Evaluation of guggulsterone derivatives as novel kidney cell protective agents against cisplatin-induced nephrotoxicity

Authors
Lee, DahaeKim, TaejungKim, Ki HyunHam, JungyeobJang, Tae SuKang, Ki SungLee, Jae Wook
Issue Date
2017-07-15
Publisher
Pergamon Press Ltd.
Citation
Bioorganic & Medicinal Chemistry Letters, v.27, no.14, pp.3156 - 3161
Abstract
Guggulsterone derivatives were prepared using [3+2] click chemistry with aryl and alkyl acetylene. The series of derivatives were evaluated for their cellular protective effects on cisplatin-treated cultured LLC-PK1 kidney epithelial cells. Among the guggulsterone-triazole derivatives, compound 6g, which contains a hydroxyl methyl group, was the most active of all the derivatives. In an additional study, we determined that inhibition of the mitogen-activated protein kinase/caspase-3 signaling cascade by 6g mediates its protective effects against cytotoxicity in cultured LLC-PK1 cells. (C) 2017 Elsevier Ltd. All rights reserved.
Keywords
NF-KAPPA-B; OXIDATIVE STRESS; NATURAL PRODUCT; IN-VITRO; ANTAGONIST; DISEASE; TRANSCRIPTION; CONSTITUENT; ACTIVATION; GINSENG; NF-KAPPA-B; OXIDATIVE STRESS; NATURAL PRODUCT; IN-VITRO; ANTAGONIST; DISEASE; TRANSCRIPTION; CONSTITUENT; ACTIVATION; GINSENG; Guggulsterone; Kidney protection; Click chemistry; MAPK
ISSN
0960-894X
URI
https://pubs.kist.re.kr/handle/201004/122520
DOI
10.1016/j.bmcl.2017.05.033
Appears in Collections:
KIST Article > 2017
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