Macrocycle derivative 14 | 1417297-71-2

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: Macrocycle derivative 14
• 英文别名: 7-oxa-10,14,19,21,22-pentazatetracyclo[13.5.2.12,6.018,21]tricosa-1(20),2(23),3,5,15(22),16,18-heptaene
• CAS: 1417297-71-2
• 化学式: C₁₇H₁₉N₅O
• 分子量: 309.371
• InChiKey: LGJSILJEEDDVAZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.1
• 重原子数：
  23
• 可旋转键数：
  0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  63.5
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  在 4-二甲氨基吡啶 、 lithium aluminium tetrahydride 、 benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate 、 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 、 N,N-二甲基甲酰胺 为溶剂， 反应 21.0h， 生成 Macrocycle derivative 14
  参考文献：
  名称：

  [EN] MACROCYCLIC COMPOUNDS AND THEIR USE AS CDK8 INHIBITORS
  [FR] COMPOSÉS MACROCYCLIQUES ET LEUR UTILISATION EN TANT QU'INHIBITEURS DE CDK8

  摘要：

  提供了具有式I的化合物，其中R1、R2、R3、R4、X、Y、Z和环A的含义如描述中所给，并且其药学上可接受的酯、酰胺、溶剂合物或盐，这些化合物在治疗需要或期望抑制蛋白质或脂质激酶（例如CDK8）的疾病中非常有用，特别是在癌症或增生性疾病的治疗中。

  公开号：

  WO2013001310A1

文献信息

• [EN] MACROCYCLIC LRRK2 KINASE INHIBITORS<br/>[FR] INHIBITEURS MACROCYCLIQUES DE LA KINASE LRRK2
  申请人：IPSEN PHARMA SAS

  公开号：WO2014140235A1

  公开（公告）日：2014-09-18

  The present invention relates to macrocyclic compounds and compositions containing said compounds acting as kinase inhibitors, in particular as inhibitors of LRRK2 kinase, for use in the diagnosis, prevention and/or treatment of LRRK2 -kinase associated diseases. Moreover, the present invention provides methods of using said compounds, for instance as a medicine or diagnostic agent. Finally, the present invention also relates to new macrocyclic compounds.

  本发明涉及大环化合物以及含有作为激酶抑制剂，特别是LRRK2激酶抑制剂的化合物的组合物，用于诊断、预防或治疗与LRRK2激酶相关的疾病。此外，本发明还提供了使用所述化合物的方法，例如作为药物或诊断剂。最后，本发明还涉及新的大环化合物。
• MACROCYCLIC LRRK2 KINASE INHIBITORS
  申请人：IPSEN PHARMA S.A.S.

  公开号：EP2970333B1

  公开（公告）日：2017-05-03
• Macrocyclic LRRK2 Kinase Inhibitors
  申请人：IPSEN PHARMA S.A.S.

  公开号：US20160031905A1

  公开（公告）日：2016-02-04

  The present invention relates to macrocyclic compounds and compositions containing said compounds acting as kinase inhibitors, in particular as inhibitors of LRRK2 kinase, for use in the diagnosis, prevention and/or treatment of LRRK2-kinase associated diseases. Moreover, the present invention provides methods of using said compounds, for instance as a medicine or diagnostic agent. Finally, the present invention also relates to new macrocyclic compounds.
• METHODS AND COMPOUNDS FOR THE TREATMENT OF GENETIC DISEASE
  申请人：Design Therapeutics, Inc.

  公开号：US20210238226A1

  公开（公告）日：2021-08-05

  The present disclosure relates to compounds and methods for modulating the expression of dmpk, atxn1, atxn2, atxn3, cacna1a, atxn7, ppp2r2br tbp, htt, jph3r ar, or atn1 and treating diseases and conditions in which dmpk, atxn1, atxn2, atxn3, cacna1a, atxn1, ppp2r2b, tbp, htt, jph3, ar, or atn1 plays an active role. The compound can be a transcription modulator molecule having a first terminus, a second terminus, and oligomeric backbone, wherein: a) the first terminus comprises a DNA-binding moiety capable of noncovalently binding to a nucleotide repeat sequence CAG or CTG; b) the second terminus comprises a protein-binding moiety binding to a regulatory molecule that modulates an expression of a gene comprising the nucleotide repeat sequence CAG or CTG; and c) the oligomeric backbone comprising a linker between the first terminus and the second terminus.