Details
Stereochemistry | ACHIRAL |
Molecular Formula | C4H4N2O2 |
Molecular Weight | 113.0794 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1N[13C](=O)NC=C1
InChI
InChIKey=ISAKRJDGNUQOIC-AZXPZELESA-N
InChI=1S/C4H4N2O2/c7-3-1-2-5-4(8)6-3/h1-2H,(H2,5,6,7,8)/i4+1
Molecular Formula | C4H4N2O2 |
Molecular Weight | 113.0794 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Otsuka Pharmaceutical was developing URACIL C-13, 2- ([2-13C]uracil) breath test for diagnosis of cancer and gastric emptying disorders. Dihydropyrimidine dehydrogenase (DPD) deficiency is critical in the predisposition to 5-fluorouracil dose-related toxicity. The phenotypic [2-(13)C]uracil breath test (UraBT) demonstrated 96% specificity and 100% sensitivity for identification of DPD deficiency. Phase II development of the breath test was ongoing. As phase II clinical study didn't exploit performance as diagnostic medicines, the development of [2-13C]uracil was discontinued.
Originator
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Pharmacokinetic modelling of [2-13C]uracil metabolism in normal and DPD-deficient dogs. | 2006 |
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The uracil breath test in the assessment of dihydropyrimidine dehydrogenase activity: pharmacokinetic relationship between expired 13CO2 and plasma [2-13C]dihydrouracil. | 2006 Jan 15 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/16428499
An aqueous solution of [2-(13)C]uracil (6 mg/kg) was orally administered to 23 healthy volunteers and 8 cancer patients.
Route of Administration:
Oral
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 07:39:29 GMT 2023
by
admin
on
Sat Dec 16 07:39:29 GMT 2023
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Record UNII |
OZF8J4VAIK
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Record Status |
Validated (UNII)
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Record Version |
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35803-45-3
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DTXSID70189336
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10171240
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OZF8J4VAIK
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admin on Sat Dec 16 07:39:29 GMT 2023 , Edited by admin on Sat Dec 16 07:39:29 GMT 2023
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