JUAREZ SALDIVAR, ALFREDO
CIENCIAS DE LA VIDA · Nivel 1
Desde 2021 es en Universidad Autónoma de Tamaulipas
| Nombre | ALFREDO JUAREZ SALDIVAR |
|---|---|
| Área | BIOLOGÍA Y QUÍMICA |
| Campo | CIENCIAS DE LA VIDA |
| Disciplina | QUÍMICA FARMACÉUTICA |
| Especialidad | BIOINFORMATICA |
| CVU | 703879 |
| Institución | |
|---|---|
| Dependencia | NO APLICA |
| Entidad | NO APLICA |
| Nivel | 1 |
| Vigencia | Inicio: 01/01/2023 |
| Fin: 31/12/2027 |
Publicaciones ORCID
- 2024
- Repositioning FDA-Approved Drug Against Chagas Disease and Cutaneous Leishmaniosis by Structure-Based Virtual Screening Archives of Medical Research
- Structure-based Virtual Screening from Natural Products as Inhibitors of SARS-CoV-2 Spike Protein and ACE2 Receptor Binding and their Biological Evaluation In vitro Medicinal Chemistry
- Unravelling the Physicochemical and Antimicrobial Mechanisms of Human Serum Albumin/Tannic Acid Coatings for Medical-Grade Polycaprolactone Scaffolds SSRN
- 2023
- Antibacterial and In Silico Evaluation of β-lactamase Inhibitory Potential of Pinus sylvestris L. (Scots Pine) Essential Oil Proceedings of the National Academy of Sciences India Section B - Biological Sciences
- In Silico Analysis of Potential Drug Targets for Protozoan Infections Medicinal Chemistry
- Ligand-Based and Structure-Based Virtual Screening of New Sodium Glucose Cotransporter Type 2 Inhibitors Medicinal Chemistry
- Triose Phosphate Isomerase Structure-Based Virtual Screening and In Vitro Biological Activity of Natural Products as Leishmania mexicana Inhibitors Pharmaceutics
- Virtual Screening of Benzimidazole Derivatives as Potential Triose Phosphate Isomerase Inhibitors with Biological Activity against Leishmania mexicana Pharmaceuticals
- 2022
- Ligand-Based Virtual Screening and Molecular Docking of Benzimidazoles as Potential Inhibitors of Triosephosphate Isomerase Identified New Trypanocidal Agents International Journal of Molecular Sciences
- Ligand-based virtual screening, molecular docking, and molecular dynamics of eugenol analogs as potential acetylcholinesterase inhibitors with biological activity against Spodoptera frugiperda Molecular Diversity
