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Tamsulosin Hydrochloride

CHEMBL1200914 Phase 4 承認済み Small molecule
Half-Life
—
Bioavailability
—
Protein Binding
—
Molecular Weight
445.0 g/mol
LogP
—
Phase
4

A hydrochloride salt form of tamsulosin with the same therapeutic properties. This medication relaxes the muscles in the prostate and bladder neck, making it easier for men with an enlarged prostate (BPH) to urinate.

分子量

445.0000 g/mol

TPSA

108.00 Ų

治療領域

Bladder Cancer Benign Prostatic Hyperplasia Pain Management Multiple Sclerosis Chronic Kidney Disease Hypertension Chronic Pain Cardiovascular Disease Prostate Cancer Colorectal Cancer

作用機序

Selective alpha-1A adrenergic receptor antagonist.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

機序

Selective alpha-1A adrenergic receptor antagonist.

2D構造

SVG PNG

Cite this structure


                        

                            
                            
                        

                    

                


                
                

                    

                    

                        
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SMILES

                    
CCOc1ccccc1OCCN[C@H](C)Cc1ccc(OC)c(S(N)(=O)=O)c1.Cl

                

                

                
                

                    
InChI

                    
InChI=1S/C20H28N2O5S.ClH/c1-4-26-17-7-5-6-8-18(17)27-12-11-22-15(2)13-16-9-10-19(25-3)20(14-16)28(21,23)24;/h5-10,14-15,22H,4,11-13H2,1-3H3,(H2,21,23,24);1H/t15-;/m1./s1

                

                

                

                    
                    

                        
Molecular Formula

                        
C20H29ClN2O5S

                    

                    
                    

                        
HBD / HBA

                        
3 / 7

                    

                    
                    

                        
回転可能結合数

                        
11

                    

                    
                    
                    

                        
重原子数

                        
29

                    

                    
                

            


            
            

                
                


    
    
        
    
    
    
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

                

                    
                    

                        
                        

                            
A hydrochloride salt form of tamsulosin with the same therapeutic properties. This medication relaxes the muscles in the prostate and bladder neck, making it easier for men with an enlarged prostate (BPH) to urinate.

                        

                    

                    

                    

                    
                    

                        
                        

                            
Selective alpha-1A adrenergic receptor antagonist.

                        

                    

                    

                    

                    

                        
                        

                            
Yes, Tamsulosin Hydrochloride 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).
                CHEMBL1200914.
                Open-access bioactivity database.
            
        
    • 
        
        
        
  • 
            
            
                PubChem — National Center for Biotechnology Information (NCBI).
                CID 5362376.
                Chemical information database.
            
        
    • 
        
        
        
        
    

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




        


        
        
    


    



    
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.