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Details

Stereochemistry ABSOLUTE
Molecular Formula C27H22F4N6O3S
Molecular Weight 586.561
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RELACORILANT

SMILES

CN1C=C(C=N1)S(=O)(=O)N2CCC3=CC4=C(C[C@@]3(C2)C(=O)C5=CC(=CC=N5)C(F)(F)F)C=NN4C6=CC=C(F)C=C6

InChI

InChIKey=WANIDIGFXJFFEL-SANMLTNESA-N
InChI=1S/C27H22F4N6O3S/c1-35-15-22(14-33-35)41(39,40)36-9-7-18-11-24-17(13-34-37(24)21-4-2-20(28)3-5-21)12-26(18,16-36)25(38)23-10-19(6-8-32-23)27(29,30)31/h2-6,8,10-11,13-15H,7,9,12,16H2,1H3/t26-/m0/s1

HIDE SMILES / InChI

Molecular Formula C27H22F4N6O3S
Molecular Weight 586.561
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 23:20:17 GMT 2025
Edited
by admin
on Mon Mar 31 23:20:17 GMT 2025
Record UNII
2158753C7E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
relacorilant [INN]
Preferred Name English
RELACORILANT
INN  
INN  
Official Name English
CORT125134
Code English
(R)-(1-(4-FLUOROPHENYL)-6-((1-METHYL-1H-PYRAZOL-4-YL)SULFONYL)-1,4,5,6,7,8-HEXAHYDRO-4AH-PYRAZOLO(3,4-G)ISOQUINOLIN-4A-YL)(4-(TRIFLUOROMETHYL)PYRIDIN-2-YL)METHANONE
Common Name English
CORT-125134
Code English
[(4aR)-1-(4-Fluorophenyl)-6-(1-methyl-1H-pyrazole-4-sulfonyl)-1,4,5,6,7,8-hexahydro-4aH-pyrazolo[3,4-g]isoquinolin-4a-yl][4-(trifluoromethyl)pyridin-2-yl]methanone
Systematic Name English
RELACORILANT [USAN]
Common Name English
METHANONE, ((4AR)-1-(4-FLUOROPHENYL)-1,4,5,6,7,8-HEXAHYDRO-6-((1-METHYL-1H-PYRAZOL-4-YL)SULFONYL)-4AH-PYRAZOLO(3,4-G)ISOQUINOLIN-4A-YL)(4-(TRIFLUOROMETHYL)-2-PYRIDINYL)-
Systematic Name English
Relacorilant [WHO-DD]
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 652118
Created by admin on Mon Mar 31 23:20:17 GMT 2025 , Edited by admin on Mon Mar 31 23:20:17 GMT 2025
FDA ORPHAN DRUG 656518
Created by admin on Mon Mar 31 23:20:17 GMT 2025 , Edited by admin on Mon Mar 31 23:20:17 GMT 2025
EU-Orphan Drug EU/3/19/2164
Created by admin on Mon Mar 31 23:20:17 GMT 2025 , Edited by admin on Mon Mar 31 23:20:17 GMT 2025
Code System Code Type Description
WIKIPEDIA
Relacorilant
Created by admin on Mon Mar 31 23:20:17 GMT 2025 , Edited by admin on Mon Mar 31 23:20:17 GMT 2025
PRIMARY
ChEMBL
CHEMBL3544957
Created by admin on Mon Mar 31 23:20:17 GMT 2025 , Edited by admin on Mon Mar 31 23:20:17 GMT 2025
PRIMARY
PUBCHEM
73051463
Created by admin on Mon Mar 31 23:20:17 GMT 2025 , Edited by admin on Mon Mar 31 23:20:17 GMT 2025
PRIMARY
EPA CompTox
DTXSID801099345
Created by admin on Mon Mar 31 23:20:17 GMT 2025 , Edited by admin on Mon Mar 31 23:20:17 GMT 2025
PRIMARY
FDA UNII
2158753C7E
Created by admin on Mon Mar 31 23:20:17 GMT 2025 , Edited by admin on Mon Mar 31 23:20:17 GMT 2025
PRIMARY
INN
10465
Created by admin on Mon Mar 31 23:20:17 GMT 2025 , Edited by admin on Mon Mar 31 23:20:17 GMT 2025
PRIMARY
DRUG BANK
DB14976
Created by admin on Mon Mar 31 23:20:17 GMT 2025 , Edited by admin on Mon Mar 31 23:20:17 GMT 2025
PRIMARY
NCI_THESAURUS
C127838
Created by admin on Mon Mar 31 23:20:17 GMT 2025 , Edited by admin on Mon Mar 31 23:20:17 GMT 2025
PRIMARY
USAN
EF-147
Created by admin on Mon Mar 31 23:20:17 GMT 2025 , Edited by admin on Mon Mar 31 23:20:17 GMT 2025
PRIMARY
SMS_ID
100000180077
Created by admin on Mon Mar 31 23:20:17 GMT 2025 , Edited by admin on Mon Mar 31 23:20:17 GMT 2025
PRIMARY
CAS
1496510-51-0
Created by admin on Mon Mar 31 23:20:17 GMT 2025 , Edited by admin on Mon Mar 31 23:20:17 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY