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1.
Eur J Med Chem ; 141: 113-137, 2017 Dec 01.
Article in English | MEDLINE | ID: mdl-29031060

ABSTRACT

Heterocyclic compounds are the interesting core structures for the development of new bioactive compounds. Fatty acids are derived from renewable raw materials and exhibit various biological activities. Several researchers are amalgamating these two bioactive components to yield bioactive hybrid molecules with some desirable features. Heterocyclic-fatty acid hybrid derivatives are a new class of heterocyclic compounds with a broad range of biological activities and significance in the field of medicinal chemistry. Over the last few years, many research articles emphasized the significance of heterocyclic-fatty acid hybrid derivatives. The present review article focuses the developments in designing and biological evaluation of heterocyclic-fatty acid hybrid molecules.


Subject(s)
Anti-Infective Agents/pharmacology , Antineoplastic Agents/pharmacology , Fatty Acids/pharmacology , Heterocyclic Compounds/pharmacology , Neoplasms/drug therapy , Animals , Anti-Infective Agents/chemistry , Antineoplastic Agents/chemistry , Bacteria/drug effects , Fatty Acids/chemistry , Fungi/drug effects , Heterocyclic Compounds/chemistry , Humans , Tuberculosis/drug therapy
2.
Sci Rep ; 6: 21624, 2016 Feb 23.
Article in English | MEDLINE | ID: mdl-26902658

ABSTRACT

The role of the unique proline-glutamic acid (PE)/proline-proline-glutamic acid (PPE) family of proteins in the pathophysiology and virulence of Mycobacterium tuberculosis is not clearly understood. One of the PE family proteins, PE11 (LipX or Rv1169c), specific to pathogenic mycobacteria is found to be over-expressed during infection of macrophages and in active TB patients. In this study, we report that M. smegmatis expressing PE11 (Msmeg-PE11) exhibited altered colony morphology and cell wall lipid composition leading to a marked increase in resistance against various environmental stressors and antibiotics. The cell envelope of Msmeg-PE11 also had greater amount of glycolipids and polar lipids. Msmeg-PE11 was found to have better survival rate in infected macrophages. Mice infected with Msmeg-PE11 had higher bacterial load, showed exacerbated organ pathology and mortality. The liver and lung of Msmeg-PE11-infected mice also had higher levels of IL-10, IL-4 and TNF-α cytokines, indicating a potential role of this protein in mycobacterial virulence.


Subject(s)
Bacterial Proteins/genetics , Cell Wall/metabolism , Mycobacterium Infections, Nontuberculous/pathology , Mycobacterium tuberculosis/pathogenicity , Transgenes , Virulence Factors/genetics , Animals , Bacterial Proteins/immunology , Cell Wall/chemistry , Gene Expression , Interleukin-10/biosynthesis , Interleukin-10/immunology , Interleukin-4/biosynthesis , Interleukin-4/immunology , Liver/microbiology , Liver/pathology , Lung/microbiology , Lung/pathology , Macrophages/microbiology , Male , Mice , Mice, Inbred BALB C , Mycobacterium Infections, Nontuberculous/genetics , Mycobacterium Infections, Nontuberculous/microbiology , Mycobacterium Infections, Nontuberculous/mortality , Mycobacterium smegmatis/genetics , Mycobacterium smegmatis/metabolism , Mycobacterium tuberculosis/genetics , Mycobacterium tuberculosis/metabolism , Organisms, Genetically Modified , Survival Analysis , Tumor Necrosis Factor-alpha/biosynthesis , Tumor Necrosis Factor-alpha/immunology , Virulence , Virulence Factors/immunology
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