3-((S)-2-azido-3-{4-[3-isopropyl-4-(triisopropylsilyloxy)benzyl]-3,5-dimethylphenyl}propionyl)-(S)-4-benzyloxazolidin-2-one | 565452-54-2

• 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-((S)-2-azido-3-{4-[3-isopropyl-4-(triisopropylsilyloxy)benzyl]-3,5-dimethylphenyl}propionyl)-(S)-4-benzyloxazolidin-2-one
• 英文别名: (4S)-3-[(2S)-2-azido-3-[3,5-dimethyl-4-[[3-propan-2-yl-4-tri(propan-2-yl)silyloxyphenyl]methyl]phenyl]propanoyl]-4-benzyl-1,3-oxazolidin-2-one
• CAS: 565452-54-2
• 化学式: C₄₀H₅₄N₄O₄Si
• 分子量: 682.979
• InChiKey: YKCBWDZOZMKDQW-UNVMMQEESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  10.38
• 重原子数：
  49
• 可旋转键数：
  14
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  70.2
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  3-((S)-2-azido-3-{4-[3-isopropyl-4-(triisopropylsilyloxy)benzyl]-3,5-dimethylphenyl}propionyl)-(S)-4-benzyloxazolidin-2-one 在 palladium on activated charcoal lithium hydroxide 、 氢气 、 双氧水 、 triethylamine tris(hydrogen fluoride) 作用下， 以 四氢呋喃 、 水 、 溶剂黄146 为溶剂， 反应 5.5h， 生成 2-Amino-3-[4-(4-hydroxy-3-isopropyl-benzyl)-3,5-dimethyl-phenyl]-propionic acid
  参考文献：
  名称：

  Structural Determinants of Selective Thyromimetics

  摘要：

  The thyromimetic GC-1 shows a preference for binding the P form of the thyroid hormone receptor (TR). GC-1 was designed as an analogue of the thyromimetic DIMIT, which has alower affinity for TR and is not selective. GC-1 has a methylene group linking its two aromatic rings and an oxyacetic acid polar side chain, while DIMIT has an ether oxygen linking its aromatic rings and an L-alanine polar side chain. The structural features of GC-1 that confer its greater affinity and selectivity compared to DIMIT were analyzed with the preparation of analogues that bear only one of their two different structural features. The analogue of GC-1 with a biaryl ether has selectivity comparable to that of GC-1, while the analogue of DIMIT with a methylene group linking its aromatic rings is only slightly selective. These results demonstrate that the oxyacetic acid side chain of GC-1 is critical in conferring TR-beta selectivity.

  DOI：

  10.1021/jm0301181
• 作为产物：
  描述：

  4-溴-2-异丙基苯酚 在 palladium on activated charcoal 吡啶 、 咪唑 、 bis-triphenylphosphine-palladium(II) chloride 、 正丁基锂 、 氢气 、 三甲基乙酰氯 、 双(三甲基硅烷基)氨基钾 、 臭氧 、 三乙胺 、 lithium chloride 作用下， 以 四氢呋喃 、 乙醇 、 正己烷 、 二氯甲烷 、 溶剂黄146 、 乙酸乙酯 、 1,2-二氯乙烷 、 N,N-二甲基甲酰胺 、 甲苯 为溶剂， -78.0~60.0 ℃ 、241.32 kPa 条件下， 反应 52.76h， 生成 3-((S)-2-azido-3-{4-[3-isopropyl-4-(triisopropylsilyloxy)benzyl]-3,5-dimethylphenyl}propionyl)-(S)-4-benzyloxazolidin-2-one
  参考文献：
  名称：

  Structural Determinants of Selective Thyromimetics

  摘要：

  The thyromimetic GC-1 shows a preference for binding the P form of the thyroid hormone receptor (TR). GC-1 was designed as an analogue of the thyromimetic DIMIT, which has alower affinity for TR and is not selective. GC-1 has a methylene group linking its two aromatic rings and an oxyacetic acid polar side chain, while DIMIT has an ether oxygen linking its aromatic rings and an L-alanine polar side chain. The structural features of GC-1 that confer its greater affinity and selectivity compared to DIMIT were analyzed with the preparation of analogues that bear only one of their two different structural features. The analogue of GC-1 with a biaryl ether has selectivity comparable to that of GC-1, while the analogue of DIMIT with a methylene group linking its aromatic rings is only slightly selective. These results demonstrate that the oxyacetic acid side chain of GC-1 is critical in conferring TR-beta selectivity.

  DOI：

  10.1021/jm0301181

文献信息

• Structural Determinants of Selective Thyromimetics
  作者：Hikari A. I. Yoshihara、James W. Apriletti、John D. Baxter、Thomas S. Scanlan

  DOI：10.1021/jm0301181

  日期：2003.7.1

  The thyromimetic GC-1 shows a preference for binding the P form of the thyroid hormone receptor (TR). GC-1 was designed as an analogue of the thyromimetic DIMIT, which has alower affinity for TR and is not selective. GC-1 has a methylene group linking its two aromatic rings and an oxyacetic acid polar side chain, while DIMIT has an ether oxygen linking its aromatic rings and an L-alanine polar side chain. The structural features of GC-1 that confer its greater affinity and selectivity compared to DIMIT were analyzed with the preparation of analogues that bear only one of their two different structural features. The analogue of GC-1 with a biaryl ether has selectivity comparable to that of GC-1, while the analogue of DIMIT with a methylene group linking its aromatic rings is only slightly selective. These results demonstrate that the oxyacetic acid side chain of GC-1 is critical in conferring TR-beta selectivity.