CbzTyr-Val-Sta-Ala-StaOH | 135467-17-3

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 肽模拟物
• 英文名称: CbzTyr-Val-Sta-Ala-StaOH
• 英文别名: Cbz-Tyr-Val-Sta-Ala-Sta-OH；(3S,4S)-3-hydroxy-4-[[(2S)-2-[[(3S,4S)-3-hydroxy-4-[[(2S)-2-[[(2S)-3-(4-hydroxyphenyl)-2-(phenylmethoxycarbonylamino)propanoyl]amino]-3-methylbutanoyl]amino]-6-methylheptanoyl]amino]propanoyl]amino]-6-methylheptanoic acid
• CAS: 135467-17-3
• 化学式: C₄₁H₆₁N₅O₁₁
• 分子量: 799.962
• InChiKey: ADXHQLZNZBMXKP-MSQJMBMRSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  57
• 可旋转键数：
  24
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.56
• 拓扑面积：
  253
• 氢给体数：
  9
• 氢受体数：
  11

反应信息

• 作为反应物：
  描述：

  cis-2-<(tert-butyldiphenyl)silyloxymethyl>-5-4-(4-aminobutyl)cytosin-1'-yl>-1,3-oxathiolane 、 CbzTyr-Val-Sta-Ala-StaOH 在 (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate 、 三乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 以56%的产率得到cis-2-(tert-butyldiphenylsilyloxymethyl)-5-4-(CbzTyr-Val-Sta-Ala-Sta-4-aminobutyl)cytosin-1'-yl>-1,3-oxathiolane
  参考文献：
  名称：

  Synthesis and anti-human immunodeficiency virus type 1 activities of new peptido-nucleoside analogues

  摘要：

  In order to investigate whether antiproteasic peptides coupled to anti-reverse transcriptase nucleosides can act as inhibitors at the different stages of the HIV life cycle, various peptido-nucleosides were synthesized using methodologies involving (benzotriazol-1-yloxy)-tris(dimethylamino)phosphonium hexafluorophosphate (BOP) as a coupling reagent between the N-4-cytosinyl moiety and the peptide carboxy terminus. The anti-HIV-1 activity in MT(4) cells of this new class of compounds and their anti-HIV protease activities were determined. Fourteen peptido-nucleosides have been synthesized and six act against both the HIV-protease and viral replication in vitro. Although the activity of the most potent compounds against HIV was found to be one order of magnitude lower than that of the parent nucleoside drug 2',3'-dideoxy-3'-thiacytidine, this new class of compound could be of biological interest. Indeed, since the in vitro half-lives (t(1/2)) of the hydrolysis of the most potent compounds in human plasma were found to be longer than 2.5 h, these analogues could reach the infected cells in their structural integrity. This observation does not exclude that these compounds may exert their antiviral effects as combined prodrugs through extracellular or intracellular hydrolysis.

  DOI：

  10.1016/0223-5234(96)88298-5

文献信息

• Synthesis and anti-human immunodeficiency virus type 1 activities of new peptido-nucleoside analogues
  作者：M Camplo、V Niddam、P Barthélémy、P Faury、N Mourier、V Simon、AS Charvet、C Trabaud、JC Graciet、JC Chermann、JL Kraus

  DOI：10.1016/0223-5234(96)88298-5

  日期：1995.1

  In order to investigate whether antiproteasic peptides coupled to anti-reverse transcriptase nucleosides can act as inhibitors at the different stages of the HIV life cycle, various peptido-nucleosides were synthesized using methodologies involving (benzotriazol-1-yloxy)-tris(dimethylamino)phosphonium hexafluorophosphate (BOP) as a coupling reagent between the N-4-cytosinyl moiety and the peptide carboxy terminus. The anti-HIV-1 activity in MT(4) cells of this new class of compounds and their anti-HIV protease activities were determined. Fourteen peptido-nucleosides have been synthesized and six act against both the HIV-protease and viral replication in vitro. Although the activity of the most potent compounds against HIV was found to be one order of magnitude lower than that of the parent nucleoside drug 2',3'-dideoxy-3'-thiacytidine, this new class of compound could be of biological interest. Indeed, since the in vitro half-lives (t(1/2)) of the hydrolysis of the most potent compounds in human plasma were found to be longer than 2.5 h, these analogues could reach the infected cells in their structural integrity. This observation does not exclude that these compounds may exert their antiviral effects as combined prodrugs through extracellular or intracellular hydrolysis.