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Details

Stereochemistry ACHIRAL
Molecular Formula C15H10Cl3NO6S
Molecular Weight 438.667
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULICRINAT

SMILES

NS(=O)(=O)C1=CC(=CC=C1Cl)C(=O)C2=CC=C(OCC(O)=O)C(Cl)=C2Cl

InChI

InChIKey=REORSPZOQXYWIT-UHFFFAOYSA-N
InChI=1S/C15H10Cl3NO6S/c16-9-3-1-7(5-11(9)26(19,23)24)15(22)8-2-4-10(14(18)13(8)17)25-6-12(20)21/h1-5H,6H2,(H,20,21)(H2,19,23,24)

HIDE SMILES / InChI

Molecular Formula C15H10Cl3NO6S
Molecular Weight 438.667
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Sulicrinat (also known as HOE 428) is a sulfamoylbenzophenone derivative patented by Hoechst A.-G. as a loop diuretic.

Approval Year

PubMed

PubMed

TitleDatePubMed
Binding of loop diuretics to their renal receptors: use as a screening model for potential diuretic activity.
1988
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:43:37 GMT 2023
Edited
by admin
on Sat Dec 16 16:43:37 GMT 2023
Record UNII
DJH1LFU42E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULICRINAT
INN  
INN  
Official Name English
sulicrinat [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C448
Created by admin on Sat Dec 16 16:43:37 GMT 2023 , Edited by admin on Sat Dec 16 16:43:37 GMT 2023
Code System Code Type Description
INN
5611
Created by admin on Sat Dec 16 16:43:37 GMT 2023 , Edited by admin on Sat Dec 16 16:43:37 GMT 2023
PRIMARY
NCI_THESAURUS
C74256
Created by admin on Sat Dec 16 16:43:37 GMT 2023 , Edited by admin on Sat Dec 16 16:43:37 GMT 2023
PRIMARY
EPA CompTox
DTXSID40238062
Created by admin on Sat Dec 16 16:43:37 GMT 2023 , Edited by admin on Sat Dec 16 16:43:37 GMT 2023
PRIMARY
PUBCHEM
213028
Created by admin on Sat Dec 16 16:43:37 GMT 2023 , Edited by admin on Sat Dec 16 16:43:37 GMT 2023
PRIMARY
SMS_ID
100000083787
Created by admin on Sat Dec 16 16:43:37 GMT 2023 , Edited by admin on Sat Dec 16 16:43:37 GMT 2023
PRIMARY
ChEMBL
CHEMBL2107610
Created by admin on Sat Dec 16 16:43:37 GMT 2023 , Edited by admin on Sat Dec 16 16:43:37 GMT 2023
PRIMARY
FDA UNII
DJH1LFU42E
Created by admin on Sat Dec 16 16:43:37 GMT 2023 , Edited by admin on Sat Dec 16 16:43:37 GMT 2023
PRIMARY
CAS
90207-12-8
Created by admin on Sat Dec 16 16:43:37 GMT 2023 , Edited by admin on Sat Dec 16 16:43:37 GMT 2023
PRIMARY
EVMPD
SUB10743MIG
Created by admin on Sat Dec 16 16:43:37 GMT 2023 , Edited by admin on Sat Dec 16 16:43:37 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY