Published August 2017 | Version v1
Journal article

Synthesis and evaluation of anticancer and PDE 5 inhibitory activity of spiro-substituted quinazolin-4-ones

  • 1. Minia University, Chemistry Department, Faculty of Science (Egypt)
  • 2. Al-Azhar University, Organic Chemistry Department, Faculty of Pharmacy (Egypt)

Description

A series of novel spiro-substituted 2,3-dihydroquinazolin-4(1H)-ones was synthesized and structurally confirmed by spectral analysis, screened for their anticancer activity at a concentration of 10 μΜ against a panel of 56 cell lines derived from nine different types of cancers, including leukemia, melanoma, lung, colon, CNS, ovarian, renal, prostate, and breast cancers. The synthesized compounds screened for their PDE 5 inhibitory activity and it showed encouraged activity compared to sildenafil. Graphical abstract: .

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Publishing Information

Journal Title
Monatshefte fuer Chemie
Journal Volume
148
Journal Issue
8
Journal Page Range
p. 1513-1523
ISSN
0026-9247
CODEN
MOCHAP

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Copyright (c) 2017 Springer-Verlag Wien