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  2. CYP3A4 - Wikipedia

    en.wikipedia.org/wiki/CYP3A4

    CYP3A4 promotes the growth of various types of human cancer cell lines in culture by producing (±)-14,15-epoxyeicosatrienoic acids, which stimulate these cells to grow. [9] The CYP3A4 enzyme is also reported to have fatty acid monooxgenase activity for metabolizing arachidonic acid to 20-Hydroxyeicosatetraenoic acid (20-HETE).

  3. Ribociclib - Wikipedia

    en.wikipedia.org/wiki/Ribociclib

    Ribociclib itself is a moderate to strong CYP3A4 inhibitor and can increase concentrations ... Simply blocking one pathway in cancer tumorigenesis can sometimes ...

  4. CYP3A - Wikipedia

    en.wikipedia.org/wiki/CYP3A

    n/a Ensembl n/a n/a UniProt n a n/a RefSeq (mRNA) NM_000775 n/a RefSeq (protein) n/a n/a Location (UCSC) n/a n/a PubMed search n/a Wikidata View/Edit Human Cytochrome P450, family 3, subfamily A, also known as CYP3A, is a human gene locus. A homologous locus is found in mice. The CYP3A locus includes all the known members of the 3A subfamily of the cytochrome P450 superfamily of genes. These ...

  5. VEGFR-2 inhibitor - Wikipedia

    en.wikipedia.org/wiki/VEGFR-2_inhibitor

    Grapefruit juice is a CYP3A4 inhibitor and should be avoided when taking pazopanib. It is also a weak inhibitor of other liver enzymes, CYP2C8 and CYP2D6. [8] Axitinib is metabolized by CYP3A4 and UGT1A1. Strong inhibitors of CYP3A4 will increase the plasma concentration of axitinib, while weak inhibitors have less effect on the plasma ...

  6. Imatinib - Wikipedia

    en.wikipedia.org/wiki/Imatinib

    Its use is advised against in people on strong CYP3A4 inhibitors such as clarithromycin, chloramphenicol, ketoconazole, ritonavir and nefazodone due to its reliance on CYP3A4 for metabolism. [26] Likewise it is a CYP3A4 , CYP2D6 and CYP2C9 inhibitor and hence concurrent treatment with substrates of any of these enzymes may increase plasma ...

  7. Exemestane - Wikipedia

    en.wikipedia.org/wiki/Exemestane

    The liver enzyme CYP3A4 oxidizes the methylidene group in position 6, and the 17-keto group (on the five-membered ring) is reduced by aldo-keto reductases to an alcohol. Of the resulting metabolites, 40% are excreted via the urine and 40% via the feces within a week. The original substance accounts for only 1% of excretion in the urine.