Artículos de revistas
Three-dimensional QSAR analysis and design of new 1,2,4-oxadiazole antibacterials
Fecha
2016-01Registro en:
Leemans, Erika; Mahasenan, Kiran V.; Kumarasiri, Malika; Spink, Edward; Ding, Derong; et al.; Three-dimensional QSAR analysis and design of new 1,2,4-oxadiazole antibacterials; Pergamon-Elsevier Science Ltd; Biorganic and Medicinal Chemistry Letters; 26; 3; 1-2016; 1011-1015
0960-894X
CONICET Digital
CONICET
Autor
Leemans, Erika
Mahasenan, Kiran V.
Kumarasiri, Malika
Spink, Edward
Ding, Derong
O'Daniel, Peter I.
Boudreau, Marc A.
Lastochkin, Elena
Testero, Sebastian Andres
Yamaguchi, Takao
Lee, Mijoon
Hesek, Dusan
Fisher, Jed F.
Chang, Mayland
Mobashery, Shahriar
Resumen
The oxadiazole antibacterials, a class of newly discovered compounds that are active against Gram-positive bacteria, target bacterial cell-wall biosynthesis by inhibition of a family of essential enzymes, the penicillin-binding proteins. Ligand-based 3D-QSAR analyses by comparative molecular field analysis (CoMFA), comparative molecular shape indices analysis (CoMSIA) and Field-Based 3D-QSAR evaluated a series of 102 members of this class. This series included inactive compounds as well as compounds that were moderately to strongly antibacterial against Staphylococcus aureus. Multiple models were constructed using different types of energy minimization and charge calculations. CoMFA derived contour maps successfully defined favored and disfavored regions of the molecules in terms of steric and electrostatic properties for substitution.