Details
Stereochemistry | ACHIRAL |
Molecular Formula | CrO4 |
Molecular Weight | 114.9424 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | -2 |
SHOW SMILES / InChI
SMILES
[O-][51Cr]([O-])(=O)=O
InChI
InChIKey=ZCDOYSPFYFSLEW-HONVGLGOSA-N
InChI=1S/Cr.4O/q;;;2*-1/i1-1;;;;
Molecular Formula | CrH2O4 |
Molecular Weight | 116.9583 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Chromate ion CR-51 is a radioactive chromium 51 in the form of sterile, nonpyrogenic aqueous solution of sodium chromate. It is a diagnostic radiopharmaceutical for intravenous administration. This agent provides Chromium 51 decays by electron capture and gamma emission with a physical half-life of 27.7 days. It is indicated for use in determining red blood cell volume or mass, studying red blood cell survival time (in conditions such as hemolytic anemia), and evaluating blood loss. No adverse reactions specifically attributable to Chromate ion CR-51 injection have been reported.
Approval Year
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Diagnostic | SODIUM CHROMATE CR 51 Approved UseCr51 is indicated for use in determining red blood cell volume or mass, studying red blood cell survival time (in conditions such as hemolytic anemia), and evaluating blood loss Launch Date1971 |
|||
Diagnostic | SODIUM CHROMATE CR 51 Approved UseCr51 is indicated for use in determining red blood cell volume or mass, studying red blood cell survival time (in conditions such as hemolytic anemia), and evaluating blood loss Launch Date1971 |
|||
Diagnostic | SODIUM CHROMATE CR 51 Approved UseCr51 is indicated for use in determining red blood cell volume or mass, studying red blood cell survival time (in conditions such as hemolytic anemia), and evaluating blood loss Launch Date1971 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.drugs.com/pro/chromitope.html#s-34068-7
The usual doses to the average patient (70 kg) are as follows: Determination of red blood cell volume or mass–0.37 to 1.11 megabecquerels (10 to 30 microcuries).
Study of red blood cell survival time–5.55 megabecquerels (150 microcuries).
Evaluation of blood loss–7.40 megabecquerels (200 microcuries).
Route of Administration:
Intravenous
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:46:43 GMT 2023
by
admin
on
Fri Dec 15 16:46:43 GMT 2023
|
Record UNII |
SVU4HTP02M
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NDF-RT |
N0000177914
Created by
admin on Fri Dec 15 16:46:43 GMT 2023 , Edited by admin on Fri Dec 15 16:46:43 GMT 2023
|
||
|
NDF-RT |
N0000000205
Created by
admin on Fri Dec 15 16:46:43 GMT 2023 , Edited by admin on Fri Dec 15 16:46:43 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
SVU4HTP02M
Created by
admin on Fri Dec 15 16:46:43 GMT 2023 , Edited by admin on Fri Dec 15 16:46:43 GMT 2023
|
PRIMARY | |||
|
3080663
Created by
admin on Fri Dec 15 16:46:43 GMT 2023 , Edited by admin on Fri Dec 15 16:46:43 GMT 2023
|
PRIMARY | |||
|
DB14537
Created by
admin on Fri Dec 15 16:46:43 GMT 2023 , Edited by admin on Fri Dec 15 16:46:43 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
IONIC MOIETY |