| 1 | Virtual and in Vitro Screening Employing a Repurposing Approach Reveal 13-cis-Retinoic Acid is a PTP1B Inhibitor | 2ᵒ autor: Cortés-Benítez F., Del Carmen Navarrete-Mondragón R., Elena Mendieta-Wejebe J., González-Andrade M., et al. | 2024 | Chemmedchem | WoS-id: 001330601700001
Scopus-id: 2-s2.0-85205921478
| 0 | 0 |
| 2 | The importance of including the C-terminal domain of PTP1B(1-400) to identify potential antidiabetic inhibitors | 2ᵒ autor: Cortes-Benitez, Francisco, Coronell-Tovar, Andrea, Gonzalez-Andrade, Martin | 2023 | JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY | WoS-id: 000961028800001
Scopus-id: 2-s2.0-85151316456
| 4 | 4 |
| 3 | Anti-Diabetic Activity of Glycyrrhetinic Acid Derivatives FC-114 and FC-122: Scale-Up, In Silico, In Vitro, and In Vivo Studies | Coautor: Cortes-Benitez, Francisco, Alvarez-Almazan, Samuel, Solis-Dominguez, Luz Cassandra, Duperou-Luna, Paulina, et al. | 2023 | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | WoS-id: 001057280700001
Scopus-id: 2-s2.0-85168715964
| 5 | 5 |
| 4 | Synthesis and Antitumor Activity of 2,3-Diphenyl-2H-indazole Derivatives as Potent Antitubulin Agents | Coautor: Cortés-Benítez F., Matadamas-Martínez F., Yépez-Mulia L., Pérez-Koldenkova V., et al. | 2022 | Chemistryselect | WoS-id: 000826509000001
Scopus-id: 2-s2.0-85134547418
| 1 | 1 |
| 5 | Design, Synthesis and Anticandidal Evaluation of Indazole and Pyrazole Derivatives | Coautor: Cortes-Benitez, Francisco, Rodriguez-Villar, Karen, Hernandez-Campos, Alicia, Yepez-Mulia, Lilian, et al. | 2021 | Pharmaceuticals | WoS-id: 000634096600001
Scopus-id: 2-s2.0-85102294099
| 10 | 11 |
| 6 | The giardicidal activity of lobendazole, fabomotizole, tenatoprazole and ipriflavone: A ligand-based virtual screening and in vitro study | Coautor: Cortés-Benítez F., Pérez-Villanueva J., Yépez-Mulia L., Rodríguez-Villar K., et al. | 2021 | EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY | WoS-id: 000639375500041
Scopus-id: 2-s2.0-85098131978
| 3 | 6 |
| 7 | Synthesis, antiprotozoal activity, and cheminformatic analysis of 2-phenyl-2h-indazole derivatives | Coautor: Cortés-Benítez F., Rodríguez-Villar K., Yépez-Mulia L., Cortés-Gines M., et al. | 2021 | Molecules | WoS-id: 000644587100001
Scopus-id: 2-s2.0-85105130720
| 16 | 19 |
| 8 | 16-Picolyl-androsterone derivative exhibits potent 17ß-HSD3 inhibitory activity, improved metabolic stability and cytotoxic effect on various cancer cells: Synthesis, homology modeling and docking studies | 1ᵉʳ autor: Cortés-Benítez F., Roy J., Perreault M., Maltais R., et al. | 2021 | JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY | WoS-id: 000652020500011
Scopus-id: 2-s2.0-85101870762
| 4 | 7 |
| 9 | Indole- and Pyrazole-Glycyrrhetinic Acid Derivatives as PTP1B Inhibitors: Synthesis, In Vitro and In Silico Studies | Coautor: Cortes-Benitez, Francisco, De-la-Cruz-Martinez, Ledyy, Duran-Becerra, Constanza, Gonzalez-Andrade, Martin, et al. | 2021 | Molecules | WoS-id: 000677385500001
Scopus-id: 2-s2.0-85111458077
| 15 | 16 |
| 10 | Synthesis and Cytotoxic Activity of Combretastatin A-4 and 2,3-Diphenyl-2H-indazole Hybrids | Coautor: Cortes-Benitez, Francisco, Perez-Villanueva, Jaime, Matadamas-Martinez, Felix, Yepez-Mulia, Lilian, et al. | 2021 | Pharmaceuticals | WoS-id: 000689796300001
Scopus-id: 2-s2.0-85113736996
| 7 | 8 |
| 11 | A- and D-Ring Structural Modifications of an Androsterone Derivative Inhibiting 17 beta-Hydroxysteroid Dehydrogenase Type 3: Chemical Synthesis and Structure-Activity Relationships | 1ᵉʳ autor: Cortes-Benitez, Francisco, Roy, Jenny, Perreault, Martin, Maltais, Rene, et al. | 2019 | JOURNAL OF MEDICINAL CHEMISTRY | WoS-id: 000480500600017
Scopus-id: 2-s2.0-85070614039
| 9 | 9 |
| 12 | Design, synthesis and biological evaluation of new anti-Candida agents | Coautor: Cortes Benitez, Juan Francisco, Rodriguez Villar, Karen, Hernandez Campos, Alicia, Drago-Serrano, Maria, et al. | 2019 | Abstracts Of Papers Of The American Chemical Society | WoS-id: 000525061502166
| 0 | 0 |
| 13 | Targeting Cytochrome P450 (CYP) 1B1 Enzyme with Four Series of A-Ring Substituted Estrane Derivatives: Design, Synthesis, Inhibitory Activity, and Selectivity | Coautor: Cortes-Benitez, Francisco, Dutour, Raphael, Roy, Jenny, Maltais, Rene, et al. | 2018 | JOURNAL OF MEDICINAL CHEMISTRY | WoS-id: 000448754900016
Scopus-id: 2-s2.0-85054690168
| 29 | 29 |
| 14 | 17ß-N-arylcarbamoylandrost-4-en-3-one derivatives as inhibitors of the enzymes 3a-hydroxysteroid dehydrogenase and 5a-reductase | Coautor: Cortés-Benítez F., Bratoeff E., Moreno I., Heuze Y., et al. | 2018 | Current Enzyme Inhibition | Scopus-id: 2-s2.0-85045375869
| 0 | 2 |
| 15 | Impact of androstane A- and D-ring inversion on 17 beta-hydroxysteroid dehydrogenase type 3 inhibitory activity, androgenic effect and metabolic stability | 1ᵉʳ autor: Cortes-Benitez, Francisco, Roy, Jenny, Maltais, Rene, Poirier, Donald | 2017 | BIOORGANIC & MEDICINAL CHEMISTRY | WoS-id: 000398650800005
Scopus-id: 2-s2.0-85013800387
| 9 | 10 |
| 16 | Structure-Based Design and Synthesis of New Estrane-Pyridine Derivatives as Cytochrome P450 (CYP) 1B1 Inhibitors | 2ᵒ autor: Cortes-Benitez, Francisco, Dutour, Raphael, Roy, Jenny, Poirier, Donald | 2017 | ACS MEDICINAL CHEMISTRY LETTERS | WoS-id: 000415140500008
| 18 | 0 |
| 17 | Identification of potent 17 beta-hydroxysteroid dehydrogenase type 3 (17 beta-HSD3) inhibitors by systematic structural modifications of the lead compound RM-532-105 | 1ᵉʳ autor: Cortes-Benitez, Francisco, Roy, Jenny, Perrault, Martin, Maltais, Rene, et al. | 2017 | Abstracts Of Papers Of The American Chemical Society | WoS-id: 000429556701285
| 0 | 0 |
| 18 | Structure-Based Design and Synthesis of New Estrane-Pyridine Derivatives as Cytochrome P450 (CYP) 1B1 Inhibitors | 2ᵒ autor: Cortés-Benítez F., Dutour R., Roy J., Poirier D. | 2017 | ACS MEDICINAL CHEMISTRY LETTERS | WoS-id: 000415140500008
Scopus-id: 2-s2.0-85033401309
| 20 | 20 |
| 19 | Activity landscape analysis of novel 5 a -reductase inhibitors | 2ᵒ autor: Cortes-Benitez, Francisco, Jesus Naveja, J., Bratoeff, Eugene, Medina-Franco, Jose L. | 2016 | MOLECULAR DIVERSITY | WoS-id: 000379259200018
Scopus-id: 2-s2.0-84977460212
| 8 | 8 |
| 20 | Synthesis of 17ß-N-arylcarbamoylandrost-4-en-3-one derivatives and their anti-proliferative effect on human androgen-sensitive LNCaP cell line | 1ᵉʳ autor: Cortés-Benítez F., Cabeza M., Teresa Ramirez-Apan, Maria, Alvarez-Manrique B., et al. | 2016 | EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY | WoS-id: 000382269700059
Scopus-id: 2-s2.0-84978252237
| 11 | 16 |
| 21 | Targeting cytochrome P450 (CYP) 1B1 with steroid derivatives | Coautor: Cortes-Benitez, Francisco, Poirier, Donald, Roy, Jenny, Dutour, Raphael | 2016 | BIOORGANIC & MEDICINAL CHEMISTRY LETTERS | WoS-id: 000389015300026
Scopus-id: 2-s2.0-84992205967
| 9 | 9 |
| 22 | Synthesis of 17 beta-N-arylcarbamoylandrost-4-en-3-one derivatives and their in vitro and in vivo effect as potent 5 alpha-reductase inhibitors | 1ᵉʳ autor: Cortes, Francisco, Cabeza, Marisa, Alvarez, Berenice, Ramirez-Apan, Maria-Teresa, et al. | 2015 | Abstracts Of Papers Of The American Chemical Society | WoS-id: 000432475701261
| 0 | 0 |
| 23 | Synthesis of 17-triazoyldehydroepiandrosterone derivatives with substituted cinnamates at C-3 and their in vitro and in vivo biological activity | Coautor: Cortes, Francisco, Mendoza Jasso, Maria Eugenia, Cabeza, Marisa, Ramirez-Apan, Maria-Teresa, et al. | 2015 | Abstracts Of Papers Of The American Chemical Society | WoS-id: 000432475701262
| 0 | 0 |
| 24 | Cytotoxic effect of novel dehydroepiandrosterone derivatives on different cancer cell lines | Coautor: Cortes, F, Bratoeff, E, Garrido, M, Cabeza, M | 2014 | Abstracts Of Papers Of The American Chemical Society | WoS-id: 000348457602453
| 0 | 0 |
| 25 | Cytotoxic effect of novel dehydroepiandrosterone derivatives on different cancer cell lines | Coautor: Cortes, F, Garrido, M, Cabeza, M, Gutierrez, J, et al. | 2013 | EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY | WoS-id: 000326902300032
Scopus-id: 2-s2.0-84882743116
| 20 | 21 |
ID's SCOPUS 