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Polycyclic phloroglucinols as PTP1B inhibitors from Hypericum longistylum: Structures, PTP1B inhibitory activities, and interactions with PTP1B

Authors
Cao, XiangrongYang, XueyuanWang, PeixiaLiang, YueLiu, FengTuerhong, MuhetaerJin, Da-QingXu, JingLee, DonghoOhizumi, YasushiGuo, Yuanqiang
Issue Date
Nov-2017
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
PTP1B inhibitors; Hypericum longistylum; Polycyclic phloroglucinol; Molecular docking; ECD
Citation
BIOORGANIC CHEMISTRY, v.75, pp.139 - 148
Indexed
SCIE
SCOPUS
Journal Title
BIOORGANIC CHEMISTRY
Volume
75
Start Page
139
End Page
148
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/81786
DOI
10.1016/j.bioorg.2017.09.001
ISSN
0045-2068
Abstract
Protein tyrosine phosphatase 1B (PTP1B) has been regarded as a target for the research and development of new drugs to treat type II diabetes and PTP1B inhibitors are potential lead compounds for this type of new drugs. A phytochemical investigation to obtain new PTP1B inhibitors resulted in the isolation of four new phloroglucinols, longistyliones A-D (1-4) from the aerial parts of Hypericum longistylum. The structures of 1-4 were elucidated on the basis of extensive 1D and 2D NMR spectroscopic data analysis, and the absolute configurations of these compounds were established by comparing their experimental electronic circular dichroism (ECD) spectra with those calculated by the time-dependent density functional theory method. Compounds 1-4 possess a rare polycyclic phloroglucinol skeleton. The following biological evaluation revealed that all of the compounds showed PTP1B inhibitory effects. The further molecular docking studies indicated the strong interactions between these bioactive compounds with the PTP1B protein, which revealed the possible mechanism of PTP1B inhibition of bioactive compounds. All of the results implied that these compounds are potentially useful for the treatment of type II diabetes. (C) 2017 Elsevier Inc. All rights reserved.
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