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"INHIBITORS, INDUCERS AND SUBSTRATES OF CYTOCHROME P450 ISOZYMES". "The Life Raft Group: Long List of Inhibitors and Inducers of CYP3A4 and CYP2D6". "DRUGBANK Online: Cytochrome P-450 Enzyme Inhibitors". "MEDICATIONS METABOLIZED BY CYTOCHROME P450 3A4" (PDF)
Cytochrome P450 inhibitors is a category of agents that inhibit Cytochrome P450. Subcategories. This category has the following 8 subcategories, out of 8 total. A.
Azole cytochrome P450 inhibitors form a dative bond with the iron center. [1] Coumarin aryl-ethers, like 8-methoxypsoralen are reactive inhibitors where the compounds are de-alkylated by the P450s. ^ pubmeddev; PR, Balding; Al., Et (2020-05-06).
Cytochrome P450 3A4 (abbreviated CYP3A4) (EC 1.14.13.97) is an important enzyme in the body, mainly found in the liver and in the intestine, which in humans is encoded by CYP3A4 gene. It oxidizes small foreign organic molecules ( xenobiotics ), such as toxins or drugs, so that they can be removed from the body.
A second electron is transferred, from either cytochrome P450 reductase, ferredoxins, or cytochrome b 5, reducing the Fe-O 2 adduct to give a short-lived peroxo state. The peroxo group formed in step 4 is rapidly protonated twice, releasing one molecule of water and forming the highly reactive species referred to as P450 Compound 1 (or just ...
Cytochrome P450 inhibitors (8 C, 7 P) Pages in category "Cytochrome P450" The following 113 pages are in this category, out of 113 total. ... Cytochrome P450 eryF; E ...
Cytochrome P450 4F2 is a protein that in humans is encoded by the CYP4F2 gene. This protein is an enzyme , a type of protein that catalyzes (helps speed up) chemical reactions inside cells . This specific enzyme is part of the superfamily of cytochrome P450 (CYP) enzymes, and the encoding gene is part of a cluster of cytochrome P450 genes ...
Cimetidine is a potent inhibitor of certain cytochrome P450 (CYP) enzymes, [20] [32] including CYP1A2, CYP2C9, CYP2C19, CYP2D6, CYP2E1, and CYP3A4. [20] [32] [33] The drug appears to primarily inhibit CYP1A2, CYP2D6, and CYP3A4, [34] of which it is described as a moderate inhibitor. [8]