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2000
Volume 14, Issue 3
  • ISSN: 1573-4080
  • E-ISSN: 1875-6662

Abstract

Background: Some of chemical syntheses are attractive because of their pharmacological application in the drug industry. Materials and Methods: In this study, water soluble peripherally and non-peripherally tetra substituted novel zinc (II) phthalocyanines, which were tagged as ZnPC, investigated against the inhibition of urease and hyaluronidase (HYA). In addition to enzyme inhibitory activities, antioxidant activity of synthesis molecules was measured by Ferric Reducing Antioxidant Power (FRAP) and DPPH radical scavenging activity assays. Results: The study also showed that four synthesis extracts exhibited a potent hyaluronidase and urease inhibitory effects with IC50 value ranges 7.095-115.878 μM and 4.227-35.678 μM respectively. Besides ZnPC-1 exhibited efficient urease and HYA inhibition, it showed good antioxidant activity with 0.341±0.001 μmol FeSO4.7H2O/mg sample for FRAP and 16.917±0.005 μM for DPPH. Also, the results obtained in the present study indicate that zinc (II) phthalocyanines compounds can be a potential source of bioactive agents.

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/content/journals/cei/10.2174/1573408014666180627143643
2018-12-01
2025-12-13
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/content/journals/cei/10.2174/1573408014666180627143643
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  • Article Type:
    Research Article
Keyword(s): DPPH; FRAP; hyaluronidase; phthalocyanines; urease; zinc
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