{"product_id":"superdrol-10mg","title":"Superdrol 10mg","description":"\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eProduct name:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e Superdrol — Paragon Pharmatech\u003c\/span\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003eStrength per capsule:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e 10 mg Superdrol\u003c\/span\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003eCapsules per bottle:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e 60 vegetarian capsules\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eOther names:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e Methasterone; Methyldrostanolone; 2α,17α-dimethyl-5α-androstan-17β-ol-3-one; designer anabolic steroid; DHT‑derived anabolic agent\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eCAS number:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e3381-88-2\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eChemical structure (summary):\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eSuperdrol (methasterone) is a synthetic derivative of dihydrotestosterone (DHT) characterized by \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e17α‑methylation\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e, which allows oral bioavailability, and \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e2α‑methyl substitution\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e, which alters anabolic and androgenic activity. The molecule contains a steroid nucleus composed of four fused cycloalkane rings with a ketone group at C3 and hydroxyl group at C17.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eMolecular formula:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e C21H34O2\u003c\/span\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003eMolecular weight:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e 318.49 g\/mol\u003c\/span\u003e\u003cbr\u003e\u003cstrong\u003e\u003cspan\u003eChemical class:\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e 17α‑alkylated anabolic‑androgenic steroid (AAS), DHT derivative\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003chr\u003e\u003c\/div\u003e\n\u003ch1\u003e\u003cspan\u003e10 Strong Points \u0026amp; Benefits \u003c\/span\u003e\u003c\/h1\u003e\n\u003col data-spread=\"false\" start=\"1\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eDemonstrates strong anabolic activity in experimental and historical pharmacologic studies of DHT‑derived compounds.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eOral bioavailability due to 17α‑alkylation allows pharmacokinetic and endocrine research without parenteral administration.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eDHT‑derived structure prevents aromatization to estrogen, enabling research on androgenic signaling without estrogenic conversion.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003ePotent stimulation of protein synthesis pathways observed in cellular and animal models of androgen receptor activation.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eIncreased nitrogen retention and lean tissue accretion documented in studies of comparable anabolic agents.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eUseful experimental model for studying androgen receptor signaling and muscle hypertrophy pathways.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eDemonstrates measurable effects on erythropoiesis and hematologic parameters in androgen research.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eProvides insights into lipid metabolism and hepatic enzyme responses to 17α‑alkylated steroids.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eValuable research tool for examining endocrine feedback mechanisms and HPG axis suppression.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eChemically stable small molecule suitable for analytical characterization using HPLC, GC‑MS, and NMR methods.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003cdiv\u003e\u003chr\u003e\u003c\/div\u003e\n\u003ch1\u003e\u003cspan\u003eOverview\u003c\/span\u003e\u003c\/h1\u003e\n\u003cp\u003e\u003cspan\u003eSuperdrol (methasterone) is a synthetic anabolic‑androgenic steroid derived from dihydrotestosterone and structurally related to drostanolone. It was originally described in pharmaceutical literature in the mid‑20th century but was never widely marketed as a prescription medication. In the early 2000s it appeared in dietary supplement markets before being prohibited in multiple jurisdictions due to its pharmacologic potency and potential toxicity.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eFrom a scientific perspective, methasterone is notable for its strong anabolic properties and resistance to aromatization. The compound binds to androgen receptors in skeletal muscle and other tissues, promoting transcription of genes involved in protein synthesis, nitrogen retention, and cellular growth.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eResearch interest in compounds such as methasterone extends beyond performance physiology into endocrinology, hepatology, and cardiovascular research. 17α‑alkylated anabolic steroids are frequently used as models for studying hepatic metabolism, lipid alterations, and hormonal feedback mechanisms.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eParagon Pharmatech manufactures Superdrol capsules under controlled conditions with identity, purity, and potency testing suitable for laboratory and scientific research applications.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003chr\u003e\u003c\/div\u003e\n\u003ch1\u003e\u003cspan\u003eHow It Works \u003c\/span\u003e\u003c\/h1\u003e\n\u003ch2\u003e\u003cspan\u003eAndrogen Receptor Activation\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eSuperdrol binds to intracellular androgen receptors, forming a ligand‑receptor complex that translocates to the nucleus and regulates transcription of androgen‑responsive genes. These genes influence protein synthesis, satellite cell activation, and muscle fiber hypertrophy.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e\u003cspan\u003eProtein Synthesis and Nitrogen Retention\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eActivation of androgen signaling increases ribosomal activity and translational efficiency, resulting in increased synthesis of contractile proteins such as actin and myosin. Nitrogen retention improves the anabolic environment of skeletal muscle tissue.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e\u003cspan\u003eErythropoiesis and Hematologic Effects\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eAndrogens stimulate erythropoietin production and bone marrow activity, increasing red blood cell mass and hemoglobin levels in experimental studies.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e\u003cspan\u003eLipid and Metabolic Effects\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003e17α‑alkylated anabolic steroids commonly reduce HDL cholesterol and may increase LDL cholesterol. These effects are widely documented and provide a model for studying steroid‑induced dyslipidemia.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e\u003cspan\u003eHepatic Metabolism\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eOral anabolic steroids undergo hepatic metabolism via cytochrome P450 enzymes. Structural alkylation at the 17α position slows hepatic breakdown but increases hepatic strain, making such compounds useful models for hepatotoxicity research.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e\u003cspan\u003eEndocrine Feedback Mechanisms\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eExogenous androgens suppress luteinizing hormone (LH) and follicle‑stimulating hormone (FSH) through negative feedback at the hypothalamus and pituitary, reducing endogenous testosterone production. This mechanism is well established in endocrine studies.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003chr\u003e\u003c\/div\u003e\n\u003ch1\u003e\u003cspan\u003eWhat Studies Have Shown \u003c\/span\u003e\u003c\/h1\u003e\n\u003ch2\u003e\u003cspan\u003eAndrogenic and Anabolic Research\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eStudies of DHT‑derived anabolic agents demonstrate increased lean mass, protein synthesis, and nitrogen retention in animal models and clinical settings involving related compounds. These findings form the mechanistic basis for understanding methasterone’s pharmacology.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e\u003cspan\u003eHepatic Effects of 17α‑Alkylated Steroids\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eClinical and toxicologic literature documents elevated liver enzymes and cholestatic injury associated with oral anabolic steroids. These observations provide important insights into steroid metabolism and hepatotoxic mechanisms.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e\u003cspan\u003eCardiovascular and Lipid Research\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eResearch consistently shows reductions in HDL cholesterol and increases in LDL cholesterol in subjects exposed to anabolic steroids. These findings have been used to study mechanisms of atherosclerosis and lipid transport.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e\u003cspan\u003eEndocrine Suppression\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eControlled endocrine studies of anabolic steroids demonstrate suppression of the hypothalamic–pituitary–gonadal axis, decreased endogenous testosterone production, and reversible hypogonadism following cessation.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e\u003cspan\u003eMuscle Physiology and Hypertrophy\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eExperimental studies of androgen receptor activation demonstrate increased myonuclear number, enhanced satellite cell activity, and increased muscle fiber cross‑sectional area.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e\u003cspan\u003eEvidence Synthesis\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eOverall evidence indicates strong anabolic and androgenic activity, well‑characterized endocrine effects, and predictable metabolic and hepatic responses consistent with other 17α‑alkylated anabolic steroids.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003chr\u003e\u003c\/div\u003e\n\u003ch1\u003e\u003cspan\u003eUsage \u0026amp; Quality Compliance \u003c\/span\u003e\u003c\/h1\u003e\n\u003cp\u003e\u003cspan\u003eSuperdrol capsules are manufactured under GMP‑aligned conditions. Each batch undergoes:\u003c\/span\u003e\u003c\/p\u003e\n\u003cul data-spread=\"false\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eIdentity testing by HPLC or LC‑MS\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003ePotency assay\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eResidual solvent testing\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eHeavy metal analysis\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eMicrobiological testing\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eStability testing\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003cspan\u003eResearch protocols may include monitoring of:\u003c\/span\u003e\u003c\/p\u003e\n\u003cul data-spread=\"false\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eHormonal panels (LH, FSH, testosterone)\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eLiver function tests (ALT, AST, ALP, bilirubin)\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eLipid profiles\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eHematology parameters\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eCardiovascular markers\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003cspan\u003eRandomized and controlled experimental designs are recommended to ensure reproducibility and safety oversight.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003chr\u003e\u003c\/div\u003e\n\u003ch1\u003e\u003cspan\u003eSafety Note\u003c\/span\u003e\u003c\/h1\u003e\n\u003cp\u003e\u003cspan\u003eMethasterone and related compounds may cause:\u003c\/span\u003e\u003c\/p\u003e\n\u003cul data-spread=\"false\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eElevation of liver enzymes and hepatotoxicity\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eAdverse lipid profile changes\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eSuppression of endogenous testosterone production\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eIncreased hematocrit\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003ePotential cardiovascular strain\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003cspan\u003eLong‑term safety data in humans are limited, and compounds of this class are regulated or prohibited in many jurisdictions. Research involving such agents should be conducted under appropriate ethical and regulatory oversight.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003chr\u003e\u003c\/div\u003e\n\u003ch1\u003e\u003cspan\u003eFull Reference List (Clickable Links)\u003c\/span\u003e\u003c\/h1\u003e\n\u003cp\u003e\u003cspan\u003eKicman AT. Pharmacology of anabolic steroids. British Journal of Pharmacology.\u003c\/span\u003e\u003cbr\u003e\u003ca disabled\u003e\u003cspan\u003ehttps:\/\/pubmed.ncbi.nlm.nih.gov\/15226172\/\u003c\/span\u003e\u003c\/a\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eBasaria S. Androgen abuse and cardiovascular risk. Journal of Clinical Endocrinology \u0026amp; Metabolism.\u003c\/span\u003e\u003cbr\u003e\u003ca disabled\u003e\u003cspan\u003ehttps:\/\/pubmed.ncbi.nlm.nih.gov\/20371619\/\u003c\/span\u003e\u003c\/a\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eHartgens F, Kuipers H. Effects of androgenic‑anabolic steroids in athletes.\u003c\/span\u003e\u003cbr\u003e\u003ca disabled\u003e\u003cspan\u003ehttps:\/\/pubmed.ncbi.nlm.nih.gov\/15248788\/\u003c\/span\u003e\u003c\/a\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eLiverTox: Anabolic Steroids and Liver Injury.\u003c\/span\u003e\u003cbr\u003e\u003ca disabled\u003e\u003cspan\u003ehttps:\/\/www.ncbi.nlm.nih.gov\/books\/NBK548931\/\u003c\/span\u003e\u003c\/a\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eNieschlag E, Behre HM. Testosterone and anabolic steroids: clinical pharmacology.\u003c\/span\u003e\u003cbr\u003e\u003ca disabled\u003e\u003cspan\u003ehttps:\/\/pubmed.ncbi.nlm.nih.gov\/2104626\/\u003c\/span\u003e\u003c\/a\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003chr\u003e\u003c\/div\u003e\n\u003cp\u003e\u003cspan\u003e© Paragon Pharmatech — Educational Material 2025. For scientific and educational purposes only.\u003cbr\u003e\u003cbr\u003e\u003cspan style=\"color: #ff2a00;\"\u003eRemember, this product is intended for research purposes only and should not be used for human consumption without proper medical guidance. As with any supplement, it is important to prioritize your health and safety, and to consult with a healthcare professional if you have any underlying health concerns before incorporating this product into your routine.\u003c\/span\u003e\u003cbr\u003e\u003cspan style=\"color: #ff2a00;\"\u003eThis product is not a food product. By acquiring this product, you are in full knowledge that it’s not a food, nor is it for human consumption and it’s for market research purposes only\u003c\/span\u003e\u003cbr\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv id=\"sconnect-is-installed\" style=\"display: none;\"\u003e2.14.0.0\u003c\/div\u003e\n\u003cdiv id=\"sconnect-is-installed\" style=\"display: none;\"\u003e2.14.0.0\u003c\/div\u003e\n\u003cdiv style=\"display: none;\" id=\"sconnect-is-installed\"\u003e2.14.0.0\u003c\/div\u003e","brand":"ProSuppz.Com","offers":[{"title":"Default Title","offer_id":56751894462796,"sku":"PP468","price":49.9,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0790\/2871\/5852\/files\/FWSuperdol002_1.png?v=1771415055","url":"https:\/\/prosuppz.com\/products\/superdrol-10mg","provider":"ProSuppz.Com","version":"1.0","type":"link"}