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Volumn 12, Issue 21, 2002, Pages 3027-3031

Novel semi-synthetic glycopeptide antibiotics active against methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci (VRE): Doubly-modified water-soluble derivatives of chloroorienticin B

Author keywords

[No Author keywords available]

Indexed keywords

CHLOROORIENTICIN B; GLYCOPEPTIDE; POLYPEPTIDE ANTIBIOTIC AGENT; VANCOMYCIN DERIVATIVE; WATER;

EID: 0037020718     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(02)00664-9     Document Type: Article
Times cited : (18)

References (21)
  • 18
    • 0010692183 scopus 로고    scopus 로고
    • Preliminary experiments revealed that the N-terminus secondary amino group of the peptide backbone was more reactive than the amino sugar nitrogen, therefore protection of N-terminus amino group was found to be necessary prior to reductive N-alkylation.
  • 19
    • 0010733392 scopus 로고    scopus 로고
    • Minimum Inhibitory Concentrations (MICs) were determined by National Committee for Clinical Laboratory Standards (NCCLS)-recommended microbroth dilution methods using cation-adjusted Mueller Hinton broth (Difco Laboratories, Detroit, MI, USA).
  • 21
    • 0010693232 scopus 로고    scopus 로고
    • Histamine dihydrochloride was used for aminomethylation of 2d.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.