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)
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 |
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[Evaluation by electrocorticogram of the protective action of piridoxilate against cerebral hypoxia in rats]. | 1977 |
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[Influence of piridoxilate on the energy metabolism of normothermic ischemic organs in the rat]. | 1980 |
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Effects of piridoxilate, a glyoxylic acid derivative, on the energy metabolism of the heart. | 1980 Nov |
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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 Jan 31 |
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Piridoxilate-associated calcium oxalate urinary calculi: a new metabolic drug-induced nephrolithiasis. | 1985 Jun 8 |
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Piridoxilate-associated nephrocalcinosis: a new form of chronic oxalate nephropathy. | 1987 |
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Piridoxilate-induced calcium oxalate calculi: a new drug-induced metabolic nephrolithiasis. | 1987 Aug |
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[13 cases of drug-induced calculi]. | 1988 |
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[Correlation of the cause and composition of renal calculi. Value of morphologic and infrared analysis]. | 1989 |
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On combination therapy with benzoate and piridoxilate. | 1989 Dec |
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Influence of protective drugs on the elevation of extracellular potassium ion concentration in the brain during ischaemia. | 1990 |
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Piridoxilate-induced oxalate nephropathy can lead to end-stage renal failure. | 1993 |
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
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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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100000081647
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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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ACTIVE MOIETY