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USD master pricing, shown in your selected country's currency. Minimum order 10 units per product.
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5-Amino-1MQ 50mg / 60 Count Capsules
50 mg per capsule
5-Amino-1MQ is a small-molecule inhibitor of nicotinamide N-methyltransferase (NNMT) studied for its influence on adipocyte energy metabolism and cellular NAD+ salvage. Research organizations investigate it in metabolic models examining fat cell bioenergetics, methylation flux, and nutrient partitioning under laboratory conditions. Supplied in capsule form, it is valued as a selective chemical probe for separating methylation-dependent effects from receptor-mediated metabolic signaling.
MOQ: 10
Priced on request
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AOD 9604 5mg
5 mg
AOD-9604 is a modified C-terminal fragment of human growth hormone studied for lipolytic signaling in adipose tissue without the broader somatotropic activity of the full hormone. It is frequently used in metabolic and adipose research examining fat mobilization pathways under controlled laboratory conditions. It allows fat metabolism to be examined without concurrent IGF-1 induction.
MOQ: 10
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Cagrilintide 10mg
10 mg
Cagrilintide is a long-acting amylin analog studied for its activity at amylin and calcitonin receptors and its role in satiety signaling. Research organizations investigate it in metabolic models examining food-intake regulation, gastric signaling, and combination approaches with incretin pathways. Its extended half-life relative to native amylin makes it practical for longitudinal preclinical designs and combination studies alongside incretin-pathway agonists.
MOQ: 10
$81.00per unit
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Cardiogen 20mg
20 mg
Cardiogen is a short synthetic peptide bioregulator studied in cardiovascular tissue models. Research interest centers on its proposed role in cellular regulation and tissue-specific gene expression, with laboratory applications in cardiac cell culture and connective tissue investigation. It is most often deployed as a comparator within a panel of short regulatory peptides to evaluate sequence-dependent effects.
MOQ: 10
Priced on request
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GW-501516 10mg/30ml Liquid
10 mg/mL
GW-501516 is a selective PPARδ agonist studied for its effects on fatty acid oxidation, mitochondrial gene expression, and substrate utilization in skeletal muscle. It is used strictly as a laboratory reference compound in metabolic and exercise-physiology research models. Following discontinuation of clinical development on toxicology grounds, it persists in science solely as a reference agonist for nuclear receptor transactivation work.
MOQ: 10
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Tesofensine 100mcg / 60 Count Capsules
100 mcg per capsule
Tesofensine is a triple monoamine reuptake inhibitor studied for its effects on noradrenaline, dopamine, and serotonin signaling. Research organizations investigate it in neuropharmacology and energy-balance models examining appetite regulation and central monoamine transmission. The lower capsule strength provides finer resolution for threshold characterization, and its central mechanism makes it a useful comparator against peripherally acting metabolic compounds.
MOQ: 10
Priced on request
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Tesofensine 250mcg / 60 Count Capsules
250 mcg per capsule
Tesofensine 250mcg capsules provide a higher-strength presentation of this triple monoamine reuptake inhibitor. Research groups use it in neuropharmacology and energy-balance studies examining combined noradrenergic, dopaminergic, and serotonergic modulation of central appetite circuitry. The higher strength reduces unit counts per condition in established protocols while preserving an identical formulation for constructing dose-response relationships across both capsule presentations.
MOQ: 10
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Tesofensine 250mcg/30ml Liquid
250 mcg/mL
Tesofensine 250mcg/30ml liquid delivers this triple monoamine reuptake inhibitor in solution, supporting flexible volumetric dosing in research protocols. It is studied in neuropharmacology and energy-balance models investigating central monoamine transmission and appetite circuitry. Solution presentation removes the granularity limits of fixed-dose capsules, supporting serial dilution and body-weight-adjusted protocols in behavioral and neuropharmacological study designs.
MOQ: 10
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BPC-157 10mg
10 mg
BPC-157 is a synthetic pentadecapeptide derived from a protein sequence identified in gastric juice. It is widely studied for angiogenic signaling and tissue-repair pathways, with laboratory applications spanning connective tissue, gastrointestinal, and vascular research models. Its notable stability in gastric conditions, unusual among peptides, has made it practical for a wide range of preclinical route-of-administration designs.
MOQ: 10
$61.00per unit
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BPC-157 500mcg / 60 Count Capsules
500 mcg per capsule
BPC-157 500mcg capsules provide this repair-associated pentadecapeptide in an oral research format. The presentation supports gastrointestinal and enteral-route study designs that exploit the peptide's reported stability in gastric conditions. The oral presentation directly serves research questions concerning gastric stability, mucosal contact, and enteral bioavailability that parenteral vials cannot address.
MOQ: 10
Priced on request
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BPC-157 5mg / TB-500 5mg Blend
BPC-157 5 mg / TB-500 5 mg
This blend combines BPC-157 and TB-500 in a single vial, pairing two peptides with complementary reported mechanisms in tissue-repair research. It is used in laboratory models investigating whether angiogenic and cytoskeletal pathways produce additive effects. Co-formulation at a fixed ratio removes the preparation variance that arises when two peptides are reconstituted and combined manually across experimental replicates.
MOQ: 10
$74.00per unit
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BPC-157 5mg
5 mg
BPC-157 5mg supplies this repair-associated pentadecapeptide in a smaller vial suited to pilot studies, assay validation, and dose-ranging work. It is studied for angiogenic signaling and cell migration in tissue-repair research models. The smaller vial suits reconstitution protocol development and assay validation before laboratories commit material to full multi-arm study series.
MOQ: 10
Priced on request
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GHK-Cu 60mg
60 mg
GHK-Cu is a naturally occurring copper-binding tripeptide studied for its influence on extracellular matrix remodeling and gene expression. Research applications include dermatological, connective tissue, and wound-repair models examining collagen synthesis and copper-dependent enzymatic activity. Its dual character as both a copper-transport peptide and a transcriptional modulator underpins its extensive use across matrix biology and dermatological research.
MOQ: 10
Priced on request
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GHKCu 2mg / 60 Count Capsules
2 mg per capsule
GHK-Cu 2mg capsules present the copper-binding tripeptide in an oral research format. The presentation supports enteral-route study designs investigating systemic copper transport, matrix signaling, and comparative bioavailability. The oral format allows enteral-versus-parenteral comparisons to be run from a consistent compound source, which is essential for interpretable bioavailability data in matrix research.
MOQ: 10
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Glow Peptide - BPC-157 10mg / TB-500 10mg / GHK-Cu 50mg Blend
BPC-157 10 mg / TB-500 10 mg / GHK-Cu 50 mg
The Glow Peptide blend combines BPC-157, TB-500, and GHK-Cu in a single vial, pairing angiogenic, cytoskeletal, and matrix-remodeling mechanisms. It is studied in dermatological and connective tissue research examining multi-pathway repair signaling. By engaging vascular supply, cellular motility, and matrix construction simultaneously, it allows repair to be studied as an integrated process rather than in isolated fragments.
MOQ: 10
$92.00per unit
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Klow Peptide – KPV 10mg/ GHK-Cu 50mg/ BPC-157 10mg/ TB-500 10mg Blend
KPV 10 mg / GHK-Cu 50 mg / BPC-157 10 mg / TB-500 10 mg
The Klow Peptide blend combines KPV, GHK-Cu, BPC-157, and TB-500, adding a melanocortin-derived anti-inflammatory tripeptide to a repair-focused peptide panel. It is studied in models examining inflammatory modulation alongside matrix and angiogenic signaling. Running it against the three-component blend isolates the specific contribution of the KPV component within an otherwise identical formulation, a clean comparative design.
MOQ: 10
$100.00per unit
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KPV 10mg
10 mg
KPV is the C-terminal tripeptide of alpha-melanocyte-stimulating hormone, studied for anti-inflammatory signaling without pigmentation activity. Research applications include inflammatory pathway investigation, cytokine profiling, and gastrointestinal and dermatological inflammation models. Because it retains anti-inflammatory activity without the pigmentation effects of full-length alpha-MSH, it permits an experimental separation the parent hormone cannot provide.
MOQ: 10
$59.00per unit
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LL-37 10mg
10 mg
LL-37 is the only human cathelicidin-derived antimicrobial peptide, studied for innate immune signaling, membrane interaction, and immunomodulatory activity. Research applications span microbiology, host defense, and inflammatory pathway investigation in laboratory models. As the only cathelicidin identified in humans, it has no direct substitute in host-defense research, and findings map directly onto human innate immune biology.
MOQ: 10
$79.00per unit
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TB 500 5mg
5 mg
TB-500 is a synthetic peptide corresponding to the active region of thymosin beta-4, studied for actin binding and cytoskeletal regulation. Research applications include cell migration, tissue repair, and cardiovascular models examining motility-dependent processes. Its actin-binding mechanism is distinct from growth-factor-driven repair signaling, making it a natural pairing partner for angiogenic peptides in combination studies.
MOQ: 10
$69.00per unit
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B12 10,000mcg/10ml
10,000 mcg/10 mL
Vitamin B12 is an essential cobalt-containing cofactor required for methylation and mitochondrial metabolism. Research organizations use this high-concentration solution in studies of one-carbon metabolism, homocysteine regulation, hematopoiesis, and neurological cofactor dependency. Because cobalamin links methylation capacity to mitochondrial substrate flux, it is a recurring control variable in metabolic, hematological, and neurological study designs.
MOQ: 10
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BAM-15 50mg/ SLU-PP-332 50mg
BAM-15 50 mg / SLU-PP-332 50 mg
This blend pairs BAM-15, a mitochondrial uncoupler, with SLU-PP-332, an estrogen-related receptor agonist. Together they engage bioenergetic and transcriptional arms of metabolism, supporting research into mitochondrial efficiency and exercise-associated gene programs. Pairing an acute bioenergetic intervention with a transcriptional one lets investigators probe whether immediate uncoupling and longer-term mitochondrial biogenesis interact in metabolic models.
MOQ: 10
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DSIP 5mg
5 mg
Delta sleep-inducing peptide is a nonapeptide studied for its association with sleep architecture and neuroendocrine regulation. Research applications include electrophysiological sleep models, circadian investigation, and studies of stress-axis modulation. Its receptor target remains unidentified despite decades of study, making the peptide both an investigational tool and an active subject of mechanistic inquiry.
MOQ: 10
$58.00per unit
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Epitalon 550mcg/10ml/320mg Spray
550 mcg/10 mL (320 mg total)
This Epitalon spray presentation delivers the tetrapeptide bioregulator in a metered solution format. It is studied in cellular senescence, telomere biology, and pineal regulation research, with the spray supporting mucosal-route experimental designs. The metered format supports transmucosal absorption research and allows controlled comparison against parenteral presentations of the same tetrapeptide across administration routes.
MOQ: 10
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Epithalon 25mg
25 mg
Epithalon is a synthetic tetrapeptide bioregulator studied for its reported influence on telomerase activity and pineal regulation. It is a widely referenced compound in cellular ageing research, senescence models, and gene-expression investigation. As the reference compound of the peptide bioregulator class, it carries a citation base that makes comparative senescence study design straightforward for laboratories.
MOQ: 10
Priced on request
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Glutathione 1500mg
1500 mg
Glutathione is the principal intracellular antioxidant tripeptide, central to redox homeostasis and phase II detoxification. Research applications include oxidative stress assays, redox ratio measurement, and studies of cellular defense against reactive oxygen species. The GSH to GSSG ratio serves as a standard quantitative index of cellular redox status, making this compound indispensable in oxidative stress work.
MOQ: 10
$102.00per unit
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Hyaluronic Acid 100G Powder
100 g
Hyaluronic acid is a high-molecular-weight glycosaminoglycan and a principal structural component of the extracellular matrix. This bulk powder supports research in matrix biology, hydrogel formulation, viscoelasticity, and CD44 receptor signaling. Its biological effects are strongly molecular-weight dependent, with high and low molecular weight fragments reported to produce opposing effects on inflammation and angiogenesis.
MOQ: 10
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MOTS-c 10mg
10 mg
MOTS-c is a mitochondrial-derived peptide encoded in mitochondrial DNA, studied for AMPK activation and metabolic homeostasis. Research applications include insulin sensitivity models, mitochondrial-nuclear signaling, and exercise-associated metabolic investigation. As one of very few characterized mitochondrial-derived peptides, it gives laboratories a direct experimental handle on retrograde mitochondrial-to-nuclear communication in metabolic research.
MOQ: 10
$64.00per unit
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NAD+ 1000mg / 60 Count Capsules
1000 mg per capsule
NAD+ 1000mg capsules supply nicotinamide adenine dinucleotide in an oral research format. The presentation supports enteral-route studies of redox cofactor availability, sirtuin-dependent signaling, and NAD+ bioavailability research. The capsule format specifically serves the contested question of whether the intact dinucleotide is absorbed enterally or first degraded to precursors before cellular uptake.
MOQ: 10
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NAD+ 500mg
500 mg
NAD+ 500mg supplies nicotinamide adenine dinucleotide as a lyophilized preparation for parenteral research protocols. It is studied in redox metabolism, sirtuin-dependent signaling, DNA repair, and cellular ageing models. The lyophilized vial gives precise control over final concentration in solution, essential for mechanistic work where cofactor availability is the independent variable.
MOQ: 10
$61.00per unit
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Selank 10mg
10 mg
Selank is a synthetic heptapeptide derived from the immunomodulatory peptide tuftsin, studied for anxiolytic-associated signaling and neuroplasticity. Research applications include behavioral neuroscience, BDNF expression studies, and neuroimmune investigation. Its origin in an immunologically active peptide gives it a dual neurological and immune character, making it a distinctive probe for neuroimmune research.
MOQ: 10
$71.00per unit
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Semax 20mg / Selank 10mg Blend
Semax 20 mg / Selank 10 mg
This blend pairs Semax with Selank, combining a neurotrophic ACTH-derived peptide with an anxiolytic-associated tuftsin analog. It supports research into concurrent neurotrophic and neuroimmune signaling in behavioral and cognitive models. Fixed-ratio co-formulation allows combination arms to be run against single-peptide controls with confidence that the ratio is identical across every experimental replicate.
MOQ: 10
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Semax 25mg
25 mg
Semax is a synthetic analog of the ACTH(4-10) fragment, studied for neurotrophic factor expression and cognitive-behavioral endpoints without corticotropic activity. Research applications include neuroprotection models, BDNF signaling, and cognitive neuroscience. Critically, it retains neurotropic activity while lacking the corticotropic effects of full-length ACTH, permitting CNS study without confounding activation of the stress axis.
MOQ: 10
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Semax 300mcg/10ml/20mg Spray
300 mcg/10 mL (20 mg total)
Semax spray delivers this ACTH-derived neurotrophic peptide in a metered solution, supporting research into transmucosal administration routes. It is studied in neuroprotection, BDNF expression, and cognitive-behavioral models. Intranasal and transmucosal routes are actively investigated as pathways that may reach the central nervous system while limiting systemic exposure and first-pass metabolism.
MOQ: 10
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SS-31 10mg
10 mg
SS-31 is a mitochondria-targeting tetrapeptide that binds cardiolipin on the inner mitochondrial membrane. It is studied for effects on cristae architecture, electron transport efficiency, and mitochondrial dysfunction in cellular models. Unusually, it acts on the inner mitochondrial membrane without depolarizing membrane potential, allowing structural and functional effects to be studied independently of uncoupling.
MOQ: 10
$64.00per unit
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Thymosin Alpha1 10mg
10 mg
Thymosin alpha-1 is a thymus-derived immunomodulatory peptide studied for T-cell maturation and innate immune signaling. Research applications include immunology, Toll-like receptor pathway investigation, and models of immune competence. Because it modulates rather than broadly stimulates or suppresses immune function, it is studied where restoration of balanced immune competence is the endpoint.
MOQ: 10
$80.00per unit
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Thymosin Alpha1 300mcg/10ml/20mg Spray
300 mcg/10 mL (20 mg total)
This Thymosin Alpha-1 spray presentation supplies the immunomodulatory peptide in a metered solution format, supporting research into mucosal-route administration and mucosal immunity alongside systemic immune signaling. Mucosal surfaces represent a distinct immune compartment, so the spray format enables research questions about mucosal-associated lymphoid tissue that parenteral presentations cannot address.
MOQ: 10
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CJC-1295 3mg / Ipamorelin 3mg / GHRP-2 3mg Blend
CJC-1295 3 mg / Ipamorelin 3 mg / GHRP-2 3 mg
This triple blend combines CJC-1295 with two growth hormone secretagogues, Ipamorelin and GHRP-2. It supports research into dual-pathway stimulation of somatotroph signaling, pairing GHRH receptor activity with ghrelin receptor agonism. Fixed-ratio co-formulation across three peptides removes compounding handling error, allowing convergent somatotroph stimulation to be tested against single-agent controls with confidence.
MOQ: 10
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CJC-1295 No DAC 5mg / GHRP-2 5mg Blend
CJC-1295 No DAC 5 mg / GHRP-2 5 mg
This blend pairs CJC-1295 without DAC with GHRP-2, combining a short-acting GHRH analog with a potent growth hormone secretagogue. It is studied in models examining pulsatile somatotroph stimulation across two receptor pathways. The No DAC variant preserves the pulsatile signaling pattern that defines physiological growth hormone release, making it appropriate where pulsatility is an experimental endpoint.
MOQ: 10
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CJC-1295 No DAC 5mg / GHRP-6 5mg Blend
CJC-1295 No DAC 5 mg / GHRP-6 5 mg
This blend pairs CJC-1295 without DAC with GHRP-6, a secretagogue noted for pronounced appetite-associated signaling. It supports research examining growth hormone release alongside ghrelin receptor effects on food intake. GHRP-6 produces the most pronounced orexigenic signature of the secretagogue family, allowing growth hormone release and appetite circuitry to be observed together in one model.
MOQ: 10
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CJC-1295 No DAC 5mg / Ipamorelin 5mg Blend
CJC-1295 No DAC 5 mg / Ipamorelin 5 mg
This blend pairs CJC-1295 without DAC with Ipamorelin, the most receptor-selective growth hormone secretagogue. It supports research requiring somatotroph stimulation with minimal off-target endocrine signaling. Ipamorelin contributes minimal cortisol, ACTH, or prolactin activity, so this pairing engages both regulatory arms of the axis while keeping the endocrine background unusually clean.
MOQ: 10
$83.00per unit
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CJC-1295 with DAC 5mg
5 mg
CJC-1295 with DAC is a long-acting GHRH analog incorporating a drug affinity complex that binds serum albumin. It is studied for sustained somatotroph stimulation and for comparing continuous versus pulsatile growth hormone signaling. The albumin-binding modification produces sustained rather than pulsatile exposure, making it the reference tool for investigating how signaling pattern alters downstream IGF-1 output.
MOQ: 10
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GHRP-2 5mg
5 mg
GHRP-2 is a synthetic growth hormone secretagogue acting at the ghrelin receptor. It is studied for potent somatotroph stimulation and for its reported effects on cortisol and prolactin, making it a useful probe of secretagogue selectivity. Its documented cortisol and prolactin activity makes it a valuable positive comparator when mapping the selectivity boundaries of growth hormone secretagogue pharmacology.
MOQ: 10
$58.00per unit
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GHRP-6 Acetate 5mg
5 mg
GHRP-6 is a growth hormone secretagogue notable for pronounced appetite-associated signaling through the ghrelin receptor. It is studied in both somatotroph stimulation and hypothalamic food-intake research models. Its pronounced orexigenic profile provides a robust, reproducible signal in feeding-behavior models that more selective secretagogues such as Ipamorelin do not generate.
MOQ: 10
$58.00per unit
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HEXARLIN 10mg
10 mg
Hexarelin is a synthetic growth hormone secretagogue studied for both ghrelin receptor agonism and reported CD36-mediated cardiovascular signaling. This dual receptor profile makes it a distinctive probe in cardiac and endocrine research. Its reported CD36 binding is not shared by other GHRPs, permitting investigation of growth-hormone-independent cardiovascular signaling within the secretagogue class.
MOQ: 10
$84.00per unit
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hGH Fragment 176-191 5mg
5 mg
hGH Fragment 176-191 is the C-terminal lipolytic region of human growth hormone, studied for fat metabolism signaling isolated from the hormone's anabolic and glucoregulatory activity. It is used in adipose and metabolic research models. This structure-function dissociation is the fragment's entire scientific value, isolating lipolytic activity from the anabolic and glucoregulatory signaling of the parent molecule.
MOQ: 10
$78.00per unit
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IGF1-Lr3 1mg
1 mg
IGF-1 LR3 is a modified analog of insulin-like growth factor 1 engineered for reduced binding-protein affinity and extended activity. It is widely used in cell culture research on proliferation, differentiation, and IGF-1 receptor signaling. Reduced binding-protein affinity is what makes it the standard growth factor for cell culture, where native IGF-1 would be sequestered unpredictably by secreted binding proteins.
MOQ: 10
$104.00per unit
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Ipamorelin 5mg
5 mg
Ipamorelin is the most receptor-selective growth hormone secretagogue in common research use, stimulating somatotroph release with minimal cortisol or prolactin activity. It is valued where clean GH-axis stimulation is required. Because it does not meaningfully activate the stress axis, observed effects can be attributed to growth hormone signaling without the interpretive ambiguity less selective compounds introduce.
MOQ: 10
$60.00per unit
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MK-677 10mg / 60 Count Capsules
10 mg per capsule
MK-677 (ibutamoren) is an orally active, non-peptide growth hormone secretagogue receptor agonist. The capsule format supports enteral-route research into sustained GH and IGF-1 axis stimulation and receptor pharmacology. Its non-peptide structure resists gastrointestinal proteolysis, making it the practical choice for enteral-route secretagogue research that injectable GHRPs cannot support.
MOQ: 10
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MK-677 Ibutamoren 20mg/30ml Liquid
20 mg/mL
MK-677 Ibutamoren 20mg/30ml liquid supplies this orally active growth hormone secretagogue in solution, supporting volumetric dosing flexibility in dose-response and pharmacokinetic research protocols. Pharmacologically it is a non-peptidic ghrelin receptor agonist reported to produce sustained elevation of growth hormone and IGF-1 with an extended duration of action.
MOQ: 10
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RAD-140 10mg / 60 Count Capsules
10 mg per capsule
RAD-140 (testolone) is a selective androgen receptor modulator studied for tissue-selective receptor activation. It is used as a laboratory reference compound in androgen receptor pharmacology and tissue-selectivity research. SARM pharmacology rests on tissue selectivity, and its depth of published characterization makes it a standard reference ligand for androgen receptor binding and transactivation assays.
MOQ: 10
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RAD-140 TESTOLONE 20mg/30ml Liquid
20 mg/mL
RAD-140 Testolone 20mg/30ml liquid supplies this selective androgen receptor modulator in solution, supporting serial dilution and fine dose-response work in androgen receptor pharmacology research. As a non-steroidal SARM it induces receptor conformations reported to drive tissue-differential coactivator recruitment, the mechanistic basis of selectivity that defines the class.
MOQ: 10
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Sermorelin 5mg / Ipamorelin 5mg Blend
Sermorelin 5 mg / Ipamorelin 5 mg
This blend pairs Sermorelin, a GHRH(1-29) analog, with Ipamorelin, a selective ghrelin receptor agonist. It supports research into dual-pathway somatotroph stimulation using the native GHRH sequence. Because Sermorelin is the native GHRH sequence rather than a stabilized analog, this pairing is preferred when physiological fidelity of pulsatile signaling matters experimentally.
MOQ: 10
$81.00per unit
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Sermorelin 5mg
5 mg
Sermorelin is a GHRH(1-29) analog representing the shortest fully active fragment of growth hormone-releasing hormone. It is studied in pituitary function research, GH pulsatility, and GHRH receptor pharmacology. As the minimal fully active fragment of native GHRH, it serves as the physiological baseline against which stabilized analogs and half-life extension are measured.
MOQ: 10
$70.00per unit
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Tesamorelin 10mg
10 mg
Tesamorelin is a stabilized GHRH analog studied for its effects on the somatotropic axis and, distinctively, on visceral adipose tissue. It is used in metabolic and endocrine research examining GH-mediated fat distribution. Its reported association with reductions in visceral rather than subcutaneous adipose tissue is anatomically selective and unusual, making it compelling for fat-distribution research.
MOQ: 10
$94.00per unit
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Tesamorelin 12mg / CJC-1295 3mg / Ipamorelin 6mg / GHRP-2 3mg Blend
Tesamorelin 12 mg / CJC-1295 3 mg / Ipamorelin 6 mg / GHRP-2 3 mg
This four-component blend combines Tesamorelin, CJC-1295, Ipamorelin, and GHRP-2, assembling two GHRH-pathway analogs with two ghrelin receptor secretagogues for comprehensive somatotroph axis research. Combining two GHRH-pathway analogs with two secretagogues of differing selectivity, it supports investigation of receptor saturation and ceiling effects across the somatotropic axis.
MOQ: 10
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Tesamorelin 6mg / Ipamorelin 2mg Blend
Tesamorelin 6 mg / Ipamorelin 2 mg
This blend pairs Tesamorelin with Ipamorelin, combining a DPP-4-resistant GHRH analog associated with visceral adipose effects and a highly selective ghrelin receptor agonist for dual-pathway metabolic research. Minimizing stress-axis activation matters here because cortisol elevation would itself alter fat distribution, corrupting precisely the body-composition endpoint under investigation.
MOQ: 10
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YK-11 12mg/30ml Liquid
12 mg/mL
YK-11 is a steroidal compound studied as a partial androgen receptor agonist with reported myostatin-pathway activity. The liquid format supports serial dilution in receptor pharmacology and muscle cell research. Its steroidal structure and reported follistatin involvement distinguish it mechanistically from conventional non-steroidal SARMs, making it a subject of active rather than settled investigation.
MOQ: 10
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YK-11 6mg / 60 Count Capsules
6 mg per capsule
YK-11 6mg capsules provide this steroidal androgen receptor partial agonist in an oral research format, supporting enteral-route protocols in muscle biology and myostatin-pathway investigation. Because follistatin antagonizes myostatin, a negative regulator of skeletal muscle mass, the compound engages muscle biology through a route separate from direct receptor transactivation.
MOQ: 10
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Gonadorelin 10mg
10 mg
Gonadorelin is a synthetic form of gonadotropin-releasing hormone, studied for its role in pituitary gonadotropin release. It is used in reproductive endocrinology research examining LH and FSH secretion and hypothalamic-pituitary-gonadal axis regulation. Pulsatile stimulation sustains gonadotropin output while continuous stimulation downregulates the receptor and suppresses the axis, a dependence on temporal pattern that makes it a classic teaching tool.
MOQ: 10
$70.00per unit
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Kisspeptin 5mg
5 mg
Kisspeptin is a neuropeptide acting upstream of GnRH as a principal gatekeeper of the reproductive axis. It is studied in neuroendocrinology research examining KISS1R signaling, pubertal onset, and hypothalamic control of reproduction. Because loss-of-function mutations in its receptor abolish pubertal onset, the pathway is non-redundant, giving experiments conducted with it unusually clear interpretive weight.
MOQ: 10
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Melanotan 2 (MT2) 10mg
10 mg
Melanotan 2 is a synthetic cyclic analog of alpha-melanocyte-stimulating hormone acting as a non-selective melanocortin receptor agonist. It is studied in pigmentation biology, melanocortin receptor pharmacology, and appetite signaling research. Its broad receptor engagement is both the source of its utility and its complexity, serving as the standard pan-agonist comparator against receptor-selective melanocortin compounds.
MOQ: 10
$60.00per unit
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Oxytocin 10mg
10 mg
Oxytocin is a nine-amino-acid neuropeptide acting at the oxytocin receptor, studied for its roles in social behavior, smooth muscle physiology, and central neuromodulation. It is widely used in behavioral neuroscience and receptor pharmacology research. Its dual peripheral and central release architecture gives it two largely distinct biologies, supporting both smooth muscle physiology and social neuroscience research programs.
MOQ: 10
$61.00per unit
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Oxytocin 150mcg/10ml/10mg Spray
150 mcg/10 mL (10 mg total)
This Oxytocin spray presentation supplies the neuropeptide in a metered solution, supporting research into intranasal and transmucosal administration — a route central to the study of centrally mediated oxytocin effects. Intranasal delivery is the dominant route in central oxytocin research, and the extent of actual brain exposure achieved remains an active methodological debate.
MOQ: 10
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PT 141 300mcg/10ml/20mg Spray
300 mcg/10 mL (20 mg total)
This PT-141 spray delivers the melanocortin receptor agonist in a metered solution format, supporting transmucosal administration research alongside studies of MC4R signaling and centrally mediated neuroendocrine pathways. Because its mechanism is centrally rather than peripherally mediated, route of administration materially affects experimental outcomes, making transmucosal formats scientifically meaningful.
MOQ: 10
Priced on request
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PT-141 10mg
10 mg
PT-141 (bremelanotide) is a cyclic melanocortin receptor agonist studied for MC4R-mediated central signaling. It is used in neuroendocrine and receptor pharmacology research examining melanocortin pathways in the central nervous system. Weighted toward centrally expressed receptor subtypes, it serves as the natural counterpart to non-selective analogs when separating central from peripheral melanocortin effects.
MOQ: 10
$69.00per unit
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PT-141 1mg / Semax 0.5mg / Oxytocin 1.5mg Blend
PT-141 1 mg / Semax 0.5 mg / Oxytocin 1.5 mg
This blend combines PT-141, Semax, and Oxytocin, pairing melanocortin, neurotrophic, and oxytocinergic signaling in a single formulation. It supports research into convergent neuropeptide modulation of central circuits. Because the three pathways are pharmacologically independent, the formulation lets investigators test whether simultaneous engagement produces integrated effects distinguishable from any single peptide.
MOQ: 10
Priced on request
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BAC-Water 3 mL
3 mL
Bacteriostatic water (3 mL) for laboratory reconstitution of lyophilized research compounds. Contains 0.9% benzyl alcohol, which supports multiple withdrawals under proper aseptic technique. Research use only.
MOQ: 10
$8.99per unit
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BAC-Water 10 mL
10 mL
Bacteriostatic water (10 mL) for laboratory reconstitution of lyophilized research compounds. Contains 0.9% benzyl alcohol, which supports multiple withdrawals under proper aseptic technique. Research use only.
MOQ: 10
$11.99per unit
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BAC-Water 30 mL
30 mL
Bacteriostatic water (30 mL) for laboratory reconstitution of lyophilized research compounds. Contains 0.9% benzyl alcohol, which supports multiple withdrawals under proper aseptic technique. Research use only.
MOQ: 10
$17.99per unit
This product is intended exclusively for laboratory research and analytical purposes. NOT FOR HUMAN CONSUMPTION. Not intended to diagnose, treat, cure, or prevent any disease.