Synthesis and in vitro evaluation of novel small molecule inhibitors of bacterial arylamine N-acetyltransferases (NATs).
The synthesis and inhibitory activity of a series of 5-substituted-(1,1-dioxo-2,3-dihydro-1H-1 lambda(6)-benzo[e][1,2]thiazin-4-ylidene)-thiazolidine-2,4-dione derivatives as competitive inhibitors of recombinant bacterial arylamine-N-acetyltransferases (NATs) are described. The most potent NAT inhi...
Príomhchruthaitheoirí: | Brooke, E, Davies, S, Mulvaney, A, Okada, M, Pompeo, F, Sim, E, Vickers, R, Westwood, I |
---|---|
Formáid: | Journal article |
Teanga: | English |
Foilsithe / Cruthaithe: |
2003
|
Míreanna comhchosúla
Míreanna comhchosúla
-
An approach to identifying novel substrates of bacterial arylamine N-acetyltransferases.
de réir: Brooke, E, et al.
Foilsithe / Cruthaithe: (2003) -
Novel small-molecule inhibitors of arylamine N-acetyltransferases: drug discovery by high-throughput screening.
de réir: Westwood, I, et al.
Foilsithe / Cruthaithe: (2011) -
Identification of arylamine N-acetyltransferase inhibitors as an approach towards novel anti-tuberculars.
de réir: Westwood, I, et al.
Foilsithe / Cruthaithe: (2010) -
Selective small molecule inhibitors of the potential breast cancer marker, human arylamine N-acetyltransferase 1, and its murine homologue, mouse arylamine N-acetyltransferase 2.
de réir: Russell, A, et al.
Foilsithe / Cruthaithe: (2009) -
Structure and mechanism of arylamine N-acetyltransferases.
de réir: Westwood, I, et al.
Foilsithe / Cruthaithe: (2006)