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酯衍生葡萄糖摄取抑制剂的类似物。

Isosteres of ester derived glucose uptake inhibitors.

机构信息

Department of Chemistry and Biochemistry, Ohio University, Athens, OH 45701, USA.

Department of Biomedical Science, Ohio University, Athens, OH 45701, USA; Program of Molecular and Cellular Biology, Ohio University, Athens, OH 45701, USA.

出版信息

Bioorg Med Chem Lett. 2020 Sep 15;30(18):127406. doi: 10.1016/j.bmcl.2020.127406. Epub 2020 Jul 15.

Abstract

Glucose transporters (GLUTs) facilitate glucose uptake and are overexpressed in most cancer cells. Inhibition of glucose transport has been shown to be an effective method to slow the growth of cancer cells both in vitro and in vivo. We have previously reported on the anticancer activity of an ester derived glucose uptake inhibitor. Due to the hydrolytic instability of the ester linkage we have prepared a series of isosteres of the ester moiety. Of all of the isosteres prepared, the amine linkage showed the most promise. Several additional analogues of the amine-linked compounds were also prepared to improve the overall activity.

摘要

葡萄糖转运蛋白(GLUTs)促进葡萄糖摄取,在大多数癌细胞中过度表达。抑制葡萄糖转运已被证明是一种有效方法,可以减缓体外和体内癌细胞的生长。我们之前曾报道过一种衍生自葡萄糖摄取抑制剂的酯类的抗癌活性。由于酯键的水解不稳定性,我们已经制备了一系列酯部分的等排体。在所制备的所有等排体中,胺键最有希望。还制备了几种胺连接化合物的其他类似物,以提高整体活性。

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