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从胡枝子中提取的黑色素合成抑制剂。

Melanin synthesis inhibitors from Lespedeza floribunda.

机构信息

Cutaneous Drug Research Department, POLA Chemical Industries, Inc, Yokohama 244-0812, Japan.

出版信息

J Nat Prod. 2009 Feb 27;72(2):194-203. doi: 10.1021/np800395j.

Abstract

In the course of our search for new melanin synthesis inhibitors from plants, 40 new flavonoids and 11 known flavonoids were isolated from the roots of Lespedeza floribunda Bunge. The structures of the new compounds were determined by MS and NMR analyses, and the absolute configurations by CD spectra. Many of the compounds inhibited melanin synthesis in normal human epidermal melanocytes (NHEM), and compounds 3, 7, 8, 11, 16, 24, 27, 29, 33, 43, 45, and 51 were particularly inhibitory. Their activities were stronger than that of hydroquinone, which is known as a major skin-lightening drug.

摘要

在从植物中寻找新型黑色素合成抑制剂的过程中,我们从胡枝子的根部分离得到了 40 种新的黄酮类化合物和 11 种已知的黄酮类化合物。通过 MS 和 NMR 分析确定了新化合物的结构,并通过 CD 光谱确定了它们的绝对构型。许多化合物抑制了正常人表皮黑素细胞(NHEM)中的黑色素合成,其中化合物 3、7、8、11、16、24、27、29、33、43、45 和 51 的抑制作用特别显著。它们的活性强于氢醌,后者是一种主要的皮肤美白药物。

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