4-amino-N-methyl-3-methylamino-benzamide | 1325676-63-8

• 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: 4-amino-N-methyl-3-methylamino-benzamide
• 英文别名: 4-amino-N-methyl-3-(methylamino)benzamide
• CAS: 1325676-63-8
• 化学式: C₉H₁₃N₃O
• 分子量: 179.222
• InChiKey: GVBZSCIIODKXIC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.5
• 重原子数：
  13
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  67.2
• 氢给体数：
  3
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  4-amino-N-methyl-3-methylamino-benzamide 、 三氟乙酸 在 盐酸 作用下， 以 水 为溶剂， 反应 24.0h， 以69%的产率得到N,1-dimethyl-2-(trifluoromethyl)-1H-benzimidazole-6-carboxamide
  参考文献：
  名称：

  Exploring the interplay of physicochemical properties, membrane permeability and giardicidal activity of some benzimidazole derivatives

  摘要：

  This study evaluated the relationship between the physicochemical properties, membrane permeability and in vitro giardicidal activity of twenty nine benzimidazole derivatives (1-7n). The retention time data from reverse phase high performance chromatography (RP-HPLC) were used to estimate aqueous solubility and lipophilicity of these compounds. The apparent permeability was determined using Caco-2 cell monolayer. The calculation of some descriptors, such as Clog P. PSA, was performed using ACD labs software. For benzimidazole derivatives with NHCOOCH3, CH3, NH2, SH and SCH3 groups at the 2-position, a quadratic type of regression model was obtained with giardicidal activity and aqueous solubility or lipophilicity. On the other hand, giardicidal activity of 2-(trifluoromethyl)-1H-benzimidazole derivatives was influenced by lipophilicity, hydrogen bond donors and molecular volume but it was not determined by their apparent permeability in Caco-2 cell line. (C) 2012 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2012.03.014
• 作为产物：
  描述：

  3-羟基-4-硝基苯甲酸 在 5%-palladium/activated carbon 、 氢气 、 sodium hydroxide 作用下， 生成 4-amino-N-methyl-3-methylamino-benzamide
  参考文献：
  名称：

  Exploring the interplay of physicochemical properties, membrane permeability and giardicidal activity of some benzimidazole derivatives

  摘要：

  This study evaluated the relationship between the physicochemical properties, membrane permeability and in vitro giardicidal activity of twenty nine benzimidazole derivatives (1-7n). The retention time data from reverse phase high performance chromatography (RP-HPLC) were used to estimate aqueous solubility and lipophilicity of these compounds. The apparent permeability was determined using Caco-2 cell monolayer. The calculation of some descriptors, such as Clog P. PSA, was performed using ACD labs software. For benzimidazole derivatives with NHCOOCH3, CH3, NH2, SH and SCH3 groups at the 2-position, a quadratic type of regression model was obtained with giardicidal activity and aqueous solubility or lipophilicity. On the other hand, giardicidal activity of 2-(trifluoromethyl)-1H-benzimidazole derivatives was influenced by lipophilicity, hydrogen bond donors and molecular volume but it was not determined by their apparent permeability in Caco-2 cell line. (C) 2012 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2012.03.014

文献信息

• Substituted Fused Imidazole Derivatives, Pharmaceutical Compositions, and Methods of Use Thereof
  申请人：Mjalli Adnan M. M.

  公开号：US20110201604A1

  公开（公告）日：2011-08-18

  Substituted fused imidazole derivatives, methods of their preparation, pharmaceutical compositions comprising a substituted fused imidazole derivative, and methods of use in treating inflammation are provided. The substituted fused imidazole derivatives may control the activity or the amount or both the activity and the amount of heme-oxygenase.

  提供了替代融合咪唑衍生物、其制备方法、包含替代融合咪唑衍生物的药物组合物，以及在治疗炎症中使用的方法。这些替代融合咪唑衍生物可能控制血红素氧合酶的活性或数量，或者同时控制活性和数量。
• Substituted fused imidazole derivatives, pharmaceutical compositions, and methods of use thereof
  申请人：Mjalli Adnan M. M.

  公开号：US08759535B2

  公开（公告）日：2014-06-24

  Substituted fused imidazole derivatives, methods of their preparation, pharmaceutical compositions comprising a substituted fused imidazole derivative, and methods of use in treating inflammation are provided. The substituted fused imidazole derivatives may control the activity or the amount or both the activity and the amount of heme-oxygenase.

  本发明提供了替代融合咪唑衍生物，它们的制备方法，包括替代融合咪唑衍生物的药物组合物以及在治疗炎症方面使用的方法。这些替代融合咪唑衍生物可以控制血红素氧化酶的活性或数量或活性和数量。
• SUBSTITUTED FUSED IMIDAZOLE DERIVATIVES, PHARMACEUTICAL COMPOSITIONS, AND METHODS OF USE THEREOF
  申请人：vTv Therapeutics LLC

  公开号：EP2536285B1

  公开（公告）日：2018-04-25
• US8759535B2
  申请人：——

  公开号：US8759535B2

  公开（公告）日：2014-06-24
• [EN] SUBSTITUTED FUSED IMIDAZOLE DERIVATIVES, PHARMACEUTICAL COMPOSITIONS, AND METHODS OF USE THEREOF<br/>[FR] DÉRIVÉS D'IMIDAZOLE FUSIONNÉS ET SUBSTITUÉS, COMPOSITIONS PHARMACEUTIQUES ET PROCÉDÉS D'UTILISATION ASSOCIÉS
  申请人：HIGH POINT PHARMACEUTICALS LLC

  公开号：WO2011103018A1

  公开（公告）日：2011-08-25

  Substituted fused imidazole derivatives, methods of their preparation, pharmaceutical compositions comprising a substituted fused imidazole derivative, and methods of use in treating inflammation are provided. The substituted fused imidazole derivatives may control of the activity or the amount or both the activity and the amount of heme-oxygenase.