Background: Xanthatin, fluoropyrimidine and thienopyrimidine, pyrazolopyrimidine, pyrimidine carboxamides, and SKLB1002 are reported as VEGFR2 tyrosine kinase inhibitors. Recently, many studies related to different heterocycles conjugated with dihydroquinazolinones are known to have very good biological activities. In this study, we are intended to explore the cytotoxic studies of piperidine conjugated dihydroquinazolinones against colorectal/colon cancer cell lines and along with molecular docking studies and DFT calculations. Methods: The colorectal/colon cell lines HCT116 and A549 cell lines were treated with these compounds and cytotoxic activities were evaluated by MTT dye uptake method. We performed molecular modelling for compound 3d...
A series of indole-aminoquinazolines was prepared via amination of the 2-aryl-4-chloroquinazolines w...
Suzuki-Miyaura cross-coupling of 6-bromo-2-styrylquinazolin-4(3H)-ones with arylboronic acids afford...
ABSTRACT A series of 4-(2-(4-substituted phenyl)-4-oxoquinazolin-3(4H)-yl)-N-(2-(4-fluorophenyl)-4-o...
1273-1278Dichloroacetate (DCA) as a small and active anticancer agent through inhibition of pyruvate...
According to data from the World Health Organization in 2014, cancer was the second biggest cause of...
A series of 7-chloro-4-[4-(substituted arylideneimino)] 2,5-dioxo-1,4 piperazinoquinoline VI was des...
In this paper, a set of 3-methylquniazolinone derivatives were designed, synthesised, and studied th...
AbstractA series of 7-chloro-4-[4-(substituted arylideneimino)] 2,5-dioxo-1,4 piperazinoquinoline VI...
In this study, a proper multicomponent process was developed for synthesis of tetrahydroquinazolinon...
<div><p></p><p>A novel series of 3-benzyl-substituted-4(3<i>H</i>)-quinazolinones were designed, syn...
P-glycoprotein (P-gp) is a transmembrane efflux pump that has been associated with ineffective cance...
267-272The present investigation deals with molecular docking, synthesis, characterization, and eval...
Development of small-molecule inhibitors targeting phosphoinositide 3-kinase (PI3K) has been an appe...
A series of indole-aminoquinazolines was prepared via amination of the 2-aryl-4-chloroquinazolines ...
The novel series of piperidine conjugated benzophenone analogs with amide link 11a–l were synthesize...
A series of indole-aminoquinazolines was prepared via amination of the 2-aryl-4-chloroquinazolines w...
Suzuki-Miyaura cross-coupling of 6-bromo-2-styrylquinazolin-4(3H)-ones with arylboronic acids afford...
ABSTRACT A series of 4-(2-(4-substituted phenyl)-4-oxoquinazolin-3(4H)-yl)-N-(2-(4-fluorophenyl)-4-o...
1273-1278Dichloroacetate (DCA) as a small and active anticancer agent through inhibition of pyruvate...
According to data from the World Health Organization in 2014, cancer was the second biggest cause of...
A series of 7-chloro-4-[4-(substituted arylideneimino)] 2,5-dioxo-1,4 piperazinoquinoline VI was des...
In this paper, a set of 3-methylquniazolinone derivatives were designed, synthesised, and studied th...
AbstractA series of 7-chloro-4-[4-(substituted arylideneimino)] 2,5-dioxo-1,4 piperazinoquinoline VI...
In this study, a proper multicomponent process was developed for synthesis of tetrahydroquinazolinon...
<div><p></p><p>A novel series of 3-benzyl-substituted-4(3<i>H</i>)-quinazolinones were designed, syn...
P-glycoprotein (P-gp) is a transmembrane efflux pump that has been associated with ineffective cance...
267-272The present investigation deals with molecular docking, synthesis, characterization, and eval...
Development of small-molecule inhibitors targeting phosphoinositide 3-kinase (PI3K) has been an appe...
A series of indole-aminoquinazolines was prepared via amination of the 2-aryl-4-chloroquinazolines ...
The novel series of piperidine conjugated benzophenone analogs with amide link 11a–l were synthesize...
A series of indole-aminoquinazolines was prepared via amination of the 2-aryl-4-chloroquinazolines w...
Suzuki-Miyaura cross-coupling of 6-bromo-2-styrylquinazolin-4(3H)-ones with arylboronic acids afford...
ABSTRACT A series of 4-(2-(4-substituted phenyl)-4-oxoquinazolin-3(4H)-yl)-N-(2-(4-fluorophenyl)-4-o...