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Zardaverine

Zardaverine is an orally active and selective PDE3/4 inhibitor (IC50) =0.58 uM/0.17 uM) with potent bronchodilator activity. Zardaverine also selectively inhibits the proliferation of HCC cells and induces apoptosis and cycle arrest (G0/G1 phase) . Zardaverine has good antitumor potential and is effective in both bronchial relaxation and reduction of inflammation in asthma[1][2][3].

Product Specifications

CAS Number

101975-10-4

UNSPSC

12352005

Hazard Statement

H302, H315, H319, H335

Target

Apoptosis; Phosphodiesterase (PDE)

Type

Reference compound

Related Pathways

Apoptosis; Metabolic Enzyme/Protease

Applications

COVID-19-immunoregulation

Field of Research

Cancer; Inflammation/Immunology

Assay Protocol

https://www.medchemexpress.com/Zardaverine.html

Concentration

10mM

Purity

98.64

Solubility

DMSO : 25 mg/mL (ultrasonic)

Smiles

O=C1C=CC(C2=CC=C(OC(F)F)C(OC)=C2)=NN1

Molecular Formula

C12H10F2N2O3

Molecular Weight

268.22

Precautions

H302, H315, H319, H335

References & Citations

[1]Sun L, et al. Phosphodiesterase 3/4 inhibitor zardaverine exhibits potent and selective antitumor activity against hepatocellular carcinoma both in vitro and in vivo independently of phosphodiesterase inhibition. PLoS One. 2014 Mar 5;9 (3) :e90627.|[2]Kips JC, et al. The effect of zardaverine, an inhibitor of phosphodiesterase isoenzymes III and IV, on endotoxin-induced airway changes in rats. Clin Exp Allergy. 1993 Jun;23 (6) :518-23. |[3]Schudt C, et al. Zardaverine: a cyclic AMP specific PDE III/IV inhibitor. Agents Actions Suppl. 1991;34:379-402.

Shipping Conditions

Room Temperature

Storage Conditions

-20°C, 3 years; 4°C, 2 years (Powder)

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Isoform

PDE3; PDE4

Available Sizes

Frequently Asked Questions

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