3-<3-<3-(tert-butyloxycarbonyl)-2,2-dimethyl-4(S)-isobutyl-5(R)-oxazolidinyl>-2(R)-isopropyl-1,3-dioxopropyl>-4(R)-methyl-5(S)-phenyl-2-oxazolidinone | 134458-54-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑烷类
• 英文名称: 3-<3-<3-(tert-butyloxycarbonyl)-2,2-dimethyl-4(S)-isobutyl-5(R)-oxazolidinyl>-2(R)-isopropyl-1,3-dioxopropyl>-4(R)-methyl-5(S)-phenyl-2-oxazolidinone
• 英文别名: tert-butyl (4S,5R)-2,2-dimethyl-5-[(2R)-3-methyl-2-[(4R,5S)-4-methyl-2-oxo-5-phenyl-1,3-oxazolidine-3-carbonyl]butanoyl]-4-(2-methylpropyl)-1,3-oxazolidine-3-carboxylate
• CAS: 134458-54-1
• 化学式: C₃₀H₄₄N₂O₇
• 分子量: 544.689
• InChiKey: ONXOYJGXKQPFDJ-IQUCOFIMSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.9
• 重原子数：
  39
• 可旋转键数：
  9
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  102
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  3-<3-<3-(tert-butyloxycarbonyl)-2,2-dimethyl-4(S)-isobutyl-5(R)-oxazolidinyl>-2(R)-isopropyl-1,3-dioxopropyl>-4(R)-methyl-5(S)-phenyl-2-oxazolidinone 在 ethandithiol 、 ruthenium trichloride 、 sodium tetrahydroborate 、 diethylphosphoryl cyanide 、 camphor-10-sulfonic acid 、 过碘酸 、 N,N-二异丙基乙胺 、 乙酰氯 、 丙酮 作用下， 以 甲醇 、 四氯化碳 、 二氯甲烷 、 水 、 乙腈 为溶剂， 反应 36.0h， 生成 (2R,3R,4R,5S)-5-Amino-3,4-dihydroxy-2-isopropyl-7-methyl-octanoic acid ((S)-2-methyl-butyl)-amide
  参考文献：
  名称：

  Inhibitors of the protease from human immunodeficiency virus: design and modeling of a compound containing a dihydroxyethylene isostere insert with high binding affinity and effective antiviral activity

  摘要：

  The peptidomimetic template and the dihydroxyethylene isostere insert that were applied successfully to the design of renin inhibitors have been extended to the related protease from human immunodeficiency virus (HIV). The present report describes the structure-activity study leading to the identification of an inhibitor with a K(i) of < 1 nM for the HIV type-1 protease (compound II). This compound, containing a diol insert, is highly effective in blocking polyprotein processing in in vitro cell culture assays. Results obtained from kinetic analysis, studies of the stereochemistry of the insert, and modeling have led to insights as to the requisites involved in the active site-inhibitor interaction.

  DOI：

  10.1021/jm00112a005
• 作为产物：
  描述：

  3-<3(R)-<3-(tert-butyloxycarbonyl)-2,2-dimethyl-4(S)-isobutyl-5(R)-oxazolidinyl>-3-hydroxy-2(R)-isopropyl-1-oxopropyl>-4(R)-methyl-5(S)-phenyl-2-oxazolidinone 在 草酰氯 、 二甲基亚砜 作用下， 以 二氯甲烷 为溶剂， 反应 0.33h， 以90%的产率得到3-<3-<3-(tert-butyloxycarbonyl)-2,2-dimethyl-4(S)-isobutyl-5(R)-oxazolidinyl>-2(R)-isopropyl-1,3-dioxopropyl>-4(R)-methyl-5(S)-phenyl-2-oxazolidinone
  参考文献：
  名称：

  Inhibitors of the protease from human immunodeficiency virus: design and modeling of a compound containing a dihydroxyethylene isostere insert with high binding affinity and effective antiviral activity

  摘要：

  The peptidomimetic template and the dihydroxyethylene isostere insert that were applied successfully to the design of renin inhibitors have been extended to the related protease from human immunodeficiency virus (HIV). The present report describes the structure-activity study leading to the identification of an inhibitor with a K(i) of < 1 nM for the HIV type-1 protease (compound II). This compound, containing a diol insert, is highly effective in blocking polyprotein processing in in vitro cell culture assays. Results obtained from kinetic analysis, studies of the stereochemistry of the insert, and modeling have led to insights as to the requisites involved in the active site-inhibitor interaction.

  DOI：

  10.1021/jm00112a005