1-(2,4-dichlorophenyl)-N-[(2S)-3-(1H-indol-3-yl)-1-(4-methylpiperazin-1-yl)-1-oxopropan-2-yl]cyclopropanecarboxamide | 1239704-29-0

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: 1-(2,4-dichlorophenyl)-N-[(2S)-3-(1H-indol-3-yl)-1-(4-methylpiperazin-1-yl)-1-oxopropan-2-yl]cyclopropanecarboxamide
• 英文别名: 1-(2,4-dichlorophenyl)-N-[(2S)-3-(1H-indol-3-yl)-1-(4-methylpiperazin-1-yl)-1-oxopropan-2-yl]cyclopropane-1-carboxamide
• CAS: 1239704-29-0
• 化学式: C₂₆H₂₈Cl₂N₄O₂
• 分子量: 499.44
• InChiKey: WFRXEZYSVYRRFE-QHCPKHFHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  34
• 可旋转键数：
  6
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  68.4
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  BOC-L-色氨酸羟基琥珀酰亚胺酯 在 盐酸 、 N,N-二异丙基乙胺 、 Methanaminium,N-[(dimethylamino)(3H-1,2,3-triazolo[4,5-b]pyridin-3-yloxy)methylene]-N-methyl-, hexafluorophosphate(1-) 作用下， 以 1,4-二氧六环 、 乙腈 为溶剂， 反应 38.0h， 生成 1-(2,4-dichlorophenyl)-N-[(2S)-3-(1H-indol-3-yl)-1-(4-methylpiperazin-1-yl)-1-oxopropan-2-yl]cyclopropanecarboxamide
  参考文献：
  名称：

  Discovery and Characterization of an Inhibitor of Glucosylceramide Synthase

  摘要：

  Targeting glycosphingolipid synthesis has emerged as a novel approach for treating metabolic diseases. 32 (EXEL-0346) represents a new class of glucosylceramide synthase (GCS) inhibitors. This report details the elaboration of hit 8 with the goal of achieving and maintaining maximum GCS inhibition in vivo. 32 inhibited GCS with an IC50 of 2 nM and achieved maximum hepatic GCS inhibition after four or five daily doses in rodents. Robust improvements in glucose tolerance in DIO mice and ZDF rats were observed after 2 weeks of q.d. dosing. Four weeks of dosing resulted in decreased plasma triglycerides and reduced hepatic fat deposition. Thus, 32 provides insight into the amount of metabolic regulation that can be restored following achievement of maximal target knockdown.

  DOI：

  10.1021/jm300122u

文献信息

• Inhibitors of gangliosides metabolism for the treatment of motor neuron diseases
  申请人：ICM (INSTITUT DU CERVEAU ET DE LA MOELLE ÉPINIÈRE)

  公开号：US11065238B2

  公开（公告）日：2021-07-20

  The present invention relates to inhibitors of gangliosides metabolism for treating motor neuron diseases, in particular hereditary spastic paraplegias.

  本发明涉及用于治疗运动神经元疾病，特别是遗传性痉挛性截瘫的神经节苷脂代谢抑制剂。
• INHIBITORS OF GANGLIOSIDES METABOLISM FOR THE TREATMENT OF MOTOR NEURON DISEASES
  申请人：ICM (INSTITUT DU CERVEAU ET DE LA MOELLE ÉPINIÈRE)

  公开号：US20190350913A1

  公开（公告）日：2019-11-21

  The present invention relates to inhibitors of gangliosides metabolism for treating motor neuron diseases, in particular hereditary spastic paraplegias.
• [EN] INHIBITORS OF GLUCOSYLCERAMIDE SYNTHASE<br/>[FR] INHIBITEURS DE LA GLUCOSYLCÉRAMIDE SYNTHASE
  申请人：EXELIXIS INC

  公开号：WO2010091164A1

  公开（公告）日：2010-08-12

  The present invention comprises glucosylceramide synthase (GCS) modulators of following structural formula (I); wherein R1, A, L, R2, R3, and m are defined herein, as well as N-oxides of them and pharmaceutically acceptable salts thereof, and methods of making said compounds. The invention further comprises compositions comprising the compounds, N-oxides, and/or pharmaceutically acceptable salts thereof. The invention also comprises use of the compounds and compositions for treating diseases in which GCS is a mediator or is implicated. The invention also comprises use of the compounds in and for the manufacture of medicaments, particularly for treating diseases in which GCS is a mediator or is implicated.
• Discovery and Characterization of an Inhibitor of Glucosylceramide Synthase
  作者：Steven Richards、Christopher J. Larson、Elena S. Koltun、Art Hanel、Vicky Chan、Jason Nachtigall、Amanda Harrison、Naing Aay、Hongwang Du、Arlyn Arcalas、Adam Galan、Jeff Zhang、Wentao Zhang、Kwang-Ai Won、Danny Tam、Fawn Qian、Tao Wang、Patricia Finn、Kathy Ogilvie、Jon Rosen、Ron Aoyama、Artur Plonowski、Belinda Cancilla、Frauke Bentzien、Michael Yakes、Raju Mohan、Peter Lamb、John Nuss、Patrick Kearney

  DOI：10.1021/jm300122u

  日期：2012.5.10

  Targeting glycosphingolipid synthesis has emerged as a novel approach for treating metabolic diseases. 32 (EXEL-0346) represents a new class of glucosylceramide synthase (GCS) inhibitors. This report details the elaboration of hit 8 with the goal of achieving and maintaining maximum GCS inhibition in vivo. 32 inhibited GCS with an IC50 of 2 nM and achieved maximum hepatic GCS inhibition after four or five daily doses in rodents. Robust improvements in glucose tolerance in DIO mice and ZDF rats were observed after 2 weeks of q.d. dosing. Four weeks of dosing resulted in decreased plasma triglycerides and reduced hepatic fat deposition. Thus, 32 provides insight into the amount of metabolic regulation that can be restored following achievement of maximal target knockdown.