首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >2,4-Bis(octadecanoylamino)benzenesulfonic acid sodium salt as a novel scavenger receptor inhibitor with low molecular weight.
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2,4-Bis(octadecanoylamino)benzenesulfonic acid sodium salt as a novel scavenger receptor inhibitor with low molecular weight.

机译:2,4-双(十八烷基氨基)苯磺酸钠盐是一种新型的低分子量清除剂受体抑制剂。

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摘要

In order to investigate the effect of the fixation of the orientations of the two long chains, three types of novel derivatives of scavenger receptor inhibitor 1 were synthesized, and their biological activities were evaluated. Among the novel derivatives, 2,4-bis(octadecanoylamino)benzenesulfonic acid sodium salt (4d) showed the most potent inhibitory activity against the incorporation of 1,1(')-dioctadecyl-3,3,3('),3(')-tetramethylindocarbocyanine perchlorate-labeled acetyl-LDL (DiI-acetyl-LDL) into macrophages. 2,5-Bis(octadecanoylamino)benzenesulfonic acid sodium salt (4c), a regioisomer of 4d, did not exhibit as potent an inhibitory activity as 4d, meaning that the substitution pattern of two long chains on the benzene ring must be important. Compound 4d exhibited 10 times more potent inhibitory activity against the binding of (125)I-labeled acetyl-LDL to the surface of macrophages than compound 1.
机译:为了研究固定两个长链的方向的作用,合成了三种类型的清道夫受体抑制剂1的新型衍生物,并评估了它们的生物学活性。在新的衍生物中,2,4-双(十八烷酰氨基)苯磺酸钠盐(4d)对1,1(')-dioctadecyl-3,3,3('),3( ')将四甲基吲哚基花青高氯酸盐标记的乙酰基-LDL(DiI-乙酰基-LDL)转化为巨噬细胞。 2,5-双(十八烷酰基氨基)苯磺酸钠盐(4c)是4d的区域异构体,没有像4d那样强大的抑制活性,这意味着苯环上两个长链的取代方式必须很重要。化合物4d对(125)I标记的乙酰基LDL与巨噬细胞表面的结合的抑制活性是化合物1的10倍。

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