Osilodrostat
Systematic (IUPAC) name | |
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4-[(5R)-6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-5-yl]-3-fluorobenzonitrile
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Clinical data | |
Routes of administration |
Oral |
Identifiers | |
CAS Number | 928134-65-0 |
PubChem | CID: 44139752 |
ChemSpider | 29340911 |
UNII | 5YL4IQ1078 |
ChEMBL | CHEMBL3099695 |
Synonyms | LCI-699 |
Chemical data | |
Formula | C13H10FN3 |
Molecular mass | 227.242 g/mol |
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Osilodrostat (INN, USAN) (developmental code name LCI-699) is an orally active, non-steroidal corticosteroid biosynthesis inhibitor which is under development by Novartis for the treatment of Cushing's syndrome and pituitary ACTH hypersecretion (a specific subtype of Cushing's syndrome).[1][2] It specifically acts as a potent and selective inhibitor of aldosterone synthase (CYP11B2) and at higher dosages of 11β-hydroxylase (CYP11B1).[2] The drug was also under development for the treatment of heart failure, hypertension, and solid tumors, but development was discontinued for these indications.[1] As of 2017, osilodrostat is in phase III and phase II clinical trials for treatment of pituitary ACTH hypersecretion and Cushing's syndrome, respectively.[1]
See also
References
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- Antiglucocorticoids
- Imidazoles
- Nitriles
- Organofluorides
- Pyrroles
- Steroid 11β-hydroxylase inhibitors
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