Rodrigo Said Razo Hernández
Rodrigo Said Razo Hernández
Centro de Investigación en Dinámica Celular, Universidad Autónoma del Estado de Morelos
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Cited by
Cited by
Design, synthesis and QSAR study of 2′-hydroxy-4′-alkoxy chalcone derivatives that exert cytotoxic activity by the mitochondrial apoptotic pathway
S Marquina, M Maldonado-Santiago, JN Sánchez-Carranza, ...
Bioorganic & Medicinal Chemistry 27 (1), 43-54, 2019
000Synthesis of new α-aminophosphonates: Evaluation as anti-inflammatory agents and QSAR studies
I Romero-Estudillo, JL Viveros-Ceballos, O Cazares-Carreño, ...
Bioorganic & Medicinal Chemistry 27 (12), 2376-2386, 2019
Synthesis and in Vitro Antioxidant Activity Evaluation of 3-Carboxycoumarin Derivatives and QSAR Study of Their DPPH• Radical Scavenging Activity
FJ Martínez-Martínez, RS Razo-Hernández, AL Peraza-Campos, ...
Molecules 17 (12), 14882-14898, 2012
QSAR study of the DPPH· radical scavenging activity of coumarin derivatives and xanthine oxidase inhibition by molecular docking
RS Razo-Hernández, K Pineda-Urbina, MA Velazco-Medel, ...
Central European Journal of Chemistry 12, 1067-1080, 2014
Silicon containing ibuprofen derivatives with antioxidant and anti-inflammatory activities: An in vivo and in silico study
DJ Pérez, MI Díaz-Reval, F Obledo-Benicio, UI Zakai, Z Gómez-Sandoval, ...
European journal of pharmacology 814, 18-27, 2017
Synthesis, characterization, antimicrobial and theoretical studies of the first main group tris(ephedrinedithiocarbamate) complexes of As(III), Sb(III), Bi(III), Ga(III) and In …
AO Ariza-Roldán, EM López-Cardoso, ME Rosas-Valdez, ...
Poyhedron 134, 221-229, 2017
Achillin increases chemosensitivity to paclitaxel, overcoming resistance and enhancing apoptosis in human hepatocellular carcinoma cell line resistant to paclitaxel (Hep3B/PTX)
JN Sanchez-Carranza, L González-Maya, RS Razo-Hernández, ...
Pharmaceutics 11 (10), 512, 2019
Removal of sulfamethoxazole, sulfadiazine, and sulfamethazine by UV radiation and HO and SO4•− radicals using a response surface model and DFT calculations
LAJ Rodríguez-Blanco, R Ocampo-Pérez, CFA Gómez-Durán, ...
Environmental Science and Pollution Research 27, 41609-41622, 2020
Synthesis of 1,4-Biphenyl-triazole Derivatives as Possible 17β-HSD1 Inhibitors: An in Silico Study
H Hernández-López, S Leyva-Ramos, CF Azael Gómez-Durán, ...
ACS omega 5 (23), 14061-14068, 2020
In silico receptor-based drug design of X,Y-benzenesulfonamide derivatives as selective COX-2 inhibitors
DJ Pérez, O Sarabia, M Villanueva-García, K Pineda-Urbina, ...
Comptes Rendus. Chimie 20 (2), 169-180, 2017
Novel-Substituted Heterocyclic GABA Analogues. Enzymatic Activity against the GABA-AT Enzyme from Pseudomonas fluorescens and In Silico Molecular Modeling
E Tovar-Gudiño, JA Guevara-Salazar, JR Bahena-Herrera, ...
Molecules 23 (5), 1128, 2018
Synthesis, crystal structure, antibacterial, antiproliferative and QSAR studies of new bismuth (III) complexes of pyrrolidineditiocarbamate of dithia-bismolane and bismane …
M López-Cardoso, H Tlahuext, M Pérez-Salgado, DG Vargas-Pineda, ...
Journal of molecular structure 1217, 128456, 2020
Berberine as source of antiproliferative hybrid compounds: In vitro antiproliferative activity and quantitative structure-activity relationship
MA Leyva-Peralta, RE Robles-Zepeda, RS Razo-Hernández, LPÁ Berber, ...
Anti-Cancer Agents in Medicinal Chemistry (Formerly Current Medicinal …, 2019
QSAR and molecular docking studies of the inhibitory activity of novel heterocyclic GABA analogues over GABA-AT
J Rodríguez-Lozada, E Tovar-Gudiño, JA Guevara-Salazar, ...
Molecules 23 (11), 2984, 2018
Synthesis and biological screening of silicon-containing ibuprofen derivatives: a study of their NF-κβ inhibitory activity, cytotoxicity, and their ability to bind IKKβ
DJ Pérez, UI Zakai, S Guo, IA Guzei, Z Gómez-Sandoval, ...
Australian Journal of Chemistry 69 (6), 662-671, 2015
In silico structure‐based design of GABAB receptor agonists using a combination of docking and QSAR
Z Martínez‐Campos, N Pastor, K Pineda‐Urbina, Z Gómez‐Sandoval, ...
Chemical Biology & Drug Design 94 (4), 1782-1798, 2019
Novel ciprofloxacin and norfloxacin-tetrazole hybrids as potential antibacterial and antiviral agents: Targeting S. aureus topoisomerase and SARS-CoV-2-MPro
J Cardoso-Ortiz, S Leyva-Ramos, KM Baines, CFA Gómez-Durán, ...
Journal of molecular structure 1274, 134507, 2023
Isatin derivatives as DNA minor groove-binding agents: A structural and theoretical study
M Maldonado-Santiago, Á Santiago, N Pastor, L Alvarez, ...
Structural Chemistry 31, 1289-1307, 2020
The TATA‐binding Protein DNA‐binding domain of eukaryotic parasites is a potentially druggable target
Á Santiago, RS Razo‐Hernández, N Pastor
Chemical Biology & Drug Design 95 (1), 130-149, 2020
Antitumor structure–activity relationship in bis-stannoxane derivatives from pyridine dicarboxylic and benzoic acids
JA Valcarcel, RS Razo-Hernández, LL Valdez-Velázquez, MV García, ...
Inorganica Chimica Acta 392, 229-235, 2012
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