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Details

Stereochemistry ABSOLUTE
Molecular Formula C13H13IN2O2
Molecular Weight 356.159
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IODOMETOMIDATE I-123, R-

SMILES

COC(=O)C1=CN=CN1[C@H](C)C2=CC=C(I)C=C2

InChI

InChIKey=KECBLXVYTIVCTG-SECBINFHSA-N
InChI=1S/C13H13IN2O2/c1-9(10-3-5-11(14)6-4-10)16-8-15-7-12(16)13(17)18-2/h3-9H,1-2H3/t9-/m1/s1

HIDE SMILES / InChI

Molecular Formula C13H13IN2O2
Molecular Weight 356.159
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Iodometomidate I-123, R- (also known as ) is phenylethylimidazole derivative studied as a diagnostic agent for adrenal imaging. Iodometomidate is a highly suitable tracer combining specific uptake in adrenocortical tissue with far lower radiation exposure compared to norcholesterol scintigraphy. Phase III clinical trial for Adrenal Gland Neoplasms imaging is currently ongoing.

Approval Year

PubMed

PubMed

TitleDatePubMed
[¹²³I]Iodometomidate imaging in adrenocortical carcinoma.
2013 Jul
Patents

Patents

Sample Use Guides

185 MBq
Route of Administration: Intravenous
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:18:41 GMT 2023
Edited
by admin
on Fri Dec 15 15:18:41 GMT 2023
Record UNII
U21CVV13SV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
IODOMETOMIDATE I-123, R-
Common Name English
123I-IODOMETOMIDATE
Common Name English
1H-IMIDAZOLE-5-CARBOXYLIC ACID, 1-((1R)-1-(4-IODOPHENYL)ETHYL)-, METHYL ESTER
Common Name English
(R)-4-(123I)IODOMETOMIDATE
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID50231064
Created by admin on Fri Dec 15 15:18:41 GMT 2023 , Edited by admin on Fri Dec 15 15:18:41 GMT 2023
PRIMARY
FDA UNII
U21CVV13SV
Created by admin on Fri Dec 15 15:18:41 GMT 2023 , Edited by admin on Fri Dec 15 15:18:41 GMT 2023
PRIMARY
PUBCHEM
11660398
Created by admin on Fri Dec 15 15:18:41 GMT 2023 , Edited by admin on Fri Dec 15 15:18:41 GMT 2023
PRIMARY
CAS
813466-05-6
Created by admin on Fri Dec 15 15:18:41 GMT 2023 , Edited by admin on Fri Dec 15 15:18:41 GMT 2023
PRIMARY
DRUG BANK
DB13021
Created by admin on Fri Dec 15 15:18:41 GMT 2023 , Edited by admin on Fri Dec 15 15:18:41 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY