Department of Organic Chemistry, Gdansk University of Technology, G. Narutowicza 11/12, 80-233, Gdansk, Poland.
Department of Organic Chemistry, Gdansk University of Technology, G. Narutowicza 11/12, 80-233, Gdansk, Poland.
Eur J Med Chem. 2020 Mar 1;189:112091. doi: 10.1016/j.ejmech.2020.112091. Epub 2020 Jan 24.
Mycophenolic acid (MPA) was coupled with amino acids and biologically active peptides including derivatives of tuftsin to modify its immunosuppressive properties. Both amino acid unit in the case of simple MPA amides and modifications within peptide moiety of MPA - tuftsin conjugates influenced the observed activity. Antiproliferative potential of the obtained conjugates was investigated in vitro and MPA amides with threonine methyl ester and conjugate of MPA with retro-tuftisin occurred to be more selective against PBMC in comparison to parent MPA. Both amino acid and peptide derivatives of MPA acted as inosine-5'-monophosphate dehydrogenaze (IMPDH) inhibitors.
将麦考酚酸(MPA)与氨基酸和生物活性肽(包括硫肽衍生物)偶联,以修饰其免疫抑制特性。在简单的 MPA 酰胺的情况下,氨基酸单元和 MPA-硫肽缀合物的肽部分内的修饰都影响了观察到的活性。在体外研究了所得缀合物的抗增殖潜力,与母体 MPA 相比,MPA 与苏氨酸甲酯的酰胺和 MPA 与 retro-tuftisin 的缀合物对 PBMC 更具选择性。MPA 的氨基酸和肽衍生物均作为肌苷-5'-单磷酸脱氢酶(IMPDH)抑制剂。