(2-naphthylthio)glycolamide | 74616-66-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: (2-naphthylthio)glycolamide
• 英文别名: (2-naphthylthio)acetamide；[2]naphthylsulfanyl-acetic acid amide；C-(Naphthyl-(2)-mercapto)-acetamid；(Naphthyl-(2)-mercapto)-essigaeure-amid；[2]Naphthylmercapto-essigsaeure-amid；Acetamide, 2-(2-naphthalenylthio)-；2-naphthalen-2-ylsulfanylacetamide
• CAS: 74616-66-3
• 化学式: C₁₂H₁₁NOS
• mdl: MFCD01210371
• 分子量: 217.291
• InChiKey: XMNWGYAHESUGCX-UHFFFAOYSA-N

物化性质

• 熔点：
  128-129 °C
• 沸点：
  442.7±28.0 °C(Predicted)
• 密度：
  1.26±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  15
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.083
• 拓扑面积：
  68.4
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (2-naphthylthio)glycolamide 在 双氧水 作用下， 以 溶剂黄146 为溶剂， 反应 2.0h， 以63.4%的产率得到(2-naphthylsulfinyl)acetamide
  参考文献：
  名称：

  Lisitsyn. V. N.; Kukalenko, L. S., Journal of Organic Chemistry USSR (English Translation), 1980, vol. 16, p. 549 - 552

  摘要：

  DOI：
• 作为产物：
  描述：

  杀螨砜 在 五氯化磷 作用下， 生成 (2-naphthylthio)glycolamide
  参考文献：
  名称：

  Gajowczyk; Suszko, Chemische Berichte, 1935, vol. 68, p. 1005,1008

  摘要：

  DOI：

文献信息

• Proteasome inhibitors and methods of using the same
  申请人：Bernadini Raffaella

  公开号：US20050107307A1

  公开（公告）日：2005-05-19

  The present invention provides boronic acid compounds, boronic esters, and compositions thereof that can modulate apoptosis such as by inhibition of proteasome activity. The compounds and compositions can be used in methods of inducing apoptosis and treating diseases such as cancer and other disorders associated directly of indirectly with proteasome activity.

  本发明提供了硼酸化合物、硼酸酯及其组合物，可以通过抑制蛋白酶体活性等方式调节细胞凋亡。这些化合物和组合物可以用于诱导细胞凋亡并治疗癌症等疾病，以及与蛋白酶体活性直接或间接相关的其他疾病。
• PROTEASOME INHIBITORS AND METHODS OF USING THE SAME
  申请人：Bernardini Raffaella

  公开号：US20090291918A1

  公开（公告）日：2009-11-26

  The present invention provides boronic acid compounds, boronic esters, and compositions thereof that can modulate apoptosis such as by inhibition of proteasome activity. The compounds and compositions can be used in methods of inducing apoptosis and treating diseases such as cancer and other disorders associated directly of indirectly with proteasome activity.

  本发明提供了硼酸化合物、硼酸酯及其组合物，可以调节细胞凋亡，例如通过抑制蛋白酶体活性。这些化合物和组合物可以用于诱导细胞凋亡和治疗癌症及其他与蛋白酶体活性直接或间接相关的疾病。
• Proteasome Inhibitors and Methods of Using the Same
  申请人：Bernardini Raffaella

  公开号：US20110144033A1

  公开（公告）日：2011-06-16

  The present invention provides boronic acid compounds, boronic esters, and compositions thereof that can modulate apoptosis such as by inhibition of proteasome activity. The compounds and compositions can be used in methods of inducing apoptosis and treating diseases such as cancer and other disorders associated directly of indirectly with proteasome activity.

  本发明提供了硼酸化合物、硼酸酯及其组合物，可以调节细胞凋亡，例如通过抑制蛋白酶体活性。这些化合物和组合物可用于诱导细胞凋亡和治疗癌症和其他与蛋白酶体活性直接或间接相关的疾病的方法。
• Proteasome Inhibitors And Methods Of Using The Same
  申请人：Cephalon, Inc.

  公开号：US20140088042A1

  公开（公告）日：2014-03-27

  The present invention provides boronic acid compounds, boronic esters, and compositions thereof that can modulate apoptosis such as by inhibition of proteasome activity. The compounds and compositions can be used in methods of inducing apoptosis and treating diseases such as cancer and other disorders associated directly of indirectly with proteasome activity.

  本发明提供了硼酸化合物、硼酸酯及其组合物，可以调节凋亡，例如通过抑制蛋白酶体活性。这些化合物和组合物可以用于诱导凋亡和治疗癌症和其他与蛋白酶体活性直接或间接相关的疾病的方法。
• Lisitsyn, V. N.; Kukalenko, L. S., Journal of Organic Chemistry USSR (English Translation), 1984, vol. 20, # 1, p. 116 - 118
  作者：Lisitsyn, V. N.、Kukalenko, L. S.

  DOI：——

  日期：——