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Total Synthesis and Biological Evaluation of Sericetin for Protection against Cisplatin-Induced Acute Kidney Injury

Authors
Kim, Eun-SunJang, HongjunChang, Sun-YoungBaek, Seung-HoonBae, Ok-NamKim, Hyoungsu
Issue Date
Dec-2018
Publisher
AMER CHEMICAL SOC
Keywords
PRENYLATED FLAVONOIDS; INDUCED NEPHROTOXICITY; OXIDATIVE STRESS; MACAKURZIN C; CELL-DEATH; IN-VITRO; INFLAMMATION; INHIBITION; MECHANISMS; APOPTOSIS
Citation
JOURNAL OF NATURAL PRODUCTS, v.81, no.12, pp.2647 - 2653
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF NATURAL PRODUCTS
Volume
81
Number
12
Start Page
2647
End Page
2653
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/5081
DOI
10.1021/acs.jnatprod.8b00434
ISSN
0163-3864
Abstract
A concise synthesis of sericetin (1) was performed in four steps from readily available 3-O-benzylgalangin (4), featuring electrocyclization to produce the tricyclic core and a sequential aromatic Claisen/Cope rearrangement to incorporate the 8-prenyl group of 1. In addition, the therapeutic potential of sericetin (1), isosericetin (2), and three prenylated tetracyclic synthetic intermediates (11, 12, and 14) against cisplatin-induced nephrotoxicity using renal tubular cells were evaluated. Compound 14 showed therapeutic potential against cisplatin-induced kidney damage.
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