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Trandolapril

CHEMBL1519 Phase 4 معتمد Small molecule
Half-Life
—
Bioavailability
—
Protein Binding
—
Molecular Weight
430.5 g/mol
LogP
2.0
Phase
4

Trandolapril is a prodrug ACE inhibitor that is hydrolyzed in the liver to its active diacid form trandolaprilat, which inhibits angiotensin-converting enzyme, reducing angiotensin II production and aldosterone secretion, leading to vasodilation and decreased sodium retention. It is approved for hypertension, heart failure post-myocardial infarction, and left ventricular dysfunction after MI, and provides cardioprotective benefits beyond its antihypertensive effects. Its high tissue ACE binding affinity and long duration of action support once-daily dosing.

الوزن الجزيئي

430,5000 g/mol

LogP

2,00

TPSA

95,90 Ų

قاعدة ليبينسكي للخمسة

ناجح

المجالات العلاجية

Stroke Obesity Type 2 Diabetes Hypertension Heart Failure

آلية العمل

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

الآلية

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

البنية ثنائية الأبعاد

SVG PNG

Cite this structure


                        

                            
                            
                        

                    

                


                
                

                    

                    

                        
Embed this structure

                        

                        

                            
                            
                        

                    

                

                

                
                

                    
SMILES

                    
CCOC(=O)[C@H](CCc1ccccc1)N[C@@H](C)C(=O)N1[C@H](C(=O)O)C[C@H]2CCCC[C@@H]21

                

                

                
                

                    
InChI

                    
InChI=1S/C24H34N2O5/c1-3-31-24(30)19(14-13-17-9-5-4-6-10-17)25-16(2)22(27)26-20-12-8-7-11-18(20)15-21(26)23(28)29/h4-6,9-10,16,18-21,25H,3,7-8,11-15H2,1-2H3,(H,28,29)/t16-,18+,19-,20-,21-/m0/s1

                

                

                

                    
                    

                        
Molecular Formula

                        
C24H34N2O5

                    

                    
                    

                        
HBD / HBA

                        
2 / 6

                    

                    
                    

                        
الروابط القابلة للدوران

                        
10

                    

                    
                    
                    

                        
الذرات الثقيلة

                        
31

                    

                    
                

            


            
            

                
                


    
    
        
    
    
    
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.

    



                
            


            
            
            

                
الأسئلة الشائعة

                

                    
                    

                        
                        

                            
Trandolapril is a prodrug ACE inhibitor that is hydrolyzed in the liver to its active diacid form trandolaprilat, which inhibits angiotensin-converting enzyme, reducing angiotensin II production and aldosterone secretion, leading to vasodilation and decreased sodium retention. It is approved for hypertension, heart failure post-myocardial infarction, and left ventricular dysfunction after MI, and provides cardioprotective benefits beyond its antihypertensive effects. Its high tissue ACE binding affinity and long duration of action support once-daily dosing.

                        

                    

                    

                    

                    
                    

                        
                        

                            
Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

                        

                    

                    

                    

                    

                        
                        

                            
Yes, Trandolapril 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).
                CHEMBL1519.
                Open-access bioactivity database.
            
        
    • 
        
        
        
  • 
            
            
                PubChem — National Center for Biotechnology Information (NCBI).
                CID 5484727.
                Chemical information database.
            
        
    • 
        
        
        
        
    

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




        


        
        
    


    



    
إخلاء المسؤولية الطبية

    

        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.