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Details

Stereochemistry ACHIRAL
Molecular Formula C21H30I3N3O9
Molecular Weight 849.191
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IOSIMIDE

SMILES

OCCN(CCO)C(=O)C1=C(I)C(C(=O)N(CCO)CCO)=C(I)C(C(=O)N(CCO)CCO)=C1I

InChI

InChIKey=KZYHGCLDUQBASN-UHFFFAOYSA-N
InChI=1S/C21H30I3N3O9/c22-16-13(19(34)25(1-7-28)2-8-29)17(23)15(21(36)27(5-11-32)6-12-33)18(24)14(16)20(35)26(3-9-30)4-10-31/h28-33H,1-12H2

HIDE SMILES / InChI

Molecular Formula C21H30I3N3O9
Molecular Weight 849.191
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Iosimide is synthetic, nonionic, monomeric contrast medium patented by Schering A.-G. In clinical trial Iosimide exhibited no differences in comparison with Ioxaglate with respect to the contrast, the neurological status or the liver or renal tolerance. In examining cardiovascular tolerance there is only a slight tendency toward liver changes with Iosimide. Examination of the general tolerance, however, shows a statistically significant lower incidence of sensation of heat and pain with iosimide than with ioxaglate.

Approval Year

PubMed

PubMed

TitleDatePubMed
Controlled, double-blind study of iosimide, a new, nonionic, monomeric contrast medium, and ioxaglate in cerebral angiography.
1989
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:53:13 GMT 2025
Edited
by admin
on Mon Mar 31 17:53:13 GMT 2025
Record UNII
3EL4NLE563
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
UNIVIST
Preferred Name English
IOSIMIDE
INN   MART.   WHO-DD  
INN  
Official Name English
N,N,N',N',N'',N''-HEXAKIS(2-HYDROXYETHYL)-2,4,6-TRIIODO-1,3,5-BENZENETRICARBOXAMIDE
Systematic Name English
ZK-36699
Code English
IOSIMIDE [MART.]
Common Name English
Iosimide [WHO-DD]
Common Name English
iosimide [INN]
Common Name English
ZK 36699
Code English
Code System Code Type Description
CAS
79211-10-2
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
INN
5439
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
EPA CompTox
DTXSID20229579
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
ECHA (EC/EINECS)
279-110-8
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
NCI_THESAURUS
C166675
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
SMS_ID
100000083110
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
MESH
C047355
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
EVMPD
SUB08251MIG
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
ChEMBL
CHEMBL2105004
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
FDA UNII
3EL4NLE563
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
PUBCHEM
60911
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY