Details
Stereochemistry | ACHIRAL |
Molecular Formula | C7H5I2NO3.C4H11NO2 |
Molecular Weight | 510.0641 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OCCNCCO.OC(=O)CN1C=C(I)C(=O)C(I)=C1
InChI
InChIKey=RERHJVNYJKZHLJ-UHFFFAOYSA-N
InChI=1S/C7H5I2NO3.C4H11NO2/c8-4-1-10(3-6(11)12)2-5(9)7(4)13;6-3-1-5-2-4-7/h1-2H,3H2,(H,11,12);5-7H,1-4H2
Molecular Formula | C7H5I2NO3 |
Molecular Weight | 404.9284 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C4H11NO2 |
Molecular Weight | 105.1356 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Iodopyracet (Diodone) is a radiocontrast agent used in urography before 1950. Renal clearance of iodopyracet is characterized by supply-limited elimination at low plasma concentrations and capacity-limited elimination at high plasma levels. Iodopyracet to be an effective agent for the estimation of renal plasma flow and tubular function has been used extensively in physiological studies. In 1945 was found, that p-aminohippuric acid was in some ways superior to diodone for these estimations in man because the urine and plasma blanks are small and because diodone penetrates human red blood cells whereas p-aminohippuric acid does not.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL1777665 Sources: https://www.ncbi.nlm.nih.gov/pubmed/14734677 |
Doses
Dose | Population | Adverse events |
---|---|---|
10 g single, intravenous Dose: 10 g Route: intravenous Route: single Dose: 10 g Co-administed with:: diphenhydramine(20 mg) Sources: |
unhealthy n = 416 Health Status: unhealthy Condition: urography Population Size: 416 Sources: |
Other AEs: Nausea and vomiting, Urticaria... Other AEs: Nausea and vomiting (severe, 2 patients) Sources: Urticaria (8 patients) Sleepiness (34 patients) |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Sleepiness | 34 patients | 10 g single, intravenous Dose: 10 g Route: intravenous Route: single Dose: 10 g Co-administed with:: diphenhydramine(20 mg) Sources: |
unhealthy n = 416 Health Status: unhealthy Condition: urography Population Size: 416 Sources: |
Urticaria | 8 patients | 10 g single, intravenous Dose: 10 g Route: intravenous Route: single Dose: 10 g Co-administed with:: diphenhydramine(20 mg) Sources: |
unhealthy n = 416 Health Status: unhealthy Condition: urography Population Size: 416 Sources: |
Nausea and vomiting | severe, 2 patients | 10 g single, intravenous Dose: 10 g Route: intravenous Route: single Dose: 10 g Co-administed with:: diphenhydramine(20 mg) Sources: |
unhealthy n = 416 Health Status: unhealthy Condition: urography Population Size: 416 Sources: |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2706315
3.0 g, administered i.v.
Route of Administration:
Intravenous
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 15:49:43 GMT 2023
by
admin
on
Sat Dec 16 15:49:43 GMT 2023
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Record UNII |
ZTK4026YJ5
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Record Status |
Validated (UNII)
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Record Version |
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C28500
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WHO-VATC |
QV08AA10
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WHO-ATC |
V08AA10
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Code System | Code | Type | Description | ||
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DTXSID1023154
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m6353
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PRIMARY | Merck Index | ||
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1763
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4449
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DIODONE
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CHEMBL2110615
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9303
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D007468
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SUB07197MIG
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C75627
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300-37-8
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206-089-4
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DB13568
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ZTK4026YJ5
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100000082852
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PRIMARY |
Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE | |||
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PARENT -> SALT/SOLVATE |
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ACTIVE MOIETY |