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Volumn 16, Issue 1, 2012, Pages 113-119

Multicomponent synthesis of acylated short peptoids with antifungal activity against plant pathogens

Author keywords

Acylated peptoids; Antifungal; Multicomponent reaction; Plant pathogen

Indexed keywords

GLYCINE; PEPTOID;

EID: 84858705925     PISSN: 13811991     EISSN: 1573501X     Source Type: Journal    
DOI: 10.1007/s11030-011-9334-1     Document Type: Article
Times cited : (16)

References (24)
  • 1
    • 33748941300 scopus 로고    scopus 로고
    • Quantification and modeling of crop losses: A review of purposes
    • DOI 10.1146/annurev.phyto.44.070505.143342
    • Savary S, Teng PS, Willocquet L, Nutter FWJr (2006) Quantification and modeling of crop losses: a review of purposes. Annu Rev Phytopathol 44: 89-112. doi:10.1146/annurev.phyto.44.070505.143342 (Pubitemid 44435699)
    • (2006) Annual Review of Phytopathology , vol.44 , pp. 89-112
    • Savary, S.1    Teng, P.S.2    Willocquet, L.3    Nutter Jr., F.W.4
  • 3
    • 14544282377 scopus 로고    scopus 로고
    • Antimicrobial peptides: Pore formers or metabolic inhibitors in bacteria
    • doi:10.1038/nrmicro1098
    • Brogden KA (2005) Antimicrobial peptides: pore formers or metabolic inhibitors in bacteria. Nat Rev Microbiol 3: 238-250. doi:10.1038/nrmicro1098
    • (2005) Nat Rev Microbiol , vol.3 , pp. 238-250
    • Brogden, K.A.1
  • 4
    • 51849112889 scopus 로고    scopus 로고
    • Identification and rational design of novel antimicrobial peptides for plant protection
    • doi:10.1146/annurev.phyto.121307.094843
    • Marcos JF, Muñoz A, Pérez-Payá E, Misra S, López-García B (2008) Identification and rational design of novel antimicrobial peptides for plant protection. Annu Rev Phytopathol 46: 273-330. doi:10.1146/annurev.phyto.121307.094843
    • (2008) Annu Rev Phytopathol , vol.46 , pp. 273-330
    • Marcos, J.F.1    Muñoz, A.2    Pérez-Payá, E.3    Misra, S.4    López-García, B.5
  • 5
    • 33748946749 scopus 로고    scopus 로고
    • Mode of action of the new antibiotic for Gram-positive pathogens daptomycin: Comparison with cationic antimicrobial peptides and lipopeptides
    • DOI 10.1016/j.bbamem.2006.02.009, PII S0005273606000435
    • Straus SK, Hancock RE (2006) Mode of action of the new antibiotic for Gram-positive pathogens daptomycin: comparison with cationic antimicrobial peptides and lipopeptides. Biochim Biophys Acta 1758: 1215-1223. doi:10.1016/j.bbamem.2006.02.009 (Pubitemid 44436068)
    • (2006) Biochimica et Biophysica Acta - Biomembranes , vol.1758 , Issue.9 , pp. 1215-1223
    • Straus, S.K.1    Hancock, R.E.W.2
  • 7
    • 35448965554 scopus 로고    scopus 로고
    • Inhibition of fungal and bacterial plant pathogens in vitro and in planta with ultrashort cationic lipopeptides
    • DOI 10.1128/AEM.01334-07
    • Makovitzki A, Viterbo A, Brotman Y, Chet I, Shai Y (2007) Inhibition of fungal and bacterial plant pathogens in vitro and in planta with ultrashort cationic lipopeptides. Appl Environ Microbiol 73: 6629-6636. doi:10.1128/AEM.01334-07 (Pubitemid 47623723)
    • (2007) Applied and Environmental Microbiology , vol.73 , Issue.20 , pp. 6629-6636
    • Makovitzki, A.1    Viterbo, A.2    Brotman, Y.3    Chet, I.4    Shai, Y.5
  • 10
    • 13844322495 scopus 로고    scopus 로고
    • Design and synthesis of an optimized positional scanning library of peptoids: Identification of novel multidrug resistance reversal agents
    • DOI 10.1016/j.bmc.2005.01.024
    • Masip I, Cortés N, AbadMJ, GuardiolaM, Pérez-Payá E, Ferragut J, Ferrer-Montiel A, Messeguer A (2005) Design and synthesis of an optimized positional scanning library of peptoids: identification of novel multidrug resistance reversal agents. Bioorg Med Chem 13: 1923-1929. doi:10.1016/j.bmc.2005.01.024 (Pubitemid 40261115)
    • (2005) Bioorganic and Medicinal Chemistry , vol.13 , Issue.6 , pp. 1923-1929
    • Masip, I.1    Cortes, N.2    Abad, M.-J.3    Guardiola, M.4    Perez-Paya, E.5    Ferragut, J.6    Ferrer-Montiel, A.7    Messeguer, A.8
  • 11
    • 0000908874 scopus 로고
    • Efficient method for the preparation of peptoids [oligo(N-substituted glycines)] by submonomer solid-phase synthesis
    • doi:10.1021/ja00052a076
    • Zuckermann RN, Kerr JM, Kent SBH, Moos WH (1992) Efficient method for the preparation of peptoids [oligo(N-substituted glycines)] by submonomer solid-phase synthesis. J Am Chem Soc 114: 10646-10647. doi:10.1021/ja00052a076
    • (1992) J Am Chem Soc , vol.114 , pp. 10646-10647
    • Zuckermann, R.N.1    Kerr, J.M.2    Kent, S.B.H.3    Moos, W.H.4
  • 13
    • 31544434530 scopus 로고    scopus 로고
    • Recent developments in isocyanide based multicomponent reactions in applied chemistry
    • doi:10.1021/cr0505728
    • Dömling A (2006) Recent developments in isocyanide based multicomponent reactions in applied chemistry.ChemRev 106: 17-89. doi:10.1021/cr0505728
    • (2006) ChemRev , vol.106 , pp. 17-89
    • Dömling, A.1
  • 14
    • 0037711784 scopus 로고    scopus 로고
    • Synthesis of PNA monomers and dimers by ugi four-component reaction
    • Xu P, Zhang T,WangW, Zou X, Zhang X, Fu Y (2003) Synthesis of PNA monomers and dimers by Ugi four-component reaction. Synthesis 8: 1171-1176. doi:10.1055/s-2003-39391 (Pubitemid 36791794)
    • (2003) Synthesis , Issue.8 , pp. 1171-1176
    • Xu, P.1    Zhang, T.2    Wang, W.3    Zou, X.4    Zhang, X.5    Fu, Y.6
  • 15
    • 33744941075 scopus 로고    scopus 로고
    • Supramolecular compounds from multiple ugi multicomponent macrocyclizations: Peptoid-based cryptands, cages, and cryptophanes
    • DOI 10.1021/ja060720r
    • Rivera DG, Wessjohann LA (2006) Supramolecular compounds from multiple Ugi multicomponent macrocyclizations: peptoid-based cryptands, cages, and cryptophanes. J Am Chem Soc 128: 7122-7123. doi:10.1021/ja060720r (Pubitemid 43849089)
    • (2006) Journal of the American Chemical Society , vol.128 , Issue.22 , pp. 7122-7123
    • Rivera, D.G.1    Wessjohann, L.A.2
  • 16
    • 38749096301 scopus 로고    scopus 로고
    • Design and synthesis of cyclic RGD pentapeptoids by consecutive Ugi reactions
    • doi:10.1021/ol702521g
    • Vercillo OE, Andrade CKZ; Wessjohann LA (2008) Design and synthesis of cyclic RGD pentapeptoids by consecutive Ugi reactions. Org Lett 10: 205-208. doi:10.1021/ol702521g
    • (2008) Org Lett , vol.10 , pp. 205-208
    • Vercillo, O.E.1    Andrade, C.K.Z.2    Wessjohann, L.A.3
  • 17
    • 77956049345 scopus 로고    scopus 로고
    • Photoaffinity-labeled peptoids and depsipeptides by multicomponent reactions
    • doi:10.1055/s-0030-1258182
    • Henze M, Kreye O, Brauch S, Nitsche C, Naumann K, Wessjohann LA,Westermann B (2010) Photoaffinity-labeled peptoids and depsipeptides by multicomponent reactions. Synthesis 17: 2997-3003. doi:10.1055/s-0030-1258182
    • (2010) Synthesis , vol.17 , pp. 2997-3003
    • Henze, M.1    Kreye, O.2    Brauch, S.3    Nitsche, C.4    Naumann, K.5    Wessjohann, L.A.6    Westermann, B.7
  • 18
    • 34848845825 scopus 로고    scopus 로고
    • Kinetics and equilibria of cis/trans isomerization of backbone amide bonds in peptoids
    • DOI 10.1021/ja0740925
    • Sui Q, Borchardt D, Rabenstein DL (2007) Kinetics and equilibria of cis/trans isomerization of backbone amide bonds in peptoids. J Am Chem Soc 129: 12042-12048. doi:10.1021/ja0740925 (Pubitemid 47512033)
    • (2007) Journal of the American Chemical Society , vol.129 , Issue.39 , pp. 12042-12048
    • Sui, Q.1    Borchardt, D.2    Rabenstein, D.L.3
  • 19
    • 0030038368 scopus 로고    scopus 로고
    • Comparing mass spectrometric characteristics of peptides and peptoids
    • doi:10.1002/(SICI)1097-0231(19960315)10:4〈459::AID-RCM501〉3.0. CO;2-J
    • Heerma W, Verluis C, de Koster CG, Kruijtzer JAW, Zigrovic I, Liskamp RMJ (1996) Comparing mass spectrometric characteristics of peptides and peptoids. Rapid Commun Mass Spectrom 10: 459-464. doi:10.1002/(SICI)1097-0231(19960315)10: 4〈459::AID-RCM501〉3.0.CO;2-J
    • (1996) Rapid Commun Mass Spectrom , vol.10 , pp. 459-464
    • Heerma, W.1    Verluis, C.2    De Koster, C.G.3    Kruijtzer, J.A.W.4    Zigrovic, I.5    Liskamp, R.M.J.6
  • 20
    • 84987419408 scopus 로고
    • Proposal for a common nomenclature for sequence ions in mass spectra of peptides
    • doi:10.1002/bms.1200111109
    • Roepstorff P, Fohlman J (1984) Proposal for a common nomenclature for sequence ions in mass spectra of peptides. Biomed Mass Spectrom 11:601. doi:10.1002/bms.1200111109
    • (1984) Biomed Mass Spectrom , vol.11 , pp. 601
    • Roepstorff, P.1    Fohlman, J.2
  • 21
    • 20344392686 scopus 로고    scopus 로고
    • Natural products and antifungal drug discovery
    • Ernst EJ, Rogers PD (eds) antifungal agents: methods and protocols 1st ed. Humana Press Inc, Totowa, NJ
    • Jacob MR, Walker LA (2005) Natural products and antifungal drug discovery. In: Ernst EJ, Rogers PD (eds) Methods in molecular medicine vol 118: antifungal agents: methods and protocols 1st ed. Humana Press Inc, Totowa, NJ pp 83-110
    • (2005) Methods in Molecular Medicine , vol.118 , pp. 83-110
    • Jacob, M.R.1    Walker, L.A.2
  • 22
    • 0034101553 scopus 로고    scopus 로고
    • Testing of antifungal natural products: Methodologies, comparability of results and assay choice
    • DOI 10.1002/(SICI)1099-1565(200005/06)11:3<137::AID-PCA514>3.0. CO;2-I
    • Hadacek F, Greger H (2000) Testing of antifungal natural products: methodologies, comparability and assay choice. Phytochem Anal 11: 137-147. doi:10.1002/(SICI)1099-1565(200005/06)11:3〈137::AID-PCA514〉3.0.CO;2-I (Pubitemid 30248992)
    • (2000) Phytochemical Analysis , vol.11 , Issue.3 , pp. 137-147
    • Hadacek, F.1    Greger, H.2
  • 23
    • 35448965554 scopus 로고    scopus 로고
    • Inhibition of fungal and bacterial plant pathogens in vitro and in planta with ultrashort cationic lipopeptides
    • DOI 10.1128/AEM.01334-07
    • Makovitzki A, Viterbo A, Brotman Y, Chet I, Shai Y (2007) Inhibition of fungal and bacterial plant pathogens in vitro and in planta with ultrashort cationic lipopeptides. Appl Environ Microbiol 73: 6629-6636. doi:10.1128/AEM.01334-07 (Pubitemid 47623723)
    • (2007) Applied and Environmental Microbiology , vol.73 , Issue.20 , pp. 6629-6636
    • Makovitzki, A.1    Viterbo, A.2    Brotman, Y.3    Chet, I.4    Shai, Y.5
  • 24
    • 0036948138 scopus 로고    scopus 로고
    • Mode of action of membrane active antimicrobial peptides
    • doi:10.1002/bip.10260
    • Shai Y (2002) Mode of action of membrane active antimicrobial peptides. Pept Sci 66: 236-248. doi:10.1002/bip.10260
    • (2002) Pept Sci , vol.66 , pp. 236-248
    • Shai, Y.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.