CHEMICAL BASIS FOR THE ANTIMICROBIAL ACTIVITY OF ACETANILIDES
In vitro antimicrobial activity of a series of substituted acetanilides against S. aureus, E. coli and C. albicans were measured at two concentrations, 250 mug/ml and 500 mug/ml. Only the structures substituted with halogens in Calpha and electron acceptors in the aromatic ring are bioactive. The results are rationalized in terms of the acid properties of the N-H bond, as calculated using AM1-MO theory
Saved in:
Main Authors: | Bravo,Hector R., Weiss-López,Boris, Lamborot,Madeleine, Copaja,Sylvia |
---|---|
Format: | Digital revista |
Language: | English |
Published: |
Sociedad Chilena de Química
2003
|
Online Access: | http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072003000400005 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
FRONTIER ORBITALS AND IR FREQUENCIES OF CYCLIC HYDROXAMIC ACIDS RELATED TO ANTIMICROBIAL ACTIVITY
by: BRAVO,HÉCTOR R, et al.
Published: (2001) -
Thermodynamic quantities of solvation and dilution for some acetanilide derivatives in octanol and water mutually saturateds
by: Baena,Y., et al.
Published: (2008) -
Eco-Friendly, Catalyst and Solvent-Free, Synthesis of Acetanilides and N-Benzothiazole-2-yl-acetamides
by: Cunha,Silvio, et al.
Published: (2017) -
Karyotypic polymorphism and evolution within and between the Liolaemus monticola (Iguanidae) "northern 2n = 38-40" chromosome race populations in central Chile
by: LAMBOROT,MADELEINE
Published: (2001) -
The physico-chemical basis of phenolic antioxidant activity
by: Laguerre, Mickaël, et al.