Ethinyl Estradiol
Synthetic estrogen (17-alpha-ethinyl-17-beta-estradiol) that is the estrogen component of nearly all combined oral contraceptives and the vaginal ring/patch. 17-alpha-ethinyl substitution blocks the primary oxidative site, giving ~40x oral potency over estradiol and a ~24 h plasma half-life. Undergoes extensive first-pass 2-hydroxylation (CYP3A4, CYP1A2) and phenolic sulfation (SULT1E1) and glucuronidation (UGT1A1). Raises hepatic SHBG, CRP, and clotting factor synthesis (VTE risk). Typical contraceptive doses 10-35 mcg/day.
Projected serum levels — 30 mcg (≈ 0.030 mg), once daily
Maintenance schedule: 30 mcg (≈ 0.030 mg) once daily (oral).
Loading schedule: 52.6 mcg on day 1, then 30 mcg (≈ 0.030 mg) once daily — reaching therapeutic levels sooner.
Modeled steady state after ~2 days: peak ≈ 0.021 mg, trough ≈ 0.010 mg body load. Population-based estimate over 15 days for a reference dose at a 70 kg reference body mass — the interactive app scales curves to your doses, timing, and body mass.
Key facts
- Category
- Hormonal Contraceptive
- Route modeled
- Oral
- Model confidence
- inferred
- Half-life
- 20 h
- Common dose
- 30 mcg (≈ 0.030 mg)
- Suggested maximum
- 50 mcg/day
- Reference dose range
- 0.020–50 mcg (single dose)
- Suggested cadence
- once daily
- Validated against
- 0.030 mg oral — Cmax 0.000 mg/L at 1.5 h
Documented interactions
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danger
7-Hydroxymitragynine (7-OH) + Ethinyl Estradiol
Ethinyl Estradiol reversible_inhibitor of CYP3A4 predicted to change 7-Hydroxymitragynine (7-OH) AUC by ~2.20x
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danger
Alfuzosin (Uroxatral) + Ethinyl Estradiol
Ethinyl Estradiol reversible_inhibitor of CYP3A4 predicted to change Alfuzosin (Uroxatral) AUC by ~3.33x
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danger
Alprazolam (Xanax) + Ethinyl Estradiol
Ethinyl Estradiol reversible_inhibitor of CYP3A4 predicted to change Alprazolam (Xanax) AUC by ~3.33x
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danger
Amlodipine (Norvasc) + Ethinyl Estradiol
Ethinyl Estradiol reversible_inhibitor of CYP3A4 predicted to change Amlodipine (Norvasc) AUC by ~3.33x
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danger
Anastrozole (Arimidex) + Ethinyl Estradiol
Ethinyl Estradiol reversible_inhibitor of CYP3A4 predicted to change Anastrozole (Arimidex) AUC by ~2.68x
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danger
Astaxanthin + Ethinyl Estradiol
Ethinyl Estradiol reversible_inhibitor of CYP3A4 predicted to change Astaxanthin AUC by ~3.33x
Serum checks 486 modeled interaction pairings for ethinyl estradiol across your whole stack — absorption conflicts, enzyme inhibition, and nutrient depletion included.
Research behind this entry
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Ethinyl estradiol and conjugated equine estrogens: pharmacokinetics and endocrine pharmacology
Definitive PK review of ethinyl estradiol establishing oral bioavailability ~43%, terminal half-life ~24h, extensive first-pass metabolism via CYP3A4 2-hydroxylation and SULT1E1/UGT1A1 conjugation.
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Pharmacokinetics of ethinylestradiol
Classic PK characterization of ethinyl estradiol documenting enterohepatic recirculation and wide interindividual variability.
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Interactions between hormonal contraception and antiepileptic drugs
Review of CYP3A4 inducer interactions demonstrating 40-80% EE AUC reductions from enzyme-inducing anticonvulsants with contraceptive failure implications.
3 published studies referenced in the app, each with a plain-language summary.