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Clindamycin Hydrochloride

CHEMBL1200588 Phase 4 承認済み Small molecule
Half-Life
—
Bioavailability
—
Protein Binding
—
Molecular Weight
461.4 g/mol
LogP
—
Phase
4

The hydrochloride salt form of clindamycin used in oral capsules for treating bacterial infections of the skin, lungs, and soft tissues. It works by inhibiting bacterial ribosomal protein synthesis.

分子量

461.4000 g/mol

TPSA

128.00 Ų

治療領域

Endometriosis Pain Management Rheumatoid Arthritis Asthma Insomnia Obesity Lymphoma Hypertension Breast Cancer Chronic Pain Malaria Heart Failure Colorectal Cancer Leukemia

作用機序

Binds 50S ribosomal subunit inhibiting protein synthesis.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

機序

Binds 50S ribosomal subunit inhibiting protein synthesis.

2D構造

SVG PNG

Cite this structure


                        

                            
                            
                        

                    

                


                
                

                    

                    

                        
Embed this structure

                        

                        

                            
                            
                        

                    

                

                

                
                

                    
SMILES

                    
CCC[C@@H]1C[C@@H](C(=O)N[C@@H]([C@H]2O[C@H](SC)[C@H](O)[C@@H](O)[C@H]2O)[C@H](C)Cl)N(C)C1.Cl

                

                

                
                

                    
InChI

                    
InChI=1S/C18H33ClN2O5S.ClH/c1-5-6-10-7-11(21(3)8-10)17(25)20-12(9(2)19)16-14(23)13(22)15(24)18(26-16)27-4;/h9-16,18,22-24H,5-8H2,1-4H3,(H,20,25);1H/t9-,10+,11-,12+,13-,14+,15+,16+,18+;/m0./s1

                

                

                

                    
                    

                        
Molecular Formula

                        
C18H34Cl2N2O5S

                    

                    
                    

                        
HBD / HBA

                        
5 / 7

                    

                    
                    

                        
回転可能結合数

                        
7

                    

                    
                    
                    

                        
重原子数

                        
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.

    



                
            


            
            
            

                
よくある質問

                

                    
                    

                        
                        

                            
The hydrochloride salt form of clindamycin used in oral capsules for treating bacterial infections of the skin, lungs, and soft tissues. It works by inhibiting bacterial ribosomal protein synthesis.

                        

                    

                    

                    

                    
                    

                        
                        

                            
Binds 50S ribosomal subunit inhibiting protein synthesis.

                        

                    

                    

                    

                    

                        
                        

                            
Yes, Clindamycin 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).
                CHEMBL1200588.
                Open-access bioactivity database.
            
        
    • 
        
        
        
  • 
            
            
                PubChem — National Center for Biotechnology Information (NCBI).
                CID 16051951.
                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.