Mycophenolic Acid

Immunosuppressant metaboliteprescriptionoral · inferred

Active species of mycophenolate mofetil after hepatic esterase hydrolysis. IMPDH inhibitor selectively depleting GTP in lymphocytes. Exhibits enterohepatic recirculation producing a secondary peak at 6-12 h.

Projected serum levels — 720 mg, twice daily

Mycophenolic Acid
Mycophenolic Acid modeled serum levels, 720 mg twice daily over 15 days Population-based pharmacokinetic estimate. Steady state reached after approximately 1 days. 0 50 100 150 200 Day 0 Day 4 Day 7 Day 11 Day 15 Time on a regular schedule ≈ steady state · day 1

Maintenance schedule: 720 mg twice daily (oral).

Modeled steady state after ~1 days: peak ≈ 189 mg, trough ≈ 0.000 mg body load. Population-based estimate over 15 days for a 720 mg dose at a 70 kg reference body mass — the interactive app scales curves to your doses, timing, and body mass.

Key facts

Category
Immunosuppressant metabolite
Route modeled
Oral
Model confidence
inferred
Half-life
12 h
Common dose
720 mg
Suggested maximum
1.4k mg/day
Reference dose range
180–1.4k mg (single dose)
Suggested cadence
twice daily
Validated against
720 mg oral — Cmax 24 mg/L at 2 h

Documented interactions

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    Mycophenolate Mofetil (CellCept) + Mycophenolic Acid Stacked effects

    Mycophenolate Mofetil (CellCept) and Mycophenolic Acid both push the impdh in the same direction.

Serum checks 1 modeled interaction pairings for mycophenolic acid across your whole stack — absorption conflicts, enzyme inhibition, and nutrient depletion included.