Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/101736
Title: Synthesis and cytotoxicity of diastereomeric benzylamides derived from maslinic acid, augustic acid and bredemolic acid
Author(s): Heise, Niels V.
Heisig, JuliaLook up in the Integrated Authority File of the German National Library
Höhlich, Linda
Hoenke, Sophie
Csuk, RenéLook up in the Integrated Authority File of the German National Library
Issue Date: 2023
Type: Article
Language: English
Abstract: 36 substituted benzylamides were prepared starting from maslinic acid, bredemolic acid, and augustic acid and evaluated for their cytotoxicity in SRB assays employing several human tumor cell lines as well as non-malignant fibroblasts. Thereby, the benzylamides of maslinic acid, however, were found to be more cytotoxic than those obtained from augustic acid or bredemolic acid. The best compound (18, derived from maslinic acid) showed an EC50 value of 1.3 μM against A375 melanoma cells. Additional staining experiments revealed that this compound acted rather by apoptosis than by necrosis.
URI: https://opendata.uni-halle.de//handle/1981185920/103683
http://dx.doi.org/10.25673/101736
Open Access: Open access publication
License: (CC BY 4.0) Creative Commons Attribution 4.0(CC BY 4.0) Creative Commons Attribution 4.0
Journal Title: Results in chemistry
Publisher: Elsevier
Publisher Place: Amsterdam
Volume: 5
Original Publication: 10.1016/j.rechem.2023.100805
Appears in Collections:Open Access Publikationen der MLU

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