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MESTEROLONA · 50 MG | Andrógeno DHT  Rendimiento y Vitalidad Masculina

Product Details

  • Technical Name: Mesterolone 50 mg, Comprimidos para Uso Humano
  • Laboratory / Brand: Kinetix Pharma
  • Active Ingredient (INN): Mesterolona (1a-Metil-4,5a-dihidrotestosterona)
  • Pharmaceutical Form: Comprimidos para Administración Oral (Tabletas)
  • Concentration: 50 mg / comprimido
  • CAS Number: 1424-00-6
  • Internal SKU: SKU-MESTEROLONE-50MG-100TABS-1424006
Kinetix Pharma Mesterolona (1a-Metil-4,5a-dihidrotestosterona) Comprimidos para Administración Oral (Tabletas) CAS: 1424-00-6
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MESTEROLONA · 50 MG | Andrógeno DHT Rendimiento y Vitalidad Masculina

New Release Recovery Longevity & Performance

100 Servings Per Container: US$1.00 / serving

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US$99.99 USD
In stock (10,000 piece)
Mesterolone 50 mg tablets, from Pharma Kinetix, made in the Czech Republic. Each package contains 100 tablets of 50 mg each. This is a pharmaceutical-grade androgen product intended for human use. The active ingredient is Mesterolone, a synthetic androgen and anabolic-androgenic steroid (AAS) that is a derivative of dihydrotestosterone (DHT). Acts as a potent androgen receptor agonist with a relative binding affinity (RBA) of 25. Does not aromatize to estrogens. Indicated for the treatment of hypogonadism, oligospermia, loss of libido, and erectile dysfunction related to androgen deficiency. CAS: 1424-00-6. Molecular formula: C₂₀H₃₂O₂. Store at 2-8°C in a dry place protected from light. WARNING: This product is a prescription medication. It is classified as a Schedule III controlled substance in the United States. Its use must be supervised by a physician.

Mesterolone is a synthetic androgen and anabolic-androgenic steroid (AAS) derived from dihydrotestosterone (DHT), developed in the 1960s for the treatment of androgen deficiencies . Its chemical name is 1α-Methyl-4,5α-dihydrotestosterone, with molecular formula C₂₀H₃₂O₂ and a molecular weight of 304.467 g/mol . Unlike other androgens, mesterolone does not aromatize (convert to estrogen), meaning it lacks estrogenic effects . It is characterized by having a strong androgenic effect but a weak anabolic effect, making it useful primarily for its masculinizing effects rather than muscle-building properties . Its mechanism of action is based on its function as an agonist of the androgen receptor (AR), the biological target of androgens such as testosterone and DHT . Upon binding to the androgen receptor in the cytoplasm, it induces a conformational change that allows its translocation to the nucleus, where it dimerizes and binds to androgen response elements (AREs) on DNA, modulating gene expression in target tissues .

The problem it solves: Androgen deficiency in males can manifest as decreased libido, erectile dysfunction, fatigue, loss of muscle mass, increased body fat, and impaired cognitive function. Mesterolone directly addresses these deficiencies by acting as a potent androgen receptor agonist, restoring androgen activity levels without the risks associated with aromatization to estrogens.

Primary Benefit: Androgenic Support and Male Vitality

At its core, Mesterolone is designed to compensate for androgen deficiency in conditions such as male hypogonadism (low testosterone due to reduced gonadal function), oligospermia (low sperm count and male infertility), loss of libido and impotence related to androgen deficiency, and the decline in physical and intellectual capacity associated with aging and lower androgen levels . It acts as an androgen receptor agonist, binding to the receptor with a relative binding affinity (RBA) of 25 in rat prostate tissue (vs. methyltrienolone as reference 100) . Mesterolone demonstrates exceptionally high affinity for sex hormone-binding globulin (SHBG), approximately four times that of DHT, which can displace endogenous testosterone and increase levels of biologically active free testosterone .

Secondary Benefits: Reproductive Function and Performance

Mesterolone's specific action on the androgen receptor offers additional benefits that impact reproductive function and physical performance:

Improved Male Fertility: Both oligospermia and Leydig cell insufficiency may be causes of infertility. Mesterolone increases sperm count and improves their quality by raising and normalizing fructose concentration in the ejaculate, contributing to increased fertilization possibilities . In cases of oligospermia, a dosage of 50-75 mg per day for a spermatogenesis cycle (approximately 90 days) is recommended .

Stimulation of Secondary Sexual Characteristic Development: Mesterolone stimulates the growth, development, and function of effector organs under androgenic influence, as well as the development of secondary male sexual characteristics in cases of pre-pubertal androgen insufficiency .

Improved Physical and Intellectual Capacity: Mesterolone is indicated for the reduction of physical and intellectual capacities in middle and advanced age associated with declining androgen levels, contributing to better quality of life and overall performance .

No Estrogenic Effects: By not aromatizing to estrogens, Mesterolone does not produce estrogenic side effects such as gynecomastia or fluid retention, making it an attractive option for those seeking androgenic benefits without the risks associated with estrogen conversion .

Pairing Strategy: Mesterolone

Mesterolone is typically administered as a standalone agent for the treatment of androgen deficiency. In cases of hypogonadism with reduced gonadotropinuria, an additional initial treatment with gonadotropins may be considered . Combination with other androgens or hormonal agents is not recommended without proper medical supervision.
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MESTEROLONA · 50 MG | Andrógeno DHT Rendimiento y Vitalidad Masculina

Marketing Description (🇪🇸 Español) - 📢 Marketing

Mesterolone: Andrógeno DHT para Rendimiento y Vitalidad Masculina

Para el hombre que busca optimizar su rendimiento físico, mantener una función sexual saludable y preservar su vitalidad general, Mesterolone representa la herramienta androgénica más confiable y libre de efectos estrogénicos. Este derivado sintético de la DHT actúa como un potente agonista del receptor de andrógenos, restaurando los niveles de actividad androgénica sin los riesgos asociados a la aromatización.

Beneficio Principal: Soporte Androgénico y Vitalidad

Mesterolone actúa como un agonista del receptor de andrógenos, con una afinidad relativa (RBA) de 25 y una afinidad excepcionalmente alta por la SHBG (aproximadamente 4x la de DHT) . Los estudios clínicos han demostrado:

Mejora de la función eréctil y la libido en casos de deficiencia androgénica .

Aumento del conteo y calidad de espermatozoides en oligospermia .

Restauración de la capacidad física e intelectual en hombres de mediana edad .

Sin efectos estrogénicos ni aromatización .

Beneficios Adicionales: Función Reproductiva y Rendimiento

Fertilidad Mejorada: Normaliza la concentración de fructosa en el eyaculado, mejorando la calidad espermática .

Desarrollo de Características Sexuales: Estimula el desarrollo de características sexuales secundarias en insuficiencia androgénica .

Sin Efectos Estrogénicos: No se aromatiza a estrógenos, evitando ginecomastia y retención de líquidos .

Alta Afinidad por SHBG: Desplaza la testosterona endógena, aumentando los niveles de testosterona libre .

Ideal para la Terapia de Reemplazo Androgénico

Mesterolone es la elección perfecta para ciclos de terapia androgénica, donde el objetivo es restaurar la función hormonal masculina sin los riesgos asociados a otros andrógenos. Su perfil de seguridad y su mecanismo de acción específico lo convierten en una opción superior para el mantenimiento de la vitalidad masculina.

Key Benefits of Mesterolone Androgen Receptor Agonist for Hormonal Support Mesterolone acts as a potent androgen receptor (AR) agonist, binding to the receptor with a relative binding affinity (RBA) of 25 in rat prostate tissue (vs. methyltrienolone as reference 100) . Upon binding to the receptor in the cytoplasm, it induces a conformational change that allows translocation to the nucleus, where it dimerizes and binds to androgen response elements (AREs) on DNA, modulating gene expression in target tissues . This mechanism restores androgenic activity in conditions of hormonal deficiency. High SHBG Affinity to Increase Free Testosterone Mesterolone demonstrates exceptionally high affinity for sex hormone-binding globulin (SHBG), approximately four times that of DHT . This high affinity allows Mesterolone to displace endogenous testosterone from SHBG, increasing levels of biologically active free testosterone in the bloodstream. This effect is particularly beneficial for men with elevated SHBG levels, where total testosterone may be normal but free testosterone is reduced. Improved Erectile Function and Libido Mesterolone is indicated for the suppression of potency disturbances due to androgen deficiency . By restoring androgenic activity, it improves erectile function and sexual desire in men with reduced androgen levels. Clinical studies have demonstrated its efficacy in the treatment of erectile dysfunction related to hormonal deficiency. Increased Sperm Count and Quality Both oligospermia and Leydig cell insufficiency may be causes of infertility. Mesterolone increases sperm count and improves their quality by raising and normalizing fructose concentration in the ejaculate, contributing to increased fertilization possibilities . In cases of oligospermia, a treatment cycle of approximately 90 days (duration of one spermatogenesis cycle) is recommended . Restoration of Physical and Intellectual Capacity Mesterolone is indicated for the reduction of physical and intellectual capacities in middle and advanced age associated with declining androgen levels . By restoring androgenic activity, it contributes to improved energy, endurance, and cognitive function in men with hormonal deficiency. Absence of Estrogenic Effects Unlike other androgens such as testosterone, Mesterolone does not aromatize (convert to estrogens), meaning it lacks estrogenic effects . This eliminates the risks of side effects such as gynecomastia (breast tissue development in men), fluid retention, and hormonal axis suppression. This characteristic makes it an attractive option for those seeking androgenic benefits without the risks associated with estrogen conversion. Stimulation of Secondary Sexual Characteristic Development Mesterolone stimulates the growth, development, and function of effector organs under androgenic influence, as well as the development of secondary male sexual characteristics in cases of pre-pubertal androgen insufficiency . This effect includes the development of body and facial hair, voice deepening, and maintenance of muscle mass.
Function and Mechanism of Action of Mesterolone Mesterolone is a synthetic androgen and anabolic-androgenic steroid (AAS) derived from dihydrotestosterone (DHT) . Its chemical name is 1α-Methyl-4,5α-dihydrotestosterone, with molecular formula C₂₀H₃₂O₂ and a molecular weight of 304.467 g/mol . It was developed in the 1960s for the treatment of androgen deficiencies and has been used medically since then . Detailed Mechanism of Action: Androgen Receptor Binding: Mesterolone acts as a potent agonist of the androgen receptor (AR), a member of the nuclear receptor superfamily . It binds to the receptor with a relative binding affinity (RBA) of 25 in rat prostate tissue (vs. methyltrienolone as reference 100) . In comparison, DHT has an RBA of 46 and testosterone has lower affinity than DHT . Nuclear Translocation and Activation: Upon binding to the receptor in the cytoplasm, Mesterolone induces a conformational change that allows dissociation of heat shock proteins (HSPs) and translocation of the receptor-ligand complex to the nucleus . In the nucleus, the receptor dimerizes and binds to specific DNA sequences known as androgen response elements (AREs) in promoter or enhancer regions of target genes . Gene Expression Modulation: The AR-ligand complex binding to AREs facilitates recruitment of coactivator or corepressor proteins, which modulate transcriptional activity of target genes . The specific set of regulated genes determines the physiological response in the target tissue, including secondary sexual characteristic development, reproductive function, and muscle mass maintenance. High SHBG Affinity: Mesterolone demonstrates exceptionally high affinity for sex hormone-binding globulin (SHBG), approximately four times that of DHT . This high affinity allows Mesterolone to displace endogenous testosterone from SHBG, increasing levels of biologically active free testosterone. Absence of Aromatization: Unlike other androgens such as testosterone, Mesterolone does not aromatize (convert to estrogens), meaning it lacks estrogenic effects . This characteristic eliminates the risks of side effects such as gynecomastia, fluid retention, and hormonal axis suppression. Weak Anabolic Effect: Mesterolone is characterized by having a strong androgenic effect but a weak anabolic effect, making it useful primarily for its masculinizing effects rather than muscle-building properties
How to Use Mesterolone Route of Administration: Oral. Mesterolone is administered as tablets for oral ingestion. Tablets should be swallowed whole with water . Dosage: Dosage should be determined by a physician according to indications and patient condition. General dosage guidelines include: Hypogonadism (Development Therapy): 75-100 mg per day (1.5-2 tablets of 50 mg) for several months for secondary sexual characteristic development . Hypogonadism (Maintenance Therapy): 50 mg per day (1 tablet of 50 mg) . Oligospermia: 50-75 mg per day (1-1.5 tablets of 50 mg) for a spermatogenesis cycle (approximately 90 days) . Initial Average Dose: 50-75 mg per day divided into 2-3 administrations . Maintenance Dose: Normally 25 mg per day (half tablet of 50 mg) . Frequency: Daily doses are divided into 2-3 administrations throughout the day . Treatment Duration: Depends on the type and intensity of symptoms. Cycles of 4-6 weeks or prolonged continuous treatment for several months are recommended. Cyclic treatments may be repeated several times if necessary . Storage: Store in a cool, dry place, protected from light and at controlled temperature (2-8°C). Keep out of reach of children. Important Notice: Product intended FOR HUMAN USE under medical supervision. Mesterolone is a prescription medication and its use must be supervised by a physician. It is classified as a Schedule III controlled substance in the United States . Contraindications include prostate carcinoma, male breast cancer, liver tumors, hypercalcemia, and known hypersensitivity to androgens . Reported side effects include excessive sexual stimulation, nervousness, hypercalcemia, fluid retention, and hypersensitivity reactions in prolonged treatments
Ingredients of Mesterolone Active Ingredient: Mesterolone (1α-Methyl-4,5α-dihydrotestosterone): A synthetic androgen and anabolic-androgenic steroid (AAS) derived from dihydrotestosterone (DHT) . Acts as a potent androgen receptor agonist, with a relative binding affinity (RBA) of 25 in rat prostate tissue . Does not aromatize to estrogens . Molecular formula: C₂₀H₃₂O₂. Molecular weight: 304.467 g/mol . CAS: 1424-00-6 . Excipients: Each 50 mg tablet contains the following excipients (according to standard mesterolone formulations such as Proviron): Lactose monohydrate: Used as an excipient and bulking agent. Corn starch: Used as a disintegrant and bulking agent. Povidone (PVP): Used as a binder. Stearic acid: Used as a lubricant. Magnesium stearate: Used as a lubricant. Microcrystalline cellulose: Used as a bulking agent and disintegrant. Note: Specific excipients may vary by manufacturer. Consult the product leaflet for the complete list of excipients. Note for Users: This product is a pharmaceutical-grade medication manufactured under strict quality control standards (GMP) in the Czech Republic by Pharma Kinetix. Each package contains 100 tablets of 50 mg each. Mesterolone is classified as a Schedule III controlled substance in the United States
Onset Time & Expected Results of Mesterolone Onset of Action (Days to Weeks): Mesterolone begins acting within the first hours or days after oral administration. Effects on erectile function, libido, and energy levels may be observed within the first days of treatment. Improvement in sperm quality and fertility parameters require a complete spermatogenesis cycle. Measurable Benefits (2-4 Weeks): The first measurable changes in sexual function, libido, and energy levels begin to be visible within the first 2-4 weeks of consistent use. Clinical studies have demonstrated improvements in erectile function and sexual desire during this period. Full Effect (12-16 Weeks): For complete improvement in sperm quality and fertility parameters, the full effect requires a complete spermatogenesis cycle of approximately 90 days (12-16 weeks) . For secondary sexual characteristic development in hypogonadism, treatment may require several months . Factors Influencing Results: The speed and magnitude of results depend on dose administered, administration frequency, adherence to the treatment protocol, the patient's baseline condition, and individual metabolism.
Clinical Research & 3rd Party Test Results of Mesterolone Scientific evidence on Mesterolone comes from clinical studies and decades of medical use, as well as laboratory studies demonstrating its mechanism of action. Clinical Evidence in Humans: Hypogonadism Treatment: Mesterolone is indicated for the treatment of male hypogonadism, stimulating the growth, development, and function of effector organs under androgenic influence . In cases of pre-pubertal hypogonadism, it promotes the development of secondary male sexual characteristics . Oligospermia Treatment: Mesterolone increases sperm count and improves their quality by raising and normalizing fructose concentration in the ejaculate . In cases of oligospermia, a cycle of 50-75 mg per day for a spermatogenesis cycle (approximately 90 days) is recommended . Erectile Dysfunction Treatment: Mesterolone suppresses potency disturbances due to androgen deficiency . The initial average dose is 50-75 mg per day divided into 2-3 administrations . Reduction of Physical and Intellectual Capacities: Mesterolone is indicated for the reduction of physical and intellectual capacities in middle and advanced age associated with declining androgen levels . Preclinical Evidence: Androgen Receptor Affinity: Competitive binding studies have demonstrated that Mesterolone has a relative binding affinity (RBA) of 25 for the androgen receptor in rat prostate tissue (vs. methyltrienolone as reference 100) . DHT has an RBA of 46 in the same assay . SHBG Affinity: Mesterolone demonstrates exceptionally high affinity for sex hormone-binding globulin (SHBG), approximately four times that of DHT . Absence of Aromatization: Studies have confirmed that Mesterolone does not aromatize to estrogens, meaning it lacks estrogenic effects . Safety Considerations: Contraindications: Prostate carcinoma, male breast cancer, liver tumors, hypercalcemia, and known hypersensitivity to androgens . Side Effects: In prolonged treatments, excessive sexual stimulation, nervousness, hypercalcemia, fluid retention, and hypersensitivity reactions may occur . Regulatory Status: Mesterolone is classified as a Schedule III controlled substance in the United States . Kinetix Pharma Quality Standards: Pharmaceutical Grade: Pharmaceutical-grade product for human use. Manufacturing: Manufactured in the Czech Republic under strict GMP standards. Quality Control: Each batch is subjected to quality control testing to ensure purity and potency.

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MESTEROLONA · 50 MG | Andrógeno DHT  Rendimiento y Vitalidad Masculina MESTEROLONA · 50 MG | Andrógeno DHT Rendimiento y Vitalidad Masculina MESTEROLONA · 50 M…
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