메뉴 건너뛰기




Volumn 311, Issue 2, 2003, Pages 267-271

3-Alkoxy-5-isoxazolidinones mimic β-lactams

Author keywords

3 Alkoxy 5 isoxazolidinone; 5 Isoxazolidinone; Penicillin binding proteins; Lactam mimics; Lactamase inhibition

Indexed keywords

BETA LACTAM DERIVATIVE; CHEMICAL COMPOUND; ISOXAZOLE DERIVATIVE; KETONE DERIVATIVE; PENICILLIN BINDING PROTEIN;

EID: 0242299770     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbrc.2003.09.210     Document Type: Article
Times cited : (7)

References (27)
  • 1
    • 0011146514 scopus 로고    scopus 로고
    • Non-β-lactam antibiotics
    • Anke T., Erkel G. Non-β-lactam antibiotics. Mycota. 10:2002;93-108.
    • (2002) Mycota , vol.10 , pp. 93-108
    • Anke, T.1    Erkel, G.2
  • 2
    • 0033830002 scopus 로고    scopus 로고
    • Version 2000: The new β-lactamases of Gram-negative bacteria at the dawn of the new millennium
    • Thomson K.S., Moland E.S. Version 2000: the new β-lactamases of Gram-negative bacteria at the dawn of the new millennium. Microbes Infect. 2:2000;1225-1236.
    • (2000) Microbes Infect. , vol.2 , pp. 1225-1236
    • Thomson, K.S.1    Moland, E.S.2
  • 3
    • 0242311532 scopus 로고    scopus 로고
    • Penicillin binding proteins, β-lactam and lactamases: Offensives, attacks, and defensive countermeasures
    • Koch A.L. Penicillin binding proteins, β-lactam and lactamases: offensives, attacks, and defensive countermeasures. Emerg. Drugs. 5:2000;347-365.
    • (2000) Emerg. Drugs , vol.5 , pp. 347-365
    • Koch, A.L.1
  • 4
    • 0003745052 scopus 로고    scopus 로고
    • Mechanisms of resistance to β-lactam antibiotics
    • Kernodle D.S. Mechanisms of resistance to β-lactam antibiotics. Gram Positive Pathogens. 2000;609-620.
    • (2000) Gram Positive Pathogens , pp. 609-620
    • Kernodle, D.S.1
  • 5
    • 1642576850 scopus 로고    scopus 로고
    • Beta-lactam antibiotics: Aspects of manufacture and therapy
    • Schmidt F.R. Beta-lactam antibiotics: aspects of manufacture and therapy. Mycota. 120:2002;69-91.
    • (2002) Mycota , vol.120 , pp. 69-91
    • Schmidt, F.R.1
  • 7
    • 0035093095 scopus 로고    scopus 로고
    • Pseudomonas, porrins, pumps and carbapenems
    • Livermore D.M. Pseudomonas, porrins, pumps and carbapenems. Antimicrob. Chemother. 47:2001;247-250.
    • (2001) Antimicrob. Chemother. , vol.47 , pp. 247-250
    • Livermore, D.M.1
  • 8
    • 0037334661 scopus 로고    scopus 로고
    • New antibiotics and new resistance
    • Amabile-Cuevas C.F. New antibiotics and new resistance. Am. Sci. 91:2003;138-149.
    • (2003) Am. Sci. , vol.91 , pp. 138-149
    • Amabile-Cuevas, C.F.1
  • 9
    • 0034252755 scopus 로고    scopus 로고
    • Extended spectrum β-lactamases: How big is the problem?
    • Rahal J.J. Extended spectrum β-lactamases: how big is the problem? Clin. Microbiol. Infect. 6(Suppl. 2):2000;2-6.
    • (2000) Clin. Microbiol. Infect. , vol.6 , Issue.SUPPL. 2 , pp. 2-6
    • Rahal, J.J.1
  • 10
    • 0034035284 scopus 로고    scopus 로고
    • Molecular basis of antibiotic resistance and β-lactamase inhibition by mechanism-based inactivations: Perspectives and future directions
    • Therrien C., Leverque R.C. Molecular basis of antibiotic resistance and β-lactamase inhibition by mechanism-based inactivations: perspectives and future directions. FEMS Microbiol. Rev. 24:2000;251-262.
    • (2000) FEMS Microbiol. Rev. , vol.24 , pp. 251-262
    • Therrien, C.1    Leverque, R.C.2
  • 11
    • 0009588086 scopus 로고
    • Non-β-lactam mimics of β-lactam antibiotics
    • Jungheim L.N., Ternansky R.J. Non-β-lactam mimics of β-lactam antibiotics. Chem. β-Lactams. 1992;306-324.
    • (1992) Chem. β-Lactams , pp. 306-324
    • Jungheim, L.N.1    Ternansky, R.J.2
  • 14
    • 85030971480 scopus 로고    scopus 로고
    • M.S. thesis, University of Cincinnati, 2001
    • X.-F. Cao, M.S. thesis, University of Cincinnati, 2001.
    • Cao, X.-F.1
  • 16
    • 85030959711 scopus 로고    scopus 로고
    • Ph.D. dissertation, University of Cincinnati, 1991
    • W.E. Gooden, Ph.D. dissertation, University of Cincinnati, 1991.
    • Gooden, W.E.1
  • 17
    • 77956996073 scopus 로고
    • End-group analysis using dansyl chloride
    • Gray W.R. End-group analysis using dansyl chloride. Methods Enzymol. 25:1972;121-138.
    • (1972) Methods Enzymol. , vol.25 , pp. 121-138
    • Gray, W.R.1
  • 18
    • 0011343882 scopus 로고    scopus 로고
    • Detection of intra-cellular protein-protein interactions: Penicillin interactive proteins and morphogene products
    • Bhardwaj S., Day R.A. Detection of intra-cellular protein-protein interactions: penicillin interactive proteins and morphogene products. Techniques in Protein Chemistry. VIII:1997;469-480.
    • (1997) Techniques in Protein Chemistry , vol.8 , pp. 469-480
    • Bhardwaj, S.1    Day, R.A.2
  • 19
    • 0031735103 scopus 로고    scopus 로고
    • Analysis of reversed phase chromatographically separated Bacillus subtilis membrane proteins
    • Bhardwaj S., Day R.A. Analysis of reversed phase chromatographically separated Bacillus subtilis membrane proteins. Anal. Lett. 31:1998;2625-2634.
    • (1998) Anal. Lett. , vol.31 , pp. 2625-2634
    • Bhardwaj, S.1    Day, R.A.2
  • 20
    • 0034022103 scopus 로고    scopus 로고
    • Improved resolution of hydrophobic penicillin binding proteins and their covalently linked complexes on a modified C18 reversed phase column
    • Simon M.J., Day R.A. Improved resolution of hydrophobic penicillin binding proteins and their covalently linked complexes on a modified C18 reversed phase column. Anal. Lett. 33:2000;861-867.
    • (2000) Anal. Lett. , vol.33 , pp. 861-867
    • Simon, M.J.1    Day, R.A.2
  • 22
    • 0005738702 scopus 로고
    • Identification of 2-D gel proteins at the femtomole level of molecular mass searching of peptide fragments in protein sequence data
    • Henzel W.J., Billeci T.M., Stults J.T., Wong S.C., Grimley C., Watanabe C. Identification of 2-D gel proteins at the femtomole level of molecular mass searching of peptide fragments in protein sequence data. Techniques in Protein Chemistry. V:1993;3-9.
    • (1993) Techniques in Protein Chemistry , vol.5 , pp. 3-9
    • Henzel, W.J.1    Billeci, T.M.2    Stults, J.T.3    Wong, S.C.4    Grimley, C.5    Watanabe, C.6
  • 24
    • 0017691247 scopus 로고
    • Reformatzky-reaktion mit ketonitronen langsame N-Inversion im 5-isoxazolidinon-ring
    • Stamm H., Steudle H. Reformatzky-reaktion mit ketonitronen langsame N-Inversion im 5-isoxazolidinon-ring. Arch. Pharm. 310:1977;873-881.
    • (1977) Arch. Pharm. , vol.310 , pp. 873-881
    • Stamm, H.1    Steudle, H.2
  • 25
    • 0032573529 scopus 로고    scopus 로고
    • Synthesis of isoxazolidin-5-ones via stereocontrolled michael additions of benzylhydroxylamine to L-serine derived α,β-unsaturated esters
    • Merina P., France S., Merchan F.L., Tejero T. Synthesis of isoxazolidin-5-ones via stereocontrolled michael additions of benzylhydroxylamine to L-serine derived α,β-unsaturated esters. Tetrahedron: Asymmetry. 9:1998;3945-3949.
    • (1998) Tetrahedron: Asymmetry , vol.9 , pp. 3945-3949
    • Merina, P.1    France, S.2    Merchan, F.L.3    Tejero, T.4
  • 26
    • 0028985422 scopus 로고    scopus 로고
    • A bifunctional monocyclic β-lactam cross-links across the active site of β-lactamase
    • Ahluwalia R., Day R.A., Nauss J. A bifunctional monocyclic β-lactam cross-links across the active site of β-lactamase. Biochem. Biophys. Res. Commun. 206:1998;577-583.
    • (1998) Biochem. Biophys. Res. Commun. , vol.206 , pp. 577-583
    • Ahluwalia, R.1    Day, R.A.2    Nauss, J.3
  • 27
    • 0242279872 scopus 로고    scopus 로고
    • Penicillin-binding proteins as antimicrobial targets: Expression, purification and assay technologies
    • H.A. et al. Kiest. New York: Dekker
    • Zhao G., Meier T.I., Yeh W.-K. Penicillin-binding proteins as antimicrobial targets: expression, purification and assay technologies. Kiest H.A.et al. Enzyme Technologies for Pharmaceutical and Biotechnological Applications. 2001;263-287 Dekker, New York.
    • (2001) Enzyme Technologies for Pharmaceutical and Biotechnological Applications , pp. 263-287
    • Zhao, G.1    Meier, T.I.2    Yeh, W.-K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.