QSAR analysis of structurally similar antitubercular isatin analogues
A series of structurally similar isatin analogues with antitubercular activity have been subjected for 2D and 3D QSAR analysis using V life MDS 3.5 software. The compounds were divided into training and test set of 44 and 11 each. Best QSAR models were selected on the basis of various statistical pa...
Guardado en:
| Autores principales: | Sawant, Ramesh L., Wadekar, Jyoti B., Lanke, Prashant D. |
|---|---|
| Formato: | Articulo |
| Lenguaje: | Inglés |
| Publicado: |
2011
|
| Materias: | |
| Acceso en línea: | http://sedici.unlp.edu.ar/handle/10915/8213 http://www.latamjpharm.org/resumenes/30/4/LAJOP_30_4_1_21.pdf |
| Aporte de: |
Ejemplares similares
-
Synthesis and QSAR analysis of oxazolo/thiazolo pyrimidine derivatives as potential antibacterial agents
por: Sawant, Ramesh L., et al.
Publicado: (2012) -
Structurally modified celecoxib analogues for selective COX-2 inhibition: a classical hansch QSAR approach
por: Manivannan, E., et al.
Publicado: (2012) -
Indice de conectividad molecular y actividad antitumoral de aminoácidos-QSAR
por: Bruno Blanch, Luis Enrique, et al.
Publicado: (1989) -
2 D QSAR and docking of novel N-substitutedAryl amine derivatives as potential inhibitors of lumazine synthase
por: Bhatia, Manish S., et al.
Publicado: (2010) -
Síntesis de nuevos compuestos heterociclícos con probable actividad biológica : estudio estructural y propiedades fisicoquímicas
por: Ortiz, Cristina Susana
Publicado: (2024)