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AVERY FISK · AF COACHING

Androgens

Tetrahydrogestrinone

A designer steroid with potent, multi-receptor activity in laboratory models, not a selective muscle-only effect.

Receptor bioassays and animal pharmacology; evidence checked 2026-10-01

Also known as: THG

Tetrahydrogestrinone molecular structure
Structure reference · C21H28O2

Practical use

Evidence interpretation and concrete review questions

Specify the assay
Ask whether the number describes binding or functional activation.
Keep other pathways visible
Read progesterone and glucocorticoid findings alongside androgen effects.
Avoid numerical safety rankings
These experiments cannot identify a safer human regimen.

Androgen and progestin activity

Broader receptor and organ effects

PubChem chemical identity; checked October 1, 2026

Overview

Tetrahydrogestrinone, or THG, is a distinct steroid related structurally to gestrinone. Its activity was examined in receptor assays and animal experiments; different assay systems do not necessarily produce the same potency ranking.

Risks and limitations

Preclinical findings include activity beyond androgen signaling and altered liver glucocorticoid-related gene expression. These raise mechanistic concerns without establishing a human toxicity rate or safe exposure.

How to read this

A binding-affinity headline should be separated from functional signaling, organ effects and clinical outcomes.

Research explained

Androgen and progestin activity

Who was studied

Yeast-based reporter systems expressing human androgen, progesterone and estrogen receptors.

What was found

THG showed potent androgen and progestin activity, without estrogenic activity in those assays.

What it cannot establish

Engineered yeast assays establish signaling properties, not clinical benefit or safety.

Read the original study

Broader receptor and organ effects

Who was studied

Receptor-binding studies plus experiments in castrated rats.

What was found

THG bound several steroid receptor classes and stimulated androgen-sensitive organs. A liver glucocorticoid-responsive gene was downregulated.

What it cannot establish

Binding is not equivalent to the same functional action at every receptor; animal effects cannot be converted into a human risk ratio.

Read the original study

No estrogen signal is not global selectivity

Other hormone receptors remained relevant to THG’s experimental profile.

Supporting source

Potency depends on the assay

Receptor binding, reporter activation and animal organ growth measure different things.

Supporting source

Claims versus findings

Incorrect

An androgen-receptor effect means the compound acts only on muscle.

The experimental profile included other receptors and organs.

Check the evidence

Common questions

Does a human receptor in yeast count as a human trial?

No. The receptor is human-derived; the experimental system is yeast.

Source

Sources

Androgen and progestin activity

Broader receptor and organ effects

PubChem chemical identity; checked October 1, 2026

Sources checked 2026-10-01.

General education; not a personal treatment plan.