Froeyen M.
24
Coauthors
5
Documentos
Volumen de publicaciones por año
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| Año de publicación | Num. Publicaciones |
|---|---|
| 2011 | 1 |
| 2012 | 1 |
| 2014 | 2 |
| 2020 | 1 |
Publicaciones por áreas de conocimiento
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| Área de conocimiento | Num. Publicaciones |
|---|---|
| Antibiótico | 3 |
| Farmacología | 2 |
| Bioquímica | 2 |
| Biotecnología | 1 |
| Biología molecular | 1 |
| Virus | 1 |
| Ciencias de la computación | 1 |
Publicaciones por áreas temáticas
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| Área temática | Num. Publicaciones |
|---|---|
| Microorganismos, hongos y algas | 2 |
| Programación informática, programas, datos, seguridad | 2 |
| Biblioteconomía y Documentación informatica | 1 |
| Medicina y salud | 1 |
| Química orgánica | 1 |
| Enfermedades | 1 |
| Ingeniería y operaciones afines | 1 |
| Literatura italiana, rumana y afines | 1 |
| Farmacología y terapéutica | 1 |
| Funcionamiento de bibliotecas y archivos | 1 |
Principales fuentes de datos
| Origen | Num. Publicaciones |
|---|---|
| Scopus | 5 |
| Google Scholar | 4 |
| RRAAE | 0 |
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Coautores destacados por número de publicaciones
| Coautor | Num. Publicaciones |
|---|---|
| Yunierkis Perez-Castillo | 5 |
| Nowé A. | 4 |
| Pérez M.A.C. | 4 |
| Taminau J. | 2 |
| Lazar C. | 2 |
| Neyts J. | 1 |
| Muigg A. | 1 |
| Paeshuyse J. | 1 |
| Leyssen P. | 1 |
| Musiu S. | 1 |
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Top Keywords
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Publicaciones del autor
Bacterial FabH: Towards the Discovery of New Broad-Spectrum Antibiotics
Book PartAbstract: The emergence of drug resistant strains of important human pathogens has made urgent the necessity oPalabras claves:drug design, FabH, FabH inhibitors, FASAutores:Froeyen M., Nowé A., Pérez M.A.C., Yunierkis Perez-CastilloFuentes:googlescopusMolecular dynamics and docking simulations as a proof of high flexibility in E. coli FabH and its relevance for accurate inhibitor modeling
ArticleAbstract: Bacterial β-ketoacyl-acyl carrier protein synthase III (FabH) has become an attractive target for thPalabras claves:FabH, Molecular docking, molecular dynamics, Multiple receptor conformations dockingAutores:Froeyen M., Nowé A., Pérez M.A.C., Yunierkis Perez-CastilloFuentes:googlescopusGA(M)E-QSAR: A novel, fully automatic genetic-algorithm-(meta)-ensembles approach for binary classification in ligand-based drug design
ArticleAbstract: Computer-aided drug design has become an important component of the drug discovery process. DespitePalabras claves:Autores:Froeyen M., Lazar C., Nowé A., Pérez M.A.C., Taminau J., Yunierkis Perez-CastilloFuentes:googlescopusToward the computer-aided discovery of FabH inhibitors. Do pbkp_redictive QSAR models ensure high quality virtual screening performance?
ArticleAbstract: Antibiotic resistance has increased over the past two decades. New approaches for the discovery of nPalabras claves:Ensemble modeling, FabH inhibitors, Ligand-Based Drug Design, QSAR, Virtual ScreeningAutores:Froeyen M., Lazar C., Maykel Cruz-Monteagudo, Nowé A., Pérez M.A.C., Taminau J., Yunierkis Perez-CastilloFuentes:scopusQuinolinecarboxamides inhibit the replication of the bovine viral diarrhea virus by targeting a hot spot for the inhibition of pestivirus replication in the RNA-dependent RNA polymerase
ArticleAbstract: The bovine viral diarrhea virus (BVDV), a pestivirus from the family of Flaviviridae is ubiquitous aPalabras claves:Bovine viral diarrhea virus, RNA-dependent RNA polymerase, Substituted quinolinecarboxamide inhibitorsAutores:Froeyen M., Leyssen P., Muigg A., Musiu S., Neyts J., Paeshuyse J., Pürstinger G., Yunierkis Perez-CastilloFuentes:googlescopus