ArtNr |
HY-B0442A-25mg |
Hersteller |
MedChem Express
|
CAS-Nr. |
224785-91-5 |
Menge |
25 mg |
Quantity options |
100 mg
10mM/1mL
200 mg
25 mg
50 mg
|
Specific against |
other |
Purity |
99.48 |
Citations |
Life Sci. 15 November 2022, 120992.<br/>Anim Cells Syst (Seoul). 2019 May 16;23(3):155-163.<br/>[1]Ashour AE, et al. Vardenafil dihydrochloride. Profiles Drug Subst Excip Relat Methodol. 2014;39:515-544.<br/>[2]Saenz de Tejada I, et al. The phosphodiesterase inhibitory selectivity and the in vitro and in vivo potency of the new PDE5 inhibitor vardenafil. Int J Impot Res. 2001;13(5):282-290.<br/>[3]Gresser U, et al. Erectile dysfunction: comparison of efficacy and side effects of the PDE-5 inhibitors sildenafil, vardenafil and tadalafil--review of the literature. Eur J Med Res. 2002 Oct 29. 7(10):435-46. <br/>[4]Oudot A, et al. Combination of BAY 60-4552 and vardenafil exerts proerectile facilitator effects in rats with cavernous nerve injury: a proof of concept study for the treatment of phosphodiesterase type 5 inhibitor failure. Eur Urol. 2011 Nov. 60(5):1020-6. <br/>[5]Ahmed N, et al. Hepatoprotective role of vardenafil against experimentally induced hepatitis in mice. J Biochem Mol Toxicol. 2017 Mar. 31(3). <br/>[6]Bódi B, et al. Long-Term PDE-5A Inhibition Improves Myofilament Function in Left and Right Ventricular Cardiomyocytes through Partially Different Mechanisms in Diabetic Rat Hearts. Antioxidants (Basel). 2021 Nov 6. 10(11):1776. |
Smiles |
CCCC1=NC(C)=C2N1N=C(C(C=C(S(=O)(N3CCN(CC)CC3)=O)C=C4)=C4OCC)NC2=O.Cl |
Lieferbar |
|
Product Description |
Vardenafil hydrochloride is a selective and orally active inhibitor of phosphodiesterase-5 (PDE5), with an IC50 of 0.7 nM. Vardenafil hydrochloride shows inhibitory towards PDE1, PDE6 with IC50s of 180 nM, and 11 nM, while IC50s are >1000 nM for PDE3 and PDE4[1]. Vardenafil hydrochloride competitively inhibits cyclic guanosine monophosphate (cGMP) hydrolysis and thus increases cGMP levels[2]. Vardenafil hydrochloride can be used for the research of erectile dysfunction, hepatitis, diabetes[1]-[6]. |
StorageTemperature |
4°C (Powder, sealed storage, away from moisture) |
Shipping |
Room Temperature |
Manufacturers Applications |
COVID-19-immunoregulation |
MolecularWeight |
525.06 |
Clinical Information |
Launched |
Manufacturers Research Area |
Endocrinology; Metabolic Disease; Inflammation/Immunology |
Solubility |
DMSO : 100 mg/mL (ultrasonic)|H2O : ≥ 100 mg/mL |
Target |
Endogenous Metabolite; Phosphodiesterase (PDE) |
Manufacturers Target |
Endogenous Metabolite; Phosphodiesterase (PDE) |
Isoform |
PDE1; PDE3; PDE4; PDE5; PDE6 |
Manufacturers Pathway |
Metabolic Enzyme/Protease |
Manufacturers Product type |
Reference compound |
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