N1-[(2-Methoxyphenyl)methyl]-1,3-propanediamine | 106353-12-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: N1-[(2-Methoxyphenyl)methyl]-1,3-propanediamine
• 英文别名: N'-[(2-methoxyphenyl)methyl]propane-1,3-diamine
• CAS: 106353-12-2
• 化学式: C₁₁H₁₈N₂O
• 分子量: 194.277
• InChiKey: IRKRYKYYQONACD-UHFFFAOYSA-N

物化性质

• 沸点：
  307.2±22.0 °C(Predicted)
• 密度：
  1.013±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.8
• 重原子数：
  14
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  47.3
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  methyl [4-(chloroacetyl)-1-(2-chlorophenyl)-5-hydroxy-1H-pyrazol-3-yl]acetate 、 N1-[(2-Methoxyphenyl)methyl]-1,3-propanediamine 在 N,N-二异丙基乙胺 作用下， 以 乙腈 为溶剂， 反应 4.0h， 生成
  参考文献：
  名称：

  Design, synthesis and biological activity of original pyrazolo-pyrido-diazepine, -pyrazine and -oxazine dione derivatives as novel dual Nox4/Nox1 inhibitors

  摘要：

  Pyrazolo-pyrido-diazepine, -pyrazine and -oxazine dione derivatives are new chemical entities with good and attractive druglikeness properties. A series of pyrazolo-pyrido-diazepine dione analogs demonstrated to be particularly amenable to lead optimization through a couple of cycles in order to improve specificity for isoforms Nox4 and Nox1 and had excellent pharmacokinetic parameters by oral route. Several molecules such as compound 7c proved to be highly potent in in vitro assays on human lung fibroblasts differentiation as well as in curative murine models of bleomycin-induced pulmonary fibrosis with superior efficiency over Pirfenidone. Pyrazolo-pyrido-diazepine dione derivatives targeting Nox4 and Nox1 isoforms appear highly promising therapeutics for the treatment of idiopathic pulmonary fibrosis. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2011.10.016

文献信息

• Nitromethylen-tetrahydropyrimidine
  申请人：NIHON TOKUSHU NOYAKU SEIZO K.K.

  公开号：EP0199974A2

  公开（公告）日：1986-12-10

  Die vorliegende Erfindung betrifft neue Nitromethylen-tetrahydropyrimidin-Derivate der Formel (I) in der R eine Alkyl-Gruppe, eine Alkoxy-Gruppe, eine Alkylthio-Gruppe, eine Nitro-Gruppe, eine Cyano-Gruppe, eine halogen-substituierte Alkyl-Gruppe, eine halogen-substituierte Alkoxy-Gruppe, eine halogen-substituierte Alkylthio-Gruppe, eine Amino-Gruppe, eine Dialkylamino-Gruppe, eine Acylamino-Gruppe, eine Carboxyl-Gruppe, eine Alkoxycarbonyl-Gruppe, eine Alkylsulfinyl-Gruppe, eine Alkylsulfonyl-Gruppe oder ein Halogen-Atom bezeichnet und n 1, 2 oder 3 bezeichnet, jedoch mit der Maßgabe, daß, wenn n für 1 steht, R nicht ein Halogen-Atom bezeichnen darf, Verfahren zur Herstellung der Verbindungen (I) sowie die Verwendung der neuen Verbindungen als Pestizide, insbesondere als Insektizide.

  本发明涉及式 (I) 的新型硝基亚甲基四氢嘧啶衍生物 其中 R 表示烷基、烷氧基、烷硫基、硝基、氰基、卤素取代的烷基、卤素取代的烷氧基、卤素取代的烷硫基、氨基、二烷基氨基、酰氨基、羧基、烷氧羰基、烷基亚磺酰基、烷基磺酰基或卤素原子，以及 n 表示 1、2 或 3，但当 n 为 1 时，R 不得表示卤素原子、 化合物(I)的制备工艺以及新化合物作为杀虫剂，特别是杀虫剂的用途。
• Naphthalene diimide-polyamine hybrids as antiproliferative agents: Focus on the architecture of the polyamine chains
  作者：Andrea Milelli、Chiara Marchetti、Maria Laura Greco、Federica Moraca、Giosuè Costa、Eleonora Turrini、Elena Catanzaro、Nibal Betari、Cinzia Calcabrini、Claudia Sissi、Stefano Alcaro、Carmela Fimognari、Vincenzo Tumiatti、Anna Minarini

  DOI：10.1016/j.ejmech.2017.01.025

  日期：2017.3

  Naphthalene diimides (NDIs) have been widely used as scaffold to design DNA-directed agents able to target peculiar DNA secondary arrangements endowed with relevant biochemical roles. Recently, we have reported disubstituted linear- and macrocyclic-NDIs that bind telomeric and non-telomeric G-quadruplex with high degree of affinity and selectivity. Herein, the synthesis, biological evaluation and molecular modelling studies of a series of asymmetrically substituted NDIs are reported. Among these, compound 9 emerges as the most interesting of the series being able to bind telomeric G-quadruplex (Delta Tm = 29 degrees C at 2.5 mu M), to inhibit the activity of DNA processing enzymes, such as topoisomerase II and TAQ-polymerase, and to exert antiproliferative effects in the NCI panel of cancer cell lines with GI(50) values in the micro-to nanomolar concentration range (i.e. SR cell line, GI50 = 76 nM). Molecular mechanisms of cell death have been investigated and molecular modelling studies have been performed in order to shed light on the antiproliferative and DNA-recognition processes. (C) 2017 Elsevier Masson SAS. All rights reserved.
• Design, synthesis and biological activity of original pyrazolo-pyrido-diazepine, -pyrazine and -oxazine dione derivatives as novel dual Nox4/Nox1 inhibitors
  作者：Francesca Gaggini、Benoît Laleu、Mike Orchard、Laetitia Fioraso-Cartier、Laurène Cagnon、Sophie Houngninou-Molango、Angelo Gradia、Guillaume Duboux、Cédric Merlot、Freddy Heitz、Cédric Szyndralewiez、Patrick Page

  DOI：10.1016/j.bmc.2011.10.016

  日期：2011.12

  Pyrazolo-pyrido-diazepine, -pyrazine and -oxazine dione derivatives are new chemical entities with good and attractive druglikeness properties. A series of pyrazolo-pyrido-diazepine dione analogs demonstrated to be particularly amenable to lead optimization through a couple of cycles in order to improve specificity for isoforms Nox4 and Nox1 and had excellent pharmacokinetic parameters by oral route. Several molecules such as compound 7c proved to be highly potent in in vitro assays on human lung fibroblasts differentiation as well as in curative murine models of bleomycin-induced pulmonary fibrosis with superior efficiency over Pirfenidone. Pyrazolo-pyrido-diazepine dione derivatives targeting Nox4 and Nox1 isoforms appear highly promising therapeutics for the treatment of idiopathic pulmonary fibrosis. (C) 2011 Elsevier Ltd. All rights reserved.