Medina-Franco JL - Search Results

1

Insights into the structure and inhibition of Giardia intestinalis arginine deiminase: homology modeling, docking, and molecular dynamics studies.

Trejo-Soto PJ, Aguayo-Ortiz R, Yépez-Mulia L, Hernández-Campos A, Medina-Franco JL, Castillo R. Trejo-Soto PJ, et al. J Biomol Struct Dyn. 2016;34(4):732-48. doi: 10.1080/07391102.2015.1051115. Epub 2015 Jun 15. J Biomol Struct Dyn. 2016. PMID: 26017138

2

Flexible docking of pyridinone derivatives into the non-nucleoside inhibitor binding site of HIV-1 reverse transcriptase.

Medina-Franco JL, Rodríguez-Morales S, Juárez-Gordiano C, Hernández-Campos A, Jiménez-Barbero J, Castillo R. Medina-Franco JL, et al. Bioorg Med Chem. 2004 Dec 1;12(23):6085-95. doi: 10.1016/j.bmc.2004.09.008. Bioorg Med Chem. 2004. PMID: 15519154

3

Docking-based CoMFA and CoMSIA studies of non-nucleoside reverse transcriptase inhibitors of the pyridinone derivative type.

Medina-Franco JL, Rodríguez-Morales S, Juárez-Gordiano C, Hernández-Campos A, Castillo R. Medina-Franco JL, et al. J Comput Aided Mol Des. 2004 May;18(5):345-60. doi: 10.1023/b:jcam.0000047816.15514.ab. J Comput Aided Mol Des. 2004. PMID: 15595461

4

Molecular docking of the highly hypolipidemic agent alpha-asarone with the catalytic portion of HMG-CoA reductase.

Medina-Franco JL, López-Vallejo F, Rodríguez-Morales S, Castillo R, Chamorro G, Tamariz J. Medina-Franco JL, et al. Bioorg Med Chem Lett. 2005 Feb 15;15(4):989-94. doi: 10.1016/j.bmcl.2004.12.046. Bioorg Med Chem Lett. 2005. PMID: 15686898

5

New fragmentation processes of pyridin-2(1H)-ones upon electron impact ionization.

Medina-Franco JL, Juárez-Gordiano C, Hernández-Campos A, Duarte-Lisci G, Guzmán M, Castillo R. Medina-Franco JL, et al. Rapid Commun Mass Spectrom. 2005;19(16):2350-4. doi: 10.1002/rcm.2059. Rapid Commun Mass Spectrom. 2005. PMID: 16041820 No abstract available.

6

Quantitative structure-activity relationship analysis of pyridinone HIV-1 reverse transcriptase inhibitors using the k nearest neighbor method and QSAR-based database mining.

Medina-Franco JL, Golbraikh A, Oloff S, Castillo R, Tropsha A. Medina-Franco JL, et al. J Comput Aided Mol Des. 2005 Apr;19(4):229-42. doi: 10.1007/s10822-005-4789-8. J Comput Aided Mol Des. 2005. PMID: 16163450

7

Molecular modeling of some 1H-benzimidazole derivatives with biological activity against Entamoeba histolytica: a comparative molecular field analysis study.

López-Vallejo F, Medina-Franco JL, Hernández-Campos A, Rodríguez-Morales S, Yépez L, Cedillo R, Castillo R. López-Vallejo F, et al. Bioorg Med Chem. 2007 Jan 15;15(2):1117-26. doi: 10.1016/j.bmc.2006.10.019. Epub 2006 Oct 18. Bioorg Med Chem. 2007. PMID: 17074492

8

Pyridin-2(1H)-ones: a promising class of HIV-1 non-nucleoside reverse transcriptase inhibitors.

Medina-Franco JL, Martínez-Mayorga K, Juárez-Gordiano C, Castillo R. Medina-Franco JL, et al. ChemMedChem. 2007 Aug;2(8):1141-7. doi: 10.1002/cmdc.200700054. ChemMedChem. 2007. PMID: 17477343 Review. No abstract available.

9

Antidiabetic activity of N-(6-substituted-1,3-benzothiazol-2-yl)benzenesulfonamides.

Moreno-Díaz H, Villalobos-Molina R, Ortiz-Andrade R, Díaz-Coutiño D, Medina-Franco JL, Webster SP, Binnie M, Estrada-Soto S, Ibarra-Barajas M, León-Rivera I, Navarrete-Vázquez G. Moreno-Díaz H, et al. Bioorg Med Chem Lett. 2008 May 1;18(9):2871-7. doi: 10.1016/j.bmcl.2008.03.086. Epub 2008 Apr 8. Bioorg Med Chem Lett. 2008. PMID: 18424136

10

Synthesis, in vitro and computational studies of protein tyrosine phosphatase 1B inhibition of a small library of 2-arylsulfonylaminobenzothiazoles with antihyperglycemic activity.

Navarrete-Vazquez G, Paoli P, León-Rivera I, Villalobos-Molina R, Medina-Franco JL, Ortiz-Andrade R, Estrada-Soto S, Camici G, Diaz-Coutiño D, Gallardo-Ortiz I, Martinez-Mayorga K, Moreno-Díaz H. Navarrete-Vazquez G, et al. Bioorg Med Chem. 2009 May 1;17(9):3332-41. doi: 10.1016/j.bmc.2009.03.042. Epub 2009 Mar 26. Bioorg Med Chem. 2009. PMID: 19362487

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