Accessing Library
Connecting to Pep Nation Lab's research database...
Connecting to Pep Nation Lab's research database...
Select Up To Four Compounds To Review Their Evidence, Targets, And Handling Side By Side.
For Laboratory Research Only



| Attribute | ||
|---|---|---|
Research Summary | Survodutide is a dual-action weight loss powerhouse. It kills your appetite so you do not want to eat, while simultaneously turning up your body's heat to burn off stubborn fat directly from the liver. | Tirzepatide is a super-advanced weight loss signal. It acts like two different hormones combined into one, stopping your hunger completely while also making your body process sugars flawlessly. |
Studied For | Obesity / overweightType 2 diabetesMASH / metabolic liver diseaseNon-alcoholic steatohepatitis (NASH)Liver fat reductionDual GLP-1 glucagon therapyHbA1c loweringBody weight reductionCardiovascular risk reductionInsulin resistanceMetabolic syndromeHepatic steatosisLipid metabolismweight lossliver fat reductionNASHNAFLDobesityenergy expenditure increase | Type 2 diabetes managementChronic weight management / obesityObstructive sleep apnea in obesity (FDA approved 2024)Non-alcoholic fatty liver disease (NAFLD/MASH)Cardiovascular risk reductionHbA1c loweringBody weight reduction superior to semaglutideInsulin resistanceMetabolic syndromePolycystic ovary syndromeKidney disease in diabetesHeart failure with obesityAppetite suppression dual pathwayLean mass preservationweight lossdiabetesfat lossappetite suppressionobesitymetabolic syndromeinsulin sensitivityA1C reduction |
Research Areas | MetabolicWeight Management & Fat Loss | MetabolicWeight Management & Fat Loss |
Best Stacked With | l-carnitineb12bac-water | l-carnitineb12lipo-cbac-water |
Overview | ||
Category | Weight Loss & Metabolism | Weight Loss & Metabolism |
Compound Class | Synthetic dual agonist: GLP-1 receptor + glucagon receptor | Dual GIP/GLP-1 receptor co-agonist (twincretin); synthetic 39-residue peptide with C18 fatty diacid for albumin binding |
Molecular Target | GLP-1R (satiety, insulin secretion) + GCGR (glucagon receptor: energy expenditure, hepatic lipid metabolism); dual incretin-glucagon signaling | GIPR (GIP receptor) + GLP-1R (GLP-1 receptor); dual incretin axis activation; pancreatic insulin secretion and hypothalamic appetite suppression |
Aliases / AKA | BI 456906BI-456906Survodutide peptideGLP-1 glucagon dual agonist BI 456906Boehringer dual agonistGCGR GLP-1R dual agonist | MounjaroZepboundLY3298176Tirzepatide peptideGIP GLP-1 dual agonistEli Lilly dual agonist |
Parent Compound | Oxyntomodulin-based | Incretin dual agonist |
Molecular Weight | 4231.63 Da | 4813.45 Da |
Amino Acid Sequence | GLP-1/glucagon dual agonist (acylated synthetic peptide) | 39-aa acylated peptide (C20 diacid) |
CAS Number | 2805997-46-8 | 2023788-19-2 |
Year Discovered | Not Listed | Not Listed |
Pro-Angiogenic | No | No |
GLP-1 Class | ||
Purity | Not Listed | Not Listed |
Identity | ||
Evidence Tier | ||
Risk Level | ||
PubMed Citations | 420 Good | 2,193 Extensive |
Clinical Trials | 88 Active | 174174 Active |
Regulatory Status | Investigational (Boehringer Ingelheim / Zealand Pharma); not FDA-approved. | FDA-approved; compounded versions are not FDA-evaluated. |
Evidence & Regulatory | ||
Half-Life | ~1 week | ~1 week |
Typical Frequency | Not Listed | Not Listed |
Administration Route | Injection Only | Injection Only |
Mechanism / PK | Not Listed | Not Listed |
Reported Findings | Pooled trial data associate 4 to 11 months of treatment with roughly 7 to 9 percent weight reduction, plus Phase 2 liver-disease activity. | Strong human trials (SURPASS, SURMOUNT), superior to semaglutide on weight in a head-to-head; FDA-approved for diabetes, obesity, and sleep apnea. |
Side Effects Noted | Predominantly gastrointestinal; glucagon agonism can raise heart rate. | Dose-dependent gastrointestinal effects; gallbladder and pancreatitis signals. |
Warnings | Investigational with no approved indication or long-term safety data; GLP-1 class considerations under study. Research use only. | FDA boxed warning for thyroid C-cell tumors; contraindicated with personal or family medullary thyroid carcinoma or MEN 2. Approved product is distinct from compounded versions. |
Pharmacology | ||
Form | lyophilized | lyophilized (research) or pen/vial |
Diluent | bacteriostatic or sterile water | bacteriostatic water |
Storage Temp | frozen/refrigerated, dark | Refrigerate 2-8°C |
Light Sensitive | Yes | Yes |
Freeze / Thaw | avoid | avoid |
Handling Notes | Note: catalog lists this as Survotutide (spelling). | Avoid freeze-thaw, heat, and shaking. |
Reconstituted Shelf Life | 28 Days Refrigerated | 28 Days Refrigerated |
Handling & Storage | ||
Pep Nation Lab's comparison tool puts research-grade peptides and compounds head to head - mechanism of action, molecular target, evidence tier, molecular weight, sequence, half-life, and documented research focus - so qualified researchers can evaluate the differences that matter. Every data point is drawn from a referenced monograph. For in vitro laboratory research use only.
The two most-studied research peptides for tissue repair and recovery.
Single GLP-1 versus dual GLP-1/GIP incretin agonists in metabolic research.
Dual versus triple incretin receptor agonists in weight-research models.
A GLP-1 agonist versus a triple-agonist incretin in metabolic research.
A GHRH analog versus a selective ghrelin-receptor secretagogue.
A ghrelin-receptor secretagogue versus a GHRH analog for growth-hormone research.
Two GHRH analogs studied on the growth-hormone axis.
The two first-generation growth-hormone releasing peptides.
An amylin analog versus a GLP-1 agonist in metabolic research.
A mitochondrial-derived peptide versus an HGH fragment in metabolic research.
Melanocortin versus kisspeptin pathways in reproductive research.
A telomerase-pathway peptide versus NAD+ metabolism in longevity research.
A potent versus a highly selective ghrelin-receptor secretagogue.
Two GHRH analogs with contrasting half-life profiles.
A direct IGF-1 analog versus a growth-hormone secretagogue.
The DAC versus non-DAC forms of the CJC-1295 GHRH analog.
Two Russian-developed nootropic and anxiolytic research peptides.
Two mitochondrial-targeted peptides in cellular-energy research.
Two immune-modulating research peptides with distinct mechanisms.
Two HGH-fragment analogs studied for fat-metabolism research.
Next-generation multi-receptor incretin agonists in metabolic research.
Two leading tissue-repair peptides with distinct healing mechanisms.
A systemic repair peptide versus a copper peptide for tissue and skin research.
A GHRH analog versus a selective ghrelin-receptor secretagogue on the GH axis.
A dual incretin agonist versus an amylin analog in metabolic research.
A triple incretin agonist versus an amylin analog in weight research.
Two metabolic research compounds targeting mitochondrial and NNMT pathways.
NAD+ metabolism versus a mitochondrial-derived peptide in longevity research.
Two copper research peptides studied for skin and hair.
A long-acting versus a short-acting GHRH analog.
A selective versus a first-generation ghrelin-receptor secretagogue.
A GLP-1 agonist versus a GLP-1/amylin combination in metabolic research.
Two peptides studied for gut and mucosal repair.
Melanocortin versus oxytocin pathways in intimacy and libido research.
Two thymic immune-modulating research peptides.
An anxiolytic nootropic versus a sleep-associated research peptide.
Direct IGF-1 signaling versus myostatin inhibition in muscle research.
A mitochondrial-targeted peptide versus NAD+ in cellular-energy research.
Single BPC-157 versus the combined BPC-157 and TB-500 blend in recovery research.
Ipamorelin alone versus the CJC-1295 and ipamorelin blend on the growth-hormone axis.
A synthetic ACTH-fragment nootropic versus a neurotrophic peptide preparation in cognitive research.
Two sleep-research compounds with distinct mechanisms.
A copper tripeptide versus an acetyl hexapeptide in cosmetic and skin research.
A senolytic peptide versus a telomerase-pathway peptide in longevity research.
Two metabolic research compounds targeting the AMPK and NNMT pathways.
A GHRH analog versus an HGH fragment in fat-metabolism research.
Two AMPK-associated mitochondrial and metabolic research compounds.
Two peptides studied for tissue protection and repair.
Two peptides studied for immune and inflammatory modulation.
Two peptide bioregulators studied in longevity and neuro research.
A glucagon/GLP-1 dual agonist versus a GIP/GLP-1 dual agonist in metabolic research.
Browse the full research catalog or the A To Z index to compare any compound.
Any research-grade compound in the library can be placed side by side - up to four at a time. The tool compares mechanism of action, molecular target, evidence tier, molecular weight, amino acid sequence, reported half-life, and what each compound has been studied for, all drawn from referenced monographs.
The evidence tier reflects how extensively a compound has been studied in the referenced literature, from early preclinical signals through to compounds with human clinical data. It is a research-quality signal only, never a safety or efficacy endorsement.
Each comparison page is generated from the same referenced compound database - a genuine side-by-side of mechanism, identity, pharmacokinetics, and evidence, plus data-derived key differences. They are curated, not auto-generated thin pages.
No. Every comparison is for in vitro laboratory research use only. Nothing here is medical advice, a treatment recommendation, or dosing guidance, and no product is for human or animal consumption.