4-(7-methoxy-1-methyl-β-carbolin-9-yl)butylamine | 1342260-99-4

• 分子结构分类: 有机化合物 - 生物碱及其衍生物 - 哈马拉生物碱
• 英文名称: 4-(7-methoxy-1-methyl-β-carbolin-9-yl)butylamine
• 英文别名: 4-(7-Methoxy-1-methylpyrido[3,4-b]indol-9-yl)butan-1-amine
• CAS: 1342260-99-4
• 化学式: C₁₇H₂₁N₃O
• 分子量: 283.373
• InChiKey: MDOYARWQQSWQJS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  21
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.35
• 拓扑面积：
  53.1
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  4-(7-methoxy-1-methyl-β-carbolin-9-yl)butylamine 在 lithium aluminium tetrahydride 、 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 、 乙醇 、 二氯甲烷 为溶剂， 反应 4.5h， 生成 N-acetyl-N-methyl-4-(7-methoxy-1-methyl-β-carbolin-9-yl)-butylamine
  参考文献：
  名称：

  Synthesis and Biological Validation of a Harmine-Based, Central Nervous System (CNS)-Avoidant, Selective, Human β-Cell Regenerative Dual-Specificity Tyrosine Phosphorylation-Regulated Kinase A (DYRK1A) Inhibitor

  摘要：

  Recently, our group identified that harmine is able to induce beta-cell proliferation both in vitro and in vivo, mediated via the DYRK1A-NFAT pathway. Since, harmine suffers from a lack of selectivity, both against other kinases and CNS off-targets, we therefore sought to expand structure-activity relationships for harmine's DYRK1A activity, to enhance selectivity for off-targets while retaining human beta-cell proliferation activity. We carried out optimization of the 9-N-position of harmine to synthesize 29 harmine-based analogs. Several novel inhibitors showed excellent DYRK1A inhibition and human beta-cell proliferation capability. An optimized DYRK1A inhibitor, 2-2c, was identified as a novel, efficacious in vivo lead candidate. 2-2c also demonstrates improved selectivity for kinases and CNS off-targets, as well as in vivo efficacy for beta-cell proliferation and regeneration at lower doses than harmine. Collectively, these findings demonstrate that 2-2c is a much improved in vivo lead candidate as compared to harmine for the treatment of diabetes.

  DOI：

  10.1021/acs.jmedchem.9b01379
• 作为产物：
  描述：

  肉叶云香碱 在 sodium hydride 、 一水合肼 作用下， 以 乙醇 、 N,N-二甲基甲酰胺 为溶剂， 反应 2.0h， 生成 4-(7-methoxy-1-methyl-β-carbolin-9-yl)butylamine
  参考文献：
  名称：

  一种去氢骆驼蓬碱修饰药、制备方法及应用

  摘要：

  本发明涉及一种去氢骆驼蓬碱修饰药、制备方法及应用。通过对去氢骆驼蓬碱进行衍生化修饰，以去氢骆驼蓬碱作为疏水内核，二硫代二丙酸作为连接臂，聚乙二醇为亲水骨架材料，合成还原敏感两亲性聚合物材料去氢骆驼蓬碱接枝聚乙二醇，即去氢骆驼蓬碱修饰药；将其在水溶液中自组装，得到一种载药纳米胶束系统，用作药物递送的载体材料。本发明提供的去氢骆驼蓬碱修饰药应用于制备纳米胶束载药系统，由于其在水溶液中可自组装形成稳定的纳米级胶束体系，从而能够高效的递送药物到肿瘤部位，提高去氢骆驼蓬碱的抗肿瘤效果，降低毒副作用，同时改善水溶性，为去氢骆驼蓬碱在抗肿瘤方面的应用提供更多可能性。

  公开号：

  CN115887376A

文献信息

• ALKYL-AMINE HARMINE DERIVATIVES FOR PROMOTING BONE GROWTH
  申请人：OssiFi Inc.

  公开号：US20140288068A1

  公开（公告）日：2014-09-25

  In one aspect, the invention provides compounds of Formula I, and salts, hydrates and isomers thereof. In another aspect, the invention provides a method of promoting bone formation in a subject in need thereof by administering to the subject a therapeutically effective amount of a compound of Formula I, Formula II, or Formula III. The present invention also provides orthopedic and periodontal devices, as well as methods for the treatment of renal disease and cancer, using a compound of Formula I, Formula II, or Formula III.

  在一个方面，该发明提供了式I的化合物，以及其盐、水合物和异构体。在另一个方面，该发明提供了一种通过向需要的受试者投予式I、式II或式III的化合物的治疗有效剂量来促进骨形成的方法。本发明还提供了骨科和牙周设备，以及使用式I、式II或式III的化合物治疗肾脏疾病和癌症的方法。
• 一种去氢骆驼蓬碱修饰药、制备方法及应用
  申请人：苏州大学

  公开号：CN115887376A

  公开（公告）日：2023-04-04

  本发明涉及一种去氢骆驼蓬碱修饰药、制备方法及应用。通过对去氢骆驼蓬碱进行衍生化修饰，以去氢骆驼蓬碱作为疏水内核，二硫代二丙酸作为连接臂，聚乙二醇为亲水骨架材料，合成还原敏感两亲性聚合物材料去氢骆驼蓬碱接枝聚乙二醇，即去氢骆驼蓬碱修饰药；将其在水溶液中自组装，得到一种载药纳米胶束系统，用作药物递送的载体材料。本发明提供的去氢骆驼蓬碱修饰药应用于制备纳米胶束载药系统，由于其在水溶液中可自组装形成稳定的纳米级胶束体系，从而能够高效的递送药物到肿瘤部位，提高去氢骆驼蓬碱的抗肿瘤效果，降低毒副作用，同时改善水溶性，为去氢骆驼蓬碱在抗肿瘤方面的应用提供更多可能性。
• Structure–activity relationship study of beta-carboline derivatives as haspin kinase inhibitors
  作者：Gregory D. Cuny、Natalia P. Ulyanova、Debasis Patnaik、Ji-Feng Liu、Xiangjie Lin、Ken Auerbach、Soumya S. Ray、Jun Xian、Marcie A. Glicksman、Ross L. Stein、Jonathan M.G. Higgins

  DOI：10.1016/j.bmcl.2012.01.028

  日期：2012.3

  Haspin is a serine/threonine kinase that phosphorylates Thr-3 of histone H3 in mitosis that has emerged as a possible cancer therapeutic target. High throughput screening of approximately 140,000 compounds identified the beta-carbolines harmine and harmol as moderately potent haspin kinase inhibitors. Based on information obtained from a structure-activity relationship study previously conducted for an acridine series of haspin inhibitors in conjunction with in silico docking using a recently disclosed crystal structure of the kinase, harmine analogs were designed that resulted in significantly increased haspin kinase inhibitory potency. The harmine derivatives also demonstrated less activity towards DYRK2 compared to the acridine series. In vitro mouse liver microsome stability and kinase profiling of a representative member of the harmine series (42, LDN-211898) are also presented. (C) 2012 Elsevier Ltd. All rights reserved.
• Beta-Carbolines as Inhibitors of Haspin and DYRK Kinases
  申请人：Higgins Jonathan

  公开号：US20130231360A1

  公开（公告）日：2013-09-05

  The present disclosure is directed to compounds of Formula (I) which are inhibitors of Haspin kinase and DYRK kinases. The compounds of the present disclosure, and compositions thereof, are useful in the treatment of disease related to Haspin kinase and DYRK kinase expression and/or activity.
• COMPOUNDS FOR BONE GROWTH
  申请人：OsteoQC, Inc

  公开号：US20170298059A1

  公开（公告）日：2017-10-19

  In one aspect, the invention provides compounds of Formula I, and salts, hydrates and isomers thereof. In another aspect, the invention provides a method of promoting bone formation in a subject in need thereof by administering to the subject a therapeutically effective amount of a compound of Formula I, Formula II, or Formula III. The present invention also provides orthopedic and periodontal devices, as well as methods for the treatment of renal disease and cancer, using a compound of Formula I, Formula II, or Formula III.