Two isopentenyl resorcinols, peperobtusin B and peperobtusin C, have been isolated from . Their structures were determined on the basis of spectroscopic methods, especially H NMR, C NMR, 2D NMR, and HR-TOF-MS. Two compounds were evaluated for cytostatic activity against G, A 549, Hela and HCT 116 cells, but cytostatic activity of both compounds is weak.
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http://dx.doi.org/10.1080/10286020.2020.1830378 | DOI Listing |
J Asian Nat Prod Res
September 2021
College of Life Science and Biotechnology, Dalian University, Dalian 116622, China.
Two isopentenyl resorcinols, peperobtusin B and peperobtusin C, have been isolated from . Their structures were determined on the basis of spectroscopic methods, especially H NMR, C NMR, 2D NMR, and HR-TOF-MS. Two compounds were evaluated for cytostatic activity against G, A 549, Hela and HCT 116 cells, but cytostatic activity of both compounds is weak.
View Article and Find Full Text PDFChem Biol Interact
January 2020
Wuya College of Innovation, School of Pharmaceutical Engineering, Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang, 110016, China; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China. Electronic address:
Protein kinases play an indispensable role in signaling pathways that regulate tumor cell functions, which represent potent therapeutic targets in cancers. Dual-specificity tyrosine phosphorylation regulated kinase 1A (DYRK1A) as a serine/threonine kinase has recently been reported to be upregulated in pancreatic ductal adenocarcinoma (PDAC) and show protumorigenic effect. By activity-guided phytochemical investigation of the extracts from Glycyrrhiza uralensis Fisch, we expect to find the effective constituents that can suppress pancreatic cancer cell proliferation and/or induce cells apoptotic by inhibiting DYRK1A.
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