Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C20H28I3N3O13 |
Molecular Weight | 899.162 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 8 / 8 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CNC(=O)C1=C(I)C(NC(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO)=C(I)C(NC(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO)=C1I
InChI
InChIKey=ASFIRRNYUOVVLY-JVOWFEOISA-N
InChI=1S/C20H28I3N3O13/c1-24-18(37)6-7(21)10(25-19(38)16(35)14(33)12(31)4(29)2-27)9(23)11(8(6)22)26-20(39)17(36)15(34)13(32)5(30)3-28/h4-5,12-17,27-36H,2-3H2,1H3,(H,24,37)(H,25,38)(H,26,39)/t4-,5-,12-,13-,14+,15+,16-,17-/m1/s1
Ioglucomide is triiodoanilide derivative patented by Mallinckrodt, Inc. as nonionic x-ray contrast media for myelography. In preclinical studies the efficacy of ioglucomide and metrizamide were comparable. However, acute toxicity after intravenous injection or installation into cerebrospinal fluid was significantly less for ioglucomide. Also, in contrast to metrizamide, ioglucomide produced no evidence of any type of convulsive activity after subarachnoid administration.
Approval Year
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C28500
Created by
admin on Fri Dec 15 16:54:46 GMT 2023 , Edited by admin on Fri Dec 15 16:54:46 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
63941-74-2
Created by
admin on Fri Dec 15 16:54:46 GMT 2023 , Edited by admin on Fri Dec 15 16:54:46 GMT 2023
|
PRIMARY | |||
|
DTXSID101024309
Created by
admin on Fri Dec 15 16:54:46 GMT 2023 , Edited by admin on Fri Dec 15 16:54:46 GMT 2023
|
PRIMARY | |||
|
4643
Created by
admin on Fri Dec 15 16:54:46 GMT 2023 , Edited by admin on Fri Dec 15 16:54:46 GMT 2023
|
PRIMARY | |||
|
SUB08225MIG
Created by
admin on Fri Dec 15 16:54:46 GMT 2023 , Edited by admin on Fri Dec 15 16:54:46 GMT 2023
|
PRIMARY | |||
|
771V8M13LT
Created by
admin on Fri Dec 15 16:54:46 GMT 2023 , Edited by admin on Fri Dec 15 16:54:46 GMT 2023
|
PRIMARY | |||
|
CHEMBL2104826
Created by
admin on Fri Dec 15 16:54:46 GMT 2023 , Edited by admin on Fri Dec 15 16:54:46 GMT 2023
|
PRIMARY | |||
|
100000083655
Created by
admin on Fri Dec 15 16:54:46 GMT 2023 , Edited by admin on Fri Dec 15 16:54:46 GMT 2023
|
PRIMARY | |||
|
C83825
Created by
admin on Fri Dec 15 16:54:46 GMT 2023 , Edited by admin on Fri Dec 15 16:54:46 GMT 2023
|
PRIMARY | |||
|
C031376
Created by
admin on Fri Dec 15 16:54:46 GMT 2023 , Edited by admin on Fri Dec 15 16:54:46 GMT 2023
|
PRIMARY | |||
|
71964
Created by
admin on Fri Dec 15 16:54:46 GMT 2023 , Edited by admin on Fri Dec 15 16:54:46 GMT 2023
|
PRIMARY |
ACTIVE MOIETY