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Cidofovir Anhydrous

CHEMBL152 Phase 4 承認済み Small molecule
Half-Life
—
Bioavailability
—
Protein Binding
—
Molecular Weight
279.2 g/mol
LogP
-3.6
Phase
4

The anhydrous form of cidofovir shares the same antiviral nucleotide analog properties as the standard formulation, targeting viral DNA polymerase in CMV infections. The anhydrous designation indicates the absence of water of crystallization in the crystalline structure. Clinical use requires the same renal protective measures as the parent compound.

分子量

279.1900 g/mol

LogP

-3.60

TPSA

146.00 Ų

リピンスキーの五則

適合

治療領域

Pain Management Epilepsy Migraine Schizophrenia Bipolar Disorder Generalized Anxiety Disorder Insomnia Chronic Kidney Disease Hypertension Chronic Pain HIV/AIDS Heart Failure

Pharmacokinetics (PK)

Pharmacodynamics (PD)

2D構造

SVG PNG

Cite this structure


                        

                            
                            
                        

                    

                


                
                

                    

                    

                        
Embed this structure

                        

                        

                            
                            
                        

                    

                

                

                
                

                    
SMILES

                    
Nc1ccn(C[C@@H](CO)OCP(=O)(O)O)c(=O)n1

                

                

                
                

                    
InChI

                    
InChI=1S/C8H14N3O6P/c9-7-1-2-11(8(13)10-7)3-6(4-12)17-5-18(14,15)16/h1-2,6,12H,3-5H2,(H2,9,10,13)(H2,14,15,16)/t6-/m0/s1

                

                

                

                    
                    

                        
Molecular Formula

                        
C8H14N3O6P

                    

                    
                    

                        
HBD / HBA

                        
4 / 6

                    

                    
                    

                        
回転可能結合数

                        
6

                    

                    
                    
                    

                        
重原子数

                        
18

                    

                    
                

            


            
            

                
                


    
    
        
    
    
    
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 anhydrous form of cidofovir shares the same antiviral nucleotide analog properties as the standard formulation, targeting viral DNA polymerase in CMV infections. The anhydrous designation indicates the absence of water of crystallization in the crystalline structure. Clinical use requires the same renal protective measures as the parent compound.

                        

                    

                    

                    

                    

                    

                    

                        
                        

                            
Yes, Cidofovir Anhydrous 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).
                CHEMBL152.
                Open-access bioactivity database.
            
        
    • 
        
        
        
  • 
            
            
                PubChem — National Center for Biotechnology Information (NCBI).
                CID 60613.
                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.