Search Results for: sermorelin

GHRP-2 5mg

GHRP-2 5mg

GHRP-2 is a synthetic hexapeptide growth hormone secretagogue that binds to the growth hormone secretagogue receptor (GHS-R1a), also known as the ghrelin receptor. In experimental models, GHRP-2 activates Gq/PLC and calcium-dependent intracellular signaling pathways that regulate growth hormone release and hypothalamic–pituitary axis feedback. Preclinical research has investigated its role in somatotropic signaling, sleep-related neuroendocrine pathways, immune-associated peptide signaling, and receptor pharmacology, including evaluation of non-injectable exposure routes under controlled laboratory conditions. 

For research use only. Not for human consumption. 

References: 
Bowers CY et al., Endocrinology, 1990 126(3):1223–1228 
Jacks T et al., Endocrinology, 1994 134(2):744–750 
Smith RG et al., Science, 1997 275(5304):1261–1264

GHRP-2 10mg

GHRP-2 10mg

GHRP-2 is a synthetic hexapeptide growth hormone secretagogue that binds to the growth hormone secretagogue receptor (GHS-R1a), also known as the ghrelin receptor. In experimental models, GHRP-2 activates Gq/PLC and calcium-dependent intracellular signaling pathways that regulate growth hormone release and hypothalamic–pituitary axis feedback. Preclinical research has investigated its role in somatotropic signaling, sleep-related neuroendocrine pathways, immune-associated peptide signaling, and receptor pharmacology, including evaluation of non-injectable exposure routes under controlled laboratory conditions. 

For research use only. Not for human consumption. 

References: 
Bowers CY et al., Endocrinology, 1990 126(3):1223–1228 
Jacks T et al., Endocrinology, 1994 134(2):744–750 
Smith RG et al., Science, 1997 275(5304):1261–1264

Gonadorelin 10mg

Gonadorelin 10mg

Gonadorelin is a research peptide corresponding to the natural gonadotropin-releasing hormone (GnRH), a decapeptide with the sequence pGlu-His-Trp-Ser-Tyr-Gly-Leu-Arg-Pro-Gly-NH₂. It binds to the GnRH receptor on pituitary gonadotrophs, activating Gq/11 protein–coupled signaling and stimulating the synthesis of gonadotropins in experimental models. Gonadorelin is utilized in studies exploring hypothalamic–pituitary axis regulation, peptide receptor kinetics, and endocrine feedback control mechanisms.

For research use only. Not for human consumption.

References:
Flanagan CA et al., Front Endocrinol (Lausanne), 2017;8:274
Millar RP et al., Front Neuroendocrinol, 2004;25(1):1–28
Limonta P et al., Peptides, 1999;20(3):347–363

Gut Inflammation (60 Capsules) (Stable BPC-157 Arginate, KPV, Larazotide)

Gut Inflammation (60 Capsules) (Stable BPC-157 Arginate

Gut Inflammation is a research formulation containing stable BPC-157, KPV, palmitoylethanolamide (PEA), and tributyrin designed for studies on intestinal barrier function and inflammatory modulation. Each component contributes to signaling pathways related to epithelial regeneration, cytokine balance, and microbiome–host interaction. This blend is used in preclinical research investigating mucosal peptide regulation and enteric homeostasis mechanisms.

References:
Sikiric P et al., Curr Pharm Des, 2018 24(18):2002–2030
Getting SJ et al., J Immunol, 1999 163(10):5959–5967
Di Paola R et al., Mol Neurobiol, 2018 55(6):4785–4799

These capsules are provided exclusively as inert containers for the dry transport, storage, and handling of laboratory research materials. They are not dosage forms and are not intended for ingestion or administration. They must not be used as drug delivery systems, consumed, or administered in any form. For Research Use Only: Not for use in humans or animals. Not for diagnostic or therapeutic purposes.

 

CJC-1295 (no DAC), Ipamorelin 10mg (Blend)

CJC-1295 (no DAC)

CJC-1295 (no DAC) and Ipamorelin is a research peptide blend combining two mechanistically distinct secretagogues that act synergistically on the growth hormone axis. CJC-1295 (Mod GRF 1–29) targets GHRH receptors, stimulating cAMP/PKA-mediated GH synthesis, while Ipamorelin binds the ghrelin receptor (GHS-R1a), activating Gq/11-linked calcium signaling pathways. Together, they serve as a model for studying peptide-induced GH pulsatility, receptor cross-talk, and hypothalamic–pituitary regulation in controlled experimental systems.

For research use only. Not for human consumption.

References:
Bowers CY et al., Endocrinology, 1990 126(2):1165–1171
Teichman SL et al., J Clin Endocrinol Metab, 2006 91(2):479–487
Kojima M et al., Nature, 1999 402(6762):656–660

DSIP 5mg

DSIP 5mg

DSIP (Delta Sleep-Inducing Peptide) is a research neuropeptide consisting of eight amino acids (Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu). It has been studied for its involvement in neuroendocrine regulation, sleep-related signaling, and stress adaptation through GABAergic and hypothalamic pathways. DSIP’s structure and physiological relevance make it an important subject in peptide neurobiology and circadian rhythm research.

For research use only. Not for human consumption.

References: 
Schoenenberger GA et al., Proc Natl Acad Sci USA, 1977 74(9):4025–4029
Graf MV et al., Neuropeptides, 1984 4(3):225–238
Antonijevic I et al., J Neuroendocrinol, 1992 4(4):431–439

FGL-S 10mg

FGL-S 10mg

FGL-S is a synthetic research peptide derived from the neural cell adhesion molecule (NCAM) sequence containing the fibroblast growth factor–like (FGL) domain. It has been shown in preclinical studies to promote neurite outgrowth, synaptogenesis, and neuroplasticity through activation of FGFR, ERK, and PI3K/Akt signaling pathways. FGL-S is used in experimental neurobiology to investigate mechanisms of neuronal regeneration, peptide-induced signaling, and synaptic remodeling.

For research use only. Not for human consumption.

References:
Cambon K et al., J Neurosci Res, 2004 77(5):730–739
Bisaz R et al., Eur J Neurosci, 2006 23(8):2045–2054
Chen ZY et al., Mol Cell Neurosci, 2010 43(3):329–339

AOD9604 6mg

AOD9604 6mg

AOD-9604 is a research peptide consisting of amino acids 177–191 of the human growth hormone sequence. Studies indicate it modulates lipid and glucose metabolism pathways without influencing IGF-1 activity, acting primarily through β-adrenergic and AMPK-related mechanisms. It is commonly used in metabolic and adipocyte differentiation research to elucidate downstream energy regulation signaling.

For research use only. Not for human consumption.

References: 
Heffernan MA et al., Eur J Endocrinol, 2001 144:511-517
Ng FM et al., Drug Dev Res, 2000 51:63-71
Ng FM et al., Metabolism, 2002 51(12):1739-1743

B7-33 6mg

B7-33 6mg

B7-33 is a single-chain relaxin-family peptide analog derived from human H2 relaxin, designed to selectively activate the RXFP1 receptor without engaging RXFP2. It modulates ERK1/2 signaling and nitric oxide synthesis in cardiac and vascular tissues under experimental conditions. B7-33 is used in receptor biology research focused on peptide-based GPCR signaling and cytoprotective mechanisms.

For research use only. Not for human consumption.

References: 
Hossain MA et al., Chem Sci, 2016 7(6):3805–3813
Chan LJ et al., Br J Pharmacol, 2012 165(8):2612–2626
Bathgate RAD et al., Front Endocrinol (Lausanne), 2013 4:13

BPC-157 10mg

BPC-157 10mg

BPC-157 is a research peptide composed of 15 amino acids (Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val), a fragment of the body protection compound found in gastric juice. Experimental data suggest it influences angiogenic and cytoprotective signaling through modulation of nitric oxide pathways, growth factor expression, and extracellular matrix remodeling. These actions make it a useful model for studying molecular repair and regenerative processes under stress conditions.

For research use only. Not for human consumption.

References: 
Sikiric P et al., Curr Pharm Des, 2018;24(18):2002–2030
Kang EA et al., Dig Dis Sci, 2013;58:3310–3317
Seiwerth S et al., Biomedicines, 2018;6(3):75

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"Note : this description is intended for research and educational purposes only and does not imply or suggest human use."
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