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Melanogenesis inhibitory pregnane glycosides from Cynanchum atratum

Authors
Jin, QinghaoHan, Xiang HuaYun, Cheong-YongLee, ChulLee, Jin WooLee, DonghoLee, Mi KyeongJung, Sang-HunHong, Jin TaeKim, YoungsooHwang, Bang Yeon
Issue Date
15-Apr-2018
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Cynanchum atratum; Asclepiadaceae; Pregnane glycosides; alpha-MSH; Melanogenesis inhibitor
Citation
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.28, no.7, pp.1252 - 1256
Indexed
SCIE
SCOPUS
Journal Title
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
Volume
28
Number
7
Start Page
1252
End Page
1256
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/76135
DOI
10.1016/j.bmcl.2018.01.004
ISSN
0960-894X
Abstract
Bioassay-guided fractionation of the methanolic extract from the roots of Cynanchum atratum has resulted in the isolation of three new pregnane glycosides (1-3) along with four known compounds (4-7). Their structures were identified by analysis of the spectroscopic data including extensive 2D NMR. All of the isolates were evaluated for their potential to inhibit the melanin production in a-melanocyte stimulating hormone (alpha-MSH)-activated B16 melanoma cells. Of these, compounds 4-7 dosedependently inhibited the melanin production with the IC50 values ranging from 4 mu M to 33 mu M. (C) 2018 Elsevier Ltd. All rights reserved.
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