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1 INNClassRoute (list)PK parameters= Cmax; Tmax; F: bioavailability; t1/2: half-life; VD: volume of distribution; Cl: clearance; PPB: plasma protein binding;(EQN means that value was calculated using VD=(Cl*t1/2)/0.693)Primary Target and PDB code of Protein-Drug complexTargets from DrugCentral Links
OSILODROSTAT

OSILODROSTAT


ATC H02CA02

HORMONES
CORTISOL SYNTHESIS INHIBITOR
TREATMENT OF CUSHING’S DISEASE
INHIBITOR OF 11 BETA-HYDROXYLASE (CYP11B1) (IC50 = 2.5 NM)

ORAL

Tmax 1 HOUR

VD 100 LITER

PPB 36.4 PERCENT

HT 4 HOUR

11 BETA-HYDROXYLASE (CYP11B1)

PDB 7M8V (HUMAN CYP11B2 IN COMPLEX WITH LCI699)

LIGAND CODE = YSY (link to the list of PDB complexes)

Download experimental 3D coordinates of YSY with added hydrogens

Cytochrome P450 11B1, mitochondrial UNIPROT P15538 CYP11B1

more at DrugCentral

EMA

ANSM (in French)

Inxight Drugs
Dailymed
Drugs.com

SIDER side effects

Chemical Probes Portal

ChEMBL
BindingDB
DrugBank



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