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Enzyme:CYP2E1: Difference between revisions

From Pharmacopedia
[checked revision][checked revision]
m MDElliottMD moved page Pharmacopedia:Pharmacogenomics sandbox/Enzyme CYP2E1 to Enzyme:CYP2E1: Migrate enzyme entity pages from Pharmacogenomics sandbox to the new Enzyme: namespace
Add scope="col" to the data-table column headers for screen-reader association (ADA audit M5; designer-claude 2026-05-22)
 
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{| class="wikitable sortable mw-collapsible mw-collapsed" style="width:100%;"
{| class="wikitable sortable mw-collapsible mw-collapsed" style="width:100%;"
|+ style="white-space:nowrap; text-align:left;" | near-complete CYP2E1 medicine-substrate table (click to expand)
|+ style="white-space:nowrap; text-align:left;" | near-complete CYP2E1 medicine-substrate table (click to expand)
! Substrate !! Therapeutic class !! CYP2E1 contribution !! Clinical notes
! scope="col" | Substrate !! scope="col" | Therapeutic class !! scope="col" | CYP2E1 contribution !! scope="col" | Clinical notes
|-
|-
| '''[[Acetaminophen]]''' || Analgesic / antipyretic (paracetamol) || partial (toxic route) || '''The clinically critical CYP2E1 substrate.''' At therapeutic doses acetaminophen is cleared mostly by glucuronidation and sulfation; a minor oxidative route, substantially CYP2E1-mediated, generates the hepatotoxic metabolite NAPQI. CYP2E1 induction (chronic alcohol, fasting) increases NAPQI formation. See Clinical implications.
| '''[[Acetaminophen]]''' || Analgesic / antipyretic (paracetamol) || partial (toxic route) || '''The clinically critical CYP2E1 substrate.''' At therapeutic doses acetaminophen is cleared mostly by glucuronidation and sulfation; a minor oxidative route, substantially CYP2E1-mediated, generates the hepatotoxic metabolite NAPQI. CYP2E1 induction (chronic alcohol, fasting) increases NAPQI formation. See Clinical implications.