Results 161 to 170 of about 7,052 (211)
Some of the next articles are maybe not open access.

Cytochrome P450

Current Opinion in Structural Biology, 1995
Since 1993, three new cytochrome P450 X-ray structures have been determined, giving a total of four known structures. Two of the new structures are in the substrate-free form and one is substrate-bound. These new structures, together with a wealth of mutagenesis studies on various P450s, have provided considerable information on what structural ...
openaire   +3 more sources

Cytochrome P450 and Steatosis

Current Drug Metabolism, 2009
The term fatty liver identifies a liver in which lipids account for more than 5% of the liver's wet weight. When fat accumulates, the lipids primarily stored as triglycerides (TG) result in steatosis and provide substrates for lipid peroxidation. Accumulation of neutral lipids in hepatocytes leads to micro- and macro-vesicular steatosis and to balloon ...
María José, Gómez-Lechón   +2 more
openaire   +2 more sources

QSAR of Cytochrome P450

Drug Metabolism Reviews, 2004
The cytochrome P450 class of enzymes is an extremely important and complex group. It has a significant place in ADME (adsorption, distribution, metabolism, elimination) that those developing new dr...
Corwin, Hansch   +3 more
openaire   +2 more sources

Cytochrome P450 Assays

Current Protocols in Pharmacology, 2001
AbstractCytochrome P450s (CYPs) play a major role in drug detoxification, and inhibition of CYP‐mediated metabolism may lead to accumulation of toxic drug levels in the plasma. To prevent adverse drug‐drug interactions, new drug candidates are routinely tested for their ability to inhibit these enzymes.
Enock, Delaporte, A David, Rodrigues
openaire   +2 more sources

Cytochrome P450 Database

SAR and QSAR in Environmental Research, 2001
This paper describes a specialized database dedicated exclusively to the cytochrome P450 superfamily. The system provides the impression of superfamily's nomenclature and describes structure and function of different P450 enzymes. Information on P450-catalyzed reactions, substrate preferences, peculiarities of induction and inhibition is available ...
A V, Lisitsa   +4 more
openaire   +2 more sources

Cytochromes P450 in crustacea

Comparative Biochemistry and Physiology Part C: Pharmacology, Toxicology and Endocrinology, 1998
Since the last review of this topic, further insight has been gained into the presence and functions of cytochrome P450 proteins in the hepatopancreas and other organs of aquatic crustacean species, although progress has been slow relative to the advances in other species.
M O, James, S M, Boyle
openaire   +2 more sources

Cytochrome P450 in trypanosomatids

Biochemical Pharmacology, 1993
Post-mitochondrial supernatant extracts prepared from bloodstream forms of Trypanosoma brucei brucei, T. cruzi epimastigotes, Leishmania donovani promastigotes and Crithidia fasciculata have been found to catalyse cytochrome P450-dependent reactions. Appreciable ethoxycoumarin deethylase and ethoxyresorufin deethylase activities were found in all of ...
Berger, Bradley J., Fairlamb, Alan H.
openaire   +3 more sources

Pharmacogenetics of the Cytochromes P450

Current Topics in Medicinal Chemistry, 2004
The cytochromes P450 are a family of heme-containing proteins with a major role in the oxidation of both xenobiotics (including prescribed drugs) and endogenous compounds. There are at least 57 human P450s (termed isoforms) which are all encoded by separate genes but only 10 of these contribute to drug metabolism, with the major contribution coming ...
openaire   +2 more sources

Induction of Cytochrome P450s by Rutaecarpine and Metabolism of Rutaecarpine by Cytochrome P450s

Planta Medica, 2004
Rutaecarpine is an alkaloid originally isolated from the unripe fruit of Evodia rutaecarpa. Recently, rutaecarpine has been characterized to have an anti-inflammatory activity through cyclooxygenase-2 inhibition. In the present studies, the effects of rutaecarpine on liver cytochrome P450 s (P450s) and P450 s involved in the metabolism of rutaecarpine ...
Sang Kyu, Lee   +8 more
openaire   +2 more sources

Cytochromes P450 in the Bioactivation of Chemicals

Current Topics in Medicinal Chemistry, 2004
The initial view that the cytochrome P450 enzyme system functions simply in the deactivation of xenobiotics is anachronistic on the face of mounting evidence that this system can also transform many innocuous chemicals to toxic products. However, not all xenobiotic-metabolising cytochrome P450 subfamilies show the same propensity in the bioactivation ...
Ioannides, C, Lewis, DFV
openaire   +4 more sources

Home - About - Disclaimer - Privacy