quantitative structure activity relationship (QSAR) against methionine aminopeptidases for the development and evaluation of anti-cancer agents. Correlation may be an adequate predictive model which can help to provide guidance in designing and subsequently yielding greatly specific compounds that may have reduced side effects and improved pharmacological activities. We have used Multiple Linear Regression (MLR) for developing QSAR model. For the validation of the developed QSAR model, statistical analysis such as cross validation test (LOO-CV), quality factor, fischers test, root mean square deviation (RMSD), variance, standard deviation etc.; have been performed and all the tests validated this QSAR model with fraction of variance r2 = 0....
Background: Traditional quantitative structure – property / activity relationships (QSPRs/QSARs) are...
Quantitative structure activity relationship (QSAR) has been established for 2-aminoquinoline-6-carb...
Cylin dependent kinases (CDKs) have emerged as novel mechanistic target due to their direct involvem...
A linear quantitative structure activity relationship model is obtained using Multiple Linear Regres...
A Quantitative Structure Activity Relationship (QSAR) study has been attempted on ciprofloxacin deri...
Objective: A novel subnanomolar anticancer hydroxamic acid containing drug candidates, inhibitors of...
AbstractProtein kinases are essential components of various signaling pathways and represent attract...
In this study, we report the quantitative structure activity relationships (QSAR) investigation to d...
In the present endeavor, for the dataset of 219 in vitro MDA-MB-231 TNBC cell antagonists, a (QSAR) ...
Two parallel approaches for quantitative structure-activity relationships (QSAR) are predominant in ...
After glucose, amino acids like glutamine, methonine, glycine, alanine, phenyl alanine are a major m...
Matrix metalloproteinase-2 (MMP-2) is a lucrative therapeutic target as far as anticancer drug disco...
Antitubercular activity of 5-nitrofuran-2-yl Derivatives series were subjected to Quantitative Struc...
International audienceQuantitative structure activity relationship (QSAR) methods have been applied ...
QSAR(Quantitative Structure Activity Relationship) studies were carried out on a set of 72 α-sulfone...
Background: Traditional quantitative structure – property / activity relationships (QSPRs/QSARs) are...
Quantitative structure activity relationship (QSAR) has been established for 2-aminoquinoline-6-carb...
Cylin dependent kinases (CDKs) have emerged as novel mechanistic target due to their direct involvem...
A linear quantitative structure activity relationship model is obtained using Multiple Linear Regres...
A Quantitative Structure Activity Relationship (QSAR) study has been attempted on ciprofloxacin deri...
Objective: A novel subnanomolar anticancer hydroxamic acid containing drug candidates, inhibitors of...
AbstractProtein kinases are essential components of various signaling pathways and represent attract...
In this study, we report the quantitative structure activity relationships (QSAR) investigation to d...
In the present endeavor, for the dataset of 219 in vitro MDA-MB-231 TNBC cell antagonists, a (QSAR) ...
Two parallel approaches for quantitative structure-activity relationships (QSAR) are predominant in ...
After glucose, amino acids like glutamine, methonine, glycine, alanine, phenyl alanine are a major m...
Matrix metalloproteinase-2 (MMP-2) is a lucrative therapeutic target as far as anticancer drug disco...
Antitubercular activity of 5-nitrofuran-2-yl Derivatives series were subjected to Quantitative Struc...
International audienceQuantitative structure activity relationship (QSAR) methods have been applied ...
QSAR(Quantitative Structure Activity Relationship) studies were carried out on a set of 72 α-sulfone...
Background: Traditional quantitative structure – property / activity relationships (QSPRs/QSARs) are...
Quantitative structure activity relationship (QSAR) has been established for 2-aminoquinoline-6-carb...
Cylin dependent kinases (CDKs) have emerged as novel mechanistic target due to their direct involvem...