ID: ac262536
Aliases: AC-262, Accadrine
Type: compound
Route/form: oral preclinical SARM context
Status: research
Evidence level: preclinical
Best data tier: non-human experimental
Support scope: non-human/mechanistic, review/regulatory
Source types: preclinical, review
Linked sources: 2
Broad outcomes: Fat loss / metabolic health, Muscle growth / performance / recovery, PEDs / AAS / thermogenics, Safety / regulatory
Reading note: These are curation notes anchored to linked sources, not a clinical recommendation or protocol.
Targets / mechanism
- androgen receptor modulator
- partial AR agonist
Optimization domains
- SARM
- body composition
- bone
- doping
Research basis
- Preclinical pharmacology supports AC-262536 as a selective AR ligand with partial agonist behavior.
- It is useful for mapping newer research-chemical SARMs that are mostly discussed without human data.
- The entry should be read as molecule identity and receptor pharmacology, not a proven mild cycle.
Limits, risks, and missing evidence
- No human efficacy package was identified in this pass.
- Forum claims should be treated as molecule-identity and dose-quality problems before performance claims.
- Partial agonism does not remove endocrine, lipid/liver, androgen-sensitive tissue, or doping concerns.
Risk flags
- research compound
- preclinical only
- sarm class risk
- product identity risk
- doping
Linked papers, labels, and reviews
- Pharmacological characterization of AC-262536, a novel SARM
preclinical / pubmed_ac262536_characterization_2008
Functional and pharmacological characterization of AC-262536. - Selective androgen receptor modulators in preclinical and clinical development
review / pubmed_sarms_preclinical_clinical_2009
SARM class review covering multiple preclinical and early clinical programs.