Abstract
Current research deals with the biology-oriented drug synthesis (BIODS) of twenty-three new thiourea analogs of pharmacologically important drug atenolol which is a well-known medicine to treat hypertension as well as cardiovascular diseases (CVDs). Structural characterization of all compounds was done by various spectroscopic techniques. Compounds 1-23 were subjected for urease inhibitory activity in vitro. Screening results revealed that whole library was found to be active having IC
ranges from 11.73 ± 0.28 to 212.24 ± 0.42 µM. It is noteworthy that several derivatives including 3 (IC
= 21.65 ± 0.31 µM), 8 (IC
= 19.26 ± 0.42 µM), 9 (IC
= 21.27 ± 0.25 µM), 12 (IC
= 21.52 ± 0.42 µM), 17 (IC
= 19.26 ± 0.42 µM), 20 (IC
= 16.78 ± 0.34 µM), and 22 (IC
= 11.73 ± 0.28 µM) showed excellent inhibitory potential than parent atenolol (IC
= 64.36 ± 0.19 µM) and standard thiourea (IC
= 21.74 ± 1.76 µM). A most probable structure-activity relationship (SAR) was anticipated by observing varying degree of inhibitory potential given by compounds. However, molecular insights regarding the binding mode of atenolol thiourea analogs within the active pocket of urease enzyme was rationalized by molecular docking studies.