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Volumn 21, Issue 4, 2011, Pages 1185-1190

Analysis of β-amino alcohols as inhibitors of the potential anti-tubercular target N-acetyltransferase

Author keywords

Amino alcohols; Arylamine N acetyltransferase; Drug discovery; Enzyme inhibition; Tuberculosis

Indexed keywords

3 [3' (4'' CYCLOPENT 2''' EN 1''' YLPHENOXY) 2' HYDROXYPROPYL] 5,5 DIMETHYLIMIDAZOLIDINE 2,4 DIONE; ACYLTRANSFERASE; ACYLTRANSFERASE INHIBITOR; AMINOALCOHOL; BETA AMINOALCOHOL; UNCLASSIFIED DRUG;

EID: 79851516691     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2010.12.099     Document Type: Article
Times cited : (26)

References (25)
  • 1
    • 33644991496 scopus 로고    scopus 로고
    • C. Dye Lancet 367 2006 938
    • (2006) Lancet , vol.367 , pp. 938
    • Dye, C.1
  • 15
    • 0344089295 scopus 로고    scopus 로고
    • E.W. Brooke, S.G. Davies, A.W. Mulvaney, F. Pompeo, E. Sim, and R.J. Vickers Bioorg. Med. Chem. 11 2003 1227 The compounds were tested using a NAT activity assay which measures the rate of hydrolysis of acetyl CoA by detection with 5,5′-dithio-bis(2-nitrobenzoic acid) (DTNB) at an absorbance of 405 nm
    • (2003) Bioorg. Med. Chem. , vol.11 , pp. 1227
    • Brooke, E.W.1    Davies, S.G.2    Mulvaney, A.W.3    Pompeo, F.4    Sim, E.5    Vickers, R.J.6
  • 20
    • 79851509423 scopus 로고    scopus 로고
    • note
    • 3) 400 MHz δ, p. H., s), 1.41 (3H, s), 1.62-1.68 (1H, m), 2.12 (1H, s), 2.32-2.52 (4H, m), 3.73-3.81 (2H, m), 3.93-4.01 (2H, m), 4.25 (1H, br s), 5.78-5.82 (1H, m), 5.91-5.95 (1H, m), 6.78-8.82 (1H, m), 6.88-7.92 (1H, m), 7.11-7.19 (2H, m).
  • 24
    • 77954661989 scopus 로고    scopus 로고
    • D. Evangelopoulos, and S. Bhakta Methods Mol. Biol. 642 2010 193 Bacteria were grown on solid agar in multiwell plates as spot cultures containing increasing concentrations of inhibitors in individual wells up to 100 μg/ml. Growth was determined by measuring the area of the spot culture over a period of up to 28 days
    • (2010) Methods Mol. Biol. , vol.642 , pp. 193
    • Evangelopoulos, D.1    Bhakta, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.