p53 Laboratory, Agency for Science Technology and Research (A*STAR), 8A Biomedical Grove, #06-04/05 Neuros/Immunos, Singapore, 138648, Singapore.
Chemistry. 2020 Jan 7;26(2):379-383. doi: 10.1002/chem.201903965. Epub 2019 Nov 19.
Peptide alcohols are clinically important compounds that are underexplored in structure-activity relationship (SAR) studies in drug discovery. One reason for this underutilization is that current syntheses are laborious and time consuming. Herein, we describe the preparation and utility of Rink, Ramage, and Sieber-chloride resins, which enables the use of a general, easy and practical method for the attachment of fluorenylmethoxycarbonyl (Fmoc)-amino alcohols to a solid support, in the synthesis of peptide alcohols. This method is the first straightforward Fmoc/tBu synthesis of peptide alcohols starting from a pre-loaded resin. The synthesized peptide alcohols can be detached from the linkers through conventional methods. Treatment with trifluoroacetic acid (TFA) (95 %) and scavengers such as triisopropylsilane and water for 2 h is sufficient to obtain a fully deprotected peptide alcohol, while treatment with 20 % hexafluoroisopropanol in dichloromethane renders a fully protected peptide alcohol that can be further modified at the C-terminus. As examples, the new resins were used in straightforward, relatively rapid syntheses of the peptide alcohols octreotide, alamethicin, and a segment of trichogin GA IV, as well as the first synthesis of stapled peptide alcohols.
肽醇是具有重要临床意义的化合物,但在药物研发的构效关系(SAR)研究中却未得到充分探索。造成这种利用不足的一个原因是,目前的合成方法既费力又耗时。在此,我们描述了 Rink、Ramage 和 Sieber-氯树脂的制备和用途,这使得使用通用、简单和实用的方法将芴甲氧羰基(Fmoc)-氨基醇连接到固体载体上,用于合成肽醇成为可能。这种方法是第一个从预载树脂开始的直接 Fmoc/tBu 合成肽醇的方法。合成的肽醇可以通过常规方法从接头上分离。用三氟乙酸(TFA)(95%)和三异丙基硅烷和水等清除剂处理 2 小时足以获得完全脱保护的肽醇,而用 20%六氟异丙醇在二氯甲烷中处理则得到完全保护的肽醇,可进一步在 C 末端修饰。作为实例,新树脂被用于直链、相对快速合成奥曲肽、alamethicin 和 trichogin GA IV 的一段肽醇,以及首次合成 stapled peptide 醇。