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5-hydroxypyrazine-2-carboxylic acid

Catalog No.
A3124
Metabolite of pyrazinamide (PZA)
Grouped product items
SizePriceStock Qty
1g
$90.00
In stock
For scientific research use only and should not be used for diagnostic or medical purposes.

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Email: [email protected]

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Background

5-hydroxypyrazine-2-carboxylic acid , a metabolite of anti-tuberculosis drug pyrazinamide (PZA).

Chemical Properties

Physical AppearanceA solid
StorageStore at -20°C
M.Wt140.1
Cas No.34604-60-9
FormulaC5H4N2O3
Solubilityinsoluble in EtOH; ≥7 mg/mL in DMSO; ≥7.63 mg/mL in H2O
Chemical Name5-hydroxypyrazine-2-carboxylic acid
SDFDownload SDF
Canonical SMILESOC1=NC=C(C(O)=O)N=C1
Shipping ConditionSmall Molecules with Blue Ice, Modified Nucleotides with Dry Ice.
General tips We do not recommend long-term storage for the solution, please use it up soon.

Protocol

Animal experiment [1]:

Animal models

Sprague-Dawley female rats

Dosage form

50mg/kg,100mg/kg(p.o.)

Application

Quantitative analysis of PZA and its three major metabolites in 24-hour urine samples were performed by reversed-phase high-performance liquid chromatography. Caffeine (100mg/kg) and PZA (50mg/kg) administered simultaneously increase the excretion of the most soluble and least toxic PZA metabolite 5-hydroxypyrazine-2-carboxylic acid (from 66.18 +/- 10.87 to 94.56 + /-8.65μM / 24 h). This effect was even more pronounced when PZA was administered at 100 mg / kg: the excretion of 5-OH-PA was increased from 113.28 +/- 70 to 173.23 +/- 17.82 μM / 24 h. These results suggest that caffeine intake can affect PZA metabolism.

Other notes

Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal.

References:

[1]. Mehmedagic A, Verite P, Menager S, Tharasse C, Chabenat C, Andre D, Lafont O. Investigation of the effects of concomitant caffeine administration on the metabolic disposition of pyrazinamide in rats. Biopharm Drug Dispos. 2002 Jul;23(5):191-5. doi: 10.1002/bdd.305. PMID: 12116050.

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