O-(N^α-tert-butoxycarbonyl-L-tert-butoxytyrosinyl) O-(S-pivaloyl-2-thioethyl) N,N-diisopropylphosphoramidite | 312750-63-3

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: O-(N^α-tert-butoxycarbonyl-L-tert-butoxytyrosinyl) O-(S-pivaloyl-2-thioethyl) N,N-diisopropylphosphoramidite
• 英文别名: tert-butyl (2S)-3-[4-[2-(2,2-dimethylpropanoylsulfanyl)ethoxy-[di(propan-2-yl)amino]phosphanyl]oxyphenyl]-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate
• CAS: 312750-63-3
• 化学式: C₃₁H₅₃N₂O₇PS
• 分子量: 628.811
• InChiKey: JXVYZJMZKXESNV-LZBJMVSRSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.4
• 重原子数：
  42
• 可旋转键数：
  19
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.71
• 拓扑面积：
  129
• 氢给体数：
  1
• 氢受体数：
  9

反应信息

• 作为反应物：
  描述：

  O-(N^α-tert-butoxycarbonyl-L-tert-butoxytyrosinyl) O-(S-pivaloyl-2-thioethyl) N,N-diisopropylphosphoramidite 在 四氮唑 、 叔丁基过氧化氢 作用下， 以 甲苯 、 乙腈 为溶剂， 生成 O-(N^α-tert-butoxycarbonyl-L-tert-butoxytyrosinyl) O-(S-pivaloyl-2-thioethyl) 3'-azido-2',3'-deoxythymidin-5'-yl phosphate
  参考文献：
  名称：

  DESIGN OF NEW MONONUCLEOTIDE PRODRUGS: ARYL (SATE) PHOSPHOTRIESTER DERIVATIVES

  摘要：

  Synthesis, biological activities and decomposition kinetics of novel phosphotriester derivatives of 3'-azido-2',3'-dideoxythymidine (AZT) bearing a S-tButyl-2-thioethyl (tBuSATE) group and L-tyrosinyl residues are reported. All the derivatives appeared to be potent inhibitors of HIV-1 replication in various cell culture experiments. The proposed decomposition process of these mixed phosphotriesters may involve successively an esterase and then a phosphodiesterase activation.

  DOI：

  10.1081/ncn-100002302
• 作为产物：
  描述：

  S-(2-羟乙基)2,2-二甲基丙硫酸盐 在 四氮唑 、 TEA 作用下， 生成 O-(N^α-tert-butoxycarbonyl-L-tert-butoxytyrosinyl) O-(S-pivaloyl-2-thioethyl) N,N-diisopropylphosphoramidite
  参考文献：
  名称：

  Rational design of a new series of mixed anti-HIV pronucleotides

  摘要：

  MonoSATE aryl phosphotriesters of AZT are able to deliver intracellularly the corresponding 5'-mononucleotide. This process requires activation by an esterase followed by a phosphodiesterase. This finding opens the way to the design of hew pronucleotide series, (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(98)00535-6

文献信息

• <i>S</i>-Acyl-2-thioethyl Aryl Phosphotriester Derivatives as Mononucleotide Prodrugs
  作者：Nathalie Schlienger、Suzanne Peyrottes、Tarek Kassem、Jean-Louis Imbach、Gilles Gosselin、Anne-Marie Aubertin、Christian Périgaud

  DOI：10.1021/jm000996o

  日期：2000.11.1

  The synthesis and biological activities of phosphotriester derivatives of 3'-azido-2',3'-dideoxythymidine (AZT) bearing a phenyl group or L-tyrosinyl residues are reported. The target compounds were obtained via either P-V or p(III) chemistry from the appropriate aryl precursors. All the derivatives were evaluated for their in vitro anti-HIV activity, and they appeared to be potent inhibitors of HIV-1 replication in various cell culture experiments, with EC50 values between the micro- and nanomolar range. Furthermore, compounds incorporating an amino-and/or acid-substituted tyrosinyl residue demonstrated significant anti-HIV effects in thymidine kinase-deficient (TK-) cells showing their ability to act as mononucleotide prodrugs. The proposed decomposition process of these mixed mononucleoside aryl phosphotriesters may involve esterase activation followed by phosphodiesterase hydrolysis.
• Rational design of a new series of mixed anti-HIV pronucleotides
  作者：Nathalie Schlienger、Thierry Beltran、Christian Périgaud、Isabelle Lefebvre、Alain Pompon、Anne-Marie Aubertin、Gilles Gosselin、Jean-Louis Imbach

  DOI：10.1016/s0960-894x(98)00535-6

  日期：1998.11

  MonoSATE aryl phosphotriesters of AZT are able to deliver intracellularly the corresponding 5'-mononucleotide. This process requires activation by an esterase followed by a phosphodiesterase. This finding opens the way to the design of hew pronucleotide series, (C) 1998 Elsevier Science Ltd. All rights reserved.
• DESIGN OF NEW MONONUCLEOTIDE PRODRUGS: ARYL (SATE) PHOSPHOTRIESTER DERIVATIVES
  作者：S. Peyrottes、N. Schlienger、T. Beltran、I. Lefebvre、A. Pompon、G. Gosselin、A.-M. Aubertin、J.-L. Imbach、C. Périgaud

  DOI：10.1081/ncn-100002302

  日期：2001.3.31

  Synthesis, biological activities and decomposition kinetics of novel phosphotriester derivatives of 3'-azido-2',3'-dideoxythymidine (AZT) bearing a S-tButyl-2-thioethyl (tBuSATE) group and L-tyrosinyl residues are reported. All the derivatives appeared to be potent inhibitors of HIV-1 replication in various cell culture experiments. The proposed decomposition process of these mixed phosphotriesters may involve successively an esterase and then a phosphodiesterase activation.