7066-32-2Relevant academic research and scientific papers
Design, synthesis and structure-activity relationship of novel quinoxalin-2-carboxamides as 5-HT3 receptor antagonists for the management of depression
Mahesh, Radhakrishnan,Devadoss, Thangaraj,Pandey, Dilip Kumar,Bhatt, Shvetank,Yadav, Shushil Kumar
scheme or table, p. 6773 - 6776 (2010/12/20)
A novel series of quinoxalin-2-carboxamides were designed based on the ligand-based approach, employing a three-point pharmacophore model; it consists of an aromatic residue and a linking carbonyl group and a basic nitrogen. The target new chemical entities were synthesized from the key intermediate, quinoxalin-2-carboxylic acid, by coupling it with various amines in the presence of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC·HCl) and 1-hydroxybenzotriazole (HOBt). The obtained compounds' structures were confirmed by spectral data. The target new chemical entities were evaluated for their 5-HT3 receptor antagonisms in longitudinal muscle myenteric plexus preparation from guinea pig ileum against 5-HT3 agonist, 2-methyl-5-HT, which was expressed in the form of pA2 value. All the synthesized compounds showed antagonism towards 5-HT3 receptor; based on this result, a structure-activity relationship was derived, which reveals that the aromatic residue in 5-HT3 receptor antagonists may have hydrophobic interaction with 5-HT3 receptor. Regardless of their antagonistic potentials, all the synthesized molecules were screened for their anti-depressant potentials by using forced swim test in mice model; interestingly none of the tested compounds affect the locomotion of mice in the tested dose levels. Compounds with significant pA2 values exhibited good anti-depressant-like activity as compared to the vehicle-treated group.
SYNTHESIS AND SPECTROSCOPIC STUDIES ON SOME NEW SUBSTITUTED 2-QUINOXALINECARBOXAMIDES AND THEIR N-OXIDES
Sabri, Salim S.,El-Abadelah, Mustafa M.,Al-Bitar, Bassam A.
, p. 699 - 711 (2007/10/02)
Series of new 2-(N-phenylcarbamoyl)-3-methylquinoxaline 1,4-dioxides (I), monoxides (II,III) and their non-oxygenated analogues (IV), as well as the corresponding series lacking the C3-methyl (V-VIII) have been prepared, and their 1H-nmr spectr
