Overview
Elcatonin, also known as carbocalcitonin, is a synthetic analogue of eel calcitonin in which the disulfide bond linking positions 1 and 7 is replaced by a carbon-carbon (ethylene) bridge, formed using an aminosuberic acid residue. This substitution makes the peptide more resistant to reduction and degradation in solution while retaining potent calcitonin receptor activity.
Elcatonin was developed in Japan by Asahi Kasei and is approved in Japan and several other Asian countries, where it has been used in the context of osteoporosis-associated pain and other bone-related conditions. It is not approved by the FDA or EMA. Much of its literature comes from Japanese clinical and in vitro studies and animal models.">preclinical studies, which have explored both its effects on osteoclasts and its distinctive analgesic actions. For researchers, elcatonin is a useful example of peptide stabilisation chemistry, in which a dicarba bridge replaces a disulfide, and a tool for osteoclast inhibition research, bone pain models and calcitonin receptor pharmacology. Comparative work with salmon calcitonin examines how structure influences potency and stability.
Mechanism studied
- Elcatonin
- Osteoclast receptor
- Bone resorption ↓
- Analgesic endpoints
Elcatonin activates the calcitonin receptor, a class B G protein-coupled receptor on osteoclasts, renal cells and neurons. Receptor activation increases cAMP and phospholipase C signalling, causing osteoclast retraction, loss of the ruffled border and reduced bone resorption, which lowers calcium release from bone. Its analgesic effects in animal models are thought to be at least partly central, involving descending serotonergic pathways from the brainstem and possibly changes in endogenous opioid signalling, and in some models they appear separable from effects on bone resorption. The ethylene bridge stabilises the ring structure needed for receptor binding.
Research highlights
- 01Developed by Asahi Kasei as a stabilised analogue of eel calcitonin.
- 02The aminosuberic acid bridge is a classic example of disulfide-to-dicarba replacement in peptide chemistry.
- 03Approved in Japan and some Asian markets; it is not approved in the United States or European Union.
- 04Rodent pain models have linked elcatonin's analgesic effects to central serotonergic pathways.
- 05Open questions include how its long-term safety profile compares with salmon calcitonin following European restrictions on calcitonin use.
Latest published research
174 papers on PubMed →Early parathyroid hormone elevation after denosumab therapy following parathyroidectomy: a diagnostic pitfall
Yamashita H et al. · JCEM case reports · 2026 Dec · PMID 42890451
Sensitive and selective quantification of elcatonin in equine plasma and urine using LC-FAIMS-MS/MS
Ohnuma K et al. · Journal of pharmaceutical and biomedical analysis · 2026 Oct 15 · PMID 42127554
Serial Calcium Monitoring Revealed Primary Hyperparathyroidism in Severe Acute Pancreatitis: A Case Report
Yokota M et al. · Acute medicine & surgery · 2026 Jan-Dec · PMID 42859844
Humoral Hypercalcemia of Malignancy Caused by Parathyroid Hormone-Related Protein-Secreting Medullary Thyroid Carcinoma: A Case Report
Hirose T et al. · Surgical case reports · 2026 · PMID 41924640
Unmasking Latent Primary Hyperparathyroidism in Guillain-Barré Syndrome: A Case Report and Literature Review
Biyajima M et al. · Cureus · 2025 Feb · PMID 40109792
Granulocyte-colony stimulating factor producing cervical cancer with elevated levels of parathyroid hormone-related protein: a case report and literature review
Matsuoka N et al. · CEN case reports · 2024 Feb · PMID 37227595
Retracted: Impact of Alendronate Sodium plus Elcatonin on Postoperative Bone Pain in Patients with Osteoporotic Fractures
International BR et al. · BioMed research international · 2023 · PMID 38188785
A case report of effective intra-articular elcatonin administration in a patient with osteonecrosis of the lunate
Nagai T et al. · International journal of surgery case reports · 2023 Apr · PMID 37001370
Live feed from PubMed (NCBI) for “Elcatonin”, updated 2026-10-30. Listing a paper is not an endorsement of its findings.
Registered studies
1 on ClinicalTrials.gov →From the public ClinicalTrials.gov registry for “Elcatonin”, updated 2026-10-30. Shown for research context only; Purity Peptides products are not for human use.
Key references
- [1]PubMed — reviews on elcatonin and bone pain
- [2]National registrations — Japan
FAQ
Elcatonin is based on eel calcitonin rather than salmon calcitonin, and it replaces the disulfide bridge between positions 1 and 7 with a stable carbon-carbon linkage. Both are fish-derived sequences with high potency at mammalian calcitonin receptors.
Disulfide bonds can be reduced or rearranged, limiting peptide stability. Replacing them with a non-reducible carbon bridge, as in elcatonin, preserves ring geometry while improving chemical robustness. This dicarba strategy is studied widely in peptide drug design.
Elcatonin is approved in Japan and several other Asian countries for bone-related indications, including pain associated with osteoporosis. It has not been approved by the US FDA or the European Medicines Agency and is supplied here for research use only.
FOR RESEARCH USE ONLY.Not for human or veterinary use. Not intended to diagnose, treat, cure, or prevent any disease.



