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Volumn 9, Issue 7, 1999, Pages 997-1002

6-(1-Hydroxyalkyl)penam sulfone derivatives as inhibitors of class A and class C β-lactamases II

Author keywords

[No Author keywords available]

Indexed keywords

6 AMINOPENICILLANIC ACID; AMOXICILLIN; AMPICILLIN; BETA LACTAMASE INHIBITOR; CEPHALOSPORINASE; CLAVULANIC ACID; PIPERACILLIN; RO 48 1220; SULBACTAM; SULFONE DERIVATIVE; TAZOBACTAM; TICARCILLIN; UNCLASSIFIED DRUG;

EID: 0033526053     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(99)00107-9     Document Type: Article
Times cited : (18)

References (23)
  • 17
    • 0013523878 scopus 로고    scopus 로고
    • note
    • 2O of these five new derivatives are summarized as follows: 7, δ: 8.11 (1H, s), 7.84 (1H, s), 5.36 (1H, d; J = 15.4 Hz), 5.17 (1H, d; J = 15.4 Hz), 4.80 (1H, d; J = 4.8 Hz), 4.74 (1H, m), 4.57 (1H, s), 4.03 (1H, dd; J = 4.8 Hz), 1.42 (3H, s), 1.34 (3H, s); 10, δ: 8.12 (1H, s), 7.85 (1H, s), 5.37 (1H, d; J = 15.4 Hz), 5.16 (1H, d; J = 15.4 Hz), 5.08 (1H, d; J = 4.6 Hz), 4.57 (1H, s), 4.38-4.31 (1H, m), 4.28-3.98 (2H, m), 1.41 (3H, s); 25, δ: 6.68 (1H, d; J = 12.4 Hz), 6.16 (1H, d; J = 12.4 Hz), 5.25 (1H, d; J = 4.7 Hz), 4.36 (1H, m), 4.22 1H, dd; 7=8.16 Hz), 4.08 (1H, dd; 7 = 8.16 Hz), 1.94 (3H, s); 26, δ: 7.08 (1H, d; J = 16.5 Hz), 6.07 (1H, d; J = 16.5 Hz), 5.2 (1H, s), 4.36 (1H, m), 4.21 (1H, dd; J = 8.10 Hz), 4.07 (1H, dd; J = 8.10 Hz), 1.64 (3H, s); 29, δ: 7.68 (1H, s), 5.18 (1H, d; J = 4.5 Hz), 4.88 (1H, s), 4.35 (1H, m), 4.2 (1H, t), 4.08 (1H, dd), 3.97 (3H, s), 1.66 (3H, s).
  • 23
    • 0013525345 scopus 로고    scopus 로고
    • note
    • 17. Molecular modelling studies using MacroModel v6.0 showed that good binding ligands fit well in the enzyme active site and remained there during the molecular dynamics simulation. Details of the molecular modelling studies will be published elsewhere.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.