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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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