Drug Design Targeting Phosphodiesterase

A special issue of Pharmaceuticals (ISSN 1424-8247). This special issue belongs to the section "Medicinal Chemistry".

Deadline for manuscript submissions: closed (22 April 2024) | Viewed by 127

Special Issue Editor


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Guest Editor
School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou 510006, China
Interests: C–H function in drug synthesis; C–H function in the discovery of biological compound discovery; natural product total synthesis
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Special Issue Information

Dear Colleagues,

Phosphodiesterases (PDEs) are a superfamily of enzymes that specifically hydrolyze the second messenger cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP), which can in turn be divided into PDE1-PDE11 subfamilies. At present, more than ten PDE inhibitors are available on the market, including heavy bomb PDE5 inhibitors sildenafil and tadalafil, as well as the PDE4 inhibitor Apremilast. On the other hand, PDE has been demonstrated to be the potential target for various diseases such as heart failure and neurodegenerative diseases. More and more inhibitors are being developed to target different PDE subtypes, which will greatly promote the emergence of new targets for second messenger-related diseases. This SI seeks to solicit research on the development of PDE inhibitors, as well as research related to the application of targeted PDE and chemical probes. Our aim is to provide a platform for discussing the latest research on PDE inhibitors and promoting the application of PDE inhibitors.

Dr. Yinuo Wu
Guest Editor

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Keywords

  • phosphodiesterase inhibitor
  • novel target
  • computer-aided drug design
  • novel treatment
  • novel mechanism

Published Papers

There is no accepted submissions to this special issue at this moment.
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