1354958-35-2Relevant academic research and scientific papers
Cytotoxicity and anti-inflammatory activity of methylsulfanyl- triazoloquinazolines
Al-Salahi, Rashad A.,Gamal-Eldeen, Amira M.,Alanazi, Amer M.,Al-Omar, Mohamed A.,Marzouk, Mohamed A.,Fouda, Moustafa M.G.
, p. 1434 - 1446 (2013/04/24)
A series of twenty five 2-methylsulfanyl-[1,2,4]triazolo[1,5-a]quinazoline derivatives 1-25 was previously synthesized. We have now investigated their cytotoxic effects against hepatocellular Hep-G2 and colon HCT-116 carcinoma cells and effect on the macr
Antimicrobial activity of newly synthesized methylsulfanyl- triazoloquinazoline derivatives
Al-Salahi, Rashad,Marzouk, Mohamed,Awad, Ghada,Al-Omar, Mohamed,Ezzeldin, Essam
, p. 790 - 797 (2013/07/19)
Objective The aim of this research was to study and evaluate the antimicrobial activity of a novel 2-methylsulfanyl-[1,2,4]triazolo[1,5-a] quinazoline and its derivatives. Antibacterial activity of the target compounds was tested against a variety of spec
Synthesis of novel 2-methylsulfanyl-4h-[1,2,4]triazolo[1,5-a]quinazolin-5- one and derivatives
Al-Salahi, Rashad,Geffken, Detlef
, p. 3512 - 3523 (2011/10/09)
A novel 2-methylsulfanyl-4H-[1,2,4]triazolo[1,5-a]quinazolin-5-one was synthesized using dimethyl-n-cyanoimidodithiocarbonate and 2-hydrazinobenzoic acid as building blocks. Chemical transformation of the inherent lactam moiety in the targeted 2-methylsulfanyl-[1,2,4]triazolo[1,5-a]quinazolin-5-one offered access to a variety of derivatives.
