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Independent research. Uncompromising purity. Prices that make sense. JayX BioSolutions was built by a researcher who got tired of overpaying for compounds that underdelivered — so we fixed it.
All products sold by JayX BioSolutions, LLC are intended strictly for in vitro research and laboratory use only. Not approved for human or veterinary use.
Research Compound Finder
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About JayX BioSolutions
JayX BioSolutions was not built in a boardroom. It was built out of necessity — by an independent researcher who spent years navigating a market full of overpriced, under-tested, and inconsistently sourced compounds. The process was frustrating. The markups were insulting. The quality was unreliable. So we decided to do something about it.
We operate as an independent research supply company, directly sourcing pharmaceutical-grade peptides and verifying every batch through third-party analytical testing. No middlemen. No inflated retail margins. No compromises on purity. What you receive is exactly what the certificate of analysis says it is — nothing more, nothing less.
Our catalog spans over 41 compounds across metabolic research, regenerative science, cognitive investigation, longevity pathways, hormonal mechanisms, and more. Every compound is lyophilized to specification, stored under controlled conditions, and shipped with full documentation. We don't cut corners because we understand, firsthand, what it means to depend on reliable materials in a research setting.
We believe high-quality research compounds shouldn't be a luxury. The best prices you'll find anywhere aren't a marketing claim — they're the result of running a lean, researcher-first operation with no unnecessary overhead. When you order from JayX BioSolutions, you're ordering directly from someone who has used these same compounds in their own work and holds them to the same standards they'd hold for themselves.
This is independent research supply done right.
Catalog
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A long-acting GLP-1 receptor agonist analogue modeled on semaglutide. Studied for glucose-dependent insulin secretion, appetite suppression signaling, and gut-brain axis research. Its extended half-life via fatty acid conjugation makes it a favored compound in chronic metabolic pathway studies.
A dual GIP and GLP-1 receptor co-agonist analogue modeled on tirzepatide. Research spans adipose tissue metabolism, beta-cell function, energy expenditure regulation, and incretin pathway synergy. The dual-receptor mechanism offers a distinct pharmacodynamic profile from single-agonist GLP-1 compounds.
A triple receptor agonist analogue modeled on retatrutide, simultaneously engaging GLP-1, GIP, and glucagon receptors. Studied for synergistic effects on energy homeostasis, lipid oxidation, and hepatic fat reduction. Represents the frontier of incretin-based research compounds.
The C-terminal fragment (residues 176-191) of human growth hormone. Studied for its selective action on fat metabolism pathways, stimulating lipolysis and inhibiting lipogenesis without affecting insulin sensitivity or IGF-1 levels — a precise tool for adipose tissue studies.
A cell-permeable small molecule inhibitor of nicotinamide N-methyltransferase (NNMT). Research shows it can reverse metabolic dysregulation associated with NNMT overexpression. Studied for fat cell size reduction and whole-body energy expenditure effects.
A synthetic GHRH analogue stabilized with a trans-3-hexenoic acid group, significantly extending its half-life. Research applications include visceral adiposity reduction models, GH secretion stimulation, and lipodystrophy-associated metabolic dysregulation studies.
A GHRH analogue modified with Drug Affinity Complex (DAC) technology allowing covalent albumin binding, extending half-life to 6-8 days. Ideal for studying sustained GH pulse elevation, IGF-1 upregulation, and long-term somatotropic axis regulation.
A synergistic combination of a GHRH analogue (CJC-1295 DAC) and a selective GH secretagogue (Ipamorelin). Studied for amplifying both frequency and amplitude of GH pulses while maintaining selectivity without significantly elevating cortisol or prolactin.
A synthetic hexapeptide and potent ghrelin mimetic acting on GHS-R1a receptors to stimulate robust GH release. Among the most potent GHRPs studied, with applications in GH pulse characterization, hypothalamic-pituitary axis studies, and appetite-regulating pathway research.
One of the original synthetic GH-releasing hexapeptides. Acts on ghrelin receptors to stimulate GH secretion and is studied for appetite pathway modulation, gastric motility research, and somatotropic axis activation. Significantly elevates ghrelin, valuable for hunger-signaling pathway research.
A recombinant long-acting IGF-1 analogue with 13 amino acid N-terminal extension reducing binding to IGF-binding proteins by over 1000-fold. With half-life ~120x longer than native IGF-1, it is a key tool for receptor binding studies, muscle cell proliferation research, and downstream signaling analysis.
The biologically active fragment GHRH(1-29)-NH2. Studied as a physiological stimulator of pituitary GH secretion, valuable for research into age-related GH decline, somatotropic axis responsiveness, and GH deficiency models.
A synthetic hexapeptide and one of the most potent GHRPs studied. Notable for research into cardioprotective mechanisms independent of GH release — hexarelin demonstrates direct cardiac receptor activity, making it uniquely valuable for cardiovascular and somatotropic research.
A 15-amino-acid peptide derived from a protective protein found in gastric juice. Extensively studied for tissue repair properties including tendon, ligament, muscle, and gut healing — through upregulation of growth factor receptors and promotion of angiogenesis. Also covers brain-gut axis and nitric oxide signaling research.
A synthetic version of the naturally occurring thymic peptide Thymosin Beta-4. Studied for actin regulation, cell migration, angiogenesis, and tissue regeneration. Research covers wound healing, inflammation reduction, and cardiac tissue repair. Particularly studied in combination with BPC-157.
A naturally occurring copper-binding tripeptide (Gly-His-Lys) found in human plasma that declines significantly with age. Research demonstrates roles in collagen and elastin synthesis, wound healing acceleration, anti-inflammatory signaling, and tissue remodeling via TGF-beta pathway modulation.
A tripeptide (Lys-Pro-Val) derived from the C-terminus of alpha-MSH. Studied for potent anti-inflammatory properties, particularly in gut mucosal research and inflammatory bowel disease models. Acts through melanocortin receptors and NF-kB pathway inhibition.
An 11-amino-acid peptide derived from the helix B region of erythropoietin that selectively activates the innate repair receptor without erythropoietic effects. Studied for neuropathy attenuation, anti-inflammatory tissue protection, and pain pathway modulation.
The N-acetyl, C-terminal amidated form of Semax with enhanced CNS stability. Studied for potent upregulation of BDNF and NGF in the hippocampus and prefrontal cortex, neuroprotective effects following ischemic events, and cognitive enhancement in memory consolidation models.
The N-acetyl, amidated form of Selank, a synthetic heptapeptide analogue of tuftsin. Studied for anxiolytic effects without sedation or dependence, modulation of GABAergic and serotonergic systems, and enhancement of cognitive performance under stress.
A hepatocyte growth factor (HGF) fragment and potent activator of the HGF/MET signaling axis. Research has shown it to be one of the most potent synaptogenic compounds identified, with effects on synaptic density and cognitive function. Studied for Alzheimer's disease modeling.
A standardized mixture of low-molecular-weight neuropeptides and amino acids derived from porcine brain proteins. Contains fragments with BDNF, NGF, CNTF, and GDNF-like activity. Studied for neuroprotective effects and neuroplasticity promotion.
A synthetic tripeptide (Glu-Asp-Arg) developed from pineal gland extract research. Studied for neuroprotective effects in retinal and cerebral tissue, circadian rhythm pathway regulation, and age-related cognitive decline models.
Delta Sleep-Inducing Peptide — a nonapeptide first isolated from rabbit cerebral venous blood during slow-wave sleep induction. Studied for sleep architecture effects, HPA axis modulation, cortisol and LH rhythm regulation, and antioxidant pathway activity.
A synthetic tetrapeptide (Ala-Glu-Asp-Gly) analogue of epithalamin from the pineal gland. Studied for its ability to activate telomerase enzyme activity and restore telomere length in somatic cells — a key area of aging and cellular senescence research.
A 16-amino-acid peptide encoded within the mitochondrial 12S rRNA gene. Studied for activation of AMPK and AICAR pathways, insulin sensitivity enhancement, skeletal muscle glucose uptake, and modulation of the mitochondrial stress response in aging-related metabolic dysfunction models.
A mitochondria-targeted tetrapeptide (D-Arg-Dmt-Lys-Phe-NH2) that concentrates in the inner mitochondrial membrane. Studied for interaction with cardiolipin to preserve cristae architecture, reduce ROS production, and protect against ischemia-reperfusion injury.
A 28-amino-acid peptide naturally secreted by thymic epithelial cells. Studied as a potent immunomodulator that promotes T-cell maturation, enhances NK cell activity, and demonstrates antiviral and antifungal properties via dendritic cell and cytokine pathway modulation.
Nicotinamide adenine dinucleotide — a foundational coenzyme central to mitochondrial electron transport, ATP synthesis, and DNA repair via PARP activation. Research applications include sirtuin pathway activation, age-related NAD+ depletion models, and neuroprotection studies.
The most abundant endogenous antioxidant tripeptide (gamma-Glu-Cys-Gly) in human cells. Central to reactive oxygen species neutralization, heavy metal detoxification, xenobiotic metabolism, and immune system support. Research applications include oxidative stress modeling and liver protection studies.
Bremelanotide — a cyclic heptapeptide acting centrally on melanocortin 3 and 4 receptors in the hypothalamus. Works through CNS pathways rather than vascular mechanisms, making it a unique research compound for sexual dysfunction pathway and melanocortin receptor binding studies.
The biologically active 10-amino-acid C-terminal fragment of kisspeptin-54. Acts as a potent agonist of the GPR54 receptor, stimulating GnRH and subsequently LH and FSH. Studied for HPG axis regulation, puberty onset modeling, and testosterone secretion pulse characterization.
Human Chorionic Gonadotropin — a glycoprotein hormone sharing the LH beta-subunit receptor binding domain. Used in research to study Leydig cell steroidogenesis, testicular function maintenance, ovarian follicle luteinization, and the LH signaling cascade.
A nine-amino-acid neuropeptide produced in the hypothalamus. Studied for social bonding and trust pathway research, HPA axis stress response modulation, uterine contractility, lactation, appetite regulation, anti-inflammatory signaling, and cardiomyocyte protection.
Vasoactive Intestinal Peptide — a 28-amino-acid neuropeptide acting on VPAC1 and VPAC2 receptors. Studied for vasodilation, smooth muscle relaxation, immune modulation, anti-inflammatory cytokine regulation, and circadian rhythm entrainment.
A linear 13-amino-acid analogue of alpha-MSH with high selectivity for MC1R. Studied for melanogenesis pathway activation, UV-independent pigmentation research, and photoprotective mechanism modeling.
A cyclic heptapeptide analogue of alpha-MSH with affinity for MC1R, MC3R, MC4R, and MC5R. Studied for melanogenesis, appetite suppression via MC4R pathway, and sexual function circuitry through central melanocortin receptors.
A precisely formulated research blend combining BPC-157's targeted tissue repair and angiogenesis promotion with TB-500's systemic cell migration and actin regulation. Studied for synergistic and complementary effects on comprehensive tissue regeneration.
A four-peptide research blend combining BPC-157 and TB-500 for tissue regeneration, GHK-Cu for collagen synthesis and connective tissue repair, and KPV for potent NF-kB-mediated anti-inflammatory modulation.
A three-peptide regenerative blend targeting angiogenesis (BPC-157), cell migration (TB-500), and collagen/elastin synthesis (GHK-Cu). Studied for synergistic skin integrity improvement, connective tissue remodeling, and wound healing.
Raw GHK-Cu powder for formulation into a topical research vehicle. Requires mixing into a scentless hyaluronic acid cream base. Studied for transdermal copper-peptide delivery, dermal collagen and elastin stimulation, and skin barrier repair research. Store refrigerated. Not for injection.
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Legal & Compliance
Last updated: June 2025
All products offered by JayX BioSolutions, LLC are sold strictly for in vitro laboratory and scientific research. These compounds are not intended, nor approved, for human or animal consumption, therapeutic use, diagnostic application, or any use other than legitimate scientific research.
By purchasing, the purchaser expressly represents and warrants they are a qualified researcher, all products will be used exclusively for lawful in vitro research, and they have verified legality in their jurisdiction.
Nothing on this website constitutes medical advice or a therapeutic recommendation.
Last updated: June 2025
Payment is due in full prior to fulfillment via Zelle, Venmo, Cash App, Bitcoin, or arranged methods. Payment notes must not reference peptides, compounds, or product names. Use your Order ID only.
USPS ($10, 3-5 business days) or UPS ($20, 2-3 business days). Orders ship within 1-3 business days of confirmed payment.
All sales are final. Damaged or purity-deficient products will be replaced upon documentation review.
Governed by Florida law. Disputes resolved via AAA arbitration in Broward County, Florida.
Last updated: June 2025
We collect name, email, organization, and order details. We do not sell or rent personal data.
Privacy questions: JayXBioSolutions@proton.me.
Last updated: June 2025
Purchaser assumes full responsibility for all risk associated with handling, storage, or use. JayX BioSolutions, LLC expressly disclaims all liability arising from misuse or unauthorized use.
To the maximum extent permitted by law, JayX BioSolutions, LLC shall not be liable for any direct, indirect, incidental, consequential, or punitive damages. Purchaser's sole remedy is limited to replacement of defective product.
Purchaser agrees to indemnify and hold harmless JayX BioSolutions, LLC from any claim, liability, or expense arising from purchaser's use of any product or breach of these terms.