor-enzyme complexes
  申请人：CORNELL RESEARCH FOUNDATION, INC.

  公开号：EP0048989B1

  公开（公告）日：1985-09-04