N-(4-bromo-1-naphthyl)-2-methylbenzamide | 928235-57-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: N-(4-bromo-1-naphthyl)-2-methylbenzamide
• 英文别名: N-(4-bromonaphthalen-1-yl)-2-methylbenzamide
• CAS: 928235-57-8
• 化学式: C₁₈H₁₄BrNO
• 分子量: 340.219
• InChiKey: GNSXOYYZOJNEQE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.1
• 重原子数：
  21
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.06
• 拓扑面积：
  29.1
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  N-(4-bromo-1-naphthyl)-2-methylbenzamide 、 N,N-二甲基甲酰胺 在 仲丁基锂 作用下， 以 四氢呋喃 、 环己烷 为溶剂， 反应 1.0h， 生成 N-(4-formyl-1-naphthyl)-2-methylbenzamide
  参考文献：
  名称：

  Design, Synthesis, and Evaluation of Naphthalene-Sulfonamide Antagonists of Human CCR8

  摘要：

  The design, synthesis, and structure-activity relationship development of naphthalene-derived human CCR8 antagonists is described. In vitro binding assay results of these investigations are reported, critical interactions of the antagonists with CCR8 are defined, and preliminary physicochemical and pharmacokinetic data for the naphthalene scaffold are presented.

  DOI：

  10.1021/jm061118e
• 作为产物：
  描述：

  4-溴-1-萘胺 、 邻甲基苯甲酰氯 在 吡啶 作用下， 以 四氢呋喃 为溶剂， 反应 17.0h， 生成 N-(4-bromo-1-naphthyl)-2-methylbenzamide
  参考文献：
  名称：

  Design, Synthesis, and Evaluation of Naphthalene-Sulfonamide Antagonists of Human CCR8

  摘要：

  The design, synthesis, and structure-activity relationship development of naphthalene-derived human CCR8 antagonists is described. In vitro binding assay results of these investigations are reported, critical interactions of the antagonists with CCR8 are defined, and preliminary physicochemical and pharmacokinetic data for the naphthalene scaffold are presented.

  DOI：

  10.1021/jm061118e

文献信息

• [EN] METHODS AND COMPOSITIONS FOR TARGETING TREGS USING CCR8 INHIBITORS<br/>[FR] MÉTHODES ET COMPOSITIONS POUR CIBLER DES TREG AU MOYEN D'INHIBITEURS DE CCR8
  申请人：NANJING IMMUNOPHAGE BIOTECH CO LTD

  公开号：WO2022000443A1

  公开（公告）日：2022-01-06

  Provided herein are compounds of Formula (I) which can be used as CCR8 inhibitors, which can be used as treatment or prevention of cancer using CCR8 inhibitors targeted tumor specific T regulatory cells.

  本文提供的是Formula (I)的化合物，可用作CCR8抑制剂，可用作使用CCR8抑制剂靶向肿瘤特异性T调节细胞的癌症治疗或预防。
• Design, Synthesis, and Evaluation of Naphthalene-Sulfonamide Antagonists of Human CCR8
  作者：Tracy J. Jenkins、Bing Guan、Mingshi Dai、Gang Li、Thomas E. Lightburn、Shan Huang、B. Scott Freeze、Douglas F. Burdi、Swanee Jacutin-Porte、Robert Bennett、Weirong Chen、Charles Minor、Shomir Ghosh、Christopher Blackburn、Kenneth M. Gigstad、Matthew Jones、Roland Kolbeck、Wei Yin、Sean Smith、Daniel Cardillo、Timothy D. Ocain、Geraldine C. Harriman

  DOI：10.1021/jm061118e

  日期：2007.2.8

  The design, synthesis, and structure-activity relationship development of naphthalene-derived human CCR8 antagonists is described. In vitro binding assay results of these investigations are reported, critical interactions of the antagonists with CCR8 are defined, and preliminary physicochemical and pharmacokinetic data for the naphthalene scaffold are presented.