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Zardaverine

From Wikipedia, the free encyclopedia
Zardaverine
Names
Preferred IUPAC name
6-[3-(Difluoromethoxy)-4-methoxyphenyl]pyridazin-3(2H)-one
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C12H10F2N2O3/c1-18-10-6-7(2-4-9(10)19-12(13)14)8-3-5-11(17)16-15-8/h2-6,12H,1H3,(H,16,17)
    Key: HJMQDJPMQIHLPB-UHFFFAOYSA-N
  • COC1=C(C=CC(=C1)C2=NNC(=O)C=C2)OC(F)F
Properties
C12H10F2N2O3
Molar mass268.220 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Zardaverine is a dual-selectivePDE3/4phosphodiesterase inhibitor.[1] Studiesin vitro suggest that it may have useful anti-cancer properties.[2]

References

[edit]
  1. ^Kümmerle, AE; Schmitt, M; Cardozo, SV; Lugnier, C; Villa, P; Lopes, AB; Romeiro, NC; Justiniano, H; Martins, MA; Fraga, CA; Bourguignon, JJ; Barreiro, EJ (2012). "Design, Synthesis, and Pharmacological Evaluation ofN-Acylhydrazones and Novel Conformationally Constrained Compounds as Selective and Potent Orally Active Phosphodiesterase-4 Inhibitors".Journal of Medicinal Chemistry.55 (17):7525–45.doi:10.1021/jm300514y.PMID 22891752.
  2. ^Corsello SM, Nagari RT, Spangler RD, et al. Discovering the anticancer potential of non-oncology drugs by systematic viability profiling.Nature Cancer (2020).doi:10.1038/s43018-019-0018-6
PDE1
PDE2
PDE3
PDE4
PDE5
PDE7
PDE9
PDE10
PDE11
Non-selective
Unsorted
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