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Dextroamphetamine

CHEMBL612 Phase 4 承認済み Small molecule
Half-Life
—
Bioavailability
—
Protein Binding
—
Molecular Weight
135.2 g/mol
LogP
1.8
Phase
4

The more pharmacologically potent d-isomer of amphetamine, a CNS stimulant that increases release of dopamine and norepinephrine; used for ADHD and narcolepsy, and historically for obesity. It carries significant potential for dependence and is a Schedule II controlled substance.

分子量

135.2100 g/mol

LogP

1.80

TPSA

26.00 Ų

リピンスキーの五則

適合

治療領域

Pain Management Asthma Schizophrenia Bipolar Disorder Generalized Anxiety Disorder Insomnia Multiple Sclerosis Stroke Obesity Hypertension Major Depressive Disorder Chronic Pain HIV/AIDS Heart Failure

Pharmacokinetics (PK)

Pharmacodynamics (PD)

2D構造

SVG PNG

Cite this structure


                        

                            
                            
                        

                    

                


                
                

                    

                    

                        
Embed this structure

                        

                        

                            
                            
                        

                    

                

                

                
                

                    
SMILES

                    
C[C@H](N)Cc1ccccc1

                

                

                
                

                    
InChI

                    
InChI=1S/C9H13N/c1-8(10)7-9-5-3-2-4-6-9/h2-6,8H,7,10H2,1H3/t8-/m0/s1

                

                

                

                    
                    

                        
Molecular Formula

                        
C9H13N

                    

                    
                    

                        
HBD / HBA

                        
1 / 1

                    

                    
                    

                        
回転可能結合数

                        
2

                    

                    
                    
                    

                        
重原子数

                        
10

                    

                    
                

            


            
            

                
                


    
    
        
    
    
    
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 more pharmacologically potent d-isomer of amphetamine, a CNS stimulant that increases release of dopamine and norepinephrine; used for ADHD and narcolepsy, and historically for obesity. It carries significant potential for dependence and is a Schedule II controlled substance.

                        

                    

                    

                    

                    

                    

                    

                        
                        

                            
Yes, Dextroamphetamine 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).
                CHEMBL612.
                Open-access bioactivity database.
            
        
    • 
        
        
        
  • 
            
            
                PubChem — National Center for Biotechnology Information (NCBI).
                CID 5826.
                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.