3-(4-Bromophenyl)sulfonyl-8-oxa-3-azabicyclo[3.2.1]octane | 1374986-85-2

• 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: 3-(4-Bromophenyl)sulfonyl-8-oxa-3-azabicyclo[3.2.1]octane
• 英文别名: 3-(4-bromophenyl)sulfonyl-8-oxa-3-azabicyclo[3.2.1]octane
• CAS: 1374986-85-2
• 化学式: C₁₂H₁₄BrNO₃S
• mdl: MFCD23229435
• 分子量: 332.218
• InChiKey: JKBZSIHDWAMPNY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  18
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  55
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  3-(4-Bromophenyl)sulfonyl-8-oxa-3-azabicyclo[3.2.1]octane 在 2,2,6,6-四甲基-3,5-庚二酮 、 caesium carbonate 、 copper(I) bromide 、 lithium hydroxide 作用下， 以 四氢呋喃 、 N-甲基吡咯烷酮 、 水 为溶剂， 反应 2.0h， 生成 3-(4-((8-oxa-3-azabicyclo[3.2.1]octan-3-yl)sulfonyl)phenoxy)-5-((3-methylbut-2-en-1-yl)oxy)benzoic acid
  参考文献：
  名称：

  Design, synthesis, and pharmacological evaluation of benzamide derivatives as glucokinase activators

  摘要：

  A series of benzamide derivatives were assembled by using the privileged-fragment-merging (PFM) strategy and their SAR studies as glucokinase activators were described. Compounds 5 and 16b were identified having a suitable balance of potency and activation profile. They showed EC50 values of 28.3 and 44.8 nM, and activation folds of 2.4 and 2.2, respectively. However, both compounds displayed a minor reduction in plasma glucose levels on imprinting control region (ICR) mice. Unfavorable pharmacokinetic profiles (PK) were also observed on these two compounds. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2012.03.008
• 作为产物：
  描述：

  8-氧杂-3-氮杂双环[3,2,1]辛烷 、 4-溴苯磺酰氯 在 吡啶 作用下， 以 二氯甲烷 为溶剂， 反应 4.0h， 生成 3-(4-Bromophenyl)sulfonyl-8-oxa-3-azabicyclo[3.2.1]octane
  参考文献：
  名称：

  Design, synthesis, and pharmacological evaluation of benzamide derivatives as glucokinase activators

  摘要：

  A series of benzamide derivatives were assembled by using the privileged-fragment-merging (PFM) strategy and their SAR studies as glucokinase activators were described. Compounds 5 and 16b were identified having a suitable balance of potency and activation profile. They showed EC50 values of 28.3 and 44.8 nM, and activation folds of 2.4 and 2.2, respectively. However, both compounds displayed a minor reduction in plasma glucose levels on imprinting control region (ICR) mice. Unfavorable pharmacokinetic profiles (PK) were also observed on these two compounds. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2012.03.008

文献信息

• Design, synthesis, and pharmacological evaluation of benzamide derivatives as glucokinase activators
  作者：Weiwei Mao、Mengmeng Ning、Zhiqing Liu、Qingzhang Zhu、Ying Leng、Ao Zhang

  DOI：10.1016/j.bmc.2012.03.008

  日期：2012.5

  A series of benzamide derivatives were assembled by using the privileged-fragment-merging (PFM) strategy and their SAR studies as glucokinase activators were described. Compounds 5 and 16b were identified having a suitable balance of potency and activation profile. They showed EC50 values of 28.3 and 44.8 nM, and activation folds of 2.4 and 2.2, respectively. However, both compounds displayed a minor reduction in plasma glucose levels on imprinting control region (ICR) mice. Unfavorable pharmacokinetic profiles (PK) were also observed on these two compounds. (C) 2012 Elsevier Ltd. All rights reserved.