Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C9H6I3NO3.C7H17NO5 |
| Molecular Weight | 752.0758 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CC(=O)NC1=C(I)C(C(O)=O)=C(I)C=C1I
InChI
InChIKey=CUNJTOHTJOOFJQ-WZTVWXICSA-N
InChI=1S/C9H6I3NO3.C7H17NO5/c1-3(14)13-8-5(11)2-4(10)6(7(8)12)9(15)16;1-8-2-4(10)6(12)7(13)5(11)3-9/h2H,1H3,(H,13,14)(H,15,16);4-13H,2-3H2,1H3/t;4-,5+,6+,7+/m.0/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| [HYSTEROSALPINGOGRAPHY WITH VASURIX 50]. | 1964 Apr |
|
| Effects of iodinated contrast media on erythrocytes. II. Effect of some drugs on alterations induced by meglumine acetrizoate. | 1973 Jul-Aug |
|
| Comparative study: Endografine (diatrizoate), Vasurix polyvidone (acetrizoate), Dimer-X (iocarmate) and Hexabrix (ioxaglate) in hysterosalpingography. | 1982 |
Patents
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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361QYH8LGO
Created by
admin on Fri Dec 15 18:08:36 GMT 2023 , Edited by admin on Fri Dec 15 18:08:36 GMT 2023
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21126676
Created by
admin on Fri Dec 15 18:08:36 GMT 2023 , Edited by admin on Fri Dec 15 18:08:36 GMT 2023
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22154-43-4
Created by
admin on Fri Dec 15 18:08:36 GMT 2023 , Edited by admin on Fri Dec 15 18:08:36 GMT 2023
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PRIMARY | |||
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131-60-2
Created by
admin on Fri Dec 15 18:08:36 GMT 2023 , Edited by admin on Fri Dec 15 18:08:36 GMT 2023
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SUB03118MIG
Created by
admin on Fri Dec 15 18:08:36 GMT 2023 , Edited by admin on Fri Dec 15 18:08:36 GMT 2023
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PRIMARY | |||
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899814-54-1
Created by
admin on Fri Dec 15 18:08:36 GMT 2023 , Edited by admin on Fri Dec 15 18:08:36 GMT 2023
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SUPERSEDED | |||
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100000086186
Created by
admin on Fri Dec 15 18:08:36 GMT 2023 , Edited by admin on Fri Dec 15 18:08:36 GMT 2023
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PRIMARY |
PARENT (SALT/SOLVATE)
PARENT (SALT/SOLVATE)
SUBSTANCE RECORD
