Approaches of Virtual Screening in Drug Discovery. Este artículo no está disponible.
Idioma: inglés
Editorial: LAP LAMBERT Academic Publishing, 2017
- Tapa blanda
- Nuevo

Librería: preigu, Osnabrück, Alemaniapreigu
Vendedor de 5 estrellas
Vendedor de IberLibro desde 5 de agosto de 2024
No disponible
Tapa blanda
Condición: Nuevo
EUR 22,50
Descripción del artículo del vendedor
Approaches of Virtual Screening in Drug Discovery | Heba Elzahabi (u. a.) | Taschenbuch | 68 S. | Englisch | 2017 | LAP LAMBERT Academic Publishing | EAN 9783330079847 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.
N° de ref. del artículo 109009657
- Título
- Approaches of Virtual Screening in Drug Discovery
- Autor
- Heba Elzahabi (u. a.)
- Editorial
- LAP LAMBERT Academic Publishing
- Año de publicación
- 2017
- Estado
- Neu
- Encuadernación
- Taschenbuch
- Idioma
- inglés
- ISBN 10
- 3330079843
- ISBN 13
- 9783330079847
- Peso del artículo
- 119 gramos
- Dimensiones
- 220 x 150 x 5 mm
- Catálogos de vendedores
- Bücher
Virtual screening has become an integral part of the drug discovery process. Through the two main streams of VS, ligand based and structure based, various interesting new scaffolds could be defined. Many interesting detailed studies were implemented in this field of research. A comparative computational study of pharmacophore model generation was explored, mentioning the advantage and disadvantage of each method. Also, an employed comparison between the two main streams was mentioned using CDK-2 as representative example with detection of the most acceptable pharmacophore model. A promising linking between the direct (ligand docking) and indirect (pharmacophore model) methods to identify the successful scaffold was explored. This linking approach using pharmacophore post filtering aims to increase the hit rates with minimizing the time used in VS process. Further, different programs that handled direct ligand docking approach was mentioned with mapping of their algorithm.
“Sinopsis” puede pertenecer a otra edición de este título.
Reseña del editor
Virtual screening has become an integral part of the drug discovery process. Through the two main streams of VS, ligand based and structure based, various interesting new scaffolds could be defined. Many interesting detailed studies were implemented in this field of research. A comparative computational study of pharmacophore model generation was explored, mentioning the advantage and disadvantage of each method. Also, an employed comparison between the two main streams was mentioned using CDK-2 as representative example with detection of the most acceptable pharmacophore model. A promising linking between the direct (ligand docking) and indirect (pharmacophore model) methods to identify the successful scaffold was explored. This linking approach using pharmacophore post filtering aims to increase the hit rates with minimizing the time used in VS process. Further, different programs that handled direct ligand docking approach was mentioned with mapping of their algorithm.
“Acerca de” puede pertenecer a otra edición de este título.