Twelve compounds grouped by the biological system researchers study them in. Every batch is HPLC purity tested and confirmed by mass spectrometry before release.
BPC-157 is a synthetic pentadecapeptide consisting of 15 amino acids. In laboratory settings, it is studied as a tool compound in endothelial signaling, epithelial cell model systems, nitric-oxide-associated pathways, and growth-factor-related signaling under controlled experimental conditions. Miss Peptides supplies BPC-157 at 5MG per vial for laboratory research use only.
GHK-Cu (Copper Peptide GHK-Cu) is a naturally occurring tripeptide-copper complex widely studied in laboratory and cosmetic research settings for its role in collagen metabolism, extracellular matrix remodeling, and wound-healing signaling pathways. Researchers use GHK-Cu as a consistent tool for exploring collagen synthesis regulation, matrix metalloproteinase (MMP) modulation, and controlled experimental models related to dermal fibroblast biology.
TB-500 (Thymosin β-4) is a naturally occurring 43-amino acid peptide widely studied in laboratory settings for its role in actin sequestration, cytoskeletal dynamics, and angiogenic signaling pathways.
Ipamorelin is a selective synthetic pentapeptide ghrelin mimetic studied in laboratory settings for its highly specific agonist activity at the growth hormone secretagogue receptor (GHS-R1a).
NAD+ (Nicotinamide Adenine Dinucleotide) is a ubiquitous biological coenzyme studied extensively in laboratory settings for its central roles in cellular energy metabolism, redox signaling, DNA repair, and sirtuin pathway regulation.
KPV (Lys-Pro-Val) is a tripeptide corresponding to the 11-13 region of alpha-melanocyte-stimulating hormone (alpha-MSH) and is studied in laboratory settings for its effects on inflammatory signaling pathways. Researchers employ KPV as a tool compound for exploring NF-kappaB-associated signaling, cytokine-regulation models, and controlled experimental systems in epithelial and immune-cell biology.
Sermorelin (GRF 1-29) is a synthetic 29-amino acid peptide corresponding to the biologically active N-terminal fragment of endogenous growth hormone-releasing hormone (GHRH). In laboratory settings, it is studied as a consistent tool for investigating GHRH receptor (GHRHR) activation, pituitary somatotroph signaling pathways, and controlled experimental models related to the hypothalamic-pituitary GH axis.
PT-141 (Bremelanotide) is a synthetic cyclic heptapeptide melanocortin receptor agonist studied in laboratory settings for its activity across multiple melanocortin receptor subtypes, including MC1R, MC3R, and MC4R.
Oxytocin is a naturally occurring nine-amino-acid (nonapeptide) hormone produced by the hypothalamic-pituitary system. It is widely studied in neuroscience, endocrinology, and receptor pharmacology for its interactions with the oxytocin receptor (OXTR) and associated downstream signaling pathways. Researchers use oxytocin as a consistent tool for exploring OXTR activation in controlled laboratory settings.
Out of stockCJC-1295 (DAC-GRF) is a synthetic GHRH analog engineered with a drug affinity complex (DAC) technology component that extends receptor interaction duration. In laboratory settings, it is studied as a consistent tool for investigating sustained GHRH receptor engagement, prolonged cAMP signaling cascades, and controlled experimental models related to GH-axis pharmacology.
AOD-9604 is a GH-derived peptide fragment, described in literature as Tyr-hGH(177-191), studied in laboratory settings for adipocyte signaling, metabolic pathway modeling, and related controlled experimental systems.
Palmitoyl Tripeptide-1 (pal-GHK) and Palmitoyl Tetrapeptide-7 (pal-GQPR) are lipid-conjugated matrikine peptides widely studied in cosmetic research settings for their roles in extracellular matrix signaling and collagen biosynthesis regulation. Researchers use these palmitoylated peptides as consistent tools for investigating matrikine receptor interactions, TGF-β pathway modulation, and controlled experimental models of dermal fibroblast signaling.