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Allopurinol Sodium

CHEMBL1200477 Phase 4 承認済み Small molecule
Half-Life
—
Bioavailability
—
Protein Binding
—
Molecular Weight
158.1 g/mol
LogP
—
Phase
4

The sodium salt form of allopurinol used as an intravenous preparation for patients who cannot take oral medication, providing the same xanthine oxidase inhibition to reduce uric acid production and prevent crystal deposition in joints, kidneys, and other tissues.

分子量

158.0900 g/mol

TPSA

77.50 Ų

治療領域

Ovarian Cancer Pancreatic Cancer Bladder Cancer Thyroid Cancer Cardiovascular Disease Non-Small Cell Lung Cancer Rheumatoid Arthritis Schizophrenia Bipolar Disorder Inflammatory Bowel Disease Chronic Kidney Disease Non-Alcoholic Fatty Liver Disease Stroke Obesity Lymphoma Type 2 Diabetes Hypertension Breast Cancer Gout Tuberculosis Heart Failure Prostate Cancer Colorectal Cancer Leukemia

作用機序

Xanthine oxidase inhibitor reducing uric acid production.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

機序

Xanthine oxidase inhibitor reducing uric acid production.

2D構造

SVG PNG

Cite this structure


                        

                            
                            
                        

                    

                


                
                

                    

                    

                        
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SMILES

                    
O=c1[n-]cnc2[nH]ncc12.[Na+]

                

                

                
                

                    
InChI

                    
InChI=1S/C5H4N4O.Na/c10-5-3-1-8-9-4(3)6-2-7-5;/h1-2H,(H2,6,7,8,9,10);/q;+1/p-1

                

                

                

                    
                    

                        
Molecular Formula

                        
C5H3N4NaO

                    

                    
                    

                        
HBD / HBA

                        
1 / 4

                    

                    
                    

                        
回転可能結合数

                        
0

                    

                    
                    
                    

                        
重原子数

                        
11

                    

                    
                

            


            
            

                
                


    
    
        
    
    
    
No targets recorded

    
    
Target interaction data is not yet available for this drug.

    



                
            


            
            

                
                


    
    
        
    
    
    
No interactions recorded

    
    
Drug interaction data is not yet available for this compound.

    



                
            


            
            

                
                


    
    
        
    
    
    
No side effects recorded

    
    
Side effect data is not yet available for this drug.

    



                
            


            
            
            

                
よくある質問

                

                    
                    

                        
                        

                            
The sodium salt form of allopurinol used as an intravenous preparation for patients who cannot take oral medication, providing the same xanthine oxidase inhibition to reduce uric acid production and prevent crystal deposition in joints, kidneys, and other tissues.

                        

                    

                    

                    

                    
                    

                        
                        

                            
Xanthine oxidase inhibitor reducing uric acid production.

                        

                    

                    

                    

                    

                        
                        

                            
Yes, Allopurinol Sodium is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

                        

                    

                

            

            

            
            

            
            

            
            
{# References & Data Sources section for drug detail pages.
   Renders standard pharmacological database links plus the drug's data_sources field. #}


    
References & Data Sources

    
    
        
        
  • 
            
            
                ChEMBL — European Bioinformatics Institute (EBI).
                CHEMBL1200477.
                Open-access bioactivity database.
            
        
    • 
        
        
        
  • 
            
            
                PubChem — National Center for Biotechnology Information (NCBI).
                CID 23662349.
                Chemical information database.
            
        
    • 
        
        
        
        
    

    
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.




        


        
        
    


    



    
医学的免責事項

    

        This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.
    

    

        Data sources:
        ChEMBL,
        PubChem,
        DailyMed.