Complete Catalog — 92 Compounds
AllPeptides
92 compounds across every goal — CoA-verified on every batch, from skin collagen to telomere extension to GLP-1 fat-loss protocols.
Showing 19 peptides · Fat Loss / Metabolic

Semaglutide
Long-half-life GLP-1 receptor agonist studied in the STEP weight-management trials. Available in five vial sizes from 3 mg through 30 mg to match research-protocol duration; all sizes draw from the same batch and CoA.

Tirzepatide
Dual incretin agonist engaging both GLP-1 and GIP receptors. Studied in SURMOUNT-1 (22.5% weight reduction at 72 weeks). Available in 15 mg, 30 mg, and 60 mg vials.

Retatrutide
Triple incretin agonist reported to produce 24.2% body-weight reduction at 48 weeks in NEJM Phase 2 data (2023). Available across four vial sizes from 10 mg through 30 mg.

CagriReta
Amylin-analogue cagrilintide combined with triple-agonist retatrutide for researchers exploring additive satiety and energy-balance pathways. Available in 5 mg and 10 mg sizes.

Cagrilintide
Acylated amylin analogue designed for once-weekly subcutaneous dosing. Studied alongside semaglutide and retatrutide for combined incretin/amylin research. Available in 5 mg and 10 mg.

AOD-9604
Modified 16-residue C-terminal fragment of human growth hormone (177-191), engineered to retain lipolytic activity without the metabolic effects of full-length hGH. Available in 2 mg, 5 mg, and 10 mg.

Adipotide (FTTP)
Fat-targeting proapoptotic peptide studied in primate adiposity models by Arap & Pasqualini. Available in 5 mg and 10 mg research vials.

BAM15
Small-molecule mitochondrial protonophore studied as a tissue-safe alternative to DNP for thermogenesis research. Available as 30 mg/mL or 50 mg/mL in 30 mL.

L-Carnitine
Quaternary ammonium compound required for long-chain fatty-acid transport into mitochondria. Available in two concentrations and a 5-pack.

SLU-PP-332 (Liquid)
Estrogen-related-receptor agonist studied for endurance and mitochondrial biogenesis. Liquid formulation in two concentrations.

SLU-PP-332 (Capsules)
Estrogen-related-receptor agonist studied for endurance and mitochondrial biogenesis. Capsule format across three strength/count combinations.

5-Amino-1MQ
Nicotinamide N-methyltransferase inhibitor studied for white-adipose NAD+ preservation and metabolic endpoints. Lyophilized research vials; 5 mg and 50 mg.

5-Amino-1MQ 50mg x60 Capsules
5-Amino-1MQ in a 60-capsule bottle at 50mg per capsule — the oral-delivery format of the NNMT inhibitor, supplying roughly two months of daily research dosing in a single bottle.

AICAR 50mg
AICAR 50mg — 5-Aminoimidazole-4-carboxamide ribonucleoside, a small-molecule AMPK activator famously described as "exercise in a pill" after the 2008 Narkar Salk Institute endurance study.

Mazdutide 6mg
Mazdutide (IBI362) — Innovent Biologics' long-acting GLP-1/glucagon dual agonist, the oxyntomodulin analog licensed from Eli Lilly that received Chinese NMPA approval in 2025 for obesity and T2D.

O-304 (ATX-304) 100mg x60 Capsules
O-304 / ATX-304 — a direct pan-AMPK activator developed by Betagenon and licensed to Atrogi, positioned as an exercise-mimetic small molecule that activates the α1β1γ1, α1β2γ1, and α2β1γ1 AMPK isoforms at low micromolar potency.

Survodutide 10mg
Survodutide (BI 456906) — the Boehringer Ingelheim/Zealand Pharma GLP-1/glucagon dual agonist that cleared Phase 2 MASH in 2024 with a 83% fibrosis-improvement response rate at the top dose.

Tesofensine 500mcg x30 Capsules
Tesofensine — a small-molecule triple monoamine reuptake inhibitor (dopamine, norepinephrine, serotonin) originally developed by NeuroSearch as an Alzheimer's candidate, reclassified into obesity research after Phase 2 showed 12.5kg mean weight loss at 1mg over 24 weeks.

Tesofensine 500mcg x30 Tablets
The pressed-tablet format — identical 500mcg tesofensine dose as the capsule variant, differentiated by faster GI disintegration kinetics and the practical option to split the tablet for lower-dose titration research.
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