(4S,6aR,6bS,8aS,12aS,12bR)-10-((3-chlorobenzylidene)amino)-6a,8a-dimethyl-3,4,5,6,6a,6b,7,8,8a,12,12a,12b-dodecahydro-1H-naphtho[2',1':4,5]indeno[1,2-d]thiazol-4-ol | 1447238-23-4

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 类固醇和类固醇衍生物
• 英文名称: (4S,6aR,6bS,8aS,12aS,12bR)-10-((3-chlorobenzylidene)amino)-6a,8a-dimethyl-3,4,5,6,6a,6b,7,8,8a,12,12a,12b-dodecahydro-1H-naphtho[2',1':4,5]indeno[1,2-d]thiazol-4-ol
• CAS: 1447238-23-4
• 化学式: C₂₇H₃₁ClN₂OS
• 分子量: 467.075
• InChiKey: QITXTHUASIZFBQ-WNPREPMYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.88
• 重原子数：
  32.0
• 可旋转键数：
  2.0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.56
• 拓扑面积：
  45.48
• 氢给体数：
  1.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  (4S,6aR,6bS,8aS,12aS,12bR)-10-((3-chlorobenzylidene)amino)-6a,8a-dimethyl-3,4,5,6,6a,6b,7,8,8a,12,12a,12b-dodecahydro-1H-naphtho[2',1':4,5]indeno[1,2-d]thiazol-4-ol 在 sodium tetrahydroborate 作用下， 以 甲醇 为溶剂， 以100%的产率得到(4S,6aR,6bS,8aS,12aS,12bR)-10-((3-chlorobenzyl)amino)-6a,8a-dimethyl-3,4,5,6,6a,6b,7,8,8a,12,12a,12b-dodecahydro-1H-naphtho[2',1':4,5]indeno[1,2-d]thiazol-4-ol
  参考文献：
  名称：

  Synthesis and biological evaluation of dehydroepiandrosterone-fused thiazole, imidazo[2,1-b]thiazole, pyridine steroidal analogues

  摘要：

  A series of steroidal[17,16-b]thiazole, steroidal[1,2-b]pyridine and steroidal[17,16-d]thiazole[2,1-b]imidazo products were synthesized through a convenient and productive method. Anti-proliferation activity against EC109 (human esophageal carcinoma), EC9706 (human esophageal carcinoma) and MGC-803 (human gastric carcinoma) cell lines was examined in vitro. Among the screened compounds, several highly potential compounds were located. (C) 2013 Elsevier Inc. All rights reserved.

  DOI：

  10.1016/j.steroids.2013.12.003
• 作为产物：
  描述：

  2'-Amino-thiazolo<5',4'-16,17>androsta-5,16-dien-3β-ol 、 3-氯苯甲醛 在 potassium carbonate 、 三乙胺 作用下， 以 四氢呋喃 、 乙醇 为溶剂， 反应 4.0h， 以94%的产率得到(4S,6aR,6bS,8aS,12aS,12bR)-10-((3-chlorobenzylidene)amino)-6a,8a-dimethyl-3,4,5,6,6a,6b,7,8,8a,12,12a,12b-dodecahydro-1H-naphtho[2',1':4,5]indeno[1,2-d]thiazol-4-ol
  参考文献：
  名称：

  Synthesis and biological evaluation of dehydroepiandrosterone-fused thiazole, imidazo[2,1-b]thiazole, pyridine steroidal analogues

  摘要：

  A series of steroidal[17,16-b]thiazole, steroidal[1,2-b]pyridine and steroidal[17,16-d]thiazole[2,1-b]imidazo products were synthesized through a convenient and productive method. Anti-proliferation activity against EC109 (human esophageal carcinoma), EC9706 (human esophageal carcinoma) and MGC-803 (human gastric carcinoma) cell lines was examined in vitro. Among the screened compounds, several highly potential compounds were located. (C) 2013 Elsevier Inc. All rights reserved.

  DOI：

  10.1016/j.steroids.2013.12.003