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Details

Stereochemistry RACEMIC
Molecular Formula C21H18N2O4S
Molecular Weight 394.444
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Aderamastat

SMILES

CC1=CC(COC2=CC=C(SC3=C(OC=C3)C4NC(=O)NC4=O)C=C2)=CC=C1

InChI

InChIKey=CXEKSVVDMIAMLF-UHFFFAOYSA-N
InChI=1S/C21H18N2O4S/c1-13-3-2-4-14(11-13)12-27-15-5-7-16(8-6-15)28-17-9-10-26-19(17)18-20(24)23-21(25)22-18/h2-11,18H,12H2,1H3,(H2,22,23,24,25)

HIDE SMILES / InChI

Molecular Formula C21H18N2O4S
Molecular Weight 394.444
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:37:21 GMT 2025
Edited
by admin
on Mon Mar 31 18:37:21 GMT 2025
Record UNII
2IZ5925NZQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Aderamastat
USAN  
Official Name English
FP-025
Preferred Name English
2,4-Imidazolidinedione, 5-[3-[[4-[(3-methylphenyl)methoxy]phenyl]thio]-2-furanyl]-
Systematic Name English
FP025
Code English
ADERAMASTAT [USAN]
Common Name English
5-(3-((4-((3-methylbenzyl)oxy)phenyl)thio)furan-2-yl)imidazolidine-2,4-dione
Systematic Name English
Code System Code Type Description
SMS_ID
300000047887
Created by admin on Mon Mar 31 18:37:21 GMT 2025 , Edited by admin on Mon Mar 31 18:37:21 GMT 2025
PRIMARY
PUBCHEM
67177374
Created by admin on Mon Mar 31 18:37:21 GMT 2025 , Edited by admin on Mon Mar 31 18:37:21 GMT 2025
PRIMARY
INN
12684
Created by admin on Mon Mar 31 18:37:21 GMT 2025 , Edited by admin on Mon Mar 31 18:37:21 GMT 2025
PRIMARY
CAS
877176-23-3
Created by admin on Mon Mar 31 18:37:21 GMT 2025 , Edited by admin on Mon Mar 31 18:37:21 GMT 2025
PRIMARY
NCI_THESAURUS
C211720
Created by admin on Mon Mar 31 18:37:21 GMT 2025 , Edited by admin on Mon Mar 31 18:37:21 GMT 2025
PRIMARY
FDA UNII
2IZ5925NZQ
Created by admin on Mon Mar 31 18:37:21 GMT 2025 , Edited by admin on Mon Mar 31 18:37:21 GMT 2025
PRIMARY
USAN
MN-91
Created by admin on Mon Mar 31 18:37:21 GMT 2025 , Edited by admin on Mon Mar 31 18:37:21 GMT 2025
PRIMARY
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ACTIVE MOIETY