Glucagon (hyperglycaemic hormone)
Glucagon (recombinant) 1 mg per vial
CAS Number39
Basic Info
| CAS Number | 16941-32-5 |
|---|---|
| Active Ingredient | Glucagon, recombinant glucagon (a recombinant peptide produced by genetic engineering of the human insulin gene) |
| Dosage Form | Lyophilised powder for injection |
| Specification & Packaging | Strength: 1 mg per vial Pack: 1 vial + 1 mL diluent Group: 03 Item No.: 39 |
Storage & Common Excipients
| Storage Conditions | 2–8 °C, protected from light. Unused pens are refrigerated; in-use storage at room temperature is limited (e.g. four weeks) depending on the product. Follow the label |
|---|---|
| Common Excipients | Typical lyophilisate: lactose, mannitol, buffer (L-histidine or phosphate), edetate disodium; reconstituted with water for injection; prefilled pens may contain propylene glycol/benzyl alcohol. Confirm against COA |
Product Introduction
A hyperglycaemic hormone secreted by pancreatic alpha cells that acts in opposition to insulin. It is used as an emergency injection (vial or nasal presentation) for the emergency treatment of severe hypoglycaemic coma. The reference products are glucagon for injection (originally porcine-sequence) and its autoinjector. **Note**: the source file describes "recombinant glucagon", whereas CAS 16941-32-5 corresponds to **porcine glucagon**. Human recombinant glucagon has a different CAS record (commonly 155701-42-3). The sequences differ (29 versus 31 amino acids), so the source of the active ingredient should be explicitly verified
Therapeutic Use
Emergency treatment of severe, consciousness-impairing hypoglycaemia in patients with diabetes (particularly those on insulin or sulfonylureas); also used to suppress gastrointestinal motility during imaging and for glucagon stimulation testing; indications follow the locally approved label
Mode of Action
Binds the hepatic Gs receptor, activates adenylyl cyclase, raises cAMP and stimulates glycogenolysis and gluconeogenesis for a rapid rise in blood glucose; rapid onset but a short half-life (minutes); secondary rebound insulin release may occur
Administration & Monitoring
Administer immediately subcutaneously, intramuscularly or intravenously in an emergency; always follow with glucose or carbohydrate to prevent recurrence; monitor glucose after administration and address the trigger; recurrent episodes require re-evaluation of the treatment plan
Important Safety Information
Pens and solutions may contain excipients such as benzyl alcohol, which requires caution in certain populations. This is an emergency medicine and does not replace long-term diabetes management. Hypoglycaemia caused by sulfonylurea or long-acting-insulin overdose may not be corrected by glucagon alone and requires glucose. Used pens must be discarded safely to prevent injury to others
Adverse Reactions
Injection-site reactions; nausea and vomiting (common); palpitations and arrhythmias (uncommon); hypokalaemia (more evident when combined with insulin)
Important Risks
Delayed meals or failure to recognise hypoglycaemic episodes can lead to serious consequences; vomiting and aspiration risk in comatose patients; recurrent episodes indicate treatment failure and require systematic review
Contraindications
Hypersensitivity to glucagon or any excipient (some formulations contain bovine/porcine-derived components or benzyl alcohol); routine use without a clear indication. Glucagon alone may be insufficient to correct hypoglycaemia caused by sulfonylurea overdose
Special Populations
Older adults and patients with renal impairment are more susceptible to hypoglycaemia and require prompt correction; weight-based dosing in children; specialist advice in pregnancy and lactation; aspiration risk with the nasal presentation when used in comatose patients
Usage Limitations
Prescription medicine. Emergency use only; storage and use must follow the label. Not for weight management or performance purposes in healthy individuals. For athletes, glucagon itself is not on the WADA Prohibited List, but its use may interfere with analytical baselines and must be proactively declared; more importantly, repeated use usually indicates concurrent use of other hypoglycaemic or metabolic-modifying agents
Anti-Doping Testing
Glucagon itself is not on the WADA Prohibited List. However, repeated use is commonly associated with TZDs, insulin and SGLT2 agents (which are prohibited or controlled), so testing often yields positive metabolic-modulator findings
Product Quality Testing
Identification (peptide mapping/MS), assay (HPLC or immunoassay), sterility and endotoxin, lyophilisate appearance and reconstitution time, clarity and stability after reconstitution, fill volume, bioactivity where applicable; COA
Source & Verification Note
**Note**: the source file states "recombinant glucagon", but CAS 16941-32-5 corresponds to **porcine** glucagon (29 aa); human recombinant glucagon is commonly 155701-42-3 (31 aa). Active-ingredient sourcing must be verified with the supplier.
Inquiry / Request for information
We will respond within 24 hours. Customized synthesis is supported.