Protein Kinase Inhibitors: Current Strategies and Future ProspectsCABALLERO, Julio.Current pharmaceutical design (Print). 2012, Vol 18, Num 20, issn 1381-6128, 145 p.Serial Issue

Molecular Dynamics of Protein Kinase-Inhibitor Complexes: A Valid Structural InformationCABALLERO, Julio; ALZATE-MORALES, Jans H.Current pharmaceutical design (Print). 2012, Vol 18, Num 20, pp 2946-2963, issn 1381-6128, 18 p.Article

Insights into the structure of urea-like compounds as inhibitors of the juvenile hormone epoxide hydrolase (JHEH) of the tobacco hornworm Manduca sexta: Analysis of the binding modes and structure-activity relationships of the inhibitors by docking and CoMFA calculationsGARRIGA, Miguel; CABALLERO, Julio.Chemosphere (Oxford). 2011, Vol 82, Num 11, pp 1604-1613, issn 0045-6535, 10 p.Article

Computational Study of the Interactions between Guanine Derivatives and Cyclin-Dependent Kinase 2 (CDK2) by CoMFA and QM/MMALZATE-MORALES, Jans; CABALLERO, Julio.Journal of chemical information and modeling. 2010, Vol 50, Num 1, pp 110-122, issn 1549-9596, 13 p.Article

QSAR modeling of matrix metalloproteinase inhibition by N -hydroxy -α -phenylsulfonylacetamide derivativesFERNANDEZ, Michael; CABALLERO, Julio.Bioorganic & medicinal chemistry. 2007, Vol 15, Num 18, pp 6298-6310, issn 0968-0896, 13 p.Article

Radiolabeled Small Molecule Inhibitors of VEGFR - Recent AdvancesKNIESS, Torsten.Current pharmaceutical design (Print). 2012, Vol 18, Num 20, pp 2867-2874, issn 1381-6128, 8 p.Article

Modeling of activity of cyclic urea HIV-1 protease inhibitors using regularized-artificial neural networksFERNANDEZ, Michael; CABALLERO, Julio.Bioorganic & medicinal chemistry. 2006, Vol 14, Num 1, pp 280-294, issn 0968-0896, 15 p.Article

Exploiting Substrate Recognition for Selective Inhibition of Protein KinasesLICHT-MURAVA, Avital; ELDAR-FINKELMAN, Hagit.Current pharmaceutical design (Print). 2012, Vol 18, Num 20, pp 2914-2920, issn 1381-6128, 7 p.Article

New Directions in Targeting Protein Kinases: Focusing Upon True Allosteric and Bivalent InhibitorsLAMBA, Vandana; GHOSH, Indraneel.Current pharmaceutical design (Print). 2012, Vol 18, Num 20, pp 2936-2945, issn 1381-6128, 10 p.Article

A CoMSIA study on the adenosine kinase inhibition of pyrrolo[2,3-d]pyrimidine nucleoside analoguesCABALLERO, Julio; FERNANDEZ, Michael; GONZALEZ-NILO, Fernando D et al.Bioorganic & medicinal chemistry. 2008, Vol 16, Num 9, pp 5103-5108, issn 0968-0896, 6 p.Article

Rho Kinase Inhibitors: Potential Treatments for Diabetes and Diabetic ComplicationsHONG ZHOU; LI, Yong-Jun.Current pharmaceutical design (Print). 2012, Vol 18, Num 20, pp 2964-2973, issn 1381-6128, 10 p.Article

Perspective of Cyclin-dependent kinase 9 (CDK9) as a Drug TargetKRYSTOF, Vladimir; BAUMLI, Sonja; FÜRST, Robert et al.Current pharmaceutical design (Print). 2012, Vol 18, Num 20, pp 2883-2890, issn 1381-6128, 8 p.Article

Conformationally Constrained Peptides as Protein Tyrosine Kinase InhibitorsTIWARI, Rakesh K; PARANG, Keykavous.Current pharmaceutical design (Print). 2012, Vol 18, Num 20, pp 2852-2866, issn 1381-6128, 15 p.Article

Structural requirements of pyrido[2,3-d]pyrimidin-7-one as CDK4/D inhibitors : 2D autocorrelation, CoMFA and CoMSIA analysesCABALLERO, Julio; FERNANDEZ, Michael; GONZALEZ-NILO, Fernando D et al.Bioorganic & medicinal chemistry. 2008, Vol 16, Num 11, pp 6103-6115, issn 0968-0896, 13 p.Article

2D Autocorrelation modeling of the negative inotropic activity of calcium entry blockers using Bayesian-regularized genetic neural networksCABALLERO, Julio; GARRIGA, Miguel; FERNANDEZ, Michael et al.Bioorganic & medicinal chemistry. 2006, Vol 14, Num 10, pp 3330-3340, issn 0968-0896, 11 p.Article

Linear and nonlinear QSAR study of N-hydroxy-2-[(phenylsulfonyl)amino]acetamide derivatives as matrix metalloproteinase inhibitorsFERNANDEZ, Michael; CABALLERO, Julio; TUNDIDOR-CAMBA, Alain et al.Bioorganic & medicinal chemistry. 2006, Vol 14, Num 12, pp 4137-4150, issn 0968-0896, 14 p.Article

Kinase Inhibitor ConjugatesHARMSEN, Stefan; KOK, Robbert Jan.Current pharmaceutical design (Print). 2012, Vol 18, Num 20, pp 2891-2900, issn 1381-6128, 10 p.Article

Cyclin-dependent kinase Inhibitors Inspired by Roscovitine: Purine BioisosteresJORDA, Radek; PARUCH, Kamil; KRYSTOF, Vladimir et al.Current pharmaceutical design (Print). 2012, Vol 18, Num 20, pp 2974-2980, issn 1381-6128, 7 p.Article

Quantitative structure-activity relationship of rubiscolin analogues as 6 opioid peptides using comparative molecular field analysis (CoMFA) and comparative molecular similarity indices analysis (CoMSIA)CABALLERO, Julio; SAAVEDRA, Mario; FERNANDEZ, Michael et al.Journal of agricultural and food chemistry (Print). 2007, Vol 55, Num 20, pp 8101-8104, issn 0021-8561, 4 p.Article

Investigation of the Differences in Activity between Hydroxycycloalkyl N1 Substituted Pyrazole Derivatives As Inhibitors of B-Raf Kinase by Using Docking, Molecular Dynamics, QM/MM, and Fragment-Based De Novo Design: Study of Binding Mode of Diastereomer CompoundsCABALLERO, Julio; ALZATE-MORALES, Jans H; VERGARA-JAQUE, Ariela et al.Journal of chemical information and modeling. 2011, Vol 51, Num 11, pp 2920-2931, issn 1549-9596, 12 p.Article

2D Autocorrelation, CoMFA, and CoMSIA modeling of protein tyrosine kinases' inhibition by substituted pyrido[2,3-d]pyrimidine derivativesCABALLERO, Julio; FERNANDEZ, Michael; SAAVEDRA, Mario et al.Bioorganic & medicinal chemistry. 2008, Vol 16, Num 2, pp 810-821, issn 0968-0896, 12 p.Article

Recent Advances in Designing Substrate-Competitive Protein Kinase InhibitorsHAN, Ki-Cheol; SO YEON KIM; EUN GYEONG YANG et al.Current pharmaceutical design (Print). 2012, Vol 18, Num 20, pp 2875-2882, issn 1381-6128, 8 p.Article

Supramolecular assembly of β-cyclodextrin-modified gold nanoparticles and Cu, Zn-superoxide dismutase on catalaseVILLALONGA, Reynaldo; CAO, Roberto; FRAGOSO, Alex et al.Journal of molecular catalysis. B, Enzymatic. 2005, Vol 35, Num 4-6, pp 79-85, issn 1381-1177, 7 p.Article

Ultrasound-assisted phase-transfer catalysis method in an aqueous medium to promote the Knoevenagel reaction: Advantages over the conventional and microwave-assisted solvent-free/catalyst-free methodDE-LA-TORRE, Pedro; OSORIO, Edison; ALZATE-MORALES, Jans H et al.Ultrasonics sonochemistry. 2014, Vol 21, Num 5, pp 1666-1674, issn 1350-4177, 9 p.Article

Synthesis, in silico, in vitro, and in vivo investigation of 5-[¹¹C]methoxy-substituted sunitinib, a tyrosine kinase inhibitor of VEGFR-2CABALLERO, Julio; MUNOZ, Camila; ALZATE-MORALES, Jans H et al.European journal of medicinal chemistry. 2012, Vol 58, pp 272-280, issn 0223-5234, 9 p.Article