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Details

Stereochemistry ABSOLUTE
Molecular Formula C18H24I3N3O9
Molecular Weight 807.1113
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IOGLUNIDE

SMILES

CN(C(C)=O)C1=C(I)C(C(=O)NCCO)=C(I)C(NC(=O)[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO)=C1I

InChI

InChIKey=ODYPLCHSCOJEIZ-GMYJMXFCSA-N
InChI=1S/C18H24I3N3O9/c1-6(27)24(2)13-10(20)8(17(32)22-3-4-25)9(19)12(11(13)21)23-18(33)16(31)15(30)14(29)7(28)5-26/h7,14-16,25-26,28-31H,3-5H2,1-2H3,(H,22,32)(H,23,33)/t7-,14-,15+,16+/m1/s1

HIDE SMILES / InChI

Molecular Formula C18H24I3N3O9
Molecular Weight 807.1113
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Ioglunide is an iodobenzene derivative patented by Laboratoires Andre Guerbet as an oil-based X-ray contrast medium. Iophendylate was commonly used in conventional myelography from the 1940s to the late 1980s before the utilization of computed tomography (CT), magnetic resonance imaging (MRI) and water-soluble contrast agents. Ioglunide, which was never shown to be safe, was initially introduced for use in small amounts for locating spinal tumors. It next appeared on the world scene for high volume, routine use, in diagnosing disc herniations.

Approval Year

PubMed

PubMed

TitleDatePubMed
Intracranial migration of iophendylate four decades after conventional myelography.
2018 Jun
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:59:28 GMT 2023
Edited
by admin
on Fri Dec 15 16:59:28 GMT 2023
Record UNII
V4XU46CRKN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
IOGLUNIDE
INN  
INN  
Official Name English
ioglunide [INN]
Common Name English
3'-((2-HYDROXYETHYL)CARBAMOYL)-2',4',6'-TRIIODO-5'-(N-METHYLACETAMIDO-D-GLUCOANILIDE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C28500
Created by admin on Fri Dec 15 16:59:28 GMT 2023 , Edited by admin on Fri Dec 15 16:59:28 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID401024027
Created by admin on Fri Dec 15 16:59:28 GMT 2023 , Edited by admin on Fri Dec 15 16:59:28 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105031
Created by admin on Fri Dec 15 16:59:28 GMT 2023 , Edited by admin on Fri Dec 15 16:59:28 GMT 2023
PRIMARY
EVMPD
SUB08226MIG
Created by admin on Fri Dec 15 16:59:28 GMT 2023 , Edited by admin on Fri Dec 15 16:59:28 GMT 2023
PRIMARY
CAS
56562-79-9
Created by admin on Fri Dec 15 16:59:28 GMT 2023 , Edited by admin on Fri Dec 15 16:59:28 GMT 2023
PRIMARY
PUBCHEM
68761
Created by admin on Fri Dec 15 16:59:28 GMT 2023 , Edited by admin on Fri Dec 15 16:59:28 GMT 2023
PRIMARY
SMS_ID
100000083636
Created by admin on Fri Dec 15 16:59:28 GMT 2023 , Edited by admin on Fri Dec 15 16:59:28 GMT 2023
PRIMARY
FDA UNII
V4XU46CRKN
Created by admin on Fri Dec 15 16:59:28 GMT 2023 , Edited by admin on Fri Dec 15 16:59:28 GMT 2023
PRIMARY
NCI_THESAURUS
C83826
Created by admin on Fri Dec 15 16:59:28 GMT 2023 , Edited by admin on Fri Dec 15 16:59:28 GMT 2023
PRIMARY
INN
4533
Created by admin on Fri Dec 15 16:59:28 GMT 2023 , Edited by admin on Fri Dec 15 16:59:28 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY