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Zardaverine

Cat. No. M27648

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Zardaverine Structure

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Quality Control & Documentation
Biological Activity

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.

Chemical Information
Molecular Weight 268.22
Formula C12H10F2N2O3
CAS Number 101975-10-4
Form Solid
Solubility (25°C) DMSO 25 mg/mL (ultrasonic)
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Donna M Cartledge, et al. Front Oncol. Cytotoxicity of Zardaverine in Embryonal Rhabdomyosarcoma from a Costello Syndrome Patient

[2] Liping Sun, et al. PLoS One. Phosphodiesterase 3/4 inhibitor zardaverine exhibits potent and selective antitumor activity against hepatocellular carcinoma both in vitro and in vivo independently of phosphodiesterase inhibition

[3] R T Schermuly, et al. Eur Respir J. Zardaverine and aerosolised iloprost in a model of acute respiratory failure

[4] C Schudt, et al. Agents Actions Suppl. Zardaverine: a cyclic AMP specific PDE III/IV inhibitor

[5] C Schudt, et al. Biochem Pharmacol. Zardaverine as a selective inhibitor of phosphodiesterase isozymes

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Keywords: Zardaverine supplier, PDE, inhibitors, activators

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