[2-bromo-4-(bromomethyl)phenyl]methanol | 345953-41-5

• 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: [2-bromo-4-(bromomethyl)phenyl]methanol
• CAS: 345953-41-5
• 化学式: C₈H₈Br₂O
• 分子量: 279.959
• InChiKey: GMYXIPBXFATPMY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  11
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  [2-bromo-4-(bromomethyl)phenyl]methanol 在 manganese(IV) oxide 、 草酰氯 、 二甲基亚砜 、 三乙胺 作用下， 生成 di-(tert-butyl)-2-bromo-4-(bromomethyl) benzoylphosphonate
  参考文献：
  名称：

  The development of potent non-peptidic PTP-1B inhibitors

  摘要：

  The SAR from our peptide libraries was exploited to design a series of potent deoxybenzoin PTP-1B inhibitors. The introduction of an ortho bromo substituent next to the difluoromethylphosphonate warhead gave up to 20-fold increase in potency compared to the desbromo analogues. In addition, these compounds were orally bioavailable and active in the animal models of non-insulin dependent diabetes mellitus (NIDDM). (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2003.11.048
• 作为产物：
  描述：

  2-溴-4-甲基苯甲酸 在 N-溴代丁二酰亚胺(NBS) 、 硼烷 作用下， 以 四氢呋喃 、 四氯化碳 为溶剂， 生成 [2-bromo-4-(bromomethyl)phenyl]methanol
  参考文献：
  名称：

  The development of potent non-peptidic PTP-1B inhibitors

  摘要：

  The SAR from our peptide libraries was exploited to design a series of potent deoxybenzoin PTP-1B inhibitors. The introduction of an ortho bromo substituent next to the difluoromethylphosphonate warhead gave up to 20-fold increase in potency compared to the desbromo analogues. In addition, these compounds were orally bioavailable and active in the animal models of non-insulin dependent diabetes mellitus (NIDDM). (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2003.11.048

文献信息

• Phosphonic acid derivatives as inhibitors of protein tyrosine phosphatase IB (PTP-IB)
  申请人：——

  公开号：US20020052344A1

  公开（公告）日：2002-05-02

  The invention encompasses the novel class of compounds represented by formula I which are inhibitors of the PTP-1B enzyme. 1 The invention also encompasses pharmaceutical compositions and methods of treating or preventing PTP-1B mediated diseases, including diabetes, obesity, and diabetes-related diseases.

  本发明包括一类新颖的化合物，这些化合物由公式I表示，是PTP-1B酶的抑制剂。 本发明还包括用于治疗或预防PTP-1B介导的疾病的药物组合物和方法，包括糖尿病、肥胖症和与糖尿病相关的疾病。
• Protein tyrosine phosphatase 1B (PTP-1B) inhibitors containing two ortho-substituted aromatic phosphonates
  申请人：——

  公开号：US20020052347A1

  公开（公告）日：2002-05-02

  The invention encompasses the novel class of compounds represented by formula I, which are inhibitors of the PTP-1B enzyme. 1 The invention also encompasses pharmaceutical compositions and methods of treating or preventing PTP-1B mediated diseases, including diabetes, obesity, and diabetes-related diseases.

  该发明涵盖了由公式I代表的新型化合物类别，这些化合物是PTP-1B酶的抑制剂。该发明还涵盖了制药组合物和治疗或预防PTP-1B介导的疾病，包括糖尿病、肥胖症和与糖尿病相关的疾病的方法。
• Phosphonic acid derivatives as inhibitors of protein tyrosine phosphatase 1B (PTP-1B)
  申请人：Merck Erosst Canada & Co.

  公开号：US06583126B2

  公开（公告）日：2003-06-24

  The invention encompasses the novel class of compounds represented by formula I which are inhibitors of the PTP-1B enzyme. The invention also encompasses pharmaceutical compositions and methods of treating or preventing PTP-1B mediated diseases, including diabetes, obesity, and diabetes-related diseases.

  该发明涵盖了由式I所代表的新型化合物类别，这些化合物是PTP-1B酶的抑制剂。该发明还涵盖了制药组合物和治疗或预防PTP-1B介导的疾病的方法，包括糖尿病、肥胖症和糖尿病相关疾病。
• AROMATIC PHOSPHONATES AS PROTEIN TYROSINE PHOSPHATASE 1B (PTP-1B) INHIBITORS
  申请人：Merck Frosst Canada & Co.

  公开号：EP1242431A1

  公开（公告）日：2002-09-25
• PHOSPHONIC ACID DERIVATIVES AS INHIBITORS OF PROTEIN TYROSINE PHOSPHATASE 1B (PTP-1B)
  申请人：MERCK FROSST CANADA INC.

  公开号：EP1242432A1

  公开（公告）日：2002-09-25