Synthesis, cytotoxicities, and carbonic anhydrase inhibition potential of 6-(3-aryl-2-propenoyl)-2(3H)-benzoxazolones
In this study, new chalcone compounds having the chemical structure of 6-(3-aryl-2-propenoyl)-2(3H)-benzoxazolones (1-8) were synthesised and were characterised by 1H-NMR, 13 C-NMR, and HRMS spectra. Cytotoxic and carbonic anhydrase (CA) inhibitory effects of the compounds were investigated. Cytotox...
Saved in:
Main Authors: | Sinan Bilginer (Author), Halise Inci Gul (Author), Feyza Sena Erdal (Author), Hiroshi Sakagami (Author), Serkan Levent (Author), Ilhami Gulcin (Author), Claudiu T. Supuran (Author) |
---|---|
Format: | Book |
Published: |
Taylor & Francis Group,
2019-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Synthesis, carbonic anhydrase I and II inhibition studies of the 1,3,5-trisubstituted-pyrazolines
by: Halise Inci Gul, et al.
Published: (2017) -
Novel sulphonamides incorporating triazene moieties show powerful carbonic anhydrase I and II inhibitory properties
by: Sinan Bilginer, et al.
Published: (2020) -
Aryl derivatives of 3H-1,2-benzoxathiepine 2,2-dioxide as carbonic anhydrase inhibitors
by: Aleksandrs Pustenko, et al.
Published: (2020) -
Designing, synthesis and bioactivities of 4-[3-(4-hydroxyphenyl)-5-aryl-4,5-dihydro-pyrazol-1-yl]benzenesulfonamides
by: Halise Inci Gul, et al.
Published: (2017) -
Aryl derivatives of 3H-1,2-benzoxaphosphepine 2-oxides as inhibitors of cancer-related carbonic anhydrase isoforms IX and XII
by: Anastasija Balašova, et al.
Published: (2023)