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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
Structure of PIRIDOXILATE

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)

HIDE SMILES / InChI
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

PubMed

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

Sample Use Guides

600 mg for 5 days
Route of Administration: Oral
Name Type Language
PIRIDOXILATE
INN   MART.   WHO-DD  
INN  
Official Name English
Piridoxilate [WHO-DD]
Common Name English
((5-HYDROXY-4-(HYDROXYMETHYL)-6-METHYL-3-PYRIDYL)METHOXY)GLYCOLIC ACID COMPOUND WITH ((4,5-BIS(HYDROXYMETHYL)-2-METHYL-3-PYRIDYL)OXY)GLYCOLIC ACID (1:1)
Systematic Name English
piridoxilate [INN]
Common Name English
PIRIDOXILATE [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C78322
Created by admin on Sat Dec 16 16:52:38 GMT 2023 , Edited by admin on Sat Dec 16 16:52:38 GMT 2023
Code System Code Type Description
EVMPD
SUB09911MIG
Created by admin on Sat Dec 16 16:52:38 GMT 2023 , Edited by admin on Sat Dec 16 16:52:38 GMT 2023
PRIMARY
CAS
24340-35-0
Created by admin on Sat Dec 16 16:52:38 GMT 2023 , Edited by admin on Sat Dec 16 16:52:38 GMT 2023
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INN
2357
Created by admin on Sat Dec 16 16:52:38 GMT 2023 , Edited by admin on Sat Dec 16 16:52:38 GMT 2023
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SMS_ID
100000081647
Created by admin on Sat Dec 16 16:52:38 GMT 2023 , Edited by admin on Sat Dec 16 16:52:38 GMT 2023
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FDA UNII
13X224L936
Created by admin on Sat Dec 16 16:52:38 GMT 2023 , Edited by admin on Sat Dec 16 16:52:38 GMT 2023
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EPA CompTox
DTXSID80947186
Created by admin on Sat Dec 16 16:52:38 GMT 2023 , Edited by admin on Sat Dec 16 16:52:38 GMT 2023
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DRUG CENTRAL
2203
Created by admin on Sat Dec 16 16:52:38 GMT 2023 , Edited by admin on Sat Dec 16 16:52:38 GMT 2023
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NCI_THESAURUS
C76588
Created by admin on Sat Dec 16 16:52:38 GMT 2023 , Edited by admin on Sat Dec 16 16:52:38 GMT 2023
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PUBCHEM
71907
Created by admin on Sat Dec 16 16:52:38 GMT 2023 , Edited by admin on Sat Dec 16 16:52:38 GMT 2023
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