Showing 33–48 of 414 resultsSorted by popularity
Anastrozole (Arimidex) is a benzyltriazole-derived Type II non-steroidal aromatase inhibitor that competitively binds the heme group of CYP19A1, blocking androgen-to-estrogen conversion. A reversible, high-fidelity tool for precise estrogen modulation research.
HCG functions biologically almost identically to pituitary-derived luteinizing hormone (LH).
TB500 (Thymosin Beta-4 Acetate) is a synthetic 43-amino acid polypeptide that binds G-actin to facilitate endothelial cell migration and tissue regeneration. It physically mobilizes reparative cells to injury sites, which makes it essential for accelerated wound healing and connective tissue repair research.
MOTS-c is a mitochondrial-derived 16-amino acid peptide encoded by the mitochondrial genome that activates AMPK to drive insulin-independent glucose uptake and fatty acid oxidation. It mimics exercise-induced metabolic adaptations and is a key tool for energy homeostasis research.
Clomiphene Citrate (Clomid) is a triarylethylene SERM that competitively blocks hypothalamic estrogen receptors, lifting negative feedback inhibition to stimulate endogenous LH and FSH secretion. A pillar compound for HPTA restoration and fertility research.
Sustanon 250 is a multi-ester testosterone blend (Propionate, Phenylpropionate, Isocaproate, Decanoate) engineered for a bimodal pharmacokinetic profile with a 15-18 day terminal half-life. It provides both immediate receptor saturation and prolonged steady-state androgen levels.
Long-acting GLP-1 receptor agonist for appetite regulation and metabolic research. Investigate weight management pathways.
KLOW is a thorough quad-peptide regenerative matrix combining GHK-Cu, BPC 157, TB-500, and KPV. It coordinates collagen remodeling, angiogenesis, cellular migration, and NF-kB anti-inflammatory signaling for combined-action soft-tissue and musculoskeletal repair.
Retatrutide (LY3437943) is an agonist of the glucose-dependent insulinotropic polypeptide, glucagon-like peptide 1, and glucagon receptors.
The data from the trials mentioned that Retatrutide is effective in reducing weight in individuals with nonsyndromic obesity.
5mg *10 vials *1 kits
AICAR (Acadesine) is a cell-permeable nucleoside analog that converts intracellularly to ZMP, potently activating AMPK to mimic exercise-induced metabolic stress. A staple tool for mitochondrial biogenesis, glucose uptake, and endurance-mimetic research.
Semaglutide is a long-acting GLP-1 receptor agonist featuring Aib substitution and fatty acid bioconjugation for DPP-4 resistance and a 7-day half-life. It stimulates glucose-dependent insulin secretion, suppresses glucagon release, and centrally modulates hypothalamic satiety pathways for strong appetite reduction.
End of content
End of content
No products in the cart.
