{"product_id":"anadrolus-oxymetholone","title":"Anadrolus (Oxymetholone)","description":"\u003ch4\u003e\u003cspan class=\"\"\u003eAbout the Product\u003c\/span\u003e\u003c\/h4\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eAnadrolus\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e is a research compound from Driada Medical, containing \u003c\/span\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eOxymetholone\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e. Oxymetholone is a synthetic anabolic-androgenic steroid (AAS) and a 17α-alkylated derivative of dihydrotestosterone (DHT)\u003c\/span\u003e\u003ca href=\"https:\/\/data.bioontology.org\/ontologies\/NCIT\/classes\/http%3A%2F%2Fncicb.nci.nih.gov%2Fxml%2Fowl%2FEVS%2FThesaurus.owl%23C723?display=all\u0026amp;apikey=8b5b7825-538d-40e0-9e9e-5ab9274a9aeb\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e. Its chemical formula is C₂₁H₃₂O₃, with a molecular weight of 332.5 g\/mol\u003c\/span\u003e\u003ca href=\"http:\/\/www.nipne.ro\/rjp\/2015_60_7-8\/RomJPhys.60.p1112.pdf#1#1\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e, a CAS number of 434-07-1\u003c\/span\u003e\u003ca href=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/S0006295219304800?via%3Dihub\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e, and a logP of 4.22\u003c\/span\u003e\u003ca href=\"http:\/\/www.nipne.ro\/rjp\/2015_60_7-8\/RomJPhys.60.p1112.pdf#1#1\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cspan class=\"\"\u003eThe compound is characterized by two key structural features:\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003e17α-methyl group\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e: Provides steric hindrance against hepatic metabolism, enabling oral bioavailability in research models, but is also associated with significant hepatotoxic effects\u003c\/span\u003e\u003ca href=\"https:\/\/read.qxmd.com\/read\/8527826\/toxic-effects-of-anabolic-androgenic-steroids-in-primary-rat-hepatic-cell-cultures?redirected=slug\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003ca href=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/105687199400073D\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003e2-hydroxymethylene modification\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e: Distinguishes it from other AAS and contributes to its unique receptor binding profile\u003c\/span\u003e\u003ca href=\"https:\/\/data.bioontology.org\/ontologies\/NCIT\/classes\/http%3A%2F%2Fncicb.nci.nih.gov%2Fxml%2Fowl%2FEVS%2FThesaurus.owl%23C723?display=all\u0026amp;apikey=8b5b7825-538d-40e0-9e9e-5ab9274a9aeb\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cspan class=\"\"\u003eThe product is intended for \u003c\/span\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003elaboratory research use only\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e and features an integrated QR code on the packaging for detailed product verification.\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eProduct Name:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e Anadrolus (Oxymetholone)\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eBrand:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e Driada Medical\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eForm:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e Solution for research applications\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eCAS:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e 434-07-1\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eFor Research Use Only.\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003chr\u003e\n\u003ch4\u003e\u003cspan class=\"\"\u003eResearch Applications \u0026amp; Mechanism of Action\u003c\/span\u003e\u003c\/h4\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eAndrogen Receptor Agonist with Low Binding Affinity:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e Oxymetholone functions as an agonist at the androgen receptor (AR). Research shows it has a \u003c\/span\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003elow binding affinity\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e for the AR but is a \u003c\/span\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003epotent activator\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e of AR-mediated signaling\u003c\/span\u003e\u003ca href=\"https:\/\/data.bioontology.org\/ontologies\/NCIT\/classes\/http%3A%2F%2Fncicb.nci.nih.gov%2Fxml%2Fowl%2FEVS%2FThesaurus.owl%23C723?display=all\u0026amp;apikey=8b5b7825-538d-40e0-9e9e-5ab9274a9aeb\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e. It demonstrates an interaction energy of -1350.53 kcal\/mol and a predicted binding free energy (ΔG) of -8.83 kcal\/mol (compared to -1400.63 and -10.06 for testosterone)\u003c\/span\u003e\u003ca href=\"http:\/\/www.nipne.ro\/rjp\/2015_60_7-8\/RomJPhys.60.p1112.pdf#1#1\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eErythropoiesis Stimulation:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e Oxymetholone enhances the production and urinary excretion of erythropoietin in research models, stimulating erythropoiesis in anemias due to deficient red cell production\u003c\/span\u003e\u003ca href=\"https:\/\/info.caremark.com\/content\/dam\/enterprise\/caremark\/microsites\/dig\/pdfs\/pa-fep\/fep-rationale\/FEP_Rationale_Oxandrin.pdf#1#1\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eProtein Anabolism:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e The primary mechanism is the ability to increase \u003c\/span\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eprotein synthesis\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e and enhance \u003c\/span\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003enitrogen retention\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e in muscle cells via androgen receptor activation\u003c\/span\u003e\u003ca href=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/S0041008X25003503\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003ca href=\"https:\/\/data.bioontology.org\/ontologies\/NCIT\/classes\/http%3A%2F%2Fncicb.nci.nih.gov%2Fxml%2Fowl%2FEVS%2FThesaurus.owl%23C723?display=all\u0026amp;apikey=8b5b7825-538d-40e0-9e9e-5ab9274a9aeb\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eSteroidogenesis Research:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e Studies demonstrate that oxymetholone decreases corticosteroid but increases dehydroepiandrosterone (DHEA) biosynthesis in H295R cells, suggesting \u003c\/span\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eCYP21A2 inhibition\u003c\/span\u003e\u003c\/strong\u003e\u003ca href=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/S0006295219304800?via%3Dihub\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003ca href=\"https:\/\/www.mendeley.com\/catalogue\/be30f103-7390-3a15-bb5f-9f2b72e67bf0\/\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eOxidative Stress Research:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e Animal studies show that oxymetholone significantly increases oxidative stress markers (MDA) while depleting antioxidant defenses (GSH, catalase, SOD), and upregulates pro-inflammatory genes (TNF-α, NF-κB, STAT3) while downregulating antioxidant genes (Nrf2, CAT, SOD)\u003c\/span\u003e\u003ca href=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/S0041008X25003503\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003ca href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC4983678\/\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eHepatotoxicity Research:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e Oxymetholone demonstrates direct toxicity to hepatocytes in vitro at 1 × 10⁻⁴ M concentrations, causing significant increases in LDH release (plasma membrane damage), decreased cell viability, and glutathione depletion within 2-6 hours\u003c\/span\u003e\u003ca href=\"https:\/\/read.qxmd.com\/read\/8527826\/toxic-effects-of-anabolic-androgenic-steroids-in-primary-rat-hepatic-cell-cultures?redirected=slug\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003ca href=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/105687199400073D\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003chr\u003e\n\u003ch4\u003e\u003cspan class=\"\"\u003eResearch \u0026amp; Scientific Background\u003c\/span\u003e\u003c\/h4\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eChemical Background:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e Oxymetholone is an orally active 17α-alkylated DHT derivative with an androgenic:anabolic ratio of 1:1 to 1:3 in rodent models. The 17α-methyl group confers oral bioavailability but is also responsible for the compound's narrow therapeutic index\u003c\/span\u003e\u003ca href=\"https:\/\/info.caremark.com\/content\/dam\/enterprise\/caremark\/microsites\/dig\/pdfs\/pa-fep\/fep-rationale\/FEP_Rationale_Oxandrin.pdf#1#1\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003ca href=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/S0041008X25003503\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003ca href=\"https:\/\/data.bioontology.org\/ontologies\/NCIT\/classes\/http%3A%2F%2Fncicb.nci.nih.gov%2Fxml%2Fowl%2FEVS%2FThesaurus.owl%23C723?display=all\u0026amp;apikey=8b5b7825-538d-40e0-9e9e-5ab9274a9aeb\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eClinical Context:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e Clinically, oxymetholone (Anadrol-50) is FDA-approved for the treatment of anemias caused by deficient red cell production, including acquired aplastic anemia, congenital aplastic anemia, myelofibrosis, and hypoplastic anemias due to myelotoxic drugs\u003c\/span\u003e\u003ca href=\"https:\/\/info.caremark.com\/content\/dam\/enterprise\/caremark\/microsites\/dig\/pdfs\/pa-fep\/fep-rationale\/FEP_Rationale_Oxandrin.pdf#1#1\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eAndrogen Receptor Binding Research:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e Computational studies demonstrate that oxymetholone is predicted to bind to multiple nuclear hormone receptors beyond the androgen receptor, including the estrogen receptor, thyroid receptor, and orphan nuclear receptors\u003c\/span\u003e\u003ca href=\"http:\/\/www.nipne.ro\/rjp\/2015_60_7-8\/RomJPhys.60.p1112.pdf#1#1\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e. This suggests potential non-specific binding that may contribute to its side-effect profile.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eHepatotoxicity Research:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e The compound has known boxed warnings for peliosis hepatitis (liver tissue replaced with blood-filled cysts), liver cell tumors, and adverse blood lipid changes. In human case reports, severe jaundice (bilirubin up to 21.9 mg\/dL) and hepatic coma have occurred within 6-8 weeks of therapy\u003c\/span\u003e\u003ca href=\"https:\/\/info.caremark.com\/content\/dam\/enterprise\/caremark\/microsites\/dig\/pdfs\/pa-fep\/fep-rationale\/FEP_Rationale_Oxandrin.pdf#1#1\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003ca href=\"https:\/\/www.be-md.ncbi.nlm.nih.gov\/books\/NBK548931\/pdf\/Bookshelf_NBK548931.pdf#9#4\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e. The direct toxicity of the 17α-alkylated structure has been confirmed in primary rat hepatic cell cultures, with oxymetholone showing significant LDH release and cell viability decreases at 1 × 10⁻⁴ M for 4 and 24 hours, and glutathione depletion within 2, 4, and 6 hours\u003c\/span\u003e\u003ca href=\"https:\/\/read.qxmd.com\/read\/8527826\/toxic-effects-of-anabolic-androgenic-steroids-in-primary-rat-hepatic-cell-cultures?redirected=slug\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003ca href=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/105687199400073D\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eOxidative Stress \u0026amp; Inflammatory Research:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e Recent rodent studies demonstrate that oxymetholone exposure increases serum ALT, AST, urea, creatinine, and MDA while depleting GSH. It upregulates pro-inflammatory genes (TNF-α, NF-κB, STAT3) and downregulates antioxidant genes (Nrf2, CAT, SOD), with histopathological examination revealing extensive liver and kidney damage\u003c\/span\u003e\u003ca href=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/S0041008X25003503\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e. Similar findings in mice (5 mg\/kg\/day for 30 days) showed significant decreases in total antioxidant capacity and catalase activity, and increased lipid peroxidation\u003c\/span\u003e\u003ca href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC4983678\/\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp class=\"ds-markdown-paragraph\"\u003e\u003cstrong\u003e\u003cspan class=\"\"\u003eGenetic Variability Research:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan class=\"\"\u003e While direct studies on oxymetholone pharmacogenomics are limited, the field of pharmacogenomics indicates that genetic variations in drug-metabolizing enzymes (e.g., CYP3A4, UGTs) can significantly influence compound response and toxicity. The compound's distinct CYP21A2 inhibition profile and receptor binding dynamics provide a basis for investigating genetic factors affecting individual susceptibility\u003c\/span\u003e\u003ca href=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/S0006295219304800?via%3Dihub\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003ca href=\"https:\/\/www.mendeley.com\/catalogue\/be30f103-7390-3a15-bb5f-9f2b72e67bf0\/\" rel=\"noreferrer\" style=\"cursor: default;\" target=\"_blank\"\u003e\u003c\/a\u003e\u003cspan class=\"\"\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"Driada","offers":[{"title":"Default Title","offer_id":58726430769477,"sku":null,"price":42.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1077\/7614\/7781\/files\/Driada-Anadrolus.jpg?v=1785449704","url":"https:\/\/genetic-peps.shop\/products\/anadrolus-oxymetholone","provider":"Genetic Peps","version":"1.0","type":"link"}