Details
| Stereochemistry | MIXED |
| Molecular Formula | 2C10H13NO6 |
| Molecular Weight | 486.4266 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=NC=C(CO)C(CO)=C1OC(O)C(O)=O.CC2=C(O)C(CO)=C(COC(O)C(O)=O)C=N2
InChI
InChIKey=TWVSQBMULZSRIJ-UHFFFAOYSA-N
InChI=1S/2C10H13NO6/c1-5-8(13)7(3-12)6(2-11-5)4-17-10(16)9(14)15;1-5-8(17-10(16)9(14)15)7(4-13)6(3-12)2-11-5/h2*2,10,12-13,16H,3-4H2,1H3,(H,14,15)
| Molecular Formula | C10H13NO6 |
| Molecular Weight | 243.2133 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
| Molecular Formula | C10H13NO6 |
| Molecular Weight | 243.2133 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Piridoxilate is a conjugation product of pyridoxine and glyoxylic acid in which pyridoxine is supposed to facilitate in vivo transformation of glyoxylic acid to glycine rather than to oxalic acid. The protective action of piridoxilate against hypoxia and metabolic inhibition of the myocardium was confirmed in the experiments on the canine heart-lung preparation using the redox potential of the myocardium and the pyridine nucleotide fluorescence of the heart as indices of cellular energy metabolism. The protective action of piridoxilate against hypoxia which may be attributable to rearrangement of the myocardial metabolism. Piridoxilate did not induce any significant changes in objective and subjective sleep variables. Long-term treatment with piridoxilate may result in overproduction of oxalic acid and in calcium oxalate nephrolithiasis. Piridoxilate should be added to the list of chemicals responsible for chronic oxalate nephropathy.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Piridoxilate-induced oxalate nephropathy can lead to end-stage renal failure. | 1993 |
|
| Influence of protective drugs on the elevation of extracellular potassium ion concentration in the brain during ischaemia. | 1990 |
|
| On combination therapy with benzoate and piridoxilate. | 1989-12 |
|
| [Correlation of the cause and composition of renal calculi. Value of morphologic and infrared analysis]. | 1989 |
|
| [13 cases of drug-induced calculi]. | 1988 |
|
| Piridoxilate-induced calcium oxalate calculi: a new drug-induced metabolic nephrolithiasis. | 1987-08 |
|
| Piridoxilate-associated nephrocalcinosis: a new form of chronic oxalate nephropathy. | 1987 |
|
| Piridoxilate-associated calcium oxalate urinary calculi: a new metabolic drug-induced nephrolithiasis. | 1985-06-08 |
|
| Potentiation by piridoxilate of the synthesis of hippurate from benzoate in isolated rat hepatocytes. An approach to the determination of new pathways of nitrogen excretion in inborn errors of urea synthesis. | 1984-01-31 |
|
| Effects of piridoxilate, a glyoxylic acid derivative, on the energy metabolism of the heart. | 1980-11 |
|
| [Influence of piridoxilate on the energy metabolism of normothermic ischemic organs in the rat]. | 1980 |
|
| [Evaluation by electrocorticogram of the protective action of piridoxilate against cerebral hypoxia in rats]. | 1977 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6396969
600 mg for 5 days
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 08:29:09 GMT 2025
by
admin
on
Wed Apr 02 08:29:09 GMT 2025
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| Record UNII |
13X224L936
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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Official Name | English | ||
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Preferred Name | English | ||
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Common Name | English | ||
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Systematic Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C78322
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SUB09911MIG
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24340-35-0
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2357
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13X224L936
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DTXSID80947186
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2203
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C76588
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71907
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