S23 10mg - 50 Tablets
S23 10mg is a SARM oral tablet formulation supplied in a 50 tablet pack. Manufactured for consistent potency, stability, and research applications.
S23 10mg is a SARM oral tablet formulation supplied in a 50 tablet pack. Manufactured for consistent potency, stability, and research applications.
S23 is a non steroidal selective androgen receptor modulator (SARM) with one of the highest documented androgen receptor binding affinities among research SARM compounds, a structural characteristic that has positioned it as a frequently referenced compound in studies examining high potency selective androgen receptor activation. F40 Biotech’s formulation delivers 10mg per tablet in a 50 count format, consistent with the concentration most commonly referenced in S23 preclinical research literature.
S23’s research profile is distinguished by its documented dual mechanism affecting both bone and skeletal muscle tissue alongside a notably pronounced HPG axis suppressive effect at the receptor level, a characteristic that differentiates it from LGD-4033 within CSD’s SARM range despite both compounds sharing the broad tissue selective androgen receptor activation principle common to the SARM class. S23 has additionally been studied as a potential male contraceptive research compound, owing to its androgen receptor binding characteristics affecting spermatogenesis related signaling. A research application that is unique among CSD’s SARM listings and reflects the compound’s particularly strong androgen receptor engagement profile compared to other selective modulators.
Like LGD-4033, S23 binds the androgen receptor through a non steroidal mechanism that avoids 5-alpha reductase and aromatase enzyme interaction, eliminating the androgenic and estrogenic conversion pathways associated with traditional anabolic steroids while still activating downstream anabolic signaling in muscle and bone tissue. The comparative research distinction between S23 and LGD-4033 centers on receptor binding affinity and the resulting differences in HPG axis suppression magnitude and tissue selectivity profile. A frequently studied comparison within SARM structure activity relationship research examining how subtle structural variations between non steroidal SARM compounds produce measurably different suppression and selectivity characteristics.
F40 Biotech formulations are stocked by Canada Steroid Depot following the same rigorous third party lab verification process applied to every product in our range. Each batch is tested for concentration accuracy and purity before being made available, with COA documentation available on request. CSD’s sourcing standards apply uniformly across all manufacturers we carry, and F40 Biotech’s S23 meets those standards consistently. All orders ship discreetly across Canada in plain, unmarked packaging with no identifying information on the exterior.
Store in a cool, dry place away from direct light and heat. Intended for research purposes only.
Commonly researched alongside LGD-4033 in comparative SARM receptor binding affinity and tissue selectivity studies. Browse CSD’s full SARM range for complete sourcing.
S23 is a non steroidal selective androgen receptor modulator (SARM) with one of the highest androgen receptor binding affinities of any SARM in the research catalogue. Producing near complete HPG axis suppression comparable to traditional anabolic steroids at research doses. It was originally investigated by GTx Inc. as a potential male hormonal contraceptive due to its potent suppression of LH, FSH, and spermatogenesis. S23 is studied for lean mass accretion, fat loss, muscle hardness, strength enhancement, and bone density improvement with a strong anabolic profile and very high tissue selectivity for muscle and bone over prostate. Its potency and suppressive profile make it one of the most aggressive SARMs in the research catalogue.
S23 is the most potent and most suppressive SARM in CSD's catalogue producing HPG axis suppression comparable to traditional anabolic steroids rather than the milder suppression associated with compounds such as Ostarine or even LGD-4033. At research doses of 10–20mg daily, S23 produces near complete suppression of LH, FSH, and endogenous testosterone; requiring a robust SERM based PCT protocol comparable to a traditional anabolic steroid cycle. In terms of anabolic potency, S23 produces the strongest lean mass, fat loss, and muscle hardness effects of any SARM. Making it the choice for researchers seeking maximum SARM efficacy at the cost of the most significant suppression management requirements.
S23 produces near complete HPG axis suppression, a full SERM based PCT protocol comparable to traditional anabolic steroid PCT is required following S23 research cycles. A common PCT protocol following S23 research uses Nolvadex 40mg daily for weeks 1–2, then 20mg daily for weeks 3–4, optionally combined with Clomiphene 50mg daily for weeks 1–2 then 25mg for weeks 3–4 for additional FSH stimulation. HCG priming before PCT commencement is also commonly researched following longer or higher dose S23 cycles to restore testicular sensitivity before SERM based HPG axis stimulation. Blood work before, during, and after the research cycle is essential.
S23 has a half-life of approximately 11.9 hours, administered once or twice daily in research protocols. Twice daily administration splitting the dose into morning and evening doses produces more stable plasma S23 levels and is preferred for tighter androgen receptor engagement throughout the day. Common research doses range from 10–20mg daily; a single 10mg tablet once daily at the conservative end, or two 10mg tablets split morning and evening for 20mg daily. The 50 tablet pack provides 500mg total, sufficient for 25–50 days of research at 10–20mg daily.
Yes! This batch has been independently HPLC tested by an accredited third party laboratory confirming concentration accuracy at 10mg per tablet and compound identity as S23. A certificate of analysis is available.
$66.14$88.20 (-25%)