Phosphodiesterase-4 (PDE4) plays an important role in treatment of asthma andchronic obstructive pulmonary disease. Thirty-one analogs displaying variable inhibition ofPDE4 were selected to develop models for establishing three-dimensional quantitativestructure-activity relationships (3D-QSAR). Comparative molecular field analysis(CoMFA) was conducted on the group of analogs to determine the structural requirementsfor potency in inhibiting PDE4. The resulting model exhibited good q2 and r2 values up to0.741 and 0.954 for CoMFA. The contributions from the steric and electrostatic fields were0.915 and 0.085 respectively. The 3D-QSAR model should be very useful for design ofnovel PDE 4 inhibitors
The phosphodiesterase 4 (PDE4) family of enzymes is a promising drug target for a variety of conditi...
Two- and three-dimensional quantitative structure-activity relationship (QSAR) and docking studies w...
AbstractContextIn recent years phosphodiesterase V acts as an attractive target for cardiovascular d...
Abstract: Phosphodiesterase-4 (PDE4) plays an important role in treatment of asthma and chronic obst...
Cyclic nucleotide phosphodiesterase IV (PDE IV) inhibitors find utility in asthma and Chronic Obstru...
Cyclic nucleotide phosphodiesterase IV (PDE IV) inhibitors find utility in asthma and Chronic Obstru...
The 3D-QSAR studies of some indole derivatives as phosphodiesterase (PDE) type IV inhibitors was per...
A quantitative structure-activity relationship (QSAR) study was performed to develop a model on a se...
A comparative molecular field analysis (CoMFA) of phthalazine class of phosphodiesterase IV (PDE IV)...
A comparative molecular field analysis (CoMFA) of phthalazine class of phosphodiesterase IV (PDE IV)...
Phosphodiesterases are a diverse family of enzymes that play a key role in regulating intracellular ...
AbstractPhosphodiesterases are a diverse family of enzymes that play a key role in regulating intrac...
In recent years there has been a resurgence of interest in inhibitors of cyclic nucleotide phosphodi...
Subtype selectivity of phosphodiesterase 4 (PDE4) has been proposed to be the most salient feature f...
Subtype selectivity of phosphodiesterase 4 (PDE4) has been proposed to be the most salient feature f...
The phosphodiesterase 4 (PDE4) family of enzymes is a promising drug target for a variety of conditi...
Two- and three-dimensional quantitative structure-activity relationship (QSAR) and docking studies w...
AbstractContextIn recent years phosphodiesterase V acts as an attractive target for cardiovascular d...
Abstract: Phosphodiesterase-4 (PDE4) plays an important role in treatment of asthma and chronic obst...
Cyclic nucleotide phosphodiesterase IV (PDE IV) inhibitors find utility in asthma and Chronic Obstru...
Cyclic nucleotide phosphodiesterase IV (PDE IV) inhibitors find utility in asthma and Chronic Obstru...
The 3D-QSAR studies of some indole derivatives as phosphodiesterase (PDE) type IV inhibitors was per...
A quantitative structure-activity relationship (QSAR) study was performed to develop a model on a se...
A comparative molecular field analysis (CoMFA) of phthalazine class of phosphodiesterase IV (PDE IV)...
A comparative molecular field analysis (CoMFA) of phthalazine class of phosphodiesterase IV (PDE IV)...
Phosphodiesterases are a diverse family of enzymes that play a key role in regulating intracellular ...
AbstractPhosphodiesterases are a diverse family of enzymes that play a key role in regulating intrac...
In recent years there has been a resurgence of interest in inhibitors of cyclic nucleotide phosphodi...
Subtype selectivity of phosphodiesterase 4 (PDE4) has been proposed to be the most salient feature f...
Subtype selectivity of phosphodiesterase 4 (PDE4) has been proposed to be the most salient feature f...
The phosphodiesterase 4 (PDE4) family of enzymes is a promising drug target for a variety of conditi...
Two- and three-dimensional quantitative structure-activity relationship (QSAR) and docking studies w...
AbstractContextIn recent years phosphodiesterase V acts as an attractive target for cardiovascular d...