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Details

Stereochemistry RACEMIC
Molecular Formula C15H12I2O3
Molecular Weight 494.0629
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0
Stereo Comments DL-IODOALPHIONIC ACID

SHOW SMILES / InChI
Structure of IODOALPHIONIC ACID

SMILES

OC(=O)C(CC1=CC(I)=C(O)C(I)=C1)C2=CC=CC=C2

InChI

InChIKey=IKYIXZSIKOYSLD-UHFFFAOYSA-N
InChI=1S/C15H12I2O3/c16-12-7-9(8-13(17)14(12)18)6-11(15(19)20)10-4-2-1-3-5-10/h1-5,7-8,11,18H,6H2,(H,19,20)

HIDE SMILES / InChI

Molecular Formula C15H12I2O3
Molecular Weight 494.0629
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Iodoalphionic acid is the contrast medium, which was used for gallbladder examination. It is rarely appeared in the colon and, therefore, rarely masked the gallbladder. The density of the shadow produced by Iodoalphionic acid was greater than that produced by iodophthalein. It was reliable peroral cholecystographic medium, which was less objectionable to take and seldom causes vomiting. Diarrhoea occurred in some cases, but not more often than with tetraiodophenolphthalein. The ingestion of Iodoalphionic acid resulted in low thyroidal radioiodine accumulation for periods ranging from a few weeks to many months.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Diagnostic
Biliselectan

Approved Use

It was used as a peroral cholecystographic agent
PubMed

PubMed

TitleDatePubMed
Pheniodol: A Contrast Medium for Cholecystography.
1943 Nov 27
Pheniodol, a new dye for cholecystography.
1946 Feb
Some experiences with priodax.
1946 Jun
The compatibility of castor oil and priodax in concurrent examination of the colon and gallbladder.
1949 Jul
[Inefficacy of iodoalphionic acid in radical cure of taeniasis].
1952 Nov-Dec
[Comparative cholecystographic study of iodopanoic acid (telepaque) and iodoalphionic acid].
1953
[Comparative study of iodopanoic acid (telepaque) and iodoalphionic acid (pheniodol) in cholecystography; densitometric and plainimetric x-ray study of 100 cases].
1954
[Duodenal intubation of acranil and iodoalphionic acid in therapy of teniasis].
1954 Jan-Mar
Cholegraphy; the new contrast medium biligrafin.
1955 May
Effects of an organic iodine compound priodax on tests of thyroid function.
1957 Jan
[A new mercurometric determination of pheniodol (Coletrast)].
1967 Aug
Unaltered bromsulphalein retention following cholecystography.
1968 Oct
[Effect of contrast agents on the iodine-absorbing function of the thyroid gland].
1982 Mar-Apr
[Effect of tri-iodine-containing x-ray contrast substances on the blood coagulation system in an experiment].
1984 Jul-Aug
[Competitive interrelations between bilirubin and x-ray contrast agents in binding with human serum albumin].
1986 Mar-Apr
Non-peptidic small-molecule inhibitors of the single-chain hepatitis C virus NS3 protease/NS4A cofactor complex discovered by structure-based NMR screening.
2004 May 6
Patents

Sample Use Guides

4.2 g. suspended in water or milk
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:15:54 GMT 2023
Edited
by admin
on Fri Dec 15 16:15:54 GMT 2023
Record UNII
060B6580LL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
IODOALPHIONIC ACID
MI  
Common Name English
COLETRAST
Brand Name English
TENAMID
Brand Name English
.BETA.-(4-HYDROXY-3,5-DIIODOPHENYL)-.ALPHA.-PHENYLPROPIONIC ACID
Systematic Name English
BILITRAST
Brand Name English
BILISELKTAN
Brand Name English
BISELECTAN
Brand Name English
3-(4-HYDROXY-3,5-DIIODOPHENYL)-2-PHENYLPROPIONIC ACID
Systematic Name English
DIKOL
Brand Name English
PHENIODOL
Common Name English
IODOALPHIONIC ACID [MI]
Common Name English
NSC-404169
Code English
BILIOGNOST
Brand Name English
TENICID
Brand Name English
JODOBIL
Brand Name English
DL-IODOALPHIONIC ACID
Common Name English
BILISELECTAN
Brand Name English
IODOBIL
Brand Name English
NSC-11854
Code English
Classification Tree Code System Code
NCI_THESAURUS C28500
Created by admin on Fri Dec 15 16:15:54 GMT 2023 , Edited by admin on Fri Dec 15 16:15:54 GMT 2023
Code System Code Type Description
CAS
577-91-3
Created by admin on Fri Dec 15 16:15:54 GMT 2023 , Edited by admin on Fri Dec 15 16:15:54 GMT 2023
PRIMARY
NCI_THESAURUS
C75626
Created by admin on Fri Dec 15 16:15:54 GMT 2023 , Edited by admin on Fri Dec 15 16:15:54 GMT 2023
PRIMARY
PUBCHEM
11350
Created by admin on Fri Dec 15 16:15:54 GMT 2023 , Edited by admin on Fri Dec 15 16:15:54 GMT 2023
PRIMARY
ECHA (EC/EINECS)
209-417-4
Created by admin on Fri Dec 15 16:15:54 GMT 2023 , Edited by admin on Fri Dec 15 16:15:54 GMT 2023
PRIMARY
ChEMBL
CHEMBL83906
Created by admin on Fri Dec 15 16:15:54 GMT 2023 , Edited by admin on Fri Dec 15 16:15:54 GMT 2023
PRIMARY
NSC
404169
Created by admin on Fri Dec 15 16:15:54 GMT 2023 , Edited by admin on Fri Dec 15 16:15:54 GMT 2023
PRIMARY
EPA CompTox
DTXSID6046131
Created by admin on Fri Dec 15 16:15:54 GMT 2023 , Edited by admin on Fri Dec 15 16:15:54 GMT 2023
PRIMARY
FDA UNII
060B6580LL
Created by admin on Fri Dec 15 16:15:54 GMT 2023 , Edited by admin on Fri Dec 15 16:15:54 GMT 2023
PRIMARY
MERCK INDEX
m6339
Created by admin on Fri Dec 15 16:15:54 GMT 2023 , Edited by admin on Fri Dec 15 16:15:54 GMT 2023
PRIMARY Merck Index
NSC
11854
Created by admin on Fri Dec 15 16:15:54 GMT 2023 , Edited by admin on Fri Dec 15 16:15:54 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY