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| CYP2C19 - Cytochrome P450 Family 2 Subfamily C Member 19 Abbreviation: CYP2C19 Type: Cytochrome P450 monooxygenase / drug-metabolizing enzyme / xenobiotic metabolism enzyme / pharmacogenetic target Function: CYP2C19 is an endoplasmic-reticulum cytochrome P450 enzyme expressed primarily in the liver and, to a lesser extent, the intestine. It oxidizes numerous xenobiotics, drugs and endogenous substrates and contributes to phase I metabolism, drug clearance and metabolic activation or inactivation. Drug and Compound Metabolism: ↕ CYP2C19 activity can increase or decrease the biological effect of a compound depending on whether metabolism inactivates the parent compound, produces an active metabolite, or activates a prodrug. Pharmacogenetics: CYP2C19 activity varies substantially between individuals. Loss-of-function alleles such as CYP2C19*2 and CYP2C19*3 can produce reduced or poor metabolism, while CYP2C19*17 is associated with increased expression and activity. Cancer: ↕ Context-dependent. CYP2C19 does not have a universal favorable cancer direction. Its importance is primarily determined by the substrate or anticancer agent being metabolized and whether CYP2C19-mediated metabolism activates, inactivates or clears that compound. Interpretation Note: When a natural product or drug inhibits CYP2C19, record CYP2C19 activity ↓ rather than assuming this is beneficial or harmful. The biological consequence depends on the affected substrate and its metabolites. |
| 8217- | LCA, | Inhibition of human cytochrome P450 enzymes by licochalcone A, a naturally occurring constituent of licorice |
| - | Study, | Nor, | NA |
Query results interpretion may depend on "conditions" listed in the research papers. Such Conditions may include : -low or high Dose -format for product, such as nano of lipid formations -different cell line effects -synergies with other products -if effect was for normal or cancerous cells
Filter Conditions: Pro/AntiFlg:% IllCat:% CanType:% Cells:% prod#:% Target#:1780 State#:% Dir#:%
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