Diltiazem Hydrochloride

CHEMBL1697 Phase 4 Approuvé Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
451.0 g/mol
LogP
Phase
4

The hydrochloride salt form of diltiazem, the standard pharmaceutical preparation used in oral and injectable formulations for hypertension, angina, and arrhythmias. It slows conduction through the AV node of the heart and dilates arteries. Available in immediate and extended-release formulations for different clinical needs.

Masse moléculaire

451,0000 g/mol

TPSA

84,40 Ų

Aires thérapeutiques

Mécanisme d'action

Benzothiazepine calcium channel blocker.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mécanisme

Benzothiazepine calcium channel blocker.

Structure 2D

SVG PNG

Cite this structure


                        

Embed this structure


                        

SMILES

COc1ccc([C@@H]2Sc3ccccc3N(CCN(C)C)C(=O)[C@@H]2OC(C)=O)cc1.Cl

InChI

InChI=1S/C22H26N2O4S.ClH/c1-15(25)28-20-21(16-9-11-17(27-4)12-10-16)29-19-8-6-5-7-18(19)24(22(20)26)14-13-23(2)3;/h5-12,20-21H,13-14H2,1-4H3;1H/t20-,21+;/m1./s1

Molecular Formula

C22H27ClN2O4S

HBD / HBA

1 / 6

Liaisons Rotatives

7

Atomes Lourds

30

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.

Foire aux questions

The hydrochloride salt form of diltiazem, the standard pharmaceutical preparation used in oral and injectable formulations for hypertension, angina, and arrhythmias. It slows conduction through the AV node of the heart and dilates arteries. Available in immediate and extended-release formulations for different clinical needs.

Benzothiazepine calcium channel blocker.

Yes, Diltiazem 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). CHEMBL1697. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 62920. Chemical information database.

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

Avertissement médical

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.