Description ACTH (1–39) is a full-length peptide form of adrenocorticotropic hormone, studied for its role in stimulating adrenal cortisol production. It is commonly used in research involving the hypothalamic-pituitary-adrenal (HPA) axis and stress response mechanisms.
Anastrozole is a powerful aromatase inhibitor (AI) that works by blocking the aromatase enzyme, responsible for converting testosterone into estrogen. It is widely used in performance enhancement cycles to control estrogen levels, preventing side effects like gynecomastia (male breast tissue development), water retention, and high blood pressure. By keeping estrogen levels low, Anastrozole helps promote a harder, more defined appearance, making it especially useful during cutting and competition preparation. It…
Boldenone Undecylenate is an esterified derivative of boldenone, a synthetic anabolic steroid structurally similar to testosterone. The undecylenate ester significantly prolongs the compound’s half-life, providing a gradual and sustained release into the bloodstream, with a half-life of approximately 14 days. This makes it suitable for long-term studies involving anabolic processes. Research on boldenone undecylenate has highlighted its capacity to promote protein…
Boldenone Undecylenate is an esterified derivative of boldenone, a synthetic anabolic steroid structurally similar to testosterone. The undecylenate ester significantly prolongs the compound’s half-life, providing a gradual and sustained release into the bloodstream, with a half-life of approximately 14 days. This makes it suitable for long-term studies involving anabolic processes. Research on boldenone undecylenate has highlighted its capacity to promote protein…
Boldenone Undecylenate is an esterified derivative of boldenone, a synthetic anabolic steroid structurally similar to testosterone. The undecylenate ester significantly prolongs the compound’s half-life, providing a gradual and sustained release into the bloodstream, with a half-life of approximately 14 days. This makes it suitable for long-term studies involving anabolic processes. Research on boldenone undecylenate has highlighted its capacity to promote protein…
Description BPC-157 is a synthetic peptide composed of 15 amino acids, derived from a partial sequence of the naturally occurring body protection compound found in human gastric juice. It has gained attention in biomedical research due to its reported cytoprotective, angiogenic, and anti-inflammatory properties. The 250 mcg oral tablet form allows for convenient administration in controlled experimental environments. Studies…
Cabex (Cabergoline) is a synthetic ergoline-based dopamine D2 receptor agonist with high affinity and long-lasting effects. It has been extensively studied for its ability to suppress prolactin secretion by acting directly on dopamine receptors in the anterior pituitary gland. This mechanism makes it relevant in research related to hyperprolactinemia, reproductive hormone regulation, and endocrine balance. In experimental contexts, cabergoline has…
Cabex (Cabergoline) is a synthetic ergoline-based dopamine D2 receptor agonist with high affinity and long-lasting effects. It has been extensively studied for its ability to suppress prolactin secretion by acting directly on dopamine receptors in the anterior pituitary gland. This mechanism makes it relevant in research related to hyperprolactinemia, reproductive hormone regulation, and endocrine balance. In experimental contexts, cabergoline has…
Description CJC-1295 with DAC (Drug Affinity Complex) is a modified version of CJC-1295, a synthetic peptide that mimics the action of growth hormone-releasing hormone (GHRH). The addition of the DAC component enables the peptide to bind covalently to albumin in the bloodstream, dramatically extending its half-life—often up to 7–10 days—compared to the few minutes seen with native GHRH. This…
Description CJC-1295 is a tetrasubstituted peptide designed to mimic the action of growth hormone-releasing hormone (GHRH) while offering enhanced stability and prolonged half-life through binding to albumin via a Drug Affinity Complex (DAC). This modification allows for sustained elevation of endogenous GH and IGF-1 levels for up to a week following administration. Research has focused on CJC-1295’s potential to…
Clenbuterol hydrochloride is a β2-adrenergic agonist that has been widely researched for its ability to stimulate the central nervous system and promote thermogenesis. It is frequently studied for its effects on increasing metabolic rate, enhancing oxygen uptake, and supporting lean tissue maintenance during catabolic conditions. Clenbuterol has also been examined for its role in improving aerobic capacity and muscle endurance by…
Clomid (Clomiphene Citrate) is a non-steroidal selective estrogen receptor modulator (SERM) that has been extensively studied for its ability to bind to estrogen receptors in the hypothalamus, thereby inhibiting negative feedback from estrogen. This mechanism stimulates the release of gonadotropins, which in turn promotes the production of luteinizing hormone (LH) and follicle-stimulating hormone (FSH), leading to an increase in endogenous testosterone…
