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Synthesis, Characterization and Glyoxalase Inhibitory Activity of 4,6-Diheteroarylpyrimidine-2-amine Derivatives: In Vitro and In Silico Studies

Abstract
New series of 4,6-diheteroarylpyrimidine-2ـamines (4a-e) and (5a-c) were prepared by cyclization of particular chalcones (2) or (3) with guanidine nitrate in the presence of potassium hydroxide. Chalcones (2) and (3) were prepared by base-catalyzed Claisen-Schmidt condensation of heteroaryl aldehydes (1) with 2-acetyl-5-chlorothiophene and 3-acetyl-2,5-dichlorothiophene, respectively. All the newl...
Keywords
In silico
In vitro
Chemistry
Amine gas treating
Inhibitory postsynaptic potential
Characterization (materials science)
Biochemistry
Combinatorial chemistry
Stereochemistry
Pharmacology
Computational biology
Biology
Organic chemistry
Nanotechnology
Neuroscience
Materials science
Gene
Sustainable Development Goals (SDG)
Clean water and sanitation



Synthesis, Characterization and Glyoxalase Inhibitory Activity of 4,6-Diheteroarylpyrimidine-2-amine Derivatives: In Vitro and In Silico Studies

Synthesis, Characterization and Glyoxalase Inhibitory Activity of 4,6-Diheteroarylpyrimidine-2-amine Derivatives: In Vitro and In Silico Studies

Abstract
New series of 4,6-diheteroarylpyrimidine-2ـamines (4a-e) and (5a-c) were prepared by cyclization of particular chalcones (2) or (3) with guanidine nitrate in the presence of potassium hydroxide. Chalcones (2) and (3) were prepared by base-catalyzed Claisen-Schmidt condensation of heteroaryl aldehydes (1) with 2-acetyl-5-chlorothiophene and 3-acetyl-2,5-dichlorothiophene, respectively. All the newl...
Keywords
In silico
In vitro
Chemistry
Amine gas treating
Inhibitory postsynaptic potential
Characterization (materials science)
Biochemistry
Combinatorial chemistry
Stereochemistry
Pharmacology
Computational biology
Biology
Organic chemistry
Nanotechnology
Neuroscience
Materials science
Gene
Sustainable Development Goals (SDG)
Clean water and sanitation