Oxyolrol 50

Price range: $20.00 through $35.00

Chemical Information and Molecular Architecture

To truly understand how oxyolrol 50 behaves in laboratory assays, chromatographic analysis, and experimental models, one must examine the intricate molecular architecture of oxymetholone.

Molecular Specifications of Oxymetholone

  • Chemical Name: 17-beta-hydroxy-2-(hydroxymethylene)-17-methyl-5-alpha-androstan-3-one
  • Base Chemical Formula: C21H32O3
  • Molecular Weight: 332.48 g/mol
  • Core Structure: Oxymetholone is a synthetic derivative of dihydrotestosterone (DHT). However, its molecular structure features two major modifications that radically alter its biological activity:
    1. Addition of a 2-hydroxymethylene group: This specific structural alteration at the carbon-2 position enhances its anabolic potency significantly while also increasing its binding affinity for estrogen receptors (despite lacking direct aromatization into estradiol).
    2. C17-alpha alkylation: The addition of a methyl group at the 17th carbon position protects the hormone from hepatic degradation, allowing it to survive oral ingestion (though in oxyolrol 50, this alkylation remains part of the molecule’s core structure).

Receptor Interactions and Pharmacodynamics

Oxymetholone is renowned for its low relative binding affinity for the classical androgen receptor, yet it exhibits extreme anabolic activity in vivo. This paradox has fascinated endocrinologists for decades, suggesting that a significant portion of oxymetholone’s anabolic signaling occurs through non-genomic pathways, upregulation of growth factors, or unique protein-synthesis cascades.

Furthermore, because oxymetholone does not convert to estrogen via the aromatase enzyme yet exhibits strong estrogenic side effects in clinical models, researchers theorize that the molecule itself (or its metabolites) may possess intrinsic estrogen receptor agonist activity. Studying these unique pathways via oxyolrol 50 provides researchers with cleaner analytical models free from oral excipient interference.

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