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Sumatriptan Succinate

CHEMBL1201150 Phase 4 Approuvé Small molecule
Half-Life
—
Bioavailability
—
Protein Binding
—
Molecular Weight
413.5 g/mol
LogP
—
Phase
4

A succinate salt form of sumatriptan with the same therapeutic properties. Designed specifically for migraine attacks, this triptan medication works by activating serotonin receptors in the brain and blood vessels, causing the swollen blood vessels responsible for migraine pain to constrict back to normal size.

Masse moléculaire

413,5000 g/mol

TPSA

148,00 Ų

Aires thérapeutiques

Pain Management Migraine Chronic Pain

Mécanisme d'action

Selective 5-HT1B/1D receptor agonist.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mécanisme

Selective 5-HT1B/1D receptor agonist.

Structure 2D

SVG PNG

Cite this structure


                        

                            
                            
                        

                    

                


                
                

                    

                    

                        
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SMILES

                    
CNS(=O)(=O)Cc1ccc2[nH]cc(CCN(C)C)c2c1.O=C(O)CCC(=O)O

                

                

                
                

                    
InChI

                    
InChI=1S/C14H21N3O2S.C4H6O4/c1-15-20(18,19)10-11-4-5-14-13(8-11)12(9-16-14)6-7-17(2)3;5-3(6)1-2-4(7)8/h4-5,8-9,15-16H,6-7,10H2,1-3H3;1-2H2,(H,5,6)(H,7,8)

                

                

                

                    
                    

                        
Molecular Formula

                        
C18H27N3O6S

                    

                    
                    

                        
HBD / HBA

                        
4 / 8

                    

                    
                    

                        
Liaisons Rotatives

                        
9

                    

                    
                    
                    

                        
Atomes Lourds

                        
28

                    

                    
                

            


            
            

                
                


    
    
        
    
    
    
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.

    



                
            


            
            
            

                
Foire aux questions

                

                    
                    

                        
                        

                            
A succinate salt form of sumatriptan with the same therapeutic properties. Designed specifically for migraine attacks, this triptan medication works by activating serotonin receptors in the brain and blood vessels, causing the swollen blood vessels responsible for migraine pain to constrict back to normal size.

                        

                    

                    

                    

                    
                    

                        
                        

                            
Selective 5-HT1B/1D receptor agonist.

                        

                    

                    

                    

                    

                        
                        

                            
Yes, Sumatriptan Succinate 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).
                CHEMBL1201150.
                Open-access bioactivity database.
            
        
    • 
        
        
        
  • 
            
            
                PubChem — National Center for Biotechnology Information (NCBI).
                CID 59772.
                Chemical information database.
            
        
    • 
        
        
        
        
    

    
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.




        


        
        
    


    



    
Avertissement médical

    

        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.