CYP

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Related to cytochrome: cytochrome c, cytochrome oxidase, Cytochrome P450

CYP

The ISO 4217 currency code for Cyprus Pound.

CYP

GOST 7.67 Latin three-letter geocode for Cyprus. The code is used for transactions to and from Cypriot bank accounts and for international shipping to Cyprus. As with all GOST 7.67 codes, it is used primarily in Cyrillic alphabets.
References in periodicals archive ?
These hemeproteins determined in the liver microsomal fraction, presented with the exception of cytochrome [b.
Reductase activity was determined by the measurement of the increasing absorbance of the preparation, corresponding to the reduction of the cytochrome C in the presence of [H.
Cytochrome C and dATP-dependent formation of Apaf-1/Caspase-9 complex initiates an apoptotic protease cascade.
Other medications that are metabolized by the 1A2 isoenzyme of cytochrome P450 include haloperidol, olanzapine, thioridazine, tacrine, amitriptyline, imipramine, clomipramine, warfarin, propranolol, methadone, verapamil, and theophylline.
It is a world leader in the discovery of cytochrome P450 genes, the identification of the function of the proteins encoded by those genes, and the discovery of highly potent and specific drugs regulating cytochrome P450 enzymes to address unmet medical needs.
Identification of a rat adrenal cytochrome P450 active in polycyclic hydrocarbon metabolism as rat CYP1B1: demonstration of a unique tissue-specific pattern of hormonal and aryl hydrocarbon receptor-linked regulation.
Many companies now conduct lab tests to see whether their drug compounds affect common metabolic pathways such as the cytochrome p450 enzymes, he notes.
03 Seizures, (d) hypotonia Patient Diagnostic criteria (a) Electron transport chain defects 1 Glutamate cytochrome reductase 0.
Cytochrome P450 comprises a family of enzymes that break down thousands of compounds in the body.
Cytochroma's novel technology platform puts it among the world's leaders in cytochrome P450-based therapeutics.
John's wort contains two compounds--hypericin and hyperforin--that induce cytochrome P450 to increase the rate of drug metabolism.
The P450 2D6 structure is a milestone in ongoing work to determine the structures of various bound substrates and inhibitors related to ligand recognition and specificity in human cytochrome systems.