Alfuzosin Hydrochloride
The hydrochloride salt form of alfuzosin, an alpha-1 receptor antagonist used to relax smooth muscle in the prostate and bladder neck to relieve urinary obstruction caused by BPH. This formulation provides the same mechanism of action as the parent compound, improving urine flow and reducing bothersome lower urinary tract symptoms in men.
Moleküler Ağırlık
425,9000 g/mol
TPSA
112,00 Ų
Terapötik Alanlar
Etki Mekanizması
Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.
2D Yapı
Cite this structure
Embed this structure
SMILES
COc1cc2nc(N(C)CCCNC(=O)C3CCCO3)nc(N)c2cc1OC.Cl
InChI
InChI=1S/C19H27N5O4.ClH/c1-24(8-5-7-21-18(25)14-6-4-9-28-14)19-22-13-11-16(27-3)15(26-2)10-12(13)17(20)23-19;/h10-11,14H,4-9H2,1-3H3,(H,21,25)(H2,20,22,23);1H
Molecular Formula
C19H28ClN5O4
HBD / HBA
3 / 8
Döndürülebilir Bağlar
8
Ağır Atomlar
29
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.
Sıkça Sorulan Sorular
The hydrochloride salt form of alfuzosin, an alpha-1 receptor antagonist used to relax smooth muscle in the prostate and bladder neck to relieve urinary obstruction caused by BPH. This formulation provides the same mechanism of action as the parent compound, improving urine flow and reducing bothersome lower urinary tract symptoms in men.
Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.
Yes, Alfuzosin Hydrochloride is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1723. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 71764. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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