ACP105 · Evidence-based safety and harm-reduction overview.
| Also known as | ACP105 |
| Category | SARM |
| development_era | Early 2000s preclinical program |
| tissue_selectivity | Intended bone and muscle preference; mechanism not fully elucidated |
| US legal status | Not FDA-approved for human use. Sold as a research chemical only. WADA-banned. No approved pharmaceutical form. |
Nonsteroidal selective androgen receptor modulator (SARM) developed for musculoskeletal conditions. Synthetic compound designed to preferentially activate androgen receptors in bone and muscle.
Selective androgen receptor agonist with reported affinity for muscle and bone tissue. Mechanism of tissue selectivity poorly understood; proposed to involve differential co-regulator expression.
Developed in early 2000s as part of academic SARM discovery program. Preclinical work discontinued; never advanced to investigational drug phase due to competitive landscape.
Preclinical and early animal evidence only. No published human Phase II/III trials. Animal studies report anabolic effects on bone and muscle. Expected androgen receptor-driven suppression of testosterone. Research is limited and older in publication timeline.
Early animal studies used escalating dose protocols to assess efficacy and tolerability thresholds. Human equivalent doses completely unknown.
This is general research/context information, not medical advice or a recommended protocol.
No validated human combinations; multi-compound use dramatically increases toxicological risk and organ-damage potential.
If you are going to research a compound, verifying identity and purity is the single most protective step. Independent analytical testing and sterile-handling supplies reduce risk.
Compare testing optionsNo. Never approved or used clinically. Research chemical only, unregulated.
Older compound; newer SARMs (RAD, LGD) received more research funding and attention.
Unknown in humans. Testosterone suppression expected, but organ impact, duration of effects, and long-term safety are unvalidated.
Only a third-party lab test can confirm identity and purity; most vendors do not provide this.
Less modern research scrutiny; preclinical work is dated and limited in scope.
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