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Volumn 57, Issue 22, 2014, Pages 9409-9423

Membrane active phenylalanine conjugated lipophilic norspermidine derivatives with selective antibacterial activity

Author keywords

[No Author keywords available]

Indexed keywords

ANTIINFECTIVE AGENT; AROMATIC AMINO ACID; COLISTIN; SPERMIDINE DERIVATIVE; VANCOMYCIN; BETA LACTAM; MICELLE; NORSPERMIDINE; PHENYLALANINE; SPERMIDINE; TETRAZOLIUM; THIAZOLE DERIVATIVE; THIAZOLYL BLUE;

EID: 84913593686     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/jm5013566     Document Type: Article
Times cited : (110)

References (47)
  • 2
    • 47749093130 scopus 로고    scopus 로고
    • The bacteria fight back
    • Taubes, G. The bacteria fight back Science 2008, 321, 356-361
    • (2008) Science , vol.321 , pp. 356-361
    • Taubes, G.1
  • 4
    • 84893089095 scopus 로고    scopus 로고
    • Prospects for new antibiotics: A molecule-centered perspective
    • Walsh, C. T.; Wencewicz, T. A. Prospects for new antibiotics: a molecule-centered perspective J. Antibiot. (Tokyo) 2014, 66, 7-22
    • (2014) J. Antibiot. (Tokyo) , vol.66 , pp. 7-22
    • Walsh, C.T.1    Wencewicz, T.A.2
  • 5
    • 10944272743 scopus 로고    scopus 로고
    • Antibacterial resistance worldwide: Causes, challenges and responses
    • Levy, S. B.; Marshall, B. Antibacterial resistance worldwide: causes, challenges and responses Nat. Med. 2004, 10, S122-S129
    • (2004) Nat. Med. , vol.10 , pp. 122-S129
    • Levy, S.B.1    Marshall, B.2
  • 6
    • 0037165196 scopus 로고    scopus 로고
    • Antimicrobial peptides of multicellular organisms
    • Zasloff, M. Antimicrobial peptides of multicellular organisms Nature 2002, 415, 389-395
    • (2002) Nature , vol.415 , pp. 389-395
    • Zasloff, M.1
  • 8
    • 84902491232 scopus 로고    scopus 로고
    • Membrane active vancomycin analogues: A strategy to combat bacterial resistance
    • Yarlagadda, V.; Akkapeddi, P.; Manjunath, G. B.; Haldar, J. Membrane active vancomycin analogues: a strategy to combat bacterial resistance J. Med. Chem. 2014, 57, 4558-4568
    • (2014) J. Med. Chem. , vol.57 , pp. 4558-4568
    • Yarlagadda, V.1    Akkapeddi, P.2    Manjunath, G.B.3    Haldar, J.4
  • 12
    • 36749053991 scopus 로고    scopus 로고
    • Bactericidal action of daptomycin against stationary-phase and nondividing Staphylococcus aureus cells
    • Mascio, C. T.; Alder, J. D.; Silverman, J. A. Bactericidal action of daptomycin against stationary-phase and nondividing Staphylococcus aureus cells Antimicrob. Agents Chemother. 2007, 51, 4255-4260
    • (2007) Antimicrob. Agents Chemother. , vol.51 , pp. 4255-4260
    • Mascio, C.T.1    Alder, J.D.2    Silverman, J.A.3
  • 13
    • 15844431142 scopus 로고    scopus 로고
    • Daptomycin: A lipopeptide antibiotic for the treatment of serious Gram-positive infections
    • Steenbergen, J. N.; Alder, J.; Thorne, G. M.; Tally, F. P. Daptomycin: a lipopeptide antibiotic for the treatment of serious Gram-positive infections J. Antimicrob. Chemother. 2005, 55, 283-288
    • (2005) J. Antimicrob. Chemother. , vol.55 , pp. 283-288
    • Steenbergen, J.N.1    Alder, J.2    Thorne, G.M.3    Tally, F.P.4
  • 14
    • 17644389620 scopus 로고    scopus 로고
    • Colistin: The revival of polymyxins for the management of multidrug-resistant Gram-negative bacterial infections
    • Falagas, M. E.; Kasiakou, S. K. Colistin: The revival of polymyxins for the management of multidrug-resistant Gram-negative bacterial infections Clin. Infect. Dis. 2005, 40, 1333-1341
    • (2005) Clin. Infect. Dis. , vol.40 , pp. 1333-1341
    • Falagas, M.E.1    Kasiakou, S.K.2
  • 15
    • 78650335200 scopus 로고    scopus 로고
    • Polymyxin B versus other antimicrobials for the treatment of pseudomonas aeruginosa bacteraemia
    • Kvitko, C. H.; Rigatto, M. H.; Moro, A. L.; Zavascki, A. P. Polymyxin B versus other antimicrobials for the treatment of pseudomonas aeruginosa bacteraemia J. Antimicrob. Chemother. 2011, 66, 175-179
    • (2011) J. Antimicrob. Chemother. , vol.66 , pp. 175-179
    • Kvitko, C.H.1    Rigatto, M.H.2    Moro, A.L.3    Zavascki, A.P.4
  • 17
    • 2442475526 scopus 로고    scopus 로고
    • Systematic peptide engineering and structural characterization to search for the shortest antimicrobial peptide analogue of gaegurin
    • Won, H. S.; Jung, S. J.; Kim, H. E.; Seo, M. D.; Lee, B. J. Systematic peptide engineering and structural characterization to search for the shortest antimicrobial peptide analogue of gaegurin J. Biol. Chem. 2004, 279, 14784-14791
    • (2004) J. Biol. Chem. , vol.279 , pp. 14784-14791
    • Won, H.S.1    Jung, S.J.2    Kim, H.E.3    Seo, M.D.4    Lee, B.J.5
  • 18
    • 16844373772 scopus 로고    scopus 로고
    • Rational design of alpha-helical antimicrobial peptides with enhanced activities and specificity/therapeutic index
    • Chen, Y. X.; Mant, C. T.; Farmer, S. W.; Hancock, R. E. W.; Vasil, M. L.; Hodges, R. S. Rational design of alpha-helical antimicrobial peptides with enhanced activities and specificity/therapeutic index J. Biol. Chem. 2005, 280, 12316-12329
    • (2005) J. Biol. Chem. , vol.280 , pp. 12316-12329
    • Chen, Y.X.1    Mant, C.T.2    Farmer, S.W.3    Hancock, R.E.W.4    Vasil, M.L.5    Hodges, R.S.6
  • 20
    • 0033616105 scopus 로고    scopus 로고
    • De novo design of antibacterial beta-peptides
    • Hamuro, Y.; Schneider, J. P.; DeGrado, W. F. De novo design of antibacterial beta-peptides J. Am. Chem. Soc. 1999, 121, 12200-12201
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 12200-12201
    • Hamuro, Y.1    Schneider, J.P.2    Degrado, W.F.3
  • 22
    • 13944267446 scopus 로고    scopus 로고
    • N, N' - Linked oligoureas as foldamers: Chain length requirements for helix formation in protic solvent investigated by circular dichroism, NMR spectroscopy, and molecular dynamics
    • Violette, A.; Averlant-Petit, M. C.; Semetey, V.; Hemmerlin, C.; Casimir, R.; Graff, R.; Marraud, M.; Briand, J. P.; Rognan, D.; Guichard, G. N, N'-Linked oligoureas as foldamers: chain length requirements for helix formation in protic solvent investigated by circular dichroism, NMR spectroscopy, and molecular dynamics J. Am. Chem. Soc. 2005, 127, 2156-2164
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 2156-2164
    • Violette, A.1    Averlant-Petit, M.C.2    Semetey, V.3    Hemmerlin, C.4    Casimir, R.5    Graff, R.6    Marraud, M.7    Briand, J.P.8    Rognan, D.9    Guichard, G.10
  • 25
    • 10044226415 scopus 로고    scopus 로고
    • Tuning the hemolytic and antibacterial activities of amphiphilic polynorbornene derivatives
    • Ilker, M. F.; Nusslein, K.; Tew, G. N.; Coughlin, E. B. Tuning the hemolytic and antibacterial activities of amphiphilic polynorbornene derivatives J. Am. Chem. Soc. 2004, 126, 15870-15875
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 15870-15875
    • Ilker, M.F.1    Nusslein, K.2    Tew, G.N.3    Coughlin, E.B.4
  • 26
    • 16244400792 scopus 로고    scopus 로고
    • Amphiphilic polymethacrylate derivatives as antimicrobial agents
    • Kuroda, K.; DeGrado, W. F. Amphiphilic polymethacrylate derivatives as antimicrobial agents J. Am. Chem. Soc. 2005, 127, 4128-4129
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 4128-4129
    • Kuroda, K.1    Degrado, W.F.2
  • 27
    • 1342290264 scopus 로고    scopus 로고
    • Biocidal activity of polystyrenes that are cationic by virtue of protonation
    • Gelman, M. A.; Weisblum, B.; Lynn, D. M.; Gellman, S. H. Biocidal activity of polystyrenes that are cationic by virtue of protonation Org. Lett. 2004, 6, 557-560
    • (2004) Org. Lett. , vol.6 , pp. 557-560
    • Gelman, M.A.1    Weisblum, B.2    Lynn, D.M.3    Gellman, S.H.4
  • 31
    • 41249093707 scopus 로고    scopus 로고
    • Antibacterial and hemolytic activities of pyridinium polymers as a function of the spatial relationship between the positive charge and the pendant alkyl tail
    • Sambhy, V.; Peterson, B. R.; Sen, A. Antibacterial and hemolytic activities of pyridinium polymers as a function of the spatial relationship between the positive charge and the pendant alkyl tail Angew. Chem., Int. Ed. 2008, 47, 1250-1254
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 1250-1254
    • Sambhy, V.1    Peterson, B.R.2    Sen, A.3
  • 32
    • 20144375391 scopus 로고    scopus 로고
    • Synthesis and antibacterial properties of novel hydrolyzable cationic amphiphiles. Incorporation of multiple head groups leads to impressive antibacterial activity
    • Haldar, J.; Kondaiah, P.; Bhattacharya, S. Synthesis and antibacterial properties of novel hydrolyzable cationic amphiphiles. Incorporation of multiple head groups leads to impressive antibacterial activity J. Med. Chem. 2005, 48, 3823-3831
    • (2005) J. Med. Chem. , vol.48 , pp. 3823-3831
    • Haldar, J.1    Kondaiah, P.2    Bhattacharya, S.3
  • 33
    • 84865476398 scopus 로고    scopus 로고
    • Cleavable cationic antibacterial amphiphiles: Synthesis, mechanism of action, and cytotoxicities
    • Hoque, J.; Akkapeddi, P.; Yarlagadda, V.; Uppu, D. S. S. M.; Kumar, P.; Haldar, J. Cleavable cationic antibacterial amphiphiles: synthesis, mechanism of action, and cytotoxicities Langmuir 2012, 28, 12225-12234
    • (2012) Langmuir , vol.28 , pp. 12225-12234
    • Hoque, J.1    Akkapeddi, P.2    Yarlagadda, V.3    Uppu, D.S.S.M.4    Kumar, P.5    Haldar, J.6
  • 35
    • 0347625845 scopus 로고    scopus 로고
    • Bestowing antifungal and antibacterial activities by lipophilic acid conjugation to d, l -amino acid-containing antimicrobial peptides: A plausible mode of action
    • Avrahami, D.; Shai, Y. Bestowing antifungal and antibacterial activities by lipophilic acid conjugation to d, l -amino acid-containing antimicrobial peptides: a plausible mode of action Biochemistry 2003, 42, 14946-14956
    • (2003) Biochemistry , vol.42 , pp. 14946-14956
    • Avrahami, D.1    Shai, Y.2
  • 37
    • 84887597873 scopus 로고    scopus 로고
    • Short antibacterial peptides with significantly reduced hemolytic activity can be identified by a systematic L-to-D exchange scan of their amino acid residues
    • Albada, H. B.; Prochnow, P.; Bobersky, S.; Langklotz, S.; Bandow, J. E.; Metzler-Nolte, N. Short antibacterial peptides with significantly reduced hemolytic activity can be identified by a systematic L-to-D exchange scan of their amino acid residues ACS Comb. Sci. 2013, 15, 585-592
    • (2013) ACS Comb. Sci. , vol.15 , pp. 585-592
    • Albada, H.B.1    Prochnow, P.2    Bobersky, S.3    Langklotz, S.4    Bandow, J.E.5    Metzler-Nolte, N.6
  • 41
    • 84887980372 scopus 로고    scopus 로고
    • Self-assembly to function: Design, synthesis, and broad spectrum antimicrobial properties of short hybrid E-vinylogous lipopeptides
    • Shankar, S. S.; Benke, S. N.; Nagendra, N.; Srivastava, P. L.; Thulasiram, H. V.; Gopi, H. N. Self-assembly to function: design, synthesis, and broad spectrum antimicrobial properties of short hybrid E-vinylogous lipopeptides J. Med. Chem. 2013, 56, 8468-8474
    • (2013) J. Med. Chem. , vol.56 , pp. 8468-8474
    • Shankar, S.S.1    Benke, S.N.2    Nagendra, N.3    Srivastava, P.L.4    Thulasiram, H.V.5    Gopi, H.N.6
  • 43
    • 47749116861 scopus 로고    scopus 로고
    • Synthetic antimicrobial peptidomimetics with therapeutic potential
    • Haug, B. E.; Stensen, W.; Kalaaji, M.; Rekdal, O.; Svendsen, J. S. Synthetic antimicrobial peptidomimetics with therapeutic potential J. Med. Chem. 2008, 51, 4306-4314
    • (2008) J. Med. Chem. , vol.51 , pp. 4306-4314
    • Haug, B.E.1    Stensen, W.2    Kalaaji, M.3    Rekdal, O.4    Svendsen, J.S.5
  • 47
    • 39449086721 scopus 로고    scopus 로고
    • Agar and broth dilution methods to determine the minimal inhibitory concentration (MIC) of antimicrobial substances
    • Wiegand, I.; Hilpert, K.; Hancock, R. E. W. Agar and broth dilution methods to determine the minimal inhibitory concentration (MIC) of antimicrobial substances Nat. Protoc. 2008, 3, 163-175
    • (2008) Nat. Protoc. , vol.3 , pp. 163-175
    • Wiegand, I.1    Hilpert, K.2    Hancock, R.E.W.3


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