Ac-Ser-Leu-Asn--Ile-Val-OMe | 127231-42-9

• 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: Ac-Ser-Leu-Asn--Ile-Val-OMe
• 英文别名: Ac-Ser-Leu-Asn-(Phe-HEA-Pro)-Ile-Val-OMe；Acetyl-seryl-leucyl-asparaginyl-phenylalanyl-psi-(2-hydroxy-1-ethylamine)-prolyl-isoleucyl-valine-methoxy；methyl (2S)-2-[[(2S,3S)-2-[[(2S)-1-[(3S)-3-[[(2S)-2-[[(2S)-2-[[(2S)-2-acetamido-3-hydroxypropanoyl]amino]-4-methylpentanoyl]amino]-4-amino-4-oxobutanoyl]amino]-2-hydroxy-4-phenylbutyl]pyrrolidine-2-carbonyl]amino]-3-methylpentanoyl]amino]-3-methylbutanoate
• CAS: 127231-42-9；127306-15-4；132748-20-0
• 化学式: C₄₂H₆₈N₈O₁₁
• 分子量: 861.049
• InChiKey: MJOXWVYKMFPFPL-OGRHDZSBSA-N

物化性质

• 沸点：
  1216.5±65.0 °C(Predicted)
• 密度：
  1?+-.0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  61
• 可旋转键数：
  26
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  288
• 氢给体数：
  9
• 氢受体数：
  12

反应信息

• 作为产物：
  描述：

  (2S)-2-amino-N-[(2S)-4-chloro-3-oxo-1-phenylbutan-2-yl]butanediamide 在 palladium dihydroxide N-甲基吗啉 、 盐酸 、 sodium tetrahydroborate 、 氢气 、 碳酸氢钠 、 1-羟基苯并三唑 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 sodium iodide 作用下， 以 1,4-二氧六环 、 甲醇 、 溶剂黄146 、 N,N-二甲基甲酰胺 为溶剂， 生成 Ac-Ser-Leu-Asn--Ile-Val-OMe
  参考文献：
  名称：

  p17 / p24底物切割位点的羟乙胺类似物是HIV蛋白酶的紧密结合抑制剂。

  摘要：

  DOI：

  10.1021/jm00167a003

文献信息

• New hydroxyethylamine HIV protease inhibitors that suppress viral replication
  作者：Daniel H. Rich、J. V. N. Vara Prasad、Chong Qing Sun、Jeremy Green、Richard Mueller、Kathryn Houseman、Debra MacKenzie、Miroslav Malkovsky

  DOI：10.1021/jm00099a008

  日期：1992.10

  The synthesis of analogues of AcSerLeuAsn[Phe-HEA-Pro]IleValOMe (1, JG-365; where HEA stands for the hydroxyethylamine unit 2), a tight-binding inhibitor of HIVP, are reported. Systematic modification of the P3 and P3' regions of the inhibitors has led to smaller HIVP inhibitors that inhibit viral replication in HIV-infected and SIV-infected cell cultures. Six aliphatic and/or aromatic derivatives were prepared by replacing residues in the P3 regions of BocLeuAsn[Phe-HEA-Pro]IleValOMe. Aromatic side chains at P3 gave better inhibitors than aliphatic side chains. The better inhibitors in this series contained a beta-naphthylalanine or a biphenyl unit at P3. A second series of HIVP inhibitors were obtained by converting the P3 group into acyl groups. CbzAsn[Phe-HEA-Pro]IlePheOMe and Qua-Asn-[Phe-HEA-Pro]-Ile-Phe-OMe (where Qua = quinolin-2-ylcarbonyl) are potent HIVP inhibitors with K(i) values equal to 1.0 and 0.1 nM, respectively. The inhibition constants were determined by using the continuous fluorometric assay developed by Toth and Marshall. The activities of the protease inhibitors for inhibition of SIV replication were determined in vitro using CEMX174 cells. Inhibition of HIV infection was determined essentially as reported by Pauwels and co-workers. The anti-HIV assay was carried out in culture using CEM cell (a CD4+ lymphocyte line) infected with virus strain HTLV-IIIb with a multiplicity of infection of 0.1. Several analogues inhibited the cytopathic effect at concentrations of 0.1-0.8 mug/mL. These results establish that good inhibitors of HIV protease that inhibit viral replication in infected lymphocytes in in vitro cell assays can be obtained from JG-365 when the AcSerLeu unit is replaced by aromatic acyl derivatives.
• Hydroxyethylamine analogs of the p17/p24 substrate cleavage site are tight-binding inhibitors of HIV protease
  作者：Daniel H. Rich、Jeremy Green、Mihaly V. Toth、Garland R. Marshall、Stephen B. H. Kent

  DOI：10.1021/jm00167a003

  日期：1990.5