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Volumn 13, Issue 23, 2003, Pages 4229-4233

Structure-activity relationship in the oxazolidinone-quinolone hybrid series: Influence of the central spacer on the antibacterial activity and the mode of action

Author keywords

[No Author keywords available]

Indexed keywords

OXAZOLIDINONE DERIVATIVE; QUINOLONE DERIVATIVE;

EID: 0242416198     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2003.07.028     Document Type: Article
Times cited : (60)

References (22)
  • 6
    • 0026766138 scopus 로고
    • Preparation of (S)-3-amino-1-pyrrolidinecarboxylic acid phenylmethyl ester and (S and R)-3-hydroxy-1-pyrrolidinecarboxylic acid phenylmethyl ester
    • Preparation of (S)-3-amino-1-pyrrolidinecarboxylic acid phenylmethyl ester and (S and R)-3-hydroxy-1-pyrrolidinecarboxylic acid phenylmethyl ester Sanchez JosephP., Domagala J.M., Heifetz C.L., Priebe S.R., Sesnie J.A., Trehan A.K. J. Med. Chem. 35:1992;1764.
    • (1992) J. Med. Chem. , vol.35 , pp. 1764
    • Sanchez Joseph, P.1    Domagala, J.M.2    Heifetz, C.L.3    Priebe, S.R.4    Sesnie, J.A.5    Trehan, A.K.6
  • 9
    • 0029568003 scopus 로고
    • Preparation of 3-hydroxy-1-piperidinecarboxylic acid phenylmethyl ester:
    • Preparation of 3-hydroxy-1-piperidinecarboxylic acid phenylmethyl ester: Apostolopoulos C.D., Haroutounian S.A. J. Heterocycl. Chem. 32:1995;1843.
    • (1995) J. Heterocycl. Chem. , vol.32 , pp. 1843
    • Apostolopoulos, C.D.1    Haroutounian, S.A.2
  • 11
    • 0030800156 scopus 로고    scopus 로고
    • Preparation of 4-hydroxyethyl-1-piperidinecarboxylic acid phenylmethyl ester:
    • Preparation of 4-hydroxyethyl-1-piperidinecarboxylic acid phenylmethyl ester: Mazzini C., Lebreton J., Alphand V., Furstoss R. J. Org. Chem. 62:1997;5215.
    • (1997) J. Org. Chem. , vol.62 , pp. 5215
    • Mazzini, C.1    Lebreton, J.2    Alphand, V.3    Furstoss, R.4
  • 14
    • 85030938740 scopus 로고    scopus 로고
    • 15 The pH of the test medium was 7.2-7.3. The bacterial strains used were from the Morphochem collection. Clinical isolates were originally obtained from the Kantonspital Basel, Switzerland, and from other European and US hospitals.
  • 15
    • 0037710633 scopus 로고    scopus 로고
    • National Committee for Clinical Laboratory Standards; Approved standard: NCCLS Document M7-A4; National Committee for Clinical Laboratory Standards: Villanova, PA, USA
    • National Committee for Clinical Laboratory Standards. Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically, 4th ed.; Approved standard: NCCLS Document M7-A4; National Committee for Clinical Laboratory Standards: Villanova, PA, USA, 1997.
    • (1997) Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically, 4th Ed.
  • 17
    • 85030944251 scopus 로고    scopus 로고
    • 18 After pre-incubation for 10 min, the reactions were initiated by adding 0. 1 μg of plasmid DNA and incubated at 37 °C for 35 min. Then, the reaction was stopped by cooling in ice, 15 μL was added to 15 μL luciferase substrate (Bright Glo, Promega, Madison, WI, USA), and luminescence was quantified in a Tecan Spectrafluor Plus plate reader.
  • 19
    • 85030943846 scopus 로고    scopus 로고
    • 50 for relaxation was determined visually, as being the compound concentration at which the relaxed band was reduced by 50% and a supercoiled band with topoisomers appeared.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.