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Citalopram

CHEMBL549 Phase 4 Đã phê duyệt Small molecule
Half-Life
35 hours
Bioavailability
—
Protein Binding
—
Molecular Weight
324.4 g/mol
LogP
3.2
Phase
4

A selective serotonin reuptake inhibitor (SSRI) that increases serotonin availability in synapses by blocking the serotonin transporter, used to treat major depressive disorder, panic disorder, and obsessive-compulsive disorder. It has a relatively favorable side effect and drug interaction profile compared to older antidepressants. QT prolongation is a dose-dependent concern, and doses above 40 mg daily are not recommended.

Khối lượng phân tử

324,3920 g/mol

LogP

3,20

TPSA

36,30 Ų

Lipinski RO5

Đạt

Lĩnh vực điều trị

Ovarian Cancer Pancreatic Cancer Bladder Cancer Thyroid Cancer Cardiovascular Disease Respiratory Disease Pain Management Non-Small Cell Lung Cancer Rheumatoid Arthritis Asthma Chronic Obstructive Pulmonary Disease Alzheimer's Disease Parkinson's Disease Epilepsy Schizophrenia Bipolar Disorder Generalized Anxiety Disorder Insomnia Infectious Disease Gastroesophageal Reflux Disease Inflammatory Bowel Disease Psoriasis Multiple Sclerosis Chronic Kidney Disease Non-Alcoholic Fatty Liver Disease Stroke Obesity Type 2 Diabetes Hypertension Major Depressive Disorder Breast Cancer Chronic Pain HIV/AIDS Hepatitis C Heart Failure Prostate Cancer Colorectal Cancer

Phân loại thuốc

N — N - Nervous System

Cơ chế tác dụng

Selective serotonin reuptake inhibitor (SSRI); racemic mixture with escitalopram as active S-enantiomer.

Pharmacokinetics (PK)

Half-Life 35 hours

Pharmacodynamics (PD)

Cơ chế

Selective serotonin reuptake inhibitor (SSRI); racemic mixture with escitalopram as active S-enantiomer.

Cấu trúc 2D

SVG PNG

Cite this structure


                        

                            
                            
                        

                    

                


                
                

                    

                    

                        
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SMILES

                    
CN(C)CCCC1(c2ccc(F)cc2)OCc2cc(C#N)ccc21

                

                

                
                

                    
InChI

                    
InChI=1S/C20H21FN2O/c1-23(2)11-3-10-20(17-5-7-18(21)8-6-17)19-9-4-15(13-22)12-16(19)14-24-20/h4-9,12H,3,10-11,14H2,1-2H3

                

                

                

                    
                    

                        
Molecular Formula

                        
C20H21FN2O

                    

                    
                    

                        
HBD / HBA

                        
- / 4

                    

                    
                    

                        
Liên kết có thể quay

                        
5

                    

                    
                    
                    

                        
Nguyên tử nặng

                        
24

                    

                    
                

            


            
            

                
                


    
    
        
    
    
    
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.

    



                
            


            
            
            

                
Câu hỏi thường gặp

                

                    
                    

                        
                        

                            
A selective serotonin reuptake inhibitor (SSRI) that increases serotonin availability in synapses by blocking the serotonin transporter, used to treat major depressive disorder, panic disorder, and obsessive-compulsive disorder. It has a relatively favorable side effect and drug interaction profile compared to older antidepressants. QT prolongation is a dose-dependent concern, and doses above 40 mg daily are not recommended.

                        

                    

                    

                    

                    
                    

                        
                        

                            
Selective serotonin reuptake inhibitor (SSRI); racemic mixture with escitalopram as active S-enantiomer.

                        

                    

                    

                    
                    

                        
                        

                            
Key pharmacokinetic parameters for Citalopram: Half-life: 35 hours.

                        

                    

                    

                    

                        
                        

                            
Yes, Citalopram is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

                        

                    

                

            

            

            
            

            
            
            

                
Related Drugs


                
                

                    
Same Drug Class

                    

                        
                        
                            Acetaminophen
                            Small molecule
                        
                        
                        
                            Aspirin
                            Small molecule
                        
                        
                        
                            Sertraline
                            Small molecule
                        
                        
                        
                            Escitalopram
                            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).
                CHEMBL549.
                Open-access bioactivity database.
            
        
    • 
        
        
        
  • 
            
            
                PubChem — National Center for Biotechnology Information (NCBI).
                CID 2771.
                Chemical information database.
            
        
    • 
        
        
        
        
    

    
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.




        


        
        
    


    



    
Tuyên bố miễn trách y tế

    

        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.