Vardenafil

Basic Information


CAS ID: 224785-90-4
Molecular Formula: C23H32N6O4S
Molecular Weight: 488.6 g/mol
Monoisotopic Mass: 488.2206 g/mol
Class: Small Molecule
Natural Product: No
Other Names: VARDENAFIL DIHYDROCHLORIDE | LEVITRA | STAXYN | VARDENAFIL HYDROCHLORIDE | VARDENAFIL
Analysis: Drug repositioning mechanism analysis

N O N NH N O S O O N N


Compound Structure and Identifier


InChI: InChI=1S/C23H32N6O4S/c1-5-8-20-24-16(4)21-23(30)25-22(26-29(20)21)18-15-17(9-10-19(18)33-7-3)34(31,32)28-13-11-27(6-2)12-14-28/h9-10,15H,5-8,11-14H2,1-4H3,(H,25,26,30) See All
InChI Key: SECKRCOLJRRGGV-UHFFFAOYSA-N
Smiles: CCCc1nc(C)c2C(=O)N=C(Nn12)c3cc(ccc3OCC)S(=O)(=O)N4CCN(CC)CC4 See All
Molfile: Download


Related Target


Target ID Name Interaction
T0431 cGMP-specific 3',5'-cyclic phosphodiesterase inhibitor

Related Fibrosis Property


Reference Record 1

PubMed ID 26410556 Target ID T0431
Uniprot ID cGMP-specific 3',5'-cyclic phosphodiesterase Name cGMP-specific 3',5'-cyclic phosphodiesterase
Model vitro Fibrosis Disease Dermal fibrosis
Process I
Process II fibroblasts differetiation
Process III
Mechanism

Reference Record 2

PubMed ID 28196856 Target ID T0431
Uniprot ID cGMP-specific 3',5'-cyclic phosphodiesterase Name cGMP-specific 3',5'-cyclic phosphodiesterase
Model vitro,mice Fibrosis Disease Cystic fibrosis
Process I attenue inflammation
Process II macrophages polarization
Process III
Mechanism Targeting PDE5- and CFTR-dependent mechanisms

Trial Record 1

ClinicalTrial ID NCT01002534 Disease Cystic fibrosis
Phase Phase 2 Status Terminated
First Received October 27, 2009 Last Verified February 25, 2019
Sponsor Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Trial Record 2

ClinicalTrial ID NCT02344823 Disease Liver fibrosis
Phase Phase 4 Status Unknown
First Received January 26, 2015 Last Verified September 25, 2015
Sponsor Medical University of Vienna

Related Link


PubChem: 110634
ChEMBL: CHEMBL1520