Andarine S4

$60.00

Andarine (S-4) is a Selective Androgen Receptor Modulator (SARM) that has been studied in various investigational and non-clinical research environments. It is characterized by its high binding affinity for androgen receptors and its potential to modulate tissue-specific anabolic activity. Research has focused on its influence on muscle preservation, bone mineral density, and androgen receptor signaling with tissue selectivity.

Research Focus Areas

Anabolic Signaling and Receptor Selectivity:
Andarine (S-4) binds selectively to androgen receptors in muscle and bone tissue, where it has been shown to stimulate anabolic signaling while avoiding unwanted stimulation in non-target tissues such as the prostate. This selectivity supports its classification as a SARM (Gao et al., 2005).

Changes in Tissue Composition:
In preclinical models, Andarine has been associated with preservation or enhancement of lean muscle mass and favorable effects on bone density without significant increases in fat or water retention

Androgen Receptor Activity and Selectivity Profile:
S-4 has demonstrated activity at muscle- and bone-related androgen receptor targets with limited interaction in reproductive and other androgen-sensitive tissues (Gao et al., 2005).

Physical Performance and Recovery Metrics:
While not approved for human use, investigational settings have explored Andarine’s role in enhancing strength indicators and recovery timelines, especially in conjunction with resistance-based models (ClinicalTrials.gov).

Potential Observations in Research

Mild Side Effect Profile:
Reported effects under investigational protocols include transient visual disturbances (e.g., yellow tint or difficulty in low light), which were generally reversible upon discontinuation. 

Precaution in Reproductive Research Contexts:
Use in reproductive, prenatal, or lactation-related research is not advised due to a lack of toxicity and teratogenicity data. No safety data exists for use during pregnancy or breastfeeding.

Handling and Dosage Information

Typical research concentrations range from 25–50 mg/mL, depending on the investigational model. Administration protocols vary by research setting, and some studies have included sublingual delivery for absorption efficiency. However, this is not considered a required route for all experimental frameworks.

Important Notice:
This product is intended for laboratory research use only. It is not intended for human consumption, medical, veterinary, or household use. Keep out of reach of children.FDA Disclaimer: The statements made within this website have not been evaluated by the US Food and Drug Administration. The statements and the products of this company are not intended to diagnose, treat, cure or prevent any disease. All products are for laboratory developmental research USE ONLY. Products are not for human consumption.

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