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Antimicrobial Efficacy of Synthetic Pyranochromenones and (Coumarinyloxy)acetamides.
Singh, Abhishek K; Prasad, Suchita; Kumar, Bipul; Kumar, Shiv; Anand, Amitesh; Kamble, Shashank S; Sharma, Sunil K; Gautam, Hemant K.
Afiliación
  • Singh AK; Department of Chemistry, University of Delhi, Delhi, 110007 India.
  • Prasad S; Department of Chemistry, University of Delhi, Delhi, 110007 India.
  • Kumar B; CSIR-Institute of Genomics and Integrative Biology, Sukhdev Vihar, Mathura Road, Delhi, 110025 India.
  • Kumar S; Department of Chemistry, University of Delhi, Delhi, 110007 India.
  • Anand A; CSIR-Institute of Genomics and Integrative Biology, Sukhdev Vihar, Mathura Road, Delhi, 110025 India.
  • Kamble SS; CSIR-Institute of Genomics and Integrative Biology, Sukhdev Vihar, Mathura Road, Delhi, 110025 India.
  • Sharma SK; Department of Chemistry, University of Delhi, Delhi, 110007 India.
  • Gautam HK; CSIR-Institute of Genomics and Integrative Biology, Sukhdev Vihar, Mathura Road, Delhi, 110025 India.
Indian J Microbiol ; 57(4): 499-502, 2017 Dec.
Article en En | MEDLINE | ID: mdl-29151652
ABSTRACT
Four (1, 2, 4 and 6) synthetic quaternary ammonium derivatives of pyranochromenones and (coumarinyloxy)acetamides were synthesized and investigated for their antimicrobial efficacy on MRSA (Methicillin-resistant Staphylococcus aureus), and multi-drug resistant Pseudomonas aeruginosa, Salmonella enteritidis and Mycobacterium tuberculosis H37Rv strain. One of the four compounds screened i.e. N,N,N-triethyl-10-((4,8,8-trimethyl-2-oxo-2,6,7,8-tetrahydropyrano[3,2-g]chromen-10-yl)oxy)decan-1-aminium bromide (1), demonstrated significant activity against S. aureus, P. aeruginosa and M. tuberculosis with MIC value of 16, 35, and 15.62 µg/ml respectively. The cytotoxicity evaluation of compound 1 on A549 cell lines showed it to be a safe antimicrobial molecule, TEM study suggested that the compound led to the rupture of the bacterial cell walls.
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