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Downloadable
pdf versions of data obtained using Cypex products presented by Cypex
and other organisations can be obtained here
Heterologously
expressed human cytochrome P450 enzymes as a tool for understanding and
predicting drug metabolism.
Urban,
G., Gasser, R., Pritchard, M., Bandera, M. & Friedberg, T.
Exp. Toxic. Pathol. 48 Suppl II pp.409-414 (1996)
Coexpression
of a human P450 (CYP3A4) and P450 reductase generates a highly
functional monooxygenase system in Escherichia coli.
Blake,
J.A.R., Pritchard, M., Ding, S., Smith, G.C.M., Burchell, B., Wolf, C.
R. & Friedberg, T.
FEBS Letters 397 pp.210-214 (1996)
A
general strategy for the expression of recombinant human cytochrome
P450s in Escherichia coli using bacterial signal
peptides: expression of CYP3A4, CYP2A6, and CYP2E1.
Pritchard, M.P., Ossetian, R., Li, D.N., Henderson, C.J., Burchell, B.,
Wolf, C.R. & Friedberg, T.
Arch. Biochem. Biophys. 345 (2) pp.342-354 (1997)
Functional
co-expression of CYP2D6 and human NADPH-cytochrome P450 reductase in Escherichia
coli.
Pritchard,
M.P., Glancey, M.J., Blake, J.A.R., Gilham, D.E., Burchell, B., Wolf,
C.R. & Friedberg, T.
Pharmacogenetics 8 pp.33-42 (1998)
Effects
of cytochrome b5
on
CYP3A4 activity and stability in vivo.
Voice,
M.W., Zhang, Y., Wolf, C.R., Burchell, B. & Friedberg, T.
Arch. Biochem. Biophys. 366 (1) pp.116-124 (1999)
Rapid
Characterisation of the major drug-metabolising human hepatic
cytochrome P-450 enzymes expressed in Escherichia coli.
McGinnity, D.F., Griffin, S.J., Moody, G.C., Voice, M., Hanlon, S.,
Friedberg, T. & Riley, R. J.
Drug Metab. Dispos. 27 (9) pp.1017-1023 (1999)
In
vivo and
in vitro recombinant DNA
technology as a powerful tool in drug development.
Friedberg,
T., Henderson, C.J., Pritchard, M.P. & Wolf, C.R.
Handbook of Drug Metabolism, Chapter 13, pp.322-362 Ed T.F. Wolf, Pub.
Marcel Dekker, Inc. (1999)
Automated
definition of the enzymology of drug oxidation by the major human drug
metabolising cytochrome P450s.
McGinnity, D.F., Parker, A.J., Soars, M. & Riley, R.J.
Drug Metab. Dispos. 28 (11) pp.1327-1334 (2000)
Amino
acid 305 determines catalytic center accessibility in CYP3A4.
Fowler, S.M., Riley, R.J., Pritchard, M.P., Sutcliffe, M.J., Friedberg,
T. & Wolf, C.R.
Biochemistry 39 (15) pp.4406-4414 (2000)
A method for the simultaneous evaluation of the
activities of seven major human drug-metabolising cytochrome P450s
using an in vitro cocktail of probe substrates and
fast gradient liquid chroimatography tandem mass spectrometry.
Dierks, E.A., Stams, K.R., Lim, H-K., Cornelius,
G., Zhang, H. & Ball, S.E.
Drug Metab. Dispos. 29 (1) pp.23-29 (2001)
Predicting drug pharmacokinetics in humans from in
vitro metabolism studies.
McGinnity, D. F. & Riley, R. J.
Biochem. Soc. Trans. 29 pp. 135-139 (2001)
The
following are made under licence from BTG International Ltd (AU730155,
EP0914446, US6566108 and other patents pending): all recombinant
cytochrome P450 products; 4'-hydroxydiclofenac; 6a-hydroxypaclitaxel.
United States Patent Nos. 5,420,027 or 5,240,831,
Great Britain Patent No. 2266719 and other patents pending.
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