Determination of pK(a) Values of Some Benzoxazoline Derivatives and the Structure-Activity Relationship
Hayati Çelik, Mahmure Büyükağa, Mustafa Celebier, Ebru Turkoz Acar, Melek Sirin Baymak, Nesrin Gökhan-Kelekci, Erhan Palaska, Hakki Erdogan
- Amer Chemıcal Soc, 2013.
The acid ionization constant (pK(a)) values of 2-(3H)-benzoxazolinone and its 17 derivatives were determined in buffered solutions by UV-vis spectrophotometry, potentiometry, and capillary zone electrophoresis techniques. The pK(a) values of the studied compounds are found to be in the range of 9.01 to 7.15. The advantages and limitations of each technique are discussed. The results suggest that the removal of a proton from the molecule occurred on the nitrogen atom of the 2-(3H)-benzoxazolinone ring and the analgesic/anti-inflammatory activities of the benzoxazolinone derivatives decrease when the pK(a) values of the compounds increase.
0021-9568
000320641100021
Near East University Article Yakın Doğu Üniversitesi Makale Antıınflammatory actıvıtıes; Capillary electrophoresis Mannıch-bases; Chemistry