Skip to content
2000
Volume 20, Issue 3
  • ISSN: 1570-1786
  • E-ISSN:

Abstract

A new series of bisthiosemicarbazide and bistriazole molecules bridged quinazolinedione was synthesized and characterized by FT-IR, 1H and 13C-NMR spectral data. Antiurease activities of all new compounds were tested according to the phenol-hypochlorite method by Weatherburn. All compounds have effective urease inhibition activities compared to the standard inhibitor thiourea and previously synthesized quinazolinones as potential inhibitors. Bistriazoles containing quinazolinedione have the best inhibition results. 1,3-Bis[(4-ethyl-5-mercapto-4H-1,2,4-triazol-3-yl)methyl]quinazoline- 2,4(1H,3H)-dione (5b) has the best inhibitory activity with 1.25 ± 0.45 μg/mL IC value.

Loading

Article metrics loading...

/content/journals/loc/10.2174/1570178619666220816121312
2023-03-01
2024-10-10
Loading full text...

Full text loading...

/content/journals/loc/10.2174/1570178619666220816121312
Loading
  • Article Type: Research Article
Keyword(s): antiurease; bisthiosemicarbazide; bistriazole; Quinazolinedione; urease; weatherburn
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test