Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/86398
Title: Platanic acid derived amides are more cytotoxic than their corresponding oximes
Author(s): Kozubek, Marie
Hoenke, Sophie
Schmidt, Theresa
Ströhl, Dieter
Csuk, René
Issue Date: 2022
Type: Article
Language: English
Abstract: Albeit platanic acid has been known since 1956, its potential to act as a valuable starting material for the synthesis of cytotoxic agents has been neglected for many years. Hereby we describe the synthesis of a small library of amides and oximes derived from 3-O-acetyl-platanic acid, and the results of their screening as cytotoxic agents for several human tumor cell lines. As a result, while the cytotoxicity of the oximes was diminished as compared to the parent amides, the homopiperazinyl amide 5 held the highest cytoxicity (EC50 = 0.9 μM for A375 human melanoma cells). Extra FACS and cell cycle measurements showed compound 5 to act onto A375 cells rather by apoptosis than by necrosis.
URI: https://opendata.uni-halle.de//handle/1981185920/88354
http://dx.doi.org/10.25673/86398
Open Access: Open access publication
License: (CC BY 4.0) Creative Commons Attribution 4.0(CC BY 4.0) Creative Commons Attribution 4.0
Sponsor/Funder: Publikationsfonds MLU
Journal Title: Medicinal chemistry research
Publisher: Birkhäuser Boston
Publisher Place: Cambridge, Mass. [u.a.]
Volume: 31
Original Publication: 10.1007/s00044-022-02902-1
Page Start: 1049
Page End: 1059
Appears in Collections:Open Access Publikationen der MLU

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