Calcitonin Salmon

drug
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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

FieldValue
ChEMBL IDCHEMBL3989767
NameCalcitonin Salmon
TypeProtein
Max phase4
FDA approvedno
PubChem CID16133812
ChEBICHEBI:3306
ATCH05BA01
Molecular formulaC145H240N44O48S2
Molecular weight3431.9
InChIKeyBBBFJLBPOGFECG-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):

TargetpChemblTypeValueUnitActivity ID
RAMP310.87EC500.01nMCHEMBL_ACT_25914952
P3221410.55IC500.03nMCHEMBL_ACT_25914664
P3221410.52IC500.03nMCHEMBL_ACT_25914682
CALCR10.18IC500.07nMCHEMBL_ACT_25914628
RAMP310.05IC500.09nMCHEMBL_ACT_25914610
RAMP16.41EC50389.1nMCHEMBL_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).

IndicationTrial phaseMONDOEFO
postmenopausal osteoporosis4MONDO:0008159EFO:0003854
bone Paget disease4MONDO:0005382EFO:0004261
hypercalcemia disease4MONDO:0001566HP:0003072
parathyroid gland disorder4MONDO:0001223EFO:0005754
bone resorption disease4MONDO:0000837MONDO:0000837
osteoporosis3MONDO:0005298EFO: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

PhaseTrials
PHASE35
PHASE14
PHASE42
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00239889PHASE4COMPLETEDEfficacy and Safety of Salmon Calcitonin Nasal Spray in Improving Muscle Strength and Reducing Pain After Forearm Fracture in Postmenopausal Women
NCT00754884PHASE4WITHDRAWNCalcitonin in the Treatment of Fibromyalgia
NCT00372099PHASE3COMPLETEDBone Microstructure in Nasal Salmon Calcitonin Treated Postmenopausal Women
NCT00414973PHASE3COMPLETEDA Study for Patients With Osteoporosis
NCT00542984PHASE3COMPLETEDComparison Medications in the Treatment of Postmenopausal Women With Osteoporosis
NCT00543023PHASE3COMPLETEDA Study of the Treatment of Postmenopausal Women With Osteoporosis
NCT00704847PHASE3TERMINATEDEfficacy and Safety of Oral Salmon Calcitonin in Patients With Knee Osteoarthritis (OA 2 Study)
NCT00376311PHASE2TERMINATEDEffects of Oral Salmon Calcitonin in Human Osteoarthritis
NCT00395395PHASE1COMPLETEDEffects of Water and Food Intake on the Pharmacokinetics and Pharmacodynamics of Oral Salmon Calcitonin in Healthy Postmenopausal Women
NCT00411125PHASE1COMPLETEDPharmacokinetics and Pharmacodynamics Study of Oral Salmon Calcitonin in Healthy Postmenopausal Women
NCT00486317PHASE1COMPLETEDPharmacokinetics/Pharmacodynamics of Oral Salmon Calcitonin in Patients With Osteoarthritis
NCT00486369PHASE1COMPLETEDSMC021A - 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.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).