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Miglustat

CHEMBL1029 Phase 4 Одобрено Small molecule
Half-Life
—
Bioavailability
—
Protein Binding
—
Molecular Weight
219.3 g/mol
LogP
-0.6
Phase
4

This oral medication reduces the production of certain fatty substances that accumulate harmfully in cells in people with specific inherited enzyme deficiency disorders. It is used to treat Gaucher disease and Niemann-Pick type C disease.

Молекулярная масса

219,2800 g/mol

LogP

-0,60

TPSA

84,20 Ų

Правило пяти Липинского

Соответствует

Pharmacokinetics (PK)

Pharmacodynamics (PD)

2D Структура

SVG PNG

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SMILES

                    
CCCCN1C[C@H](O)[C@@H](O)[C@H](O)[C@H]1CO

                

                

                
                

                    
InChI

                    
InChI=1S/C10H21NO4/c1-2-3-4-11-5-8(13)10(15)9(14)7(11)6-12/h7-10,12-15H,2-6H2,1H3/t7-,8+,9-,10-/m1/s1

                

                

                

                    
                    

                        
Molecular Formula

                        
C10H21NO4

                    

                    
                    

                        
HBD / HBA

                        
4 / 5

                    

                    
                    

                        
Вращаемые Связи

                        
4

                    

                    
                    
                    

                        
Тяжёлые Атомы

                        
15

                    

                    
                

            


            
            

                
                


    
    
        
    
    
    
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.

    



                
            


            
            
            

                
Часто задаваемые вопросы

                

                    
                    

                        
                        

                            
This oral medication reduces the production of certain fatty substances that accumulate harmfully in cells in people with specific inherited enzyme deficiency disorders. It is used to treat Gaucher disease and Niemann-Pick type C disease.

                        

                    

                    

                    

                    

                    

                    

                        
                        

                            
Yes, Miglustat 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).
                CHEMBL1029.
                Open-access bioactivity database.
            
        
    • 
        
        
        
  • 
            
            
                PubChem — National Center for Biotechnology Information (NCBI).
                CID 51634.
                Chemical information database.
            
        
    • 
        
        
        
        
    

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




        


        
        
    


    



    
Медицинский отказ от ответственности

    

        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.