2-Amino-3-(4-bromothiophen-3-yl)propanoic acid | 1270323-91-5

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: 2-Amino-3-(4-bromothiophen-3-yl)propanoic acid
• 英文别名: 2-amino-3-(4-bromothiophen-3-yl)propanoic acid
• CAS: 1270323-91-5
• 化学式: C₇H₈BrNO₂S
• 分子量: 250.116
• InChiKey: NYJITXFTOKUNQZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -1
• 重原子数：
  12
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  91.6
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  2-Amino-3-(4-bromothiophen-3-yl)propanoic acid 在 碳酸氢钠 、 三甲基硅烷化重氮甲烷 作用下， 以 四氢呋喃 、 二氯甲烷 、 水 为溶剂， 生成 Methyl 3-(4-bromothiophen-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate
  参考文献：
  名称：

  Design and synthesis of thiophene dihydroisoquinolines as novel BACE1 inhibitors

  摘要：

  Utilizing a structure based design approach, combined with extensive medicinal chemistry execution, highly selective, potent and novel BACE1 inhibitor 8 (BACE1 Alpha assay IC50=8nM) was made from a weak μM potency hit in an extremely efficient way. The detailed SAR and general design approaches will be discussed.

  DOI：

  10.1016/j.bmcl.2013.03.009
• 作为产物：
  描述：

  3-溴-4-甲基噻吩 在 N-溴代丁二酰亚胺(NBS) 、 偶氮二异丁腈 、 氢溴酸 、 caesium carbonate 作用下， 以 四氯化碳 、 乙腈 为溶剂， 反应 3.0h， 生成 2-Amino-3-(4-bromothiophen-3-yl)propanoic acid
  参考文献：
  名称：

  Design and synthesis of thiophene dihydroisoquinolines as novel BACE1 inhibitors

  摘要：

  Utilizing a structure based design approach, combined with extensive medicinal chemistry execution, highly selective, potent and novel BACE1 inhibitor 8 (BACE1 Alpha assay IC50=8nM) was made from a weak μM potency hit in an extremely efficient way. The detailed SAR and general design approaches will be discussed.

  DOI：

  10.1016/j.bmcl.2013.03.009

文献信息

• Design and synthesis of thiophene dihydroisoquinolines as novel BACE1 inhibitors
  作者：Ying-zi Xu、Shendong Yuan、Simeon Bowers、Roy K. Hom、Wayman Chan、Hing L. Sham、Yong L. Zhu、Paul Beroza、Hu Pan、Eric Brecht、Nanhua Yao、Julie Lougheed、Jiangli Yan、Danny Tam、Zhao Ren、Lany Ruslim、Michael P. Bova、Dean R. Artis

  DOI：10.1016/j.bmcl.2013.03.009

  日期：2013.5

  Utilizing a structure based design approach, combined with extensive medicinal chemistry execution, highly selective, potent and novel BACE1 inhibitor 8 (BACE1 Alpha assay IC50=8nM) was made from a weak μM potency hit in an extremely efficient way. The detailed SAR and general design approaches will be discussed.