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Details

Stereochemistry ACHIRAL
Molecular Formula C19H15Cl3N2O5S
Molecular Weight 489.757
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VONAFEXOR

SMILES

OC(=O)C1=CC2=C(Cl)C(=CC=C2O1)N3CCN(CC3)S(=O)(=O)C4=C(Cl)C=CC=C4Cl

InChI

InChIKey=XLGQSYUNOIJBNR-UHFFFAOYSA-N
InChI=1S/C19H15Cl3N2O5S/c20-12-2-1-3-13(21)18(12)30(27,28)24-8-6-23(7-9-24)14-4-5-15-11(17(14)22)10-16(29-15)19(25)26/h1-5,10H,6-9H2,(H,25,26)

HIDE SMILES / InChI

Molecular Formula C19H15Cl3N2O5S
Molecular Weight 489.757
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 14:05:25 GMT 2023
Edited
by admin
on Sat Dec 16 14:05:25 GMT 2023
Record UNII
XG6DG6A1UN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VONAFEXOR
INN  
Official Name English
Vonafexor [WHO-DD]
Common Name English
2-BENZOFURANCARBOXYLIC ACID, 4-CHLORO-5-(4-((2,6-DICHLOROPHENYL)SULFONYL)-1-PIPERAZINYL)-
Systematic Name English
vonafexor [INN]
Common Name English
Code System Code Type Description
PUBCHEM
67202717
Created by admin on Sat Dec 16 14:05:25 GMT 2023 , Edited by admin on Sat Dec 16 14:05:25 GMT 2023
PRIMARY
CAS
2156704-25-3
Created by admin on Sat Dec 16 14:05:25 GMT 2023 , Edited by admin on Sat Dec 16 14:05:25 GMT 2023
NO STRUCTURE GIVEN
INN
11223
Created by admin on Sat Dec 16 14:05:25 GMT 2023 , Edited by admin on Sat Dec 16 14:05:25 GMT 2023
PRIMARY
SMS_ID
300000023645
Created by admin on Sat Dec 16 14:05:25 GMT 2023 , Edited by admin on Sat Dec 16 14:05:25 GMT 2023
PRIMARY
NCI_THESAURUS
C174946
Created by admin on Sat Dec 16 14:05:25 GMT 2023 , Edited by admin on Sat Dec 16 14:05:25 GMT 2023
PRIMARY
FDA UNII
XG6DG6A1UN
Created by admin on Sat Dec 16 14:05:25 GMT 2023 , Edited by admin on Sat Dec 16 14:05:25 GMT 2023
PRIMARY
CAS
1192171-69-9
Created by admin on Sat Dec 16 14:05:25 GMT 2023 , Edited by admin on Sat Dec 16 14:05:25 GMT 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY