Oxipurinol

Modify Date: 2024-01-02 14:10:59

Oxipurinol Structure
Oxipurinol structure
Common Name Oxipurinol
CAS Number 2465-59-0 Molecular Weight 152.11
Density 2.19g/cm3 Boiling Point 662.9ºC at 760 mmHg
Molecular Formula C5H4N4O2 Melting Point 300 °C
MSDS Chinese USA Flash Point 354.7ºC
Symbol GHS07
GHS07
Signal Word Warning

 Use of Oxipurinol


Oxipurinol (Oxipurinol), the major active metabolite of Allopurinol, is an inhibitor of xanthine oxidase. Oxipurinol can be used to regulate blood urate levels and treat gout[1].

 Names

Name alloxanthine
Synonym More Synonyms

 Oxipurinol Biological Activity

Description Oxipurinol (Oxipurinol), the major active metabolite of Allopurinol, is an inhibitor of xanthine oxidase. Oxipurinol can be used to regulate blood urate levels and treat gout[1].
Related Catalog
Target

Human Endogenous Metabolite

In Vitro Allopurinol is rapidly metabolized (half-life approximately 1 h) to its active metabolite oxypurinol. Oxypurinol is an inhibitor of xanthine oxidoreductase and has a considerably longer elimination half-life (approximately 23 h)[1].
References

[1]. Stocker SL, et al. The pharmacokinetics of oxypurinol in people with gout. Br J Clin Pharmacol. 2012 Sep;74(3):477-89.

 Chemical & Physical Properties

Density 2.19g/cm3
Boiling Point 662.9ºC at 760 mmHg
Melting Point 300 °C
Molecular Formula C5H4N4O2
Molecular Weight 152.11
Flash Point 354.7ºC
Exact Mass 152.03300
PSA 94.92000
Vapour Pressure 3.5E-18mmHg at 25°C
Index of Refraction 1.989
Storage condition -20°C Freezer

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi: Irritant;
Risk Phrases R36/37/38
Safety Phrases S36
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2933990090

 Customs

HS Code 2933990090
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles40

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Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.

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Drug-induced liver injury is one of the main causes of drug attrition. The ability to predict the liver effects of drug candidates from their chemical structures is critical to help guide experimental...

Evaluation of neuronal protective effects of xanthine oxidoreductase inhibitors on severe whole-brain ischemia in mouse model and analysis of xanthine oxidoreductase activity in the mouse brain.

Neurol. Med. Chir. (Tokyo) 55(1) , 77-85, (2015)

Global cerebral ischemia and reperfusion (I/R) often result in high mortality. Free radicals play an important role in global cerebral I/R. Xanthine oxidoreductase (XOR) inhibitors, such as allopurino...

Systematic and Molecular Basis of the Antibacterial Action of Quinoxaline 1,4-Di-N-Oxides against Escherichia coli.

PLoS ONE 10 , e0136450, (2015)

Quinoxaline 1,4-di-N-oxides (QdNOs) are widely known as potent antibacterial agents, but their antibacterial mechanisms are incompletely understood. In this study, the transcriptomic and proteomic pro...

 Synonyms

OXYPURINOL
BW-55-5
Alloxanthine
OXIPURINOL
1H-pyrazolo[3,4-d]pyrimidine-4,6-diol
4,6-Dihydropyrazolo Pyrimidine
MFCD00056934
1,7-Dihydro
4,6-DIHYDROXYPYRAZOLO[3,4-D]PYRIMIDINE
4,6-Dihydroxy-1H-pyrazolo[3,4-d]pyrimidine
EINECS 219-570-9
Oxyprim
Oxoallopurinol
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