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GLP-1 S 10mg

Research Specifications

INN Name:
Semaglutide
CAS Number:
910463-68-2
Molecular Weight:
4113.6 Da
Side Chain:
C18 fatty acid (albumin binding, ~7-day half-life)
Form:
Lyophilized powder
Purity:
≥98% (HPLC verified)
Storage:
−20°C long-term / 4°C up to 4 weeks reconstituted
Price per mg:
$10.00

GLP-1 S 10mg

The original GLP-1 breakthrough. STEP-1 trial: 14.9% mean body weight reduction. The proven foundation of incretin-based research.

−14.9%

Mean Weight Reduction

STEP-1, 2.4mg/week (NEJM 2021)

94%

Homology to Human GLP-1

Sequence alignment

4113 Da

Molecular Weight

NCBI PubChem

Receptor Targets

GLP-1R↓ appetite, ↓ gastric emptying, ↑ insulin secretion, ↓ glucagon
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≥98% Purity Verified Free Shipping $200+ HPLC Tested

GLP-1 Receptor Agonism: The Incretin Foundation

Semaglutide (Ozempic/Wegovy) is a GLP-1 receptor agonist with 94% homology to human GLP-1 and a C18 fatty acid side chain for albumin binding (half-life ~7 days, enabling once-weekly dosing). GLP-1R activation reduces appetite via hypothalamic signaling, slows gastric emptying, enhances glucose-stimulated insulin secretion, and suppresses glucagon. It is the reference compound against which all newer dual and triple agonists are compared.

Research Highlights

STEP-1 Trial (NEJM 2021)

1,961 participants at 2.4mg/week for 68 weeks. Mean weight reduction of 14.9% (vs 2.4% placebo). 70% of participants achieved ≥10% weight loss. The STEP program established GLP-1 agonism as a viable pharmacological approach to obesity management, setting the baseline for subsequent dual and triple agonist research.

SUSTAIN-6 Cardiovascular Outcomes

The SUSTAIN-6 CVOT trial demonstrated Semaglutide reduced major adverse cardiovascular events (MACE) by 26% vs placebo. The SELECT trial (2023) further confirmed 20% MACE reduction in people without diabetes — establishing cardiovascular benefits independent of glucose control.

Reference Compound Status

Semaglutide serves as the active comparator in most newer GLP-1 class research. SURPASS-2 used Semaglutide 1mg as the comparator for Tirzepatide. Understanding Semaglutide's mechanism is foundational to understanding the incremental benefits of dual and triple agonism.

Research FAQ

How does Semaglutide work?
Semaglutide activates GLP-1 receptors in the hypothalamus, pancreas, and GI tract. This reduces appetite via brain satiety signaling, slows gastric emptying (prolonging fullness), and enhances insulin secretion in response to glucose. The net effect is significant caloric restriction with improved metabolic efficiency.
Why would a researcher choose Semaglutide over Tirzepatide or Retatrutide?
Semaglutide has the largest body of long-term human data (STEP program, SUSTAIN-6, SELECT), making it the best-characterized reference compound. For research requiring well-established baselines with extensive safety and efficacy data, Semaglutide remains the foundational GLP-1 agonist. Tirzepatide and Retatrutide offer greater potency but with less long-term human data.
What is the difference between Semaglutide doses in research?
The 5mg, 10mg, and 15mg vials represent different supply quantities for research protocols. A weekly research dose of 0.25–2.4mg (per published protocols) would be drawn from these vials, with larger vials supporting extended protocols or multiple research subjects.

Research Use Only. This product is intended for in-vitro laboratory research only. Not for human consumption, injection, or therapeutic use. Not medical advice. Always consult applicable regulations in your jurisdiction.

Price Comparison

SupplierPurityPriceShipping
Apollo (via ClavTides)>98% HPLC$99.99Free over $200
Generic Research SuppliersVaries (often <95%)Similar–HigherVaries
Pharmaceutical (Rx only)Pharmaceutical gradeNot available for researchRx required

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