Pasireotide
From Infogalactic: the planetary knowledge core
Systematic (IUPAC) name | |
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[(3S,6S,9S,12R,15S,18S,20R)-9-(4-aminobutyl)-3-benzyl-12-(1H-indol-3-ylmethyl)-2,5,8,11,14,17-hexaoxo-15-phenyl-6-[(4-phenylmethoxyphenyl)methyl]-1,4,7,10,13,16-hexazabicyclo[16.3.0]henicosan-20-yl] N-(2-aminoethyl)carbamate
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Clinical data | |
Trade names | Signifor |
Licence data | EMA:Link |
Legal status |
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Routes of administration |
Subcutaneous |
Identifiers | |
CAS Number | 396091-73-9 |
ATC code | H01CB05 (WHO) |
PubChem | CID: 9941444 |
IUPHAR/BPS | 2018 |
DrugBank | DB06663 |
ChemSpider | 8117062 |
UNII | 98H1T17066 |
KEGG | D10147 |
ChEBI | CHEBI:72312 |
Synonyms | SOM230 |
Chemical data | |
Formula | C58H66N10O9 |
Molecular mass | 1047.21 g/mol[1] |
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Pasireotide (SOM230, trade name Signifor[2]) is an orphan drug approved in the U.S. and Europe for the treatment of Cushing's disease and acromegaly in patients who fail or are ineligible for surgical therapy.[3][4] It was developed by Novartis. Pasireotide is a somatostatin analog with a 40-fold increased affinity to somatostatin receptor 5 compared to other somatostatin analogs.
Pasireotide was approved for Cushing's disease by the EMEA in October 2009[5] and by the FDA in December 2012.[6]
Pasireotide LAR was approved by the FDA for treatment of acromegaly in December 2014, and had been approved for this indication by the EMEA one month earlier.[7]
References
- ↑ Pasireotide | C58H66N10O9 - PubChem http://pubchem.ncbi.nlm.nih.gov/compound/Pasireotide
- ↑ Signifor® (pasireotide) Official Website for healthcare professionals outside the US http://www.signifor.com/
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ EMEA Approval for Pasireotide
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ Tucker, Miriam E. FDA Approves Pasireotide for Treating Acromegaly, Medscape, December 17, 2014, Retrieved 2015-08-21
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