TY - JOUR
T1 - MIA-QSAR, PCA-ranking and least-squares support-vector machines in the accurate prediction of the activities of phosphodiesterase type 5 (PDE-5) inhibitors
AU - Goodarzi, Mohammad
AU - Freitas, Matheus P.
N1 - Funding Information:
The authors are grateful to the Young Researcher Club of Islamic Azad University and FAPEMIG for the financial support of this research, as well as to CNPq for the fellowship (to M.P.F.).
PY - 2010/9
Y1 - 2010/9
N2 - Phosphodiesterase type-5 (PDE-5) is a key enzyme involved in the erection process. PDE-5 inhibitors, such as Sildenafil (Viagra™), Vardenafil (Levitra™) and Tadalafil (Cialis™), are used for the treatment of erectile dysfunction. Computer-assisted modelling of biological activities of PDE-5 inhibitors may make quantitative structure-activity relationship (QSAR) models useful for the development of safer (low side effects) and more potent drugs. The multivariate image analysis applied to QSAR (MIA-QSAR) method, coupled to partial least-squares (PLS) regression, has provided highly predictive QSAR models. Nevertheless, regression methods which take into account nonlinearity, such as least-squares support-vector machines (LS-SVMs), are supposed to predict biological activities more accurately than the usual linear methods. Thus, together with prior variable selection using principal component analysis ranking, MIA-QSAR and LS-SVM regression were applied to model the bioactivities of a series of cyclic guanine derivatives (PDE-5 inhibitors), and the results were compared with those based on linear methodologies. MIA-QSAR/LS-SVM was found to improve greatly the prediction performance when compared with MIA-QSAR/PLS, MIA-QSAR/N-PLS, CoMFA/PLS and CoMSIA/PLS models.
AB - Phosphodiesterase type-5 (PDE-5) is a key enzyme involved in the erection process. PDE-5 inhibitors, such as Sildenafil (Viagra™), Vardenafil (Levitra™) and Tadalafil (Cialis™), are used for the treatment of erectile dysfunction. Computer-assisted modelling of biological activities of PDE-5 inhibitors may make quantitative structure-activity relationship (QSAR) models useful for the development of safer (low side effects) and more potent drugs. The multivariate image analysis applied to QSAR (MIA-QSAR) method, coupled to partial least-squares (PLS) regression, has provided highly predictive QSAR models. Nevertheless, regression methods which take into account nonlinearity, such as least-squares support-vector machines (LS-SVMs), are supposed to predict biological activities more accurately than the usual linear methods. Thus, together with prior variable selection using principal component analysis ranking, MIA-QSAR and LS-SVM regression were applied to model the bioactivities of a series of cyclic guanine derivatives (PDE-5 inhibitors), and the results were compared with those based on linear methodologies. MIA-QSAR/LS-SVM was found to improve greatly the prediction performance when compared with MIA-QSAR/PLS, MIA-QSAR/N-PLS, CoMFA/PLS and CoMSIA/PLS models.
KW - LS-SVM
KW - MIA-QSAR
KW - PCA ranking
KW - PDE-5
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U2 - 10.1080/08927022.2010.490261
DO - 10.1080/08927022.2010.490261
M3 - Article
AN - SCOPUS:77958181638
SN - 0892-7022
VL - 36
SP - 871
EP - 877
JO - Molecular Simulation
JF - Molecular Simulation
IS - 11
ER -