ABSTRACT
Catalytic ozonation of Methylene Blue, Methyl Green, Methyl Orange and Methyl-thymol Blue was investigated in the presence of ion-exchanged montmorillonite (NaMt and Fe(II)Mt), crude bentonite and acid-activated counterparts. An original approach never tackled so far consisted in correlating the basicity and hydrophilic character to the dye-catalyst interactions occurring on the catalyst surface. This was achieved through CO2 and water thermal programmed desorption. Kinetics study revealed that ozonation starts in the bulk solution, and dye adsorption turns out to be an essential requirement for high catalytic effectiveness. On NaMt, dye molecules appear to adsorb mainly via hydrophobic interaction. On Fe(II)Mt, the contributions of hydrophobic interaction, cation-exchange and Fe2+ mobility to the catalytic activity prevail. Acid activated clay catalysts exhibited lowest hydrophilic character favoring adsorption through organophilic interaction and affording thorough and fast dye mineralization. This was explained in terms of increased number of silanols and -Si-O-Si- groups. For all catalysts, short ozonation of all dye molecules resulted in similar end-chain products, which were totally eliminated after prolonged reaction times. This result is of great importance because it provides valuable theoretical findings that allow envisaging total mineralization of organic molecules by recyclable metal-free clay catalysts.
ABSTRACT
HCV NS5B RNA-dependent RNA polymerase (NS5B) is essential for viral replication and is therefore considered a target for antiviral drug development. From our ongoing screening effort in the search for new anti-HCV agents, a novel inhibitor 1 with low microM activity against the HCV NS5B polymerase was identified. SAR analysis indicated the optimal substitution pattern required for activity, for example, carboxylic acid group at 2-position of thiophene ring. We describe the steps taken to identify and solve the bioactive conformation of derivative 6 through the use of the transferred NOE method (trNOE).
Subject(s)
Antiviral Agents/chemical synthesis , RNA-Dependent RNA Polymerase/antagonists & inhibitors , Sulfonamides/chemical synthesis , Viral Nonstructural Proteins/antagonists & inhibitors , Antiviral Agents/chemistry , Humans , Magnetic Resonance Spectroscopy , Models, Molecular , Molecular Conformation , Pyridines/chemistry , RNA-Dependent RNA Polymerase/chemistry , Structure-Activity Relationship , Sulfonamides/chemistry , Thiophenes/chemistry , Viral Nonstructural Proteins/chemistryABSTRACT
To determine the proportion of hospitalisations for gastroenteritis caused by rotavirus, we tested for rotavirus stool samples of all children under the age of five hospitalised for gastroenteritis between 1 December 1999 and 30 May 2000 in seven community and specialised hospitals in Quebec. Of 944 children hospitalised, 565 (59.9%) were screened for rotavirus and 405 (71.7%) tested positive. From December to April, the proportion of positive results rose from 51.6 to 78.1%. Compared with children whose test results were negative, children who tested positive presented vomiting more frequently upon admission (88.9 versus 60.4%) and needed IV fluids in greater proportion (94.1 versus 78.0%), but spent less time in hospital (2.8 versus 3.3 days). Aside from dehydration, no complications were noted. In Quebec, a large majority of winter and spring hospitalisations for gastroenteritis in children is attributable to rotavirus.
Subject(s)
Gastroenteritis/epidemiology , Gastroenteritis/virology , Rotavirus Infections/epidemiology , Rotavirus Infections/virology , Rotavirus , Child, Preschool , Dehydration/etiology , Feces/virology , Female , Fluid Therapy , Hospitalization/statistics & numerical data , Humans , Infant , Male , Quebec/epidemiology , Rotavirus Infections/complicationsABSTRACT
The discovery of a novel class of HCV NS5B polymerase inhibitors, 3-arylsulfonylamino-5-phenyl-thiophene-2-carboxylic acids is described. SAR studies have yielded several potent inhibitors of HCV polymerase as well as of HCV subgenomic RNA replication in Huh-7 cells.
Subject(s)
Enzyme Inhibitors/pharmacology , Hepacivirus/enzymology , RNA, Viral/metabolism , Sulfonamides/pharmacology , Thiophenes/pharmacology , Viral Nonstructural Proteins/antagonists & inhibitors , Carboxylic Acids , Carcinoma, Hepatocellular/chemistry , Carcinoma, Hepatocellular/enzymology , Carcinoma, Hepatocellular/virology , Enzyme Inhibitors/chemistry , Genome, Viral , Humans , Liver Neoplasms/chemistry , Liver Neoplasms/enzymology , Liver Neoplasms/virology , RNA-Dependent RNA Polymerase/antagonists & inhibitors , Replicon/drug effects , Structure-Activity Relationship , Sulfonamides/chemistry , Thiophenes/chemistry , Virus Replication/drug effectsABSTRACT
Further SAR studies on the thiophene-2-carboxylic acids are reported. These studies led to the identification of a series of tertiary amides that show inhibition of both HCV NS5B polymerase in vitro and HCV subgenomic RNA replication in Huh-7 cells. Structural insights about the bioactive conformation of this class of molecules were deduced from a combination of modeling and transferred NOE (trNOE) studies.
Subject(s)
Amides/pharmacology , Enzyme Inhibitors/pharmacology , Hepacivirus/enzymology , RNA, Viral/metabolism , Thiophenes/pharmacology , Viral Nonstructural Proteins/antagonists & inhibitors , Amides/chemistry , Carboxylic Acids , Carcinoma, Hepatocellular/chemistry , Carcinoma, Hepatocellular/enzymology , Carcinoma, Hepatocellular/virology , Enzyme Inhibitors/chemistry , Genome, Viral , Humans , Liver Neoplasms/chemistry , Liver Neoplasms/enzymology , Liver Neoplasms/virology , Magnetic Resonance Spectroscopy , Molecular Conformation , Molecular Structure , RNA-Dependent RNA Polymerase/antagonists & inhibitors , Replicon/drug effects , Structure-Activity Relationship , Thiophenes/chemistry , Virus Replication/drug effectsABSTRACT
Herein, we describe the structure-activity relationship (SAR) of N,N-disubstituted phenylalanine series of NS5B polymerase inhibitors of hepatitis C. The NS5B polymerase inhibitory activity of the most active compound exhibited an IC(50) of 2.7 microM.
Subject(s)
Enzyme Inhibitors/chemistry , Hepacivirus/enzymology , RNA-Dependent RNA Polymerase/antagonists & inhibitors , Viral Nonstructural Proteins/antagonists & inhibitors , Enzyme Inhibitors/pharmacology , Hepacivirus/drug effects , Humans , Structure-Activity Relationship , Viral Nonstructural Proteins/metabolismABSTRACT
An unusually high prevalence of pyrazinamide (PZA) monoresistance in Mycobacterium tuberculosis has been observed in Quebec. In the absence of a recognized outbreak, we hypothesized that these isolates most likely represented reactivation of an old endemic strain in this low-incidence area. A case-control study of 77 PZA-resistant isolates with a specific Quebec mutation and 253 PZA-susceptible control M. tuberculosis isolates was undertaken. By molecular analysis, all 77 case isolates shared a unique mutation profile in the pncA gene which was not present in control isolates. While control isolates manifested diverse IS6110 restriction fragment length polymorphism (RFLP) patterns, spoligotypes, and major genetic groups, case isolates had similar but nonidentical IS6110 RFLP patterns, had common spoligotypes, and were confined to one major genetic group, suggesting a common clonal ancestor. By epidemiologic and geographic analyses, however, there were no significant differences between the cases and the controls. We conclude that a clonally related family of PZA-monoresistant M. tuberculosis isolates in Quebec represents historic rather than recent transmission.
Subject(s)
Antitubercular Agents/pharmacology , Drug Resistance, Bacterial , Mycobacterium tuberculosis/drug effects , Pyrazinamide/pharmacology , Tuberculosis, Pulmonary/epidemiology , Amidohydrolases/genetics , Case-Control Studies , DNA Transposable Elements , Genotype , Humans , Incidence , Mutation , Mycobacterium tuberculosis/genetics , Oligonucleotides/analysis , Polymorphism, Restriction Fragment Length , Quebec/epidemiology , Tuberculosis, Pulmonary/microbiologyABSTRACT
The HCV NS5B RNA dependent RNA polymerase plays an essential role in viral replication. The discovery of a novel class of inhibitors based on an N,N-disubstituted phenylalanine scaffold and structure-activity relationships studies to improve potency are described.