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Enclomiphene

Enclomiphene acts as an estrogen receptor antagonist primarily at hypothalamic and pituitary sites. By blocking estrogen-mediated negative feedback on GnRH neurons, it increases pulsatile GnRH secretion, which in turn elevates pituitary LH and FSH release. The resulting gonadotropin surge stimulates testicular Leydig cell testosterone production and may support spermatogenesis. Unlike the cis-isomer zuclomiphene, enclomiphene clears more rapidly, which is thought to reduce cumulative estrogenic side effects seen with the racemic mixture.

Molecular Profile
small-molecule
10 AA Sequence
Evidence grade (Limited): Mostly preclinical or low-quality human studies. This grade reflects the overall quality of available research on this compound and does not constitute a clinical recommendation.
CAS
15690-57-0
Mol. weight
406 g/mol
Onset and duration

Injectable esters release over days to weeks depending on the ester; oral agents act within hours. Hormonal effects accrue over weeks, and dosing is individualized by a clinician.

Storage and reconstitution

Oral tablet or capsule (compounded); store at controlled room temperature in a dry location per compounding pharmacy labeling.

Clinical Evidence

What the literature says

Pharmacokinetics

Routes
Oral

Last reviewed: 2026-06-15

Research Guide

How users approach this compound

The following reflects patterns observed in research literature and community protocols. This is not medical advice and does not constitute a clinical recommendation.

Reported Uses

  • Investigated in Phase 2/3 trials for secondary (hypogonadotropic) hypogonadism in males
  • Studied as an alternative to exogenous testosterone in men wishing to preserve fertility

Key Research Benefits

  • Studied for raising endogenous LH, FSH, and testosterone in males with secondary hypogonadism while potentially preserving spermatogenesis, based on clinical trial data

Potential Side Effects

Visual disturbances (reported less frequently than with racemic clomiphene in some studies)
Mood changes
Hot flashes or estrogen-related vasomotor symptoms
Headache

Considerations and Cautions

Labs to monitor

Educational context only, not a testing mandate. Any bloodwork decisions belong with your clinician.

  • Estradiol (E2): SERM mechanism affects estrogen feedback; E2 monitoring guides adequacy and avoids estrogen deficiency.
  • LH and FSH: Primary pharmacodynamic endpoints confirming gonadotropin response to SERM blockade.
  • Lipid panel: SERMs can affect lipid metabolism; baseline and follow-up monitoring prudent.

Dose Calculator

Peptide Reconstitution Calculator

mg

Total amount of peptide in the vial.

mL

Volume of water used to mix.

mcg

Draw to this mark

10 Units

or 0.10 mL on a U-100 syringe

Concentration:2.50 mg/mL
Peptide per Unit:25.00 mcg/unit
*Always double-check your calculations. This tool is for educational purposes only.

Related Tools

Not medical advice

Information on DoseVault is for educational purposes only and is not a substitute for medical advice, diagnosis, or treatment from a qualified healthcare provider.