化学
塔夫辛
肽
结合
氨基酸
部分
立体化学
苏氨酸
霉酚酸
寡肽
体外
生物化学
酶
移植
丝氨酸
外科
数学分析
医学
数学
作者
Agnieszka Siebert,Grzegorz Cholewiński,Piotr Trzonkowski,Janusz Rachoń
标识
DOI:10.1016/j.ejmech.2020.112091
摘要
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.
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