Fmoc-L-Lys-Gly-L-Tyr-Gly-Gly-L-Phe-L-Leu-L-Pro(5-{5-[3-(2-{2-[2-(3,4,5-tris-octadecyloxy-benzoylamino)ethoxy]ethoxy}ethylcarbamoyl)allyl]})-Pro-OMe | 1190605-05-0

• 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: Fmoc-L-Lys-Gly-L-Tyr-Gly-Gly-L-Phe-L-Leu-L-Pro(5-{5-[3-(2-{2-[2-(3,4,5-tris-octadecyloxy-benzoylamino)ethoxy]ethoxy}ethylcarbamoyl)allyl]})-Pro-OMe
• CAS: 1190605-05-0
• 化学式: C₁₃₃H₂₀₈N₁₂O₂₀
• 分子量: 2295.18
• InChiKey: LPGMHLIWWCWQAR-JGLZVCHVSA-N

反应信息

• 作为产物：
  描述：

  在 盐酸 、 水 作用下， 以 二氯甲烷 为溶剂， 反应 3.0h， 生成 Fmoc-L-Lys-Gly-L-Tyr-Gly-Gly-L-Phe-L-Leu-L-Pro(5-{5-[3-(2-{2-[2-(3,4,5-tris-octadecyloxy-benzoylamino)ethoxy]ethoxy}ethylcarbamoyl)allyl]})-Pro-OMe
  参考文献：
  名称：

  Synthesis of hydrophobic phase-tagged prolyl peptides featuring rapid reaction/separation

  摘要：

  Hydrophobically tagged prolyl peptides were synthesized using an electrochemically modified prolyl moiety. The hydrophobic tag served a useful handle for the repetitive reaction/separation steps during solution-phase peptide synthesis. Furthermore, the tag was also effective as an anchor on solid phases for the evaluation of activity of immobilized peptides. (C) 2009 Published by Elsevier Ltd.

  DOI：

  10.1016/j.tet.2009.07.045