Complexes of N- and O-Donor Ligands as Potential Urease Inhibitors
Author(s) -
Syed Raza Shah,
Zarbad Shah,
Mohammed Khiat,
Ajmal Khan,
Leila R. Hill,
Shakeel Ahmed Khan,
Javid Hussain,
René Csük,
Muhammad U. Anwar,
Ahmed AlHarrasi
Publication year - 2020
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.0c01089
Subject(s) - chemistry , barbituric acid , urease , stereochemistry , nicotinamide , single crystal , enzyme , crystallography , nuclear chemistry , organic chemistry
We report five new transition-metal complexes that inhibit the urease enzyme. Barbituric acid ( BTA ), thiobarbituric acid ( TBA ), isoniazid ( INZ ), and nicotinamide ( NCA ) ligands were employed in complexation reactions. The resulting complexes were characterized using a variety of analytical techniques including infra-red and UV-vis spectroscopy, 1 H NMR spectroscopy, elemental analysis, and single-crystal X-ray diffraction analysis. We describe two mononuclear complexes with a general formula {[M( NCA ) 2 (H 2 O) 4 ]( BTA ) 2 (H 2 O)}, where M = Co ( 1 ) and Zn ( 2 ), a mononuclear complex {[Ni( NCA ) 2 (H 2 O) 4 ]( TBA ) 2 (H 2 O)} ( 3 ), and two polymeric chains of a general formula {[M( INZ ) (H 2 O) 3 ]( BTA ) 2 (H 2 O) 3 }, where M = Co ( 4 ) and Zn ( 5 ). These complexes displayed significant urease enzyme inhibition with IC 50 values in the range of 3.9-19.9 μM.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom