Researcher Verification

Retatrutide

Retatrutide is a triple agonist at GLP-1, GIP, and glucagon receptors studied for unprecedented weight-loss magnitude in metabolic disease research. Investigations map receptor co-activation, energy expenditure via glucagon, and cardiovascular risk biomarker changes.

From $1158 variants

GLP-1 / Metabolic

Tirzepatide

Tirzepatide is a dual GIP and GLP-1 receptor agonist studied for superior weight loss and glycemic control versus GLP-1-only agents. Research maps incretin co-agonism, adipose tissue remodeling, and cardiovascular outcome biomarker improvements.

From $8510 variants

GLP-1 / Metabolic

Semaglutide

Semaglutide is a GLP-1 receptor agonist with albumin-binding modification for extended half-life, studied for glycemic control and weight reduction. Research maps GLP-1R internalization, cardiovascular outcome benefits, and dose-escalation tolerability profiles.

From $706 variants

GH / GHRP

HGH 191AA

Recombinant 191-amino-acid somatropin is the canonical human growth hormone used to study IGF-1 axis activation, lipolysis, and linear growth. Laboratory models characterize receptor dimerization, JAK-STAT signaling, and tissue-specific GH responsiveness.

From $907 variants

GH / GHRP

Ipamorelin

Ipamorelin is a selective ghrelin-receptor agonist prized in research for clean GH release without significant cortisol or prolactin elevation. Studies characterize dose-dependent GH pulses, synergy with GHRH analogs, and pituitary selectivity profiles.

From $753 variants

Tanning

Melanotan II

Melanotan II is a cyclic melanocortin agonist studied for MC1R tanning and MC4R-mediated appetite and sexual arousal pathways. Research distinguishes pigmentary effects from central melanocortin signaling and examines dose-dependent nausea profiles.

Healing

BPC-157

BPC-157 is a pentadecapeptide derived from gastric juice protein, extensively studied for angiogenesis, tendon fibroblast migration, and nitric-oxide-mediated tissue repair. Models include tendon transection, inflammatory bowel injury, and growth-hormone receptor crosstalk in healing tissue.

GH / GHRP

CJC-1295 (no DAC)

Modified GRF 1-29 (CJC without DAC) is a short-acting GHRH analog used to model physiologic GH pulses when paired with ghrelin mimetics. Research focuses on receptor binding at pituitary somatotrophs and synergy with GHRP-class peptides.

From $1302 variants

GH / GHRP

Tesamorelin

Tesamorelin is a stabilized GHRH analog studied for GH-mediated visceral adipose reduction in lipodystrophy and metabolic research. Research examines IGF-1 elevation, liver fat reduction, and preferential trunk-fat mobilization patterns.

From $954 variants

Healing

TB-500 (TB4)

Thymosin beta-4 is a 43-amino-acid actin-sequestering peptide studied for wound healing, angiogenesis, and cardiac repair after ischemia. Research examines G-actin buffering, cell migration, and hair-regrowth follicle stem-cell mobilization.

From $1303 variants

Cosmetic

GHK-Cu

GHK-Cu is a copper-binding tripeptide extensively researched for wound healing, collagen synthesis, and stem-cell activation in dermal models. Studies map its effects on TGF-beta signaling, superoxide dismutase activity, and cosmetic anti-aging transcriptomics.

From $752 variants

GLP-1 / Metabolic

NAD+

Nicotinamide adenine dinucleotide is a central redox cofactor researched for sirtuin activation, DNA repair, and mitochondrial health in aging models. Studies examine NAD+ repletion strategies, CD38 inhibition synergy, and metabolic disease biomarker reversal.

From $854 variants

Sexual Health

PT-141

PT-141 (bremelanotide) is a melanocortin MC3R/MC4R agonist studied for central sexual arousal without direct vascular PDE5 mechanisms. Research maps hypothalamic activation, desire-phase endpoints, and distinction from peripheral erectogenic agents.

Tanning

Melanotan I

Melanotan I (afamelanotide) is a linear alpha-MSH analog studied for MC1R-mediated eumelanin production and photoprotection research. Investigations map melanocyte stimulation, tanning kinetics without significant erectogenic activity, and vitiligo repigmentation models.

Orals / SARMs

MK-677 (Ibutamoren)

Ibutamoren (MK-677) is an oral ghrelin-receptor agonist researched for sustained GH and IGF-1 elevation without injectable secretagogue protocols. Studies characterize appetite stimulation, sleep-quality changes, and lean-mass accrual in GH-deficiency models.

From $401 variant

GH / GHRP

Sermorelin

Sermorelin is a GHRH(1-29) analog studied for pulsatile GH stimulation and IGF-1 elevation with physiological secretory patterns. Research compares sermorelin versus GHRP combinations on somatotropic axis integrity and pituitary reserve.

From $1303 variants

GH / GHRP

CJC-1295 (DAC)

CJC-1295 with Drug Affinity Complex is a long-acting GHRH analog studied for extended GH and IGF-1 elevation through albumin binding. Investigators characterize half-life prolongation, pulsatility blunting, and somatotropic axis saturation kinetics.

From $1303 variants

GLP-1 / Metabolic · Orals / SARMs

Semaglutide Oral

Oral semaglutide uses SNAC absorption enhancer technology for gastric GLP-1 delivery without injection in metabolic research. Studies examine bioavailability challenges, fasting dosing requirements, and comparative efficacy to subcutaneous semaglutide.

From $303 variants

GH / GHRP

IGF-1 LR3

IGF-1 LR3 is a long-acting insulin-like growth factor analog with reduced IGF-binding protein affinity, studied for potent anabolic signaling. Research examines PI3K-Akt-mTOR activation, muscle hypertrophy, and mitogenic effects relative to native IGF-1.

From $852 variants

GH / GHRP

MOTS-c

MOTS-c is a mitochondrial-encoded peptide studied for metabolic homeostasis, insulin sensitivity, and exercise-mimetic AMPK activation. Research examines nuclear translocation, folate-methionine cycle modulation, and age-related metabolic decline reversal.

From $1202 variants

GLP-1 / Metabolic · Cartridges

Retatrutide Cartridge

Retatrutide cartridge delivery systems are studied for pre-filled dosing precision and patient-protocol compliance in metabolic research. Research examines peptide stability in cartridge format, subcutaneous absorption kinetics, and dose-accuracy versus vial reconstitution.

From $126 variants

GLP-1 / Metabolic · Cartridges

Tirzepatide Cartridge

Tirzepatide cartridge systems deliver pre-measured incretin doses for standardized metabolic research protocols. Studies examine dual-agonist peptide stability in cartridge format, absorption consistency, and dosing precision versus reconstituted vials.

From $144 variants

GH / GHRP

GHRP-6

GHRP-6 is a hexapeptide growth hormone secretagogue investigated for ghrelin receptor activation and somatotroph GH secretion. Studies note pronounced appetite stimulation alongside GH release, making it useful for dissecting central versus pituitary ghrelin effects.

From $852 variants

GH / GHRP

GHRP-2

GHRP-2 is a synthetic ghrelin-receptor agonist studied for potent GH release with moderate cortisol and prolactin co-stimulation. Research characterizes GHS-R1a signaling, dose-dependent GH pulses, and appetite-stimulating ghrelin pathway activation.

From $752 variants

Nootropic

Selank

Selank is a synthetic tuftsin analog studied for anxiolytic activity via GABAergic modulation and enkephalinase inhibition without sedation. Research examines stress-induced behavior, immune modulation, and BDNF expression in neuropsychiatric models.

Nootropic

Semax

Semax is an ACTH(4-10) analog studied for BDNF upregulation, stroke recovery, and attention enhancement in Russian neuropharmacology research. Models examine NGF/BDNF expression, dopaminergic modulation, and neuroprotection under hypoxic stress.

GLP-1 / Metabolic

AOD-9604

AOD-9604 is a modified fragment of human growth hormone (amino acids 176–191) researched for lipolytic activity without GH-receptor-mediated IGF-1 elevation. Studies examine adipocyte lipolysis, lipid mobilization, and cartilage-repair signaling in obesity and joint-tissue models.

From $903 variants

Orals / SARMs

HCG

Human chorionic gonadotropin is a glycoprotein hormone studied for LH-receptor activation on Leydig cells and intra-testicular testosterone support. Research examines gonadotropin replacement, testicular volume maintenance, and HPG-axis recovery after suppression.

From $903 variants

Oils

Testosterone Cypionate

Testosterone cypionate is the most widely studied long-ester testosterone for TRT pharmacokinetics and anabolic research. Models characterize 8-day half-life approximations, estradiol aromatization, and steady-state trough/peak management.

From $952 variants

Oils

Testosterone Enanthate

Testosterone enanthate is a foundational testosterone ester researched for androgen replacement and muscle anabolism across decades of literature. Studies examine enanthate cleavage kinetics, DHT/estradiol metabolite ratios, and injection-interval optimization.

Bioregulators

Epithalon

Epithalon (Epitalon) is a tetrapeptide studied for telomerase activation, pineal melatonin regulation, and circadian gene expression in aging models. Research examines telomere elongation in somatic cells, antioxidant enzyme upregulation, and lifespan endpoints in rodent studies.

From $903 variants

Healing

Thymosin Alpha-1

Thymosin alpha-1 is an immunomodulatory peptide studied for TLR-mediated dendritic cell activation and antiviral T-cell responses. Research examines hepatitis, sepsis, and cancer adjuvant models with emphasis on interferon-gamma upregulation.

Nootropic

DSIP

Delta sleep-inducing peptide (DSIP) is a neuropeptide studied for sleep-architecture modulation, stress-axis attenuation, and EEG delta-wave promotion. Research examines hypothalamic-pituitary interactions, analgesic correlates, and circadian rhythm effects in rodent sleep models.

Healing

KPV

KPV is the C-terminal tripeptide of alpha-MSH studied for NF-κB inhibition and anti-inflammatory activity without melanocortin pigmentation effects. Research targets IBD models, mast-cell stabilization, and antimicrobial properties in epithelial tissue.

GH / GHRP

Hexarelin

Hexarelin is a hexapeptide ghrelin-receptor agonist researched for strong GH release with notable cardiac CD36 receptor binding. Studies examine cardioprotective ischemia-reperfusion models alongside somatotropic axis stimulation and appetite effects.

From $802 variants

Sexual Health

Tadalafil (Cialis)

Tadalafil is a long-acting PDE5 inhibitor studied for extended cGMP elevation in erectile tissue and lower urinary tract models. Research examines 36-hour functional windows, BPH symptom relief via smooth-muscle relaxation, and nitric-oxide synergy.

Sexual Health

Sildenafil (Viagra)

Sildenafil is a PDE5 inhibitor studied for cGMP accumulation and smooth-muscle relaxation in penile, pulmonary, and cardiac vasculature. Research examines rapid-onset erectile response kinetics, nitric-oxide pathway synergy, and selective PDE5 versus PDE6 ocular effects.

GLP-1 / Metabolic

Liraglutide

Liraglutide is a daily GLP-1 receptor agonist with 97% homology to native GLP-1, studied for glucose-dependent insulin secretion and weight loss. Research maps GLP-1R signaling in pancreatic beta cells, gastric emptying delay, and cardiovascular risk biomarkers.

From $1403 variants

GLP-1 / Metabolic

Cagrilintide

Cagrilintide is a long-acting amylin analog investigated for satiety, gastric emptying delay, and weight reduction complementary to incretin therapy. Studies map AMY receptor activation, nausea dose-finding, and combination strategies with GLP-1 agonists.

From $1403 variants

GLP-1 / Metabolic

Survodutide

Survodutide (BI 456906) is a dual GLP-1 and glucagon receptor agonist studied for metabolic liver disease and obesity research. Investigations examine MASH histology improvement, glucagon-driven energy expenditure, and weight-loss durability.

From $3501 variant

GLP-1 / Metabolic

Orforglipron

Orforglipron is a small-molecule oral GLP-1 receptor agonist studied for non-peptide incretin mimetic activity and weight management. Research examines oral bioavailability, GLP-1R conformational activation, and glycemic control without injectable delivery.

From $1302 variants

Orals / SARMs

RAD-140

Testolone (RAD-140) is a SARM studied for potent muscle anabolism with reduced prostate stimulation in preclinical models. Research characterizes neuroprotective claims, tissue selectivity indices, and dose-dependent HPG-axis suppression.

Orals / SARMs

Ostarine (MK-2866)

Ostarine (MK-2866) is one of the most studied SARMs for lean-mass preservation in sarcopenia and cachexia models. Research characterizes tissue-selective AR activation, dose-dependent testosterone suppression, and bone mineral density effects.

Orals / SARMs

LGD-4033

Ligandrol (LGD-4033) is a non-steroidal SARM researched for tissue-selective androgen receptor agonism in muscle and bone. Studies characterize anabolic indices, suppression of endogenous testosterone, and partial versus full agonism across tissues.

From $401 variant

Oils

Trenbolone Acetate

Trenbolone acetate is the short-ester 19-nor studied for potent nutrient partitioning, progestogenic activity, and androgen-receptor binding. Research maps daily injection kinetics, prolactin elevation, and recomp body-composition endpoints.

Oils

Deca (Nandrolone Decanoate)

Nandrolone decanoate is the canonical long-ester nandrolone formulation used in androgen anabolic research and joint-tissue studies. Investigators quantify nandrolone and metabolite pharmacokinetics, aromatization to estradiol, and 5α-reduction to DHN.

Orals / SARMs

Anavar

Oxandrolone (Anavar) is a mild 17α-alkylated androgen researched for lean-mass preservation with relatively low androgenic activity in burn and sarcopenia models. Work focuses on protein anabolism, lipolysis, and hepatic enzyme profiles at therapeutic versus supraphysiologic exposures.

From $503 variants

Orals / SARMs

Dianabol

Methandrostenolone (Dianabol) is a 17α-alkylated oral androgen researched for rapid nitrogen retention and glycogen supercompensation in muscle. Studies characterize hepatotoxicity, aromatization to methyl-estradiol, and strength-endpoint changes in short-cycle models.

From $304 variants

Orals / SARMs

Clomid

Clomiphene citrate is a selective estrogen receptor modulator used to study HPG-axis restart via hypothalamic estrogen antagonism. Research models ovulation induction, gonadotropin rebound after androgen suppression, and enantiomer-specific ER binding.

Orals / SARMs

Nolvadex (Tamoxifen)

Tamoxifen citrate is a SERM studied for estrogen-receptor antagonism in breast tissue and agonism in bone, used in PCT research. Laboratory work maps ERα/ERβ selectivity, gonadotropin rebound, and endometrial proliferation risk modeling.

Supplies

BAC Water

Bacteriostatic water for injection contains 0.9% benzyl alcohol and serves as the standard diluent for multi-dose reconstitution of research peptides. Its preservative system is studied for sterility maintenance and compatibility with lyophilized biologics over repeated needle entries.

From $252 variants

GLP-1 / Metabolic

5-Amino-1MQ

5-Amino-1MQ is a small-molecule NNMT (nicotinamide N-methyltransferase) inhibitor studied for its effects on adipocyte metabolism and energy expenditure in preclinical models. Researchers examine how NNMT blockade may shift methyl-donor balance and support fat-mass reduction pathways without classical sympathomimetic mechanisms.

GLP-1 / Metabolic

SLU-PP-332

SLU-PP-332 is a small-molecule ERRα/β/γ agonist studied as an exercise mimetic for mitochondrial biogenesis and endurance phenotype induction. Research examines PGC-1α activation, fatty-acid oxidation, and metabolic rate without classical stimulant mechanisms.

From $505 variants

GLP-1 / Metabolic

Mazdutide

Mazdutide is a dual GLP-1 and glucagon receptor agonist studied for enhanced energy expenditure combined with incretin satiety effects. Preclinical and clinical research examines weight-loss magnitude, hepatic fat reduction, and glucagon-mediated thermogenesis.

From $1902 variants

GH / GHRP

Gonadorelin

Gonadorelin (GnRH) is the decapeptide hypothalamic hormone studied for pituitary LH and FSH pulse initiation in reproductive endocrinology. Research models HPG-axis stimulation, pulsatile versus continuous GnRH desensitization, and fertility-protocol pharmacodynamics.

GH / GHRP

MGF

Mechano growth factor is an IGF-1 splice variant studied for local muscle repair and satellite-cell activation after mechanical loading. Research examines E-domain peptide signaling, hypertrophy versus hyperplasia responses, and injury-site administration models.

GH / GHRP

Kisspeptin-10

Kisspeptin-10 is the active decapeptide fragment of kisspeptin studied for GnRH pulse initiation and reproductive hormone cascade activation. Research examines puberty onset mechanisms, fertility protocol modeling, and HPG-axis synchronization.

From $952 variants

GH / GHRP

SS-31

SS-31 (elamipretide) is a mitochondrial-targeted peptide studied for cardiolipin stabilization and electron-transport efficiency. Research examines heart-failure models, skeletal-muscle fatigue resistance, and age-related mitochondrial dysfunction.

GLP-1 / Metabolic

Glutathione

Reduced glutathione is the primary intracellular antioxidant tripeptide researched for redox homeostasis, detoxification, and melanin pathway modulation. Studies examine GSH depletion in oxidative stress models, hepatic conjugation capacity, and skin-lightening mechanisms.

Cosmetic

Botulinum Toxin

Botulinum neurotoxin type A cleaves SNARE proteins to block acetylcholine release at neuromuscular junctions, widely studied in models of focal paralysis and hyperhidrosis. Cosmetic research examines rhytid reduction, muscle atrophy reversibility, and dose-spreading in dermal applications.

From $2401 variant

Cosmetic

Snap-8

Snap-8 is an octapeptide studied as a topical botulinum-mimetic that modulates SNARE complex formation for wrinkle reduction. Cosmetic research compares Snap-8 versus Botox on expression-line depth, peptide penetration, and reversible neuromuscular effects.

Cosmetic

Matrixyl

Matrixyl (palmitoyl pentapeptide-4) is a collagen-stimulating signal peptide studied for dermal extracellular-matrix renewal in cosmetic models. Research quantifies procollagen I synthesis, fibronectin production, and wrinkle-depth reduction in fibroblast assays.

Nootropic

Dihexa

Dihexa is an oligopeptide hepatocyte growth factor mimetic studied for potent synaptogenesis and cognitive enhancement in neurodegeneration models. Research targets Ang-Tie2 signaling, dendritic spine density, and memory consolidation in Alzheimer's-like rodent paradigms.

Bioregulators

Thymalin

Thymalin is a thymic peptide extract studied for T-cell differentiation, immune reconstitution, and immunosenescence reversal in aging research. Khavinson investigations map thymic involution markers, cytokine normalization, and infection-resistance correlates.

Bioregulators

Pinealon

Pinealon is a tripeptide (Glu-Asp-Arg) bioregulator studied for pinealocyte function, melatonin synthesis, and circadian rhythm normalization. Research examines neuroprotection in brain ischemia models and epigenetic regulation of aging clocks.

From $1003 variants

Sexual Health

Dapoxetine

Dapoxetine is a short-acting SSRI researched for serotonin reuptake inhibition in models of ejaculatory latency and spinal reflex control. Studies map 5-HT transporter occupancy, on-demand pharmacokinetics, and sympathetic-parasympathetic balance in sexual-function assays.

From $192 variants

Sexual Health

Oxytocin

Oxytocin is a hypothalamic nonapeptide studied for social bonding, uterine contraction, and orgasmic reflex modulation in neuroendocrine research. Studies map OT receptor signaling in brain reward circuits and pelvic autonomic pathways.

From $803 variants

Blends

CJC (no DAC) + Ipamorelin

This blend combines modified GRF 1-29 (CJC without DAC) with Ipamorelin to study pulsatile GH release via dual GHRH-mimetic and ghrelin-receptor agonism. Research measures GH burst amplitude, cortisol sparing versus older secretagogues, and IGF-1 area-under-curve profiles.

From $1802 variants

Blends

Tesamorelin + Ipamorelin

This GH secretagogue blend pairs tesamorelin with ipamorelin for dual GHRH and ghrelin-receptor pathway stimulation research. Studies examine synergistic GH pulse amplitude, visceral fat reduction, and IGF-1 kinetics versus monotherapy.

From $3501 variant

Blends

BPC-157 + TB-500

A dual-peptide blend pairing BPC-157 with TB-500 (thymosin beta-4) for combined angiogenic and actin-regulatory repair research. Studies examine accelerated collagen organization, reduced adhesion formation, and synergistic effects on musculoskeletal recovery timelines.

Blends

Reta + Cagri Blend

This blend combines retatrutide and cagrilintide for triple-agonist plus amylin satiety research in advanced metabolic models. Studies examine additive weight-loss mechanisms, nausea management, and glucoregulatory synergy beyond GLP-1 monotherapy.

From $2201 variant

GLP-1 / Metabolic · Orals / SARMs

Tirzepatide Oral

Oral tirzepatide formulations are researched for non-injectable dual GIP/GLP-1 agonism using absorption-enhancer technology. Studies address bioavailability hurdles, fasting-state requirements, and comparative weight-loss efficacy to injectable tirzepatide.

GLP-1 / Metabolic

Dulaglutide

Dulaglutide is a once-weekly GLP-1 receptor agonist with an Fc fusion domain studied for sustained incretin signaling and glycemic control. Research examines GLP-1R internalization, weight-loss kinetics, and cardiovascular outcome biomarkers in metabolic disease models.

Pharma

Anastrozole

Anastrozole is a non-steroidal aromatase inhibitor used to study estrogen suppression via cytochrome P450 aromatase blockade. Laboratory applications include modeling gonadal and peripheral aromatization, feedback on the HPG axis, and estrogen-dependent tissue proliferation.

From $191 variant

Pharma

Finasteride

Finasteride is a type-II 5α-reductase inhibitor studied for DHT reduction in prostate and androgenic alopecia research models. Laboratory work examines neurosteroid alterations, androgen balance shifts, and tissue-specific dihydrotestosterone suppression.

From $303 variants

Orals / SARMs

Cardarine (GW-501516)

GW-501516 (Cardarine) is a PPARδ agonist researched for fatty-acid oxidation, endurance phenotype induction, and mitochondrial gene expression in muscle. Despite SARM-adjacent labeling, its mechanism is nuclear receptor-mediated rather than androgen-receptor based.

From $351 variant

Orals / SARMs

Enclomiphene

Enclomiphene is the trans-isomer of clomiphene studied for selective estrogen receptor antagonism and LH-driven testosterone restoration. Research compares enclomifene versus zuclomifene on gonadotropin pulses, testicular testosterone output, and HPG-axis recovery.

Oils

Masteron Propionate

Drostanolone propionate is the short-ester Masteron formulation used in androgen receptor binding and lean-mass retention research. Studies examine rapid peak concentrations, lack of estrogen conversion, and skeletal-muscle androgen sensitivity.

Oils

Primobolan Enanthate

Methenolone enanthate is a mild DHT-derived injectable androgen studied for lean-mass preservation with minimal water retention. Research characterizes low androgenic indices, favorable lipid effects relative to 19-nors, and collagen synthesis support.

From $4702 variants

Oils

Boldenone (Equipoise)

Boldenone undecylenate is a long-ester anabolic androgen researched for steady-state androgen exposure, erythropoiesis, and collagen synthesis in equine and rodent models. Studies characterize aromatization rates, appetite effects, and lean-mass accrual kinetics.

From $1503 variants

Supplies

AA Water

Sterile 0.9% benzyl alcohol bacteriostatic water is used in laboratory settings to reconstitute lyophilized peptide and protein preparations. The benzyl alcohol preservative allows multi-dose withdrawal from a single vial while maintaining sterility over repeated access in controlled research workflows.

GH / GHRP

ACE-031

ACE-031 is a soluble activin type IIB receptor fusion protein investigated for its ability to antagonize myostatin and related TGF-beta ligands in muscle biology research. Preclinical studies focus on lean-mass signaling, satellite-cell activity, and neuromuscular function under conditions of muscle wasting.

From $1401 variant

Nootropic

Adamax

Adamax is a modified Semax analog with an adamantane moiety designed to enhance lipophilicity and blood-brain barrier penetration in neuropharmacology studies. Researchers evaluate BDNF upregulation, attention-related behavior, and neuroprotective responses under oxidative and ischemic stress.

From $2401 variant

GLP-1 / Metabolic

Adipotide

Adipotide (FTPP) is a peptidomimetic that targets prohibitin on adipose vasculature, studied for selective ablation of white-fat blood supply in obesity models. Preclinical work measures fat-depot regression, insulin sensitivity changes, and vascular specificity versus lean tissue.

From $1402 variants

Cosmetic

AHK-Cu

AHK-Cu is a copper tripeptide (alanine-histidine-lysine) studied alongside GHK-Cu for dermal matrix remodeling and hair-follicle biology. Laboratory work examines collagen synthesis, angiogenic signaling, and extracellular-matrix turnover in skin and scalp tissue models.

From $1401 variant

GLP-1 / Metabolic

AICAR

AICAR (acadesine) is an AMPK-activating adenosine analog used to study cellular energy sensing, glucose uptake, and mitochondrial biogenesis in metabolic research. Investigators apply it to model exercise-mimetic signaling and probe endurance-related transcriptional programs in skeletal muscle.

Orals / SARMs

AICAR Oral

Oral AICAR formulations are studied for comparative bioavailability and AMPK pathway engagement relative to injectable routes in rodent metabolic models. Research emphasizes oral dosing kinetics, tissue distribution, and downstream effects on glycogen handling and fatty-acid oxidation.

Sexual Health

Alprostadil

Alprostadil (prostaglandin E1) is a vasodilatory prostaglandin studied in laboratory models of penile smooth-muscle relaxation and pelvic hemodynamics. Research examines cyclic AMP signaling, cavernosal blood flow, and erectile-tissue pharmacodynamics.

Orals / SARMs

Anadrol

Oxymetholone (Anadrol) is a 17α-alkylated anabolic androgen studied for erythropoiesis, nitrogen retention, and androgen-receptor-mediated anabolism in muscle-wasting research. Investigators characterize hepatotoxicity profiles, hematologic shifts, and dose-dependent anabolic indices.

From $452 variants

Pharma

Anastrozole (Arimidex)

Anastrozole (Arimidex) is the branded form of a third-generation aromatase inhibitor employed in endocrine research on estrogen biosynthesis. Studies quantify estradiol reduction kinetics, bone-metabolism markers, and aromatase inhibition potency in comparative endocrine assays.

Orals / SARMs

Andarine S4

Andarine (S4) is a selective androgen receptor modulator studied for partial agonism in muscle and bone with reduced prostate stimulation in preclinical models. Research examines tissue-selective AR signaling, vision-related metabolite effects, and dose-response on lean mass.

Healing

ARA-290

ARA-290 is an 11-amino-acid peptide derived from erythropoietin that activates the innate repair receptor (IRR) without erythropoietic effects. Research targets neuropathic pain modulation, anti-inflammatory tissue repair, and microvascular protection in diabetic and ischemic injury models.

Pharma

Armodafinil

Armodafinil is the R-enantiomer of modafinil investigated for wake-promoting effects through dopamine transporter inhibition and orexin pathway modulation. Laboratory studies assess vigilance, sleep-deprivation recovery, and neurochemical correlates of alertness.

Pharma

Armodafinil (Artvigil)

Armodafinil (Artvigil) is a branded enantiopure modafinil formulation used in comparative pharmacokinetic and wakefulness research. Studies map plasma half-life, receptor occupancy, and cognitive performance endpoints against racemic modafinil.

Pharma

Armodafinil (Waklert)

Armodafinil (Waklert) is studied as a long-acting eugeroic for modeling sustained dopaminergic tone and histamine release in alertness assays. Researchers evaluate dose-duration relationships and receptor-level mechanisms underlying reduced sleep propensity.

Cosmetic

Azelaic Acid Gel

Azelaic acid is a dicarboxylic acid researched for keratinocyte differentiation, tyrosinase inhibition, and anti-inflammatory activity in acne and hyperpigmentation models. Topical gel formulations are used to study follicular keratinization and rosacea-related vascular inflammation.

From $401 variant

Pharma

B12 Injectable

Cyanocobalamin injectable preparations are used in research on one-carbon metabolism, methionine synthase activity, and erythropoiesis support. Studies examine B12 tissue stores, homocysteine remethylation, and neurological marker changes under deficiency-repletion paradigms.

From $501 variant

GLP-1 / Metabolic

BAM15

BAM15 is a mitochondrial uncoupler researched for increasing energy expenditure by dissipating the proton gradient without inhibiting ATP synthase. Preclinical models investigate thermogenesis, insulin sensitivity, and selective uncoupling versus classical DNP toxicity profiles.

Cosmetic

Bimatoprost Eye Drops

Bimatoprost is a prostaglandin F2α analog studied for FP receptor activation in intraocular pressure reduction and lash-growth research. Ophthalmic drops are used to model trabecular outflow, melanogenesis in follicles, and periorbital adipose changes.

From $601 variant

Blends

BPC + TB + KPV

This triple-peptide blend combines BPC-157, TB-500, and KPV for synergistic gastrointestinal, musculoskeletal, and anti-inflammatory pathway research. Investigators compare multi-target repair signaling against single-peptide controls in tendon, gut, and wound-healing models.

From $2801 variant

Orals / SARMs

BPC + TB Oral Blend

An oral combination of BPC-157 and TB-500 analogs studied for mucosal absorption and systemic exposure relative to injectable routes. Research focuses on gut-integrity markers, oral bioavailability challenges, and comparative healing endpoints in GI injury models.

Healing

BPC-157 Arg

BPC-157 Arg is an arginine salt form of BPC-157 studied for improved solubility and stability while preserving gastric pentadecapeptide repair activity. Research compares salt versus acetate forms on angiogenic VEGF signaling and tendon outgrowth assays.

Orals / SARMs

BPC-157 Oral

Oral BPC-157 is investigated for stability through the GI tract and effects on mucosal healing, NSAID-induced gut injury, and systemic repair markers. Studies address peptide degradation kinetics and oral dose equivalence to parenteral administration in rodent models.

From $451 variant

Bioregulators

Bronchogen

Bronchogen is a Khavinson-class short peptide bioregulator derived from bronchial tissue, studied for gene-expression normalization in pulmonary cell lines. Research examines bronchial epithelial repair, mucociliary function markers, and age-related transcriptomic shifts.

Pharma

Bupropion SR

Bupropion is a norepinephrine-dopamine reuptake inhibitor researched for dopaminergic reward pathways, smoking-cessation neurochemistry, and antidepressant mechanisms. Sustained-release formulations are used to model steady plasma levels and seizure-threshold pharmacology.

From $151 variant

Pharma

Cabergoline

Cabergoline is a long-acting ergot-derived dopamine D2 agonist studied for prolactin suppression and lactotroph inhibition. Laboratory work examines dopaminergic feedback on the HPG axis, valvulopathy risk modeling, and hyperprolactinemia reversal kinetics.

From $192 variants

Blends

Cagri + Sema Blend

A co-formulated blend of cagrilintide and semaglutide studied for dual amylin and GLP-1 receptor engagement in metabolic research. Preclinical models investigate synergistic satiety signaling, weight-loss magnitude, and glucoregulatory effects beyond monotherapy.

Bioregulators

Cardiogen

Cardiogen is a cardiac-tissue-derived Khavinson peptide bioregulator studied for cardiomyocyte stress resistance and post-ischemic remodeling. Research examines apoptotic signaling, fibrosis markers, and age-related cardiac gene-expression normalization.

Cosmetic

Careprost (Bimatoprost)

Careprost is a bimatoprost ophthalmic solution repurposed in lash-growth research for prostaglandin-mediated follicle cycling and melanogenesis. Studies quantify lash length, thickness, iris pigmentation risk, and periorbital fat changes in cosmetic models.

Bioregulators

Cartalax

Cartalax is a cartilage-derived peptide bioregulator investigated for chondrocyte matrix production and aggrecan/collagen II expression. Research targets osteoarthritis models, cartilage degradation enzymes, and joint-tissue regenerative signaling.

Nootropic

Cerebrolysin

Cerebrolysin is a porcine brain-derived peptide mixture studied for neurotrophic factor mimicry, stroke recovery, and synaptic plasticity in CNS injury models. Investigators measure BDNF pathways, cognitive recovery timelines, and blood-brain barrier penetration of low-molecular-weight fractions.

Bioregulators

Chonluten

Chonluten is a lung/bronchial peptide bioregulator researched for pulmonary surfactant regulation and bronchial epithelial gene expression. Studies examine COPD-like inflammation models, mucus production, and Khavinson-class transcriptomic normalization.

GLP-1 / Metabolic

Clenbuterol

Clenbuterol is a beta-2 adrenergic agonist studied for sympathomimetic thermogenesis, skeletal-muscle hypertrophy, and lipolytic signaling. Research characterizes receptor desensitization, cardiac chronotropy, and lean-mass effects in livestock and rodent models.

Orals / SARMs

Clomiphene

Clomiphene is the active compound in Clomid, investigated for SERM activity at hypothalamic estrogen receptors and downstream LH/FSH release. Laboratory work compares zuclomifene and enclomifene contributions to gonadotropin stimulation profiles.

Sexual Health

Cock Bombs (Viagra+Cialis)

This sildenafil and tadalafil combination is studied for dual PDE5 inhibition kinetics covering rapid onset and extended duration in erectile-tissue models. Research examines overlapping cGMP signaling, hemodynamic duration, and receptor-level synergy in smooth-muscle relaxation assays.

Bioregulators

Cortagen

Cortagen is a cerebral-cortex-derived peptide bioregulator studied for cortical neuron stress responses and age-related cognitive decline markers. Research maps neurotrophic gene expression, synaptic density correlates, and Khavinson bioregulator transcriptomic effects.

Bioregulators

Crystagen

Crystagen is an immune-cell peptide bioregulator investigated for thymus-dependent lymphocyte function and immunosenescence models. Studies examine T-cell repertoire markers, cytokine balance, and peptide-mediated normalization of immune gene expression.

Oils

Deca

Nandrolone decanoate (Deca) is a 19-nortestosterone ester studied for anabolic activity with relatively low androgenic conversion in muscle and joint research. Models examine collagen synthesis, joint lubrication markers, and progestogenic feedback on the HPG axis.

From $2101 variant

Rare

Dermorphin

Dermorphin is a hepta-peptide opioid agonist from amphibian skin studied for ultra-potent mu-opioid receptor activation and analgesic pharmacology. Research examines receptor selectivity, respiratory-depression profiles, and structure-activity relationships versus endogenous endorphins.

From $1001 variant

Oils

DHB (1-Test Cyp)

Dihydroboldenone cypionate (1-testosterone) is a 5α-reduced boldenone analog studied for high anabolic potency with reduced estrogenic conversion. Research characterizes androgen-receptor binding, lipid profile shifts, and comparative anabolic indices versus testosterone esters.

From $402 variants

GLP-1 / Metabolic

DNP

2,4-Dinitrophenol is a proton ionophore researched historically for uncoupling oxidative phosphorylation and dramatically increasing metabolic rate. Laboratory studies focus on thermogenic mechanisms, mitochondrial toxicity thresholds, and hyperthermia risk modeling.

From $701 variant

Pharma

Dutasteride

Dutasteride is a dual 5α-reductase inhibitor (types I and II) studied for suppression of DHT synthesis from testosterone. Laboratory models investigate prostate volume reduction, hair-follicle miniaturization reversal, and neurosteroid pathway effects.

From $302 variants

Pharma

EPO

Erythropoietin is a glycoprotein hormone researched for erythropoiesis via EPO receptor activation on bone-marrow progenitors. Studies examine hematocrit kinetics, oxygen-delivery modeling, and tissue-protective non-hematopoietic EPO receptor signaling.

FGFR3 · Rare

Erdafitinib

Erdafitinib is a pan-FGFR tyrosine kinase inhibitor researched for FGFR-driven tumor proliferation and urothelial carcinoma signaling. Laboratory studies map receptor autophosphorylation blockade, downstream MAPK attenuation, and selectivity across FGFR isoforms.

From $1801 variant

Pharma

Exemestane

Exemestane is a steroidal aromatase inactivator (suicide inhibitor) studied for irreversible estrogen synthesis blockade. Research compares exemestane versus non-steroidal aromatase inhibitors on estradiol suppression depth, androgenic metabolites, and bone turnover markers.

Pharma

Exemestane (Aromasin)

Exemestane (Aromasin) is the branded steroidal aromatase inactivator used in breast-cancer and endocrine modeling research. Studies quantify irreversible enzyme binding, androgen precursor accumulation, and estrogen-feedback effects on gonadotropins.

From $1101 variant

Rare

FOXO4-DRI

FOXO4-DRI is a D-retro-inverso peptide that disrupts FOXO4-p53 interaction to selectively induce senescent-cell apoptosis. Research focuses on senolytic clearance, tissue rejuvenation markers, and chemotherapy- or radiation-induced senescence models.

From $5201 variant

Pharma

Gabapentin

Gabapentin is a gabapentinoid studied for voltage-gated calcium channel modulation and neuropathic pain pathway attenuation. Research examines GABA synthesis effects, neurotransmitter release inhibition, and analgesic efficacy in nerve-injury models.

From $132 variants

Cosmetic

GHK Basic

GHK (glycyl-L-histidyl-L-lysine) without copper is studied for innate copper-chelating activity and gene-expression modulation in skin fibroblasts. Research compares apo-GHK versus GHK-Cu on collagen, elastin, and wound-contraction signaling pathways.

Blends

GHK-Cu + Glutathione Blend

This blend pairs GHK-Cu with reduced glutathione for combined extracellular-matrix remodeling and antioxidant defense research. Investigators examine synergistic effects on fibroblast migration, melanin regulation, and oxidative-stress biomarkers in skin models.

Blends

GLOW-50 Blend

GLOW-50 is a cosmetic peptide blend combining GHK-Cu, BPC-157, and TB-500 for multi-pathway skin and subcutaneous repair research. Studies examine dermal collagen deposition, angiogenesis, and combined anti-inflammatory signaling versus individual peptides.

From $2401 variant

Blends

GLOW-70 Blend

GLOW-70 is a higher-concentration variant of the GHK-Cu, BPC-157, and TB-500 cosmetic repair blend for dose-response skin research. Investigators compare GLOW-70 versus GLOW-50 on fibroblast proliferation, wound closure rates, and matrix metalloproteinase regulation.

From $3001 variant

Oils

Halotestin

Fluoxymesterone (Halotestin) is a potent oral halogenated androgen studied for CNS-mediated aggression and strength endpoints with minimal mass gain. Research characterizes extreme androgenic receptor binding, hepatic strain, and hematologic stimulation.

GLP-1 / Metabolic

HGH Frag 176-191

The HGH 176–191 fragment is the lipolytic domain of growth hormone studied for fat mobilization without significant IGF-1 elevation. Research compares fragment-induced adipocyte lipolysis versus full-length GH and examines cartilage repair claims in joint models.

From $902 variants

Pharma

HMG

Human menopausal gonadotropin combines FSH and LH activity for research on folliculogenesis and spermatogenesis stimulation. Studies model IVF gonadotropin protocols, ovarian response, and Leydig/Sertoli cell stimulation kinetics.

GH / GHRP

Humanin

Humanin is a mitochondrial-derived peptide studied for cytoprotection against amyloid toxicity, oxidative stress, and apoptosis in neuronal models. Research maps Bax suppression, insulin sensitivity improvements, and longevity-associated mitochondrial signaling.

From $2701 variant

Cosmetic

Hyaluronic Acid

Hyaluronic acid is a glycosaminoglycan researched for dermal hydration, viscoelastic matrix properties, and joint lubrication in osteoarthritis models. Cosmetic studies examine molecular-weight-dependent penetration, volume restoration, and CD44 receptor interactions.

From $381 variant

Blends

Immune Enhancement Blend

This multi-peptide immune blend combines thymosin alpha-1, LL-37, and related immunomodulators for innate and adaptive immunity research. Studies examine T-cell activation markers, antimicrobial peptide activity, and cytokine storm attenuation models.

FGFR3 · Rare

Infigratinib

Infigratinib is a selective FGFR3 kinase inhibitor researched for chondrocyte signaling in achondroplasia and FGFR-driven oncology models. Laboratory work maps receptor phosphorylation blockade, growth-plate biology, and downstream STAT pathway modulation.

From $3701 variant

Cosmetic

Isotretinoin

Isotretinoin (13-cis-retinoic acid) is studied for sebocyte apoptosis, sebum suppression, and keratinocyte differentiation in acne models. Research examines retinoid receptor signaling, teratogenicity mechanisms, and mucocutaneous side-effect profiling.

From $352 variants

Cosmetic

Isotretinoin (Accutane)

Isotretinoin (Accutane) is the branded oral retinoid formulation used in severe acne and sebaceous-gland research. Studies quantify sebum output reduction, follicular keratinization normalization, and pharmacokinetic variability under fed versus fasted conditions.

Pharma

Ivermectin

Ivermectin is a macrocyclic lactone studied for glutamate-gated chloride channel activation in parasitic models and emerging antiviral screening. Research also examines neuroinflammation modulation and P2X4 receptor interactions at higher exposure levels.

Blends

KLOW-80 Blend

KLOW-80 combines KPV, BPC-157, GHK-Cu, and TB-500 for integrated anti-inflammatory and regenerative pathway research. Investigators study gut-skin axis markers, mast-cell stabilization, and multi-tissue repair signaling in comparative blend assays.

Orals / SARMs

KPV Oral

Oral KPV is investigated for mucosal anti-inflammatory activity and stability through digestive environments in colitis models. Studies compare oral versus injectable routes on intestinal permeability, cytokine reduction, and peptide absorption kinetics.

Cosmetic

Lemon Bottle

Lemon Bottle is a fat-dissolving cosmetic injection blend (riboflavin, lecithin, bromelain) studied for localized adipocyte disruption in subcutaneous models. Research examines phosphatidylcholine-mediated cell lysis, inflammation profiles, and contouring endpoint measurements.

Pharma

Letrozole

Letrozole is a potent non-steroidal aromatase inhibitor studied for near-complete estrogen suppression in endocrine research. Laboratory models investigate feedback on gonadotropins, bone mineral density changes, and tissue-specific estradiol depletion kinetics.

From $302 variants

GLP-1 / Metabolic

Lipo Mino Mix

Lipo Mino Mix is an injectable lipotropic blend (methionine, inositol, choline, B vitamins) studied for hepatic fat export and methylation support. Research examines steatosis reduction markers, homocysteine metabolism, and adjunctive weight-management protocols.

GLP-1 / Metabolic

Lipo-B 216

Lipo-B 216 is a concentrated lipotropic injection formula researched for choline-driven VLDL export and methionine cycle support in fatty-liver models. Studies quantify hepatic triglyceride changes, energy metabolism, and B12/folate cofactor interactions.

GLP-1 / Metabolic

Lipo-C 120

Lipo-C 120 combines lipotropics with L-carnitine for fatty-acid transport and mitochondrial beta-oxidation research. Investigators study carnitine palmitoyltransferase activity, exercise recovery markers, and adipose mobilization endpoints.

From $751 variant

GLP-1 / Metabolic

Lipo-C FAT BLASTER

Lipo-C FAT BLASTER is an enhanced lipotropic-carnitine blend studied for aggressive hepatic lipid mobilization in metabolic protocols. Research compares formulation potencies on liver echogenicity surrogates, ketone production, and body-composition endpoints.

From $1601 variant

GLP-1 / Metabolic

Lipo-C FOCUS

Lipo-C FOCUS adds nootropic cofactors to lipotropic bases for combined metabolic and cognitive performance research. Studies examine acetylcholine precursor availability, mental clarity correlates, and lipolytic pathway engagement in dual-outcome models.

From $1401 variant

Bioregulators

Livagen

Livagen is a liver-derived Khavinson peptide bioregulator studied for hepatocyte regeneration and detoxification enzyme expression. Research examines liver fibrosis markers, cytochrome P450 normalization, and age-related hepatic transcriptomic shifts.

Healing

LL-37

LL-37 is the sole human cathelicidin antimicrobial peptide studied for innate immunity, wound re-epithelialization, and angiogenesis. Research examines bacterial membrane disruption, autophagy modulation, and dual pro/anti-inflammatory context-dependent signaling.

Oils

Masteron Enanthate

Drostanolone enanthate is a long-ester DHT derivative studied for anti-estrogenic hardness and 5α-reduced androgen activity without aromatization. Research models contest-prep muscle preservation, SHBG binding, and androgenic alopecia correlates.

From $5201 variant

Oils

MENT (Trestolone Acetate)

Trestolone (MENT) is a 7α-methyl-19-nortestosterone studied for potent anabolic activity without 5α-reduction to dihydro metabolites. Research characterizes progestogenic activity, rapid clearance of acetate ester, and contraceptive-development origins.

From $4101 variant

GLP-1 / Metabolic

Methylene Blue

Methylene blue is a phenothiazine dye studied for mitochondrial electron-transport modulation and neuroprotective antioxidant cycling. Research examines low-dose redox buffering, memory enhancement models, and methemoglobin reduction kinetics.

Orals / SARMs

Methylstenbolone

Methylstenbolone is a designer oral anabolic studied for high potency 17α-methylated androgen activity with structural kinship to DHT derivatives. Research characterizes hepatotoxicity thresholds, rapid strength endpoints, and androgen receptor transactivation profiles.

From $501 variant

Orals / SARMs

Metribolone

Metribolone (R1881) is an extremely potent oral androgen used primarily as a radiolabeled tracer in androgen-receptor binding assays. Laboratory applications include AR competitive binding studies, tissue distribution mapping, and resistance-model characterization.

Cosmetic

Minoxidil Oral

Oral minoxidil is studied for systemic vasodilation and hair-growth promotion via potassium channel opening in follicular dermal papilla. Research examines low-dose protocols, pericardial effusion risk modeling, and comparative efficacy versus topical routes.

Cosmetic

Minoxidil Solution

Topical minoxidil is a vasodilator researched for KATP channel activation in hair-follicle angiogenesis and anagen-phase prolongation. Studies quantify vellus-to-terminal hair conversion, prostaglandin synthase-1 induction, and androgenetic alopecia models.

From $1202 variants

Pharma

Modafinil

Modafinil is a racemic wakefulness agent studied for dopamine transporter inhibition, orexin activation, and histamine release in alertness models. Research compares enantiomer contributions and examines cognitive enhancement without classical amphetamine mechanisms.

From $192 variants

Bioregulators

N-Acetyl Epitalon Amidate

N-Acetyl Epitalon Amidate is a stabilized Epithalon analog studied for enhanced bioavailability and telomerase-activation research. Investigators compare amidated forms on pineal melatonin rhythms, telomere elongation assays, and antioxidant gene expression.

From $952 variants

Nootropic

NA Selank Amidate

N-Acetyl Selank Amidate is a modified anxiolytic peptide studied for enhanced stability and GABAergic modulation without sedation. Research examines enkephalinase inhibition, BDNF expression, and stress-induced behavior in rodent anxiety models.

Nootropic

NA Semax Amidate

N-Acetyl Semax Amidate is a stabilized nootropic peptide analog researched for BDNF upregulation and cognitive recovery after hypoxia. Studies compare amidated versus native Semax on attention tasks, neurotrophin signaling, and blood-brain barrier penetration.

Blends

NAD+ / Mots-c / 5AM Blend

This metabolic blend combines NAD+, MOTS-c, and 5-amino-1MQ for multi-target mitochondrial and NNMT pathway research. Investigators study synergistic effects on cellular energy status, fat oxidation, and NAD+ salvage pathway flux.

From $2101 variant

Rare · Cartridges

NAD+ Cartridge

NAD+ cartridge formulations deliver pre-measured subcutaneous doses for standardized redox-cofactor repletion research protocols. Studies examine cartridge stability, injection convenience effects on compliance modeling, and steady NAD+ tissue levels.

From $152 variants

Pharma

Naltrexone

Naltrexone is an opioid receptor antagonist studied for mu-receptor blockade in addiction models and low-dose immunomodulation research. Studies examine TLR4 interactions, endorphin rebound, and alcohol-craving pathway attenuation.

Oils

Nandromix

Nandromix combines fast and slow nandrolone esters for blended-release androgen research on joint and muscle anabolism. Investigators study dual-peak pharmacokinetics, steady nandrolone levels, and comparative collagen biomarker responses.

From $3101 variant

Oils

NPP

Nandrolone phenylpropionate is a shorter-ester nandrolone studied for faster peak concentrations and joint-support collagen synthesis research. Models compare NPP versus decanoate ester pharmacokinetics and progestogenic HPG-axis feedback.

Bioregulators

Ovagen

Ovagen is a liver-derived tetrapeptide bioregulator studied for hepatocyte gene-expression normalization and detoxification capacity. Khavinson-class research examines cytoprotection, albumin synthesis markers, and age-related hepatic functional decline.

Nootropic

P21

P21 is a CNTF-mimetic peptide studied for neurogenesis promotion and cognitive recovery in traumatic brain injury models. Research examines hippocampal neurogenesis, synaptic plasticity markers, and memory consolidation after neuronal damage.

Nootropic

P21 Adamantane

P21 Adamantane incorporates an adamantyl group for enhanced CNS penetration in neuroregenerative peptide research. Studies compare adamantane-modified versus native P21 on neurogenesis endpoints and blood-brain barrier transport.

From $4201 variant

Bioregulators

Pancragen

Pancragen is a pancreatic peptide bioregulator investigated for islet-cell function and digestive enzyme gene-expression normalization. Khavinson research maps insulin secretion correlates, exocrine pancreatic markers, and age-related metabolic decline.

Nootropic

PE-22-28

PE-22-28 is a TREK-1 potassium channel blocker studied for antidepressant-like effects and neurogenesis promotion. Research examines rapid-acting mood models, BDNF-independent pathways, and TREK-1 role in stress resilience.

GH / GHRP

PEG MGF

PEGylated mechano growth factor extends the half-life of the IGF-1 splice variant for sustained local muscle repair research. Studies examine pegylation effects on satellite-cell activation duration and site-specific hypertrophy responses.

Rare

PNC-27

PNC-27 is a p53-derived peptide studied for selective membranolysis of cancer cells expressing mdm-2 while sparing normal tissue. Research examines pore formation in malignant membranes, HDM-2 binding, and tumor-cell necrosis kinetics.

From $1702 variants

GLP-1 / Metabolic

Pramlintide

Pramlintide is an amylin analog studied for postprandial glucagon suppression and gastric emptying delay in diabetes research. Models examine amylin receptor activation, satiety signaling complementary to insulin, and weight effects in type 1 diabetes.

From $1902 variants

Pharma

Pregabalin

Pregabalin is a gabapentinoid studied for alpha-2-delta subunit binding and calcium-channel-mediated neurotransmitter release inhibition. Research examines neuropathic pain models, anxiolytic correlates, and GABAergic modulation without direct GABA-A activity.

From $153 variants

Orals / SARMs

Primobolan Oral

Methenolone acetate oral (Primobolan) is a 1-methylated DHT derivative studied for anabolic activity with reduced hepatic toxicity versus C17-alkylated orals. Models examine nitrogen balance, immune modulation, and relatively mild HPG-axis suppression.

From $503 variants

Bioregulators

Prostamax

Prostamax is a prostate-derived peptide bioregulator studied for prostatic epithelial gene-expression normalization in BPH models. Khavinson research examines stromal proliferation markers, inflammation reduction, and urodynamic correlates.

Pharma

Proviron

Mesterolone (Proviron) is a 1-methylated DHT oral studied for SHBG binding, free-androgen modulation, and mild androgenic support. Research examines estrogen antagonism via aromatase interaction and fertility-parameter effects on spermatogenesis.

From $352 variants

Rare

PTD-DBM

PTD-DBM is a cell-penetrating peptide inhibitor of CXXC5 studied for hair-regeneration signaling via Wnt pathway disinhibition. Research examines wound-induced hair neogenesis, beta-catenin stabilization, and follicle stem-cell activation.

From $3701 variant

Oils

Ripex Blend

Ripex is a multi-ester testosterone and trenbolone blend studied for combined androgenic-anabolic pharmacokinetics in preclinical protocols. Research maps dual-peak release profiles, estrogen management requirements, and lean-mass endpoint variability.

From $3101 variant

Blends

Semax + Selank Blend

This nootropic blend pairs Semax and Selank for combined cognitive enhancement and anxiolytic research without sedative overlap. Studies examine synergistic BDNF/GABAergic signaling, stress-resilience endpoints, and dual-peptide pharmacokinetics.

From $1601 variant

Oils

Shred Blend

Shred Blend combines short-ester androgens with lipolytic agents for body-composition research on simultaneous fat loss and muscle retention. Studies map pharmacokinetic interactions, estrogen management, and cutting-phase endpoint measurements.

Orals / SARMs

SR-9009

SR-9009 (Stenabolic) is a REV-ERB agonist researched for circadian metabolic regulation, mitochondrial count, and endurance capacity in rodent models. Despite SARM-adjacent categorization, its mechanism operates through nuclear receptor Rev-Erbα/β, not androgen receptors.

From $451 variant

Oils

Super Shred Blend

Super Shred Blend is an intensified cutting-stack oil formulation studied for accelerated fat mobilization with anabolic preservation. Research examines multi-compound synergy, cardiovascular strain markers, and comparative leanness endpoints versus standard shred blends.

Orals / SARMs

Superdrol

Methasterone (Superdrol) is a potent oral anabolic studied for rapid lean-mass gains without aromatization or progesterone activity. Research characterizes severe hepatotoxicity profiles, lipid perturbation, and dry-muscle accrual kinetics in short cycles.

From $352 variants

Oils

Supertest

Supertest blends multiple testosterone esters for broad pharmacokinetic coverage in androgen replacement and anabolic research. Studies map combined peak/trough profiles, steady-state testosterone levels, and ester-specific release kinetics.

Oils

Sustanon

Sustanon is a four-ester testosterone blend studied for multi-phase release kinetics mimicking physiologic testosterone fluctuations. Research compares Sustanon versus single-ester protocols on stable serum testosterone, estradiol aromatization, and injection-frequency modeling.

GLP-1 / Metabolic

T3 (Liothyronine)

Liothyronine (T3) is the active thyroid hormone studied for basal metabolic rate elevation via nuclear thyroid receptor activation. Research examines deiodinase regulation, cardiac chronotropy, muscle catabolism risk, and hypothyroid replacement kinetics.

From $252 variants

GLP-1 / Metabolic

T4

Levothyroxine (T4) is a prohormone studied for peripheral T4-to-T3 conversion via deiodinase enzymes in thyroid research. Models map TSH feedback, tissue-specific conversion rates, and metabolic rate changes under supplementation.

Cosmetic

Tazarotene Cream

Tazarotene is a topical retinoid prodrug studied for RAR-β/γ activation in psoriasis, acne, and photoaging models. Research examines keratinocyte differentiation, parakeratosis correction, and retinoid irritation dose-response profiling.

Healing

TB-500 FRAG

TB-500 FRAG is a truncated thymosin beta-4 fragment studied for retaining actin-binding repair activity in a smaller peptide sequence. Research compares full-length TB4 versus fragment on cell migration, angiogenesis, and dosing efficiency.

Pharma

Telmisartan

Telmisartan is an angiotensin II receptor blocker studied for AT1 antagonism, blood-pressure reduction, and partial PPAR-γ agonist activity. Research examines cardiometabolic benefits beyond blood pressure, including insulin sensitivity and anti-inflammatory effects.

GLP-1 / Metabolic

Teriparatide

Teriparatide is recombinant PTH(1-34) studied for anabolic bone formation via intermittent osteoblast activation in osteoporosis research. Investigations map Wnt signaling, bone mineral density gains, and osteosarcoma risk modeling at sustained high exposures.

From $2701 variant

Pharma

Tesofensine

Tesofensine is a triple monoamine reuptake inhibitor studied for potent appetite suppression and weight loss in obesity models. Research examines dopamine, norepinephrine, and serotonin transporter blockade and cardiovascular monitoring requirements.

From $451 variant

Bioregulators

Testagen

Testagen is a testicular peptide bioregulator studied for Leydig and Sertoli cell gene-expression normalization in aging models. Khavinson research examines testosterone synthesis markers, spermatogenesis correlates, and HPG-axis support.

Oils

Testosterone Base (no ester)

Testosterone suspension without ester is studied for immediate peak serum testosterone and rapid clearance kinetics. Research models pre-workout androgen spikes, injection-frequency requirements, and crystallization pain correlates in aqueous carriers.

Oils

Testosterone Propionate

Testosterone propionate is a short-ester testosterone studied for rapid peak concentrations and frequent injection pharmacokinetics. Research maps sharper peak/trough cycles, lower water retention versus long esters, and micro-dosing protocols.

From $1102 variants

Oils

Testosterone Suspension

Testosterone aqueous suspension delivers unesterified testosterone for immediate serum elevation in acute androgen research. Studies examine microcrystal depot formation, same-day peak levels, and comparative anabolic timing versus esterified forms.

From $1101 variant

Oils

Testosterone Undecanoate

Testosterone undecanoate in oil (TU) is studied for ultra-long half-life androgen delivery with infrequent injection intervals. Research examines castor-oil depot absorption, steady testosterone levels, and fertility preservation relative to shorter esters.

Oils

Tren / Mast / Test Blend

This triple-compound oil blend combines trenbolone, masteron, and testosterone for advanced androgenic-anabolic synergy research. Studies map progestogenic, anti-estrogenic, and aromatizable androgen interactions on body composition and lipid profiles.

Oils

Tren / Mast Blend

A trenbolone and masteron blend studied for complementary 19-nor anabolic and DHT-derived anti-estrogenic activity without testosterone base. Research examines prolactin management, hardness endpoints, and combined receptor-activation profiles.

From $5801 variant

Oils

Tren Hex (Parabolan)

Trenbolone hexahydrobenzylcarbonate is a longer-acting trenbolone ester studied for sustained 19-nor androgen exposure and recomp effects. Research characterizes parabolan-era pharmacokinetics, progestogenic activity, and night-sweat cardiovascular correlates.

Oils

Tren Mix

Tren Mix combines multiple trenbolone esters for blended-release pharmacokinetics in 19-nor androgen research. Studies examine combined acetate/enanthexy/hydroxybenzoate peaks, steady trenbolone levels, and dose-response on lean mass.

From $3101 variant

Oils

Trenbolone Base

Trenbolone without ester (base) is studied for rapid serum elevation and short half-life 19-nor androgen pharmacology. Models examine immediate peak concentrations, injection-site irritation, and acute nutrient-partitioning effects.

Oils

Trenbolone Enanthate

Trenbolone enanthate provides longer-acting 19-nor exposure for sustained androgenic-anabolic research with less frequent dosing. Studies compare enanthate versus acetate on prolactin kinetics, cardiovascular strain markers, and lean-mass accrual.

From $2002 variants

Cosmetic

Tretinoin Cream

Tretinoin (all-trans retinoic acid) cream is studied for RAR-mediated keratinocyte turnover, collagen induction, and photoaging reversal. Research quantifies fine-wrinkle reduction, pigment normalization, and retinization irritation timelines.

From $302 variants

Cosmetic

Tretinoin Gel

Tretinoin gel formulations are researched for acne vulgaris comedolysis and accelerated epidermal desquamation. Studies compare gel versus cream vehicle penetration, irritation profiles, and sebaceous-gland size reduction kinetics.

Oils

Tri-Tren

Tri-Tren blends three trenbolone esters for multi-phase 19-nor release in advanced androgen research protocols. Investigators study overlapping peak concentrations, steady trenbolone exposure, and comparative side-effect kinetics.

From $4101 variant

Orals / SARMs

Turinabol

Chlorodehydromethyltestosterone (Turinabol) is a chlor-substituted Dianabol analog studied for anabolic activity without estrogenic conversion. Research characterizes lean dry gains, SHBG binding, and East German sports-pharmacology historical datasets.

From $353 variants

Bioregulators

Vesugen

Vesugen is a vascular-wall peptide bioregulator studied for endothelial function and microcirculatory gene-expression normalization. Khavinson research examines vasomotor tone, atherosclerosis risk markers, and age-related vascular stiffness correlates.

Bioregulators

Vilon

Vilon (Lys-Glu) is a dipeptide bioregulator studied for thymic immune modulation and chromatin decondensation in aging research. Studies examine CD4/CD8 ratios, melatonin pathway interactions, and epigenetic rejuvenation markers.

Nootropic

VIP

Vasoactive intestinal peptide (VIP) is a 28-amino-acid neuropeptide studied for vasodilation, circadian regulation, and anti-inflammatory immunomodulation. Research examines PACAP/VIP receptor signaling in neuroprotection, gut motility, and pulmonary hypertension models.

From $1402 variants

Pharma

Vitamin D3 Injectable

Injectable cholecalciferol is studied for rapid vitamin D repletion and calcium-phosphate homeostasis in deficiency models. Research examines 25(OH)D elevation kinetics, parathyroid hormone suppression, and bone mineralization markers.

FGFR3 · Rare

Vosoritide

Vosoritide is a C-type natriuretic peptide analog studied for FGFR3-negative chondrocyte proliferation in achondroplasia research. Investigations map growth-plate histology, linear growth velocity, and NPR-B receptor activation without blood-pressure effects.

From $1,8501 variant

Orals / SARMs

Winstrol

Stanozolol (Winstrol) is a DHT-derived anabolic studied for SHBG lowering, lean-muscle preservation, and collagen-fragility concerns. Research compares oral versus injectable routes on liver strain, joint dryness, and hematologic stimulation.

From $303 variants

Oils

Winstrol (oil base)

Oil-based stanozolol suspension is studied for injectable DHT-anabolic delivery bypassing first-pass hepatic metabolism. Research examines depot absorption, injection-site crystallization, and comparative hepatotoxicity versus oral stanozolol.

Oils

Winstrol (water base)

Aqueous stanozolol microcrystal suspension is researched for rapid serum stanozolol elevation and daily injection protocols. Studies map painful microcrystal depot formation, short half-life kinetics, and dry-lean physique endpoints.