1-Androstenediol
The diol form of the 1-testosterone pathway, converting to 1-testosterone (dihydroboldenone) via one fewer oxidation step than 1-DHEA. A non-aromatising, dry-gain prohormone with the same DHT-type side effect and suppression profile. DASCA-scheduled in the US.
01 Overview
1-Androstenediol (1-androstene-3-beta,17-beta-diol) is closely related to 1-DHEA but is already reduced at C17, so it converts to 1-testosterone with one enzymatic step. Downstream it delivers the same active androgen, dihydroboldenone, giving lean, non-estrogenic gains.
Like the rest of the 1-ene series, it has no controlled human trials; its properties are extrapolated from 1-testosterone and anecdotal use. It is a scheduled anabolic steroid under DASCA.
02 Mechanism
Oxidised by 17-beta-HSD to 1-testosterone (dihydroboldenone), a non-aromatising androgen resistant to 5-alpha reduction.
03 Dosing
| Tier | Dose | Route | Notes |
|---|---|---|---|
| Community-typical | 100–300 mg/day | Oral | Reported prohormone dosing; not medically validated. |
Ester comparison
| Ester | Half-life | Injection freq. | Testosterone by mass |
|---|
04 Effects
| Effect | Magnitude | Evidence | |
|---|---|---|---|
| Lean, dry mass gainsReported to give the same dry lean gains as 1-DHEA with slightly more efficient conversion. | Modest lean gain (reported) | Anecdotal | |
| No aromatisationEnd product does not convert to estrogen. | Non-aromatising | Preclinical |
05 Side effects
| Effect | Severity | Frequency | Evidence | Countermeasures |
|---|---|---|---|---|
| LethargyFatigue similar to other 1-testosterone precursors. | Moderate | Commonly reported | Anecdotal | |
| HPTA suppressionStrong suppression of natural testosterone. | Moderate | Near-universal | Anecdotal |