Please use this identifier to cite or link to this item: https://libjncir.jncasr.ac.in/xmlui/handle/10572/2303
Full metadata record
DC FieldValueLanguage
dc.contributor.authorGhosh, Chandradhish
dc.contributor.authorManjunath, Goutham B.
dc.contributor.authorKonai, Mohini M.
dc.contributor.authorUppu, Divakara S. S. M.
dc.contributor.authorParamanandham, Krishnamoorthy
dc.contributor.authorShome, Bibek R.
dc.contributor.authorRavikumar, Raju
dc.contributor.authorHaldar, Jayanta
dc.date.accessioned2017-01-24T09:11:14Z-
dc.date.available2017-01-24T09:11:14Z-
dc.date.issued2016
dc.identifier.citationGhosh, C.; Manjunath, G. B.; Konai, M. M.; Uppu, Dssm; Paramanandham, K.; Shome, B. R.; Ravikumar, R.; Haldar, J., Aryl-alkyl-lysines: Membrane-Active Small Molecules Active against Murine Model of Burn Infection. Acs Infectious Diseases 2016, 2 (2), 111-122 http://dx.doi.org/10.1021/acsinfecdis.5b00092en_US
dc.identifier.citationACS Infectious Diseasesen_US
dc.identifier.citation2en_US
dc.identifier.citation2en_US
dc.identifier.issn2373-8227
dc.identifier.urihttps://libjncir.jncasr.ac.in/xmlui/10572/2303-
dc.descriptionRestricted Accessen_US
dc.description.abstractInfections caused by drug-resistant Gramnegative pathogens continue to be significant contributors to human morbidity. The recent advent of New Delhi metallo-beta-lactamase-1 (blaNDM-1) producing pathogens, against which few drugs remain active, has aggravated the problem even further. This paper shows that aryl-alkyl-lysines, membrane active small molecules, are effective in treating infections caused by Gram-negative pathogens. One of the compounds of the study was effective in killing planktonic cells as well as dispersing biofilms of Gram-negative pathogens. The compound was extremely effective in disrupting preformed biofilms and did not select resistant bacteria in multiple passages. The compound retained activity in different physiological conditions and did not induce any toxic effect in female Balb/c mice until concentrations of 17.5 mg/kg. In a murine model of Acinetobacter baumannii burn infection, the compound was able to bring the bacterial burden down significantly upon topical application for 7 days.en_US
dc.description.urihttp://dx.doi.org/10.1021/acsinfecdis.5b00092en_US
dc.language.isoEnglishen_US
dc.publisherAmerican Chemical Societyen_US
dc.rights@American Chemical Society, 2016en_US
dc.subjectPharmacology & Pharmacyen_US
dc.subjectInfectious Diseasesen_US
dc.subjectantimicrobial peptidesen_US
dc.subjectantibioticsen_US
dc.subjectantimicrobial resistanceen_US
dc.subjectGram-negativeen_US
dc.subjectpersistersen_US
dc.subjectbiofilmen_US
dc.subjectburn infectionen_US
dc.subjectCombat Bacterial-Resistanceen_US
dc.subjectDe-Novo Designen_US
dc.subjectAntimicrobial Peptidesen_US
dc.subjectAcinetobacter-Baumanniien_US
dc.subjectPersister Cellsen_US
dc.subjectAntibacterial Agentsen_US
dc.subjectStationary-Phaseen_US
dc.subjectCystic-Fibrosisen_US
dc.subjectAntibioticsen_US
dc.subjectDaptomycinen_US
dc.titleAryl-alkyl-lysines: Membrane-Active Small Molecules Active against Murine Model of Burn Infectionen_US
dc.typeArticleen_US
Appears in Collections:Research Papers (Jayanta Haldar)

Files in This Item:
File Description SizeFormat 
79.pdf
  Restricted Access
4.45 MBAdobe PDFView/Open Request a copy


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.