ChemInform Abstract: OXIDATION OF N-NITROSODIBENZYLAMINE AND RELATED COMPOUNDS BY METALLOPORPHYRIN-CATALYZED MODEL SYSTEMS FOR THE CYTOCHROME P450 DEPENDENT MONO-OXYGENASES

1984 ◽  
Vol 15 (22) ◽  
Author(s):  
J. R. L. SMITH ◽  
M. W. NEE ◽  
J. B. NOAR ◽  
T. C. BRUICE
2019 ◽  
Vol 63 (12) ◽  
pp. 6477-6488 ◽  
Author(s):  
Natalia Mast ◽  
Peter Verwilst ◽  
Clayton J. Wilkey ◽  
F. Peter Guengerich ◽  
Irina A. Pikuleva

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Bruno Alves Rocha ◽  
Anderson Rodrigo Moraes de Oliveira ◽  
Murilo Pazin ◽  
Daniel Junqueira Dorta ◽  
Andresa Piacezzi Nascimento Rodrigues ◽  
...  

Monensin A is a commercially important natural product isolated fromStreptomyces cinnamonensinsthat is primarily employed to treat coccidiosis. Monensin A selectively complexes and transports sodium cations across lipid membranes and displays a variety of biological properties. In this study, we evaluated the Jacobsen catalyst as a cytochrome P450 biomimetic model to investigate the oxidation of monensin A. Mass spectrometry analysis of the products from these model systems revealed the formation of two products: 3-O-demethyl monensin A and 12-hydroxy monensin A, which are the same ones found inin vivomodels. Monensin A and products obtained in biomimetic model were tested in a mitochondrial toxicity model assessment and an antimicrobial bioassay againstStaphylococcus aureus, S. aureusmethicillin-resistant,Staphylococcus epidermidis, Pseudomonas aeruginosa,andEscherichia coli.Our results demonstrated the toxicological effects of monensin A in isolated rat liver mitochondria but not its products, showing that the metabolism of monensin A is a detoxification metabolism. In addition, the antimicrobial bioassay showed that monensin A and its products possessed activity against Gram-positive microorganisms but not for Gram-negative microorganisms. The results revealed the potential of application of this biomimetic chemical model in the synthesis of drug metabolites, providing metabolites for biological tests and other purposes.


1998 ◽  
Vol 120 (48) ◽  
pp. 12524-12530 ◽  
Author(s):  
Jason Hart-Davis ◽  
Pierrette Battioni ◽  
Jean-Luc Boucher ◽  
Daniel Mansuy

Agronomy ◽  
2018 ◽  
Vol 8 (8) ◽  
pp. 142 ◽  
Author(s):  
Miriam Lenk ◽  
Marion Wenig ◽  
Felicitas Mengel ◽  
Finni Häußler ◽  
A. Vlot

Plants are exposed to numerous pathogens and fend off many of these with different phytohormone signalling pathways. Much is known about defence signalling in the dicotyledonous model plant Arabidopsisthaliana, but it is unclear to which extent knowledge from model systems can be transferred to monocotyledonous plants, including cereal crops. Here, we investigated the defence-inducing potential of Arabidopsis resistance-inducing compounds in the cereal crop barley. Salicylic acid (SA), folic acid (Fol), and azelaic acid (AzA), each inducing defence against (hemi-)biotrophic pathogens in Arabidopsis, were applied to barley leaves and the treated and systemic leaves were subsequently inoculated with Xanthomonastranslucens pv. cerealis (Xtc), Blumeria graminis f. sp. hordei (powdery mildew, Bgh), or Pyrenophora teres. Fol and SA reduced Bgh propagation locally and/or systemically, whereas Fol enhanced Xtc growth in barley. AzA reduced Bgh propagation systemically and enhanced Xtc growth locally. Neither SA, Fol, nor AzA influenced lesion sizes caused by the necrotrophic fungus P. teres, suggesting that the tested compounds exclusively affected growth of (hemi-)biotrophic pathogens in barley. In addition to SA, Fol and AzA might thus act as resistance-inducing compounds in barley against Bgh, although adverse effects on the growth of pathogenic bacteria, such as Xtc, are possible.


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