Glucagon
Also known as: GlucaGen, Cloridrato de Glucagon, Glucagon Hydrochloride
Molecular Identifiers
Molecular Formula
C153H225N43O49S
CAS Number
16941-32-5
PubChem CID
16132283Molecular Weight
3485 Da
Overview
Pancreatic peptide hormone composed of 29 amino acids with a molecular weight of approximately 3,482.75 Da. Produced by alpha cells of the islets of Langerhans, it acts as the primary counter-regulatory hormone to insulin, promoting hepatic glycogenolysis and gluconeogenesis.
FDA-approved as GlucaGen (injection) and Baqsimi (nasal spray, 2019) for emergency treatment of severe hypoglycemia in diabetic patients. Available in emergency kits for use by caregivers.
The essential clinical effect of glucagon is a rapid rise in blood glucose through hepatic GCGR activation, driving glycogenolysis and gluconeogenesis, with additional effects on lipolysis, thermogenesis, and cardiac function. It is the counter-regulatory hormone to insulin and the pharmacological tool of choice for rapid reversal of severe hypoglycemia.
Glucagon is currently approved and marketed for emergency treatment of severe hypoglycemia in diabetic patients, in kits for caregiver use, with subcutaneous, intramuscular, or intravenous administration as an injectable (GlucaGen) and as a nasal spray (Baqsimi, approved in 2019). In metabolic research, it continues to be studied as a component of dual and triple agonists (GLP-1/glucagon, GLP-1/GIP/glucagon) for weight loss and metabolic hepatic disease. In emergencies it is a single dose; chronic cycles are not standard practice.
Glucagon was one of the earliest peptide hormones to be sequenced, with the sequence elucidated by Bromer and colleagues in the late 1950s, supporting the consolidation of the insulin-glucagon antagonist pair hypothesis in glycemic regulation.
HSQGTFTSDYSKYLDSRRAQDFVQWLMNT His-Ser-Gln-Gly-Thr-Phe-Thr-Ser-Asp-Tyr-Ser-Lys-Tyr-Leu-Asp-Ser-Arg-Arg-Ala-Gln-Asp-Phe-Val-Gln-Trp-Leu-Met-Asn-Thr Half-life
~8-18 minutes
Administration Route
Subcutaneous, intramuscular or intravenous
Category
Metabolic & Fat Loss
Mechanism of Action
- Activation of the glucagon receptor (GCGR) in hepatocytes
- Promotion of hepatic glycogenolysis (conversion of glycogen to glucose)
- Stimulation of hepatic gluconeogenesis
- Increased lipolysis in adipose tissue
- Thermogenic effect via increased energy expenditure
- Positive inotropic and chronotropic effect on the heart
Dosage Protocol
Data compiled from the literature. This does not constitute medical advice.
| Parameter | Value |
|---|---|
| Dose | 0.5-1 mg per injection (hypoglycemic emergency); research doses vary |
| Frequency | Single dose in emergency; as per protocol in research |
| Timing | Immediately in hypoglycemic emergency |
| Duration | Single dose (emergency) or as per research protocol |
Reported Side Effects
Adverse effects described in the literature. Severity and frequency vary between individuals.
- Nausea
- Vomiting
- Hyperglycemia
- Headache
Product Properties
| Purity | >98% |
| Appearance | White lyophilized powder |
| Solubility | Soluble in water and dilute acidic solutions |
| Source | Solid-phase peptide synthesis (SPPS) or recombinant DNA technology |
| Storage | Lyophilized: -20°C for up to 2 years, 2-8°C for up to 6 months. Reconstituted: use immediately or within 24 hours at 2-8°C. Very unstable in solution. Protect from light and moisture. |
Presentations & Preparation
Vials of Glucagon found in the research market:
Reconstitution
- Diluent: Accompanying diluent (sterile water)
- Volume: 1 ml per 1 mg vial
- Inject the diluent into the lyophilized powder vial
- Gently swirl until fully dissolved — never shake
- Use immediately after reconstitution
- Solution should be clear and colorless
Storage
- Lyophilized: Controlled room temperature (15-30°C)
- Reconstituted: Use immediately after reconstitution
- Do not refrigerate the reconstituted solution
- Discard unused solution
- Regularly check expiration date on emergency kits
Scientific Studies
Published studies on Glucagon.
Intranasal Glucagon for Treatment of Insulin-Induced Hypoglycemia in Adults With Type 1 Diabetes - A Randomized Crossover Noninferiority Study
Rickels MR, Ruedy KJ, Foster NC, Piché CA, Dulude H, Sherr JL, Tamborlane WV, Bethin KE, DiMeglio LA, Wadwa RP, Ahmann AJ, Haller MJ, Nathan BM, Marcovina SM, Rampakakis E, Meng L, Beck RW
Glucagon Nasal Powder - A Promising Alternative to Intramuscular Glucagon in Youth With Type 1 Diabetes
Sherr JL, Ruedy KJ, Foster NC, Piché CA, Dulude H, Rickels MR, Tamborlane WV, Bethin KE, DiMeglio LA, Fox LA, Wadwa RP, Schatz DA, Nathan BM, Marcovina SM, Rampakakis E, Meng L, Beck RW
Related Peptides
5-Amino-1MQ
50 mg per capsule · 1-2 times daily
Adipotide
0.03 mg/kg body weight (Phase 1 trial starting dose) · Once daily
AICAR
0.1 mg/kg/min by intravenous infusion (CABG trial dose) · Single continuous infusion
AOD 9604
300-600 mcg per injection · Once daily
Cagrilintide
1.2-4.5 mg per week (subcutaneous) · Once weekly
Dulaglutide
0.75-4.5 mg per week (subcutaneous) · Once weekly