Osilodrostat

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Osilodrostat
Systematic (IUPAC) name
4-[(5R)-6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-5-yl]-3-fluorobenzonitrile
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
  • C1CC2=CN=CN2[C@H]1C3=C(C=C(C=C3)C#N)F
  • InChI=1S/C13H10FN3/c14-12-5-9(6-15)1-3-11(12)13-4-2-10-7-16-8-17(10)13/h1,3,5,7-8,13H,2,4H2/t13-/m1/s1
  • Key:USUZGMWDZDXMDG-CYBMUJFWSA-N

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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External links


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  1. 1.0 1.1 1.2 http://adisinsight.springer.com/drugs/800026342
  2. 2.0 2.1 Lua error in package.lua at line 80: module 'strict' not found.