Submit Manuscript  

Article Details


Synthesis and In-vitro Phosphodiesterase 5 and 5A Inhibitory Activity of Novel 3-(3-thioxo-3h-1,2-dithiol-5-yl)phenyl4-[(1e)-3-oxo-3-phenylprop-1- en-1yl]benzoate and their Analogues

[ Vol. 14 , Issue. 2 ]

Author(s):

Manish S. Bhatia, Amol S. Sherikar* and Rakesh P. Dhavale   Pages 85 - 91 ( 7 )

Abstract:


Introduction: 3-(3-thioxo-3H-1,2-dithiol-5-yl)phenyl 4-[(1E)-3-oxo-3-phenylprop-1-en-1- yl]benzoate and their analogues were synthesized on the basis of Claisen-Schmidt condensation reaction wherein chalcone intermediates were synthesized by the reaction of substituted aldehydes and acetophenones. Final products were synthesized by reacting chalcone intermediates with 5-(4- hydroxyphenyl)-3H-1,2-dithiole-3-thione.

Conclusion: The compounds were characterized by IR, 1H NMR, 13C NMR and elemental analysis. In in-vitro Phosphodiesterase 5 inhibitory activity, compounds G4 and G8 exhibited a significant inhibitory effect against human platelet Phosphodiesterase 5 (PDE 5) while compound G3 exhibited a significant inhibitory effect on both human platelet PDE 5 and bovine recombinant Phosphodiesterase 5A (PDE 5A). This work will be highly fruitful to design novel compounds for dealing with problems associated with vasculature.

Keywords:

Bovine recombinant, claisen-schmidt, in-vitro, phosphodiesterase 5, vasculature, analogues.

Affiliation:

Department of Pharmaceutical Chemistry, Bharati Vidyapeeth College of Pharmacy, Kolhapur, 416 013 (MS), Department of Pharmaceutical Chemistry, Tatyasaheb Kore College of Pharmacy, Warananagar, Tal-Panhala, Dist-Kolhapur-416 113 (MS), Department of Pharmaceutical Chemistry, Bharati Vidyapeeth College of Pharmacy, Kolhapur, 416 013 (MS)

Graphical Abstract:



Read Full-Text article