Watanabe T, Takeuchi T, Otsuka M, Tanaka S, Umezawa K
Institute of Microbial Chemistry, Tokyo, Japan.
J Antibiot (Tokyo). 1995 Dec;48(12):1460-6. doi: 10.7164/antibiotics.48.1460.
We have synthesized derivatives of dephostatin, a protein tyrosine phosphatase (PTPase) inhibitor, to study the structure-activity relationships of this inhibitor. Inactive analogs revealed some insight into structural requirements or PTPase inhibitory activity of dephostatin. Both a nitroso group and phenolic hydroxyl groups were found to be essential for the inhibitory activity. Among the dephostatin derivative synthesized, one of the regioisomers of dephostatin showed PTPase inhibitory activity equivalent to that of dephostatin, and also had increased stability.
我们合成了去磷酸化酶抑制剂(一种蛋白质酪氨酸磷酸酶(PTPase)抑制剂)的衍生物,以研究该抑制剂的构效关系。无活性类似物揭示了去磷酸化酶抑制剂的结构要求或PTPase抑制活性的一些见解。发现亚硝基和酚羟基对于抑制活性都是必不可少的。在合成的去磷酸化酶抑制剂衍生物中,去磷酸化酶抑制剂的一种区域异构体显示出与去磷酸化酶抑制剂相当的PTPase抑制活性,并且稳定性也有所提高。