Details
| Stereochemistry | MIXED |
| Molecular Formula | C31H36I6N6O14 |
| Molecular Weight | 1478.0762 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 0 / 4 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)C1=C(I)C(C(=O)NCC(O)CO)=C(I)C(N(CC(O)CO)C(=O)CC(=O)N(CC(O)CO)C2=C(I)C(C(=O)NCC(O)CO)=C(I)C(C(N)=O)=C2I)=C1I
InChI
InChIKey=DLPPIGPJCKKVBA-UHFFFAOYSA-N
InChI=1S/C31H36I6N6O14/c32-20-16(28(38)54)22(34)26(24(36)18(20)30(56)40-2-10(48)6-44)42(4-12(50)8-46)14(52)1-15(53)43(5-13(51)9-47)27-23(35)17(29(39)55)21(33)19(25(27)37)31(57)41-3-11(49)7-45/h10-13,44-51H,1-9H2,(H2,38,54)(H2,39,55)(H,40,56)(H,41,57)
| Molecular Formula | C31H36I6N6O14 |
| Molecular Weight | 1478.0762 |
| Charge | 0 |
| Count |
|
| Stereochemistry | MIXED |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 4 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Iosimenol, is a synthetic non-ionic dimeric contrast medium with lower molecular weight patented by Schering A.-G. In clinical trials Iosimenol was not metabolized, had a distribution volume corresponding to the extracellular space, and was rapidly excreted through the kidneys by glomerular filtration. The area under the plasma concentration curve and the peak plasma concentration was proportional to dose, while clearance was independent of dose. Iosimenol upon intravenous as well as upon intra-arterial injection exhibits a safety profile and shows an efficacy similar to that of iodixanol.
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/24895062
0.5, 1.5 or 3.0 mL/kg, equivalent to approximately 0.2, 0.5, or 1.0 gI/kg
Route of Administration:
Intravenous
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:20:44 GMT 2025
by
admin
on
Mon Mar 31 18:20:44 GMT 2025
|
| Record UNII |
QPG0485VLS
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Official Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
C174895
Created by
admin on Mon Mar 31 18:20:44 GMT 2025 , Edited by admin on Mon Mar 31 18:20:44 GMT 2025
|
PRIMARY | |||
|
213045
Created by
admin on Mon Mar 31 18:20:44 GMT 2025 , Edited by admin on Mon Mar 31 18:20:44 GMT 2025
|
PRIMARY | |||
|
CHEMBL2104971
Created by
admin on Mon Mar 31 18:20:44 GMT 2025 , Edited by admin on Mon Mar 31 18:20:44 GMT 2025
|
PRIMARY | |||
|
300000034278
Created by
admin on Mon Mar 31 18:20:44 GMT 2025 , Edited by admin on Mon Mar 31 18:20:44 GMT 2025
|
PRIMARY | |||
|
DTXSID90939496
Created by
admin on Mon Mar 31 18:20:44 GMT 2025 , Edited by admin on Mon Mar 31 18:20:44 GMT 2025
|
PRIMARY | |||
|
181872-90-2
Created by
admin on Mon Mar 31 18:20:44 GMT 2025 , Edited by admin on Mon Mar 31 18:20:44 GMT 2025
|
PRIMARY | |||
|
QPG0485VLS
Created by
admin on Mon Mar 31 18:20:44 GMT 2025 , Edited by admin on Mon Mar 31 18:20:44 GMT 2025
|
PRIMARY | |||
|
SS-45
Created by
admin on Mon Mar 31 18:20:44 GMT 2025 , Edited by admin on Mon Mar 31 18:20:44 GMT 2025
|
PRIMARY | |||
|
8189
Created by
admin on Mon Mar 31 18:20:44 GMT 2025 , Edited by admin on Mon Mar 31 18:20:44 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |
|