Calcitonin Salmon
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Also known as CalcimarCalcitonin (salmon synthetic)Calcitonin salmon recombinantCalcitonin-salmonForcaltoninForticalMiacalcinRecombinant salmon calcitoninScalcitoninCALCITONINEs-CalcitoninSalmon calcitonin
Summary
Calcitonin Salmon (CHEMBL3989767) is an approved protein bone density conservation agent (ATC H05BA01); indicated across 8 conditions including postmenopausal osteoporosis and bone paget disease.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Protein
- ATC class: H05BA01
- Indications: 8 conditions
- Clinical trials: 12
- Chemistry: 3431.9 Da · C145H240N44O48S2
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL3989767 |
| Name | Calcitonin Salmon |
| Type | Protein |
| Max phase | 4 |
| FDA approved | no |
| PubChem CID | 16133812 |
| ChEBI | CHEBI:3306 |
| ATC | H05BA01 |
| Molecular formula | C145H240N44O48S2 |
| Molecular weight | 3431.9 |
| InChIKey | BBBFJLBPOGFECG-VJVYQDLKSA-N |
SMILES: C[C@H]([C@H]1C(=O)N[C@@H](CSSC[C@@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N1)CO)CC(C)C)CC(=O)N)CO)N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC2=CNC=N2)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC3=CC=C(C=C3)O)C(=O)N4CCC[C@H]4C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H]([C@@H](C)O)C(=O)NCC(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H]([C@@H](C)O)C(=O)N5CCC[C@H]5C(=O)N)O
IUPAC name: (4S)-4-[[(2S)-5-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-6-amino-2-[[2-[[(2S)-2-[[(2S)-2-[[(4R,7S,10S,13S,16S,19S,22R)-22-amino-16-(2-amino-2-oxoethyl)-7-[(1R)-1-hydroxyethyl]-10,19-bis(hydroxymethyl)-13-(2-methylpropyl)-6,9,12,15,18,21-hexaoxo-1,2-dithia-5,8,11,14,17,20-hexazacyclotricosane-4-carbonyl]amino]-3-methylbutanoyl]amino]-4-methylpentanoyl]amino]acetyl]amino]hexanoyl]amino]-4-methylpentanoyl]amino]-3-hydroxypropanoyl]amino]-5-oxopentanoyl]amino]-5-[[(2S)-1-[[(2S)-1-[[(2S)-6-amino-1-[[(2S)-1-[[(2S)-5-amino-1-[[(2S,3R)-1-[[(2S)-1-[(2S)-2-[[(2S)-1-[[(2S,3R)-1-[[(2S)-4-amino-1-[[(2S,3R)-1-[[2-[[(2S)-1-[[2-[[(2S,3R)-1-[(2S)-2-carbamoylpyrrolidin-1-yl]-3-hydroxy-1-oxobutan-2-yl]amino]-2-oxoethyl]amino]-3-hydroxy-1-oxopropan-2-yl]amino]-2-oxoethyl]amino]-3-hydroxy-1-oxobutan-2-yl]amino]-1,4-dioxobutan-2-yl]amino]-3-hydroxy-1-oxobutan-2-yl]amino]-5-carbamimidamido-1-oxopentan-2-yl]carbamoyl]pyrrolidin-1-yl]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amino]-3-hydroxy-1-oxobutan-2-yl]amino]-1,5-dioxopentan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-1-oxohexan-2-yl]amino]-3-(1H-imidazol-4-yl)-1-oxopropan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-5-oxopentanoic acid
ChEBI definition: A 32-membered heterodetic cyclic peptide comprising the sequence Cys-Ser-Asn-Leu-Ser-Thr-Cys-Val-Leu-Gly-Lys-Leu-Ser-Gln-Glu-Leu-His-Lys-Leu-Gln-Thr-Tyr-Pro-Arg-Thr-Asn-Thr-Gly-Ser-Gly-Thr-Pro-NH2 cyclised by a disulfide bridge between the two Cys residues at positions 1 and 7.
Pharmacological roles (ChEBI): bone density conservation agent.
Other ChEBI roles (chemical / environmental): metabolite.
Also known as: Calcimar, Calcitonin (salmon synthetic), Calcitonin salmon, Calcitonin salmon recombinant, Calcitonin-salmon, Forcaltonin, Fortical, Miacalcin, Recombinant salmon calcitonin, Scalcitonin, CALCITONIN SALMON, CALCITONINE
Patent coverage: 274 distinct patent families (666 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 619 (93%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.
Targets
Targets
Broader ChEMBL bioactivity targets: 5 (assay-derived). Sample: Calcitonin receptor, Calcitonin-gene-related peptide receptor, CALCRL/RAMP1, Amylin receptor AMY3; CALCR/RAMP3, Amylin receptor AMY3; CALCR/RAMP3, Calcitonin receptor.
Bioactivity
ChEMBL activities: 6 potent at pChembl ≥ 5 of 6 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| RAMP3 | 10.87 | EC50 | 0.01 | nM | CHEMBL_ACT_25914952 |
| P32214 | 10.55 | IC50 | 0.03 | nM | CHEMBL_ACT_25914664 |
| P32214 | 10.52 | IC50 | 0.03 | nM | CHEMBL_ACT_25914682 |
| CALCR | 10.18 | IC50 | 0.07 | nM | CHEMBL_ACT_25914628 |
| RAMP3 | 10.05 | IC50 | 0.09 | nM | CHEMBL_ACT_25914610 |
| RAMP1 | 6.41 | EC50 | 389.1 | nM | CHEMBL_ACT_25914956 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
8 indications (5 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| postmenopausal osteoporosis | 4 | MONDO:0008159 | EFO:0003854 |
| bone Paget disease | 4 | MONDO:0005382 | EFO:0004261 |
| hypercalcemia disease | 4 | MONDO:0001566 | HP:0003072 |
| parathyroid gland disorder | 4 | MONDO:0001223 | EFO:0005754 |
| bone resorption disease | 4 | MONDO:0000837 | MONDO:0000837 |
| osteoporosis | 3 | MONDO:0005298 | EFO:0003882 |
2 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 12.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE3 | 5 |
| PHASE1 | 4 |
| PHASE4 | 2 |
| PHASE2 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00239889 | PHASE4 | COMPLETED | Efficacy and Safety of Salmon Calcitonin Nasal Spray in Improving Muscle Strength and Reducing Pain After Forearm Fracture in Postmenopausal Women |
| NCT00754884 | PHASE4 | WITHDRAWN | Calcitonin in the Treatment of Fibromyalgia |
| NCT00372099 | PHASE3 | COMPLETED | Bone Microstructure in Nasal Salmon Calcitonin Treated Postmenopausal Women |
| NCT00414973 | PHASE3 | COMPLETED | A Study for Patients With Osteoporosis |
| NCT00542984 | PHASE3 | COMPLETED | Comparison Medications in the Treatment of Postmenopausal Women With Osteoporosis |
| NCT00543023 | PHASE3 | COMPLETED | A Study of the Treatment of Postmenopausal Women With Osteoporosis |
| NCT00704847 | PHASE3 | TERMINATED | Efficacy and Safety of Oral Salmon Calcitonin in Patients With Knee Osteoarthritis (OA 2 Study) |
| NCT00376311 | PHASE2 | TERMINATED | Effects of Oral Salmon Calcitonin in Human Osteoarthritis |
| NCT00395395 | PHASE1 | COMPLETED | Effects of Water and Food Intake on the Pharmacokinetics and Pharmacodynamics of Oral Salmon Calcitonin in Healthy Postmenopausal Women |
| NCT00411125 | PHASE1 | COMPLETED | Pharmacokinetics and Pharmacodynamics Study of Oral Salmon Calcitonin in Healthy Postmenopausal Women |
| NCT00486317 | PHASE1 | COMPLETED | Pharmacokinetics/Pharmacodynamics of Oral Salmon Calcitonin in Patients With Osteoarthritis |
| NCT00486369 | PHASE1 | COMPLETED | SMC021A - Absorption, Efficacy and Tolerance in Patients With Osteoarthritis. A Placebo-Controlled 14-Days Study |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).