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
Molecular Formula | C20H28I3N3O13 |
Molecular Weight | 899.162 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 8 / 8 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
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
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:54:45 GMT 2023
by
admin
on
Fri Dec 15 16:54:45 GMT 2023
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Record UNII |
771V8M13LT
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Record Status |
Validated (UNII)
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Record Version |
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-
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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
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63941-74-2
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DTXSID101024309
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4643
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SUB08225MIG
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771V8M13LT
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CHEMBL2104826
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100000083655
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C83825
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admin on Fri Dec 15 16:54:46 GMT 2023 , Edited by admin on Fri Dec 15 16:54:46 GMT 2023
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C031376
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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
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Related Record | Type | Details | ||
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ACTIVE MOIETY |