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au.\*:("FARACI, W. S")

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Mechanism of inhibition of RTEM-2β-lactamase by cephamycins: relative importance of the 7α-methoxy group and the 3' leaving groupFARACI, W. S; PRATT, R. F.Biochemistry (Easton). 1986, Vol 25, Num 10, pp 2934-2941, issn 0006-2960Article

Nucleophilic re-activation of the PC1 β-lactamase of Staphylococcus aureus and of the DD-peptidase of Streptomyces R61 after their inactivation by cephalosporins and cephamycinsFARACI, W. S; PRATT, R. F.Biochemical journal (London. 1906). 1987, Vol 246, Num 3, pp 651-658, issn 0006-2936Article

Subcloning, expression, and purification of the enterobactin biosynthetic enzyme 2,3-dihydroxybenzoate-AMP ligase: demonstration of enzyme-bound (2,3-dihydroxybenzoyl)adenylate productRUSNAK, F; FARACI, W. S; WALSH, C. T et al.Biochemistry (Easton). 1989, Vol 28, Num 17, pp 6827-6835, issn 0006-2960, 9 p.Article

Direct observation by 1H NMR of cephalosporoate intermediates in aqueous solution during the hydrazinolysis and β-lactamase-catalyzed hydrolysis of cephalosporins with 3' leaving groups: kinetics and equilibria of the 3' elimination reactionPRATT, R. F; FARACI, W. S.Journal of the American Chemical Society. 1986, Vol 108, Num 17, pp 5328-5333, issn 0002-7863Article

Interactions of cephalosporins with the Streptomyces R61 DD-transpeptidase/carboxypeptidase: influence of the 3'-substituentFARACI, W. S; PRATT, R. F.Biochemical journal (London. 1906). 1986, Vol 238, Num 1, pp 309-312, issn 0006-2936Article

Mechanism of inhibition of RTEM-2β-lactamase by cephamycins: relative importance of the 7α-methoxy group and the 3' leaving groupFARACI, W. S; PRATT, R. F.Biochemistry (Easton). 1986, Vol 25, Num 10, pp 2934-2941, issn 0006-2960Article

Synthesis, sar and pharmacology of CP-293,019 : A potent, selective dopamine D4 receptor antagonistSANNER, M. A; CHAPPIE, T. A; MAJCHRZAK, M. J et al.Bioorganic & medicinal chemistry letters (Print). 1998, Vol 8, Num 7, pp 725-730, issn 0960-894XArticle

Synthesis and oral efficacy of a 4-(butylethylamino)pyrrolo[2,3-d]pyrimidine: A centrally active corticotropin-releasing Factor1 receptor antagonistCHEN, Y. L; MANSBACH, R. S; SCHULZ, D. W et al.Journal of medicinal chemistry (Print). 1997, Vol 40, Num 11, pp 1749-1754, issn 0022-2623Article

Inhibition of alanine racemase by alanine phosphonate: detection of an imine linkage to pyridoxal 5'-phosphate in the enzyme-inhibitor complex by solid-state 15N nuclear magnetic resonanceCOPIE, V; FARACI, W. S; WALSH, C. T et al.Biochemistry (Easton). 1988, Vol 27, Num 14, pp 4966-4970, issn 0006-2960Article

A direct spectrophotometry assay for D-alanine carboxypeptidases and for the esterase activity of β-lactamasesPRATT, R. F; FARACI, W. S; GOVARDHAN, C. P et al.Analytical biochemistry. 1985, Vol 144, Num 1, pp 24-206, issn 0003-2697Article

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