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GLP 2 (T)
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GLP-1 Research Peptides

GLP 2 (T)

TirzepatideLY3298176Dual GIP/GLP-1
β˜…β˜…β˜…β˜…β˜†4.9(100 reviews)
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A GLP-2 receptor agonist with applications in metabolic research. Tirzepatide-class peptide studied for body composition and metabolic function.

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Exact labeled amount
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βœ“99%+ net purity β€” independently verified via HPLC
βœ“Net content confirmed β€” exact labeled amount in every vial
βœ“Certificate of Analysis with every batch
βœ“Third-party HPLC + mass spectrometry tested
βœ“Lyophilized, sealed for maximum stability
πŸ”¬ View research & study references for this compound β†’

Compound Profile

Pharmaceutical Data Sheet

EVO Labs ResearchResearch Grade Β· 99%+ Purity

GLP-1 Research Peptides

GLP 2 (T)

Tirzepatide

CAS Number

2023788-19-2

Molecular Formula

Cβ‚‚β‚‚β‚…Hβ‚ƒβ‚„β‚ˆNβ‚„β‚ˆOβ‚†β‚ˆ

Molecular Weight

4,813.46 g/mol

Purity

> 99% HPLC

Designation

RUO Β· Research Use Only

Not for human or veterinary consumption. For in vitro laboratory research only.

GLP 2 (T)

Third-Party Tested Β· Certificate of Analysis Included Β· Ships from Tampa, FL USA

Batch VerifiedLyophilized
22.5%
Body Weight Reduction (Phase 3)
Dual
GIP + GLP-1 Receptor Agonism
72 wk
SURMOUNT-1 Trial Duration
FDA
Approved Analog (Type 2 Diabetes)

Mechanism of Action

How GLP 2 (T) Works

Tirzepatide (GLP 2 T) was engineered as a balanced dual agonist at both GIP and GLP-1 receptors, with equal or slightly preferential GIP activity. The GIP receptor component provides incretin amplification and reduces the GI side effect burden of pure GLP-1 agonism, while GLP-1R activity drives appetite suppression and insulin secretion.

GIP
GIP Receptor
Primary β€” Differentiating Activity
  • Drives adiponectin release from adipocytes
  • Enhances beta-cell preservation and regeneration
  • Reduces GI adverse events vs. pure GLP-1
  • Promotes fat redistribution via lipolysis
GLP-1
GLP-1 Receptor
Primary β€” Weight & Glycemic Control
  • Reduces food intake via CNS satiety signaling
  • Stimulates insulin secretion glucose-dependently
  • Decreases glucagon secretion postprandially
  • Delays gastric emptying
INS
Insulin Signaling
Downstream β€” Metabolic Normalization
  • Improves peripheral insulin sensitivity
  • Reduces fasting and postprandial glucose
  • Lowers HbA1c through sustained glycemic control
  • Protects pancreatic beta-cell mass
Key Mechanism
GIPR + GLP-1R Balanced Co-Agonism

Unlike semaglutide which acts on GLP-1R alone, tirzepatide simultaneously activates GIPR (which historically was thought to promote fat storage but at pharmacological doses drives lipolysis and adiponectin release) and GLP-1R. This co-agonism produces superior weight loss to GLP-1 monotherapy while improving tolerability.

Primary Source

Frias JP et al., N Engl J Med (2021): SURPASS-2 trial demonstrating superiority of tirzepatide over semaglutide.

Preclinical Findings

Research Models

Adipose Tissue Reduction vs. Vehicle92%
Fasting Insulin Normalization88%
Hepatic Steatosis Reduction85%
Food Intake Reduction vs. Control79%

Clinical Data

22.5% Mean Weight Loss β€” SURMOUNT-1 Trial

Phase 3 β€” NEJM 2022

The SURMOUNT-1 Phase 3 trial (72 weeks, n=2,539) demonstrated 22.5% mean body weight reduction at the highest dose (15mg), with 63% of participants achieving β‰₯20% weight loss β€” surpassing all prior approved weight loss therapeutics.

Mean Body Weight Reduction (15mg)23%
Participants Achieving β‰₯20% Weight Loss63%
Reduction in Waist Circumference77%
Source

Jastreboff AM et al., N Engl J Med (2022); SURMOUNT-1 Trial.

Phase 3 RCT, n=2,539, 72-week follow-up

Research Outcomes

Key Research Success Metrics

63%
of participants (15mg)
Achieved β‰₯20% weight loss
SURMOUNT-1 primary endpoint
90%
of T2D patients (SURPASS)
Reached HbA1c target <7%
SURPASS-1 glycemic endpoint
23%
mean body weight
Reduced in highest dose group
72-week SURMOUNT-1

Safety Profile

Research Safety Notes

  • Nausea and GI side effects are dose-dependent, most common during titration phase
  • No increased risk of major adverse cardiovascular events (MACE) in trials
  • Rare: injection-site reactions, mild hypoglycemia (when combined with insulin)
  • Contraindicated in personal/family history of MTC or MEN2 syndrome
  • Regular monitoring of lipase and amylase recommended in long-term protocols
Research Disclaimer

GLP 2 (T) / Tirzepatide clinical data cited relates to the FDA-approved compound analog. For research use only.

Research Grade Quality
βœ“99%+ Net Purity (HPLC Verified)
βœ“Net Content Confirmed Per Vial
βœ“Batch-Specific COA Available
βœ“Lyophilized for Stability

About GLP 2 (T)

A GLP-2 receptor agonist with applications in metabolic research. Tirzepatide-class peptide studied for body composition and metabolic function.

All EVO Labs Research compounds are manufactured to research-grade standards and independently tested by Janoshik Analytical (Prague, est. 2013). The Certificate of Analysis for this compound includes full HPLC chromatography data, mass spectrometry confirmation, net purity percentage, and net content verification.

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Research Use Only

This product is strictly for in vitro research and laboratory use only. Not for human or veterinary consumption. By purchasing, you confirm use in a controlled research setting.

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