Synthesis, Cytotoxicity and Molecular Docking Studies of the 9-Substituted 5-Styryltetrazolo[1,5-c]quinazoline Derivatives
In this paper, we describe the synthesis of the 5-styryltetrazolo[1,5-c]quinazolines substituted at the 9-position with a 4-fluorophenyl ring directly or via a conjugated π-spacer (C=C or C≡C bond) based on the 6-bromo-4-chloro-2-styrylquinazoline scaffold. The structures of the synthesized compound...
Main Authors: | Malose J. Mphahlele, Samantha Gildenhuys, Nishal Parbhoo |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2017-10-01
|
Series: | Molecules |
Subjects: | |
Online Access: | https://www.mdpi.com/1420-3049/22/11/1719 |
Similar Items
-
Quinazoline-containing Hydrazydes of Dicarboxylic Acids and Products of Their Structural Modification – A Novel Class of Anti-inflammatory Agents
by: Nataliia Krasovska, et al.
Published: (2021-06-01) -
Synthesis of 6-N-R-Tetrazolo[1,5-c]quinazolin-5(6H)-ones and Their Anticancer Activity
by: Oleksii Mykolayovych Antypenko, et al.
Published: (2016-08-01) -
Synthesis and Reactivity of [1,2,4]Triazolo-annelated Quinazolines
by: Rashad A. Al-Salahi
Published: (2010-10-01) -
Potential of N-aryl(benzyl,heteryl)-2-(tetrazolo[1,5-c]quinazolin-5-ylthio)acetamides as anticancer and antimicrobial agents
by: Oleksii M. Antypenko, et al.
Published: (2016-11-01) -
Novel Polycarbo-Substituted Imidazo[1,2-c]quinazolines: Synthesis and Cytotoxicity Study
by: Tebogo Ankie Khoza, et al.
Published: (2015-12-01)