Therapeutic Targets Database
BIDD Pharmainformatics Databases
 
   
 

 

TTD Drug ID: DAP001302

Drug Information
NameSalmon Calcitonin    
Synonymssalmon calcitonin (1-32); EINECS 256-342-8; Staporos; Oseototal; Stalcin; synthetic salmon calcitonin; Porostenina; Calcitonina; Miacalcin (TN); Salmon calcitonin-(I-32); LS-48624; Miacalcic; Kalsimin; Biocalcin; Calcitonin salmon; TZ-CT; Ipocalcin; Miracalcic; Eptacalcin; Karil; Rulicalcin; Calcitonin salmon (USAN/INN); Calcitonin (salmon); C06865; Fortical (TN); Calogen; Isi-calcin; D00249; Salcat; Osteobion; Prontocalcin; Ostostabil; Calco; 47931-85-1; C145H239N43O48S2; Miacalcin; Calcitonin salmon (synthesis); Calcitonine de saumon; Calcitonin, salmar; recombinant salmon calcitonin; Quosten; UNII-7SFC6U2VI5; Calcimar (TN); Steocin; Fortical; Caltine; Calsynar; Cadens; Calcitonin-salmon; Tonocalcin; Calcimar; Cibacalcine; Casalm; Calcinil; Catonin; Calcitonin vom lachs; Calcimonta; Riostin; Ostosalm; Osteovis; Calcihexal; Bionocalcin; Calcitoran; Salmofar; Calcioton; Calcitonin,salmon; Osseocalcina; Ucecal; Salmocalcin; C028815; Salcatonin; Astronin; Thyrocalcitonin (salmon); CALCITONIN, SALMON; Salcatyn; Salmon calcitonin; Calcitonin salmon (synthesis) (JAN); Salmon calcitonin I; Calcitonin [USAN:INN:BAN:JAN]; Citonina; Cibacalcin; 135506-95-5; Calcitonin, salmon, for bioassay; Sical; Calciben; Calsynar Lyo L; Forcaltonin    
IndicationOsteoporosisApproved    [1]
Structure

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Therapeutic ClassAntiosteporotic Agents    
CAS NumberCAS 47931-85-1
FormularC145H240N44O48S2    
PubChem Compound IDCID 16129616.    
PubChem Substance IDSID 9082.    
TargetCalcitonin receptorBinder[2][3]
Ref 1Natural products as sources of new drugs over the last 25 years. J Nat Prod. 2007 Mar;70(3):461-77. Epub 2007 Feb 20. To Reference
Ref 2Improved absorption of salmon calcitonin by ultraflexible liposomes through intranasal delivery. Peptides. 2009 Jul;30(7):1288-95. Epub 2009 Apr 7. To Reference
Ref 3Purification and characterization of calcitonin receptors in rat kidney membranes by covalent cross-linking techniques. Eur J Biochem. 1986 Feb 17;155(1):141-7. To Reference



 

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