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Details

Stereochemistry RACEMIC
Molecular Formula C15H18I3NO5
Molecular Weight 673.0205
Optical Activity ( + / - )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IOPRONIC ACID

SMILES

CC[C@@H](COCCOC1=C(I)C=C(I)C(NC(C)=O)=C1I)C(O)=O

InChI

InChIKey=YMFIJXDFAPHJIN-VIFPVBQESA-N
InChI=1S/C15H18I3NO5/c1-3-9(15(21)22)7-23-4-5-24-14-11(17)6-10(16)13(12(14)18)19-8(2)20/h6,9H,3-5,7H2,1-2H3,(H,19,20)(H,21,22)/t9-/m0/s1

HIDE SMILES / InChI

Molecular Formula C15H18I3NO5
Molecular Weight 673.0205
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Iopronic acid is a triiodide derivative of aminophenol. In the 1980s it was used as a contrast medium for oral cholecystography. Iopronic acid was marketed under tradenames Bilimiro, Bilimiron, Oravue, Videobil.

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:05:21 GMT 2023
Edited
by admin
on Fri Dec 15 18:05:21 GMT 2023
Record UNII
4P675153BV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
IOPRONIC ACID
INN   MART.   MI   USAN   WHO-DD  
INN   USAN  
Official Name English
IOPRONIC ACID [MI]
Common Name English
BILIMIRON
Brand Name English
(±)-2-((2-(3-ACETAMIDO-2,4,6-TRIIODOPHENOXY)ETHOXY)METHYL)BUTYRIC ACID
Systematic Name English
iopronic acid [INN]
Common Name English
B-11420
Code English
SO-21983
Code English
IOPRONIC ACID [MART.]
Common Name English
BUTANOIC ACID, 2-((2-(3-(ACETYLAMINO)-2,4,6-TRIIODOPHENOXY)ETHOXY)METHYL)-, (±)-
Systematic Name English
IOPRONIC ACID [USAN]
Common Name English
SQ-21983
Code English
SQ 21983
Code English
Iopronic acid [WHO-DD]
Common Name English
B 11420
Code English
Code System Code Type Description
SMS_ID
100000083107
Created by admin on Fri Dec 15 18:05:21 GMT 2023 , Edited by admin on Fri Dec 15 18:05:21 GMT 2023
PRIMARY
ECHA (EC/EINECS)
253-643-6
Created by admin on Fri Dec 15 18:05:21 GMT 2023 , Edited by admin on Fri Dec 15 18:05:21 GMT 2023
PRIMARY
MESH
C006754
Created by admin on Fri Dec 15 18:05:21 GMT 2023 , Edited by admin on Fri Dec 15 18:05:21 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105012
Created by admin on Fri Dec 15 18:05:21 GMT 2023 , Edited by admin on Fri Dec 15 18:05:21 GMT 2023
PRIMARY
FDA UNII
4P675153BV
Created by admin on Fri Dec 15 18:05:21 GMT 2023 , Edited by admin on Fri Dec 15 18:05:21 GMT 2023
PRIMARY
EVMPD
SUB08245MIG
Created by admin on Fri Dec 15 18:05:21 GMT 2023 , Edited by admin on Fri Dec 15 18:05:21 GMT 2023
PRIMARY
PUBCHEM
76959803
Created by admin on Fri Dec 15 18:05:21 GMT 2023 , Edited by admin on Fri Dec 15 18:05:21 GMT 2023
PRIMARY
INN
3281
Created by admin on Fri Dec 15 18:05:21 GMT 2023 , Edited by admin on Fri Dec 15 18:05:21 GMT 2023
PRIMARY
NCI_THESAURUS
C166773
Created by admin on Fri Dec 15 18:05:21 GMT 2023 , Edited by admin on Fri Dec 15 18:05:21 GMT 2023
PRIMARY
EPA CompTox
DTXSID201031997
Created by admin on Fri Dec 15 18:05:21 GMT 2023 , Edited by admin on Fri Dec 15 18:05:21 GMT 2023
PRIMARY
MERCK INDEX
m6376
Created by admin on Fri Dec 15 18:05:21 GMT 2023 , Edited by admin on Fri Dec 15 18:05:21 GMT 2023
PRIMARY Merck Index
CAS
37723-78-7
Created by admin on Fri Dec 15 18:05:21 GMT 2023 , Edited by admin on Fri Dec 15 18:05:21 GMT 2023
PRIMARY
DRUG CENTRAL
3200
Created by admin on Fri Dec 15 18:05:21 GMT 2023 , Edited by admin on Fri Dec 15 18:05:21 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY