Formyltrienolone (RU-2341)
Formyltrienolone (RU-2341) is a highly potent trenbolone-family (estra-4,9,11-triene) synthetic steroid characterised chiefly in preclinical endocrine research. It is an extremely strong androgen-receptor and progesterone-receptor ligand from the same Roussel-Uclaf lineage as metribolone and trenbolone, with no clinical use and essentially no human data.
01 Overview
Formyltrienolone belongs to the 19-nor trienic steroid series that includes trenbolone (Finaplix), metribolone (R1881) and dimethyltrienolone. These compounds are prized in laboratories as reference androgens because of their exceptionally high receptor affinity and resistance to metabolism.
RU-2341 itself is a research chemical rather than a marketed drug, and any bodybuilding presence would be as an extremely potent, non-aromatising but strongly progestogenic and suppressive designer androgen. Its potency and the near-total absence of human safety data make it one of the higher-risk trenbolone relatives.
02 Mechanism
Very high-affinity agonist at the androgen receptor with substantial progesterone-receptor activity; the 4,9,11-triene system prevents aromatisation and 5-alpha reduction while boosting binding potency.
03 Dosing
| Tier | Dose | Route | Notes |
|---|---|---|---|
| No established human dose | 1–5 mg/day | Oral | Speculative only; no validated human dosing exists |
Ester comparison
| Ester | Half-life | Injection freq. | Testosterone by mass |
|---|
04 Effects
| Effect | Magnitude | Evidence | |
|---|---|---|---|
| Potent androgen-receptor activationVery high AR affinity predicts strong anabolic and androgenic signalling in vitro. | Preclinical | ||
| No aromatisationTriene structure blocks conversion to estrogen. | Preclinical |
05 Side effects
| Effect | Severity | Frequency | Evidence | Countermeasures |
|---|---|---|---|---|
| Progestogenic side effectsStrong progesterone-receptor activity can drive progestin-mediated gynecomastia and libido suppression, as seen across the trenbolone family. | Moderate | Predicted | Preclinical | |
| Severe HPTA suppressionHigh-potency androgens of this class strongly suppress endogenous testosterone. | Severe | Predicted | Preclinical |