Linagliptin

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Identification

Molecular formula
C11H11BrN4O
CAS Number
43200-77-1
IUPAC Name
1-(4-bromophenyl)-2-(6-methyl-4-oxo-1H-pyrimidin-2-yl)guanidine
Molecular Weight
175.92g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.6930g/cm3
Interesting facts

Interesting Facts about 1-(4-bromophenyl)-2-(6-methyl-4-oxo-1H-pyrimidin-2-yl)guanidine

This compound, 1-(4-bromophenyl)-2-(6-methyl-4-oxo-1H-pyrimidin-2-yl)guanidine, is a fascinating example of a guanidine derivative that has garnered attention in various fields, particularly in medicinal chemistry. Here are some interesting aspects of this compound:

  • Diverse Biological Activity: This compound has been studied for its potential therapeutic effects. The presence of the guanidine group can facilitate interactions with biomolecular targets, making it a candidate for drug development.
  • Significance of Substituents: The incorporation of the 4-bromophenyl group and the 6-methyl-4-oxo-1H-pyrimidin-2-yl moiety enhances the compound's bioactivity. The halogen substituent, in particular, can influence both the electronic properties and lipophilicity of the molecule.
  • Potential as an Antibacterial Agent: Research has suggested that similar guanidine derivatives exhibit antibacterial activity. This opens doors for exploring this compound in the development of new antimicrobial agents.
  • Involvement in Biological Pathways: Compounds like this one can also serve as probes in studying specific biological pathways, especially those linked to nucleic acid interactions and enzyme inhibition.
  • Structure-Activity Relationship (SAR): Understanding the SAR of this compound can lead to the optimization of its potency and selectivity, aiding in the design of more effective therapeutic agents.

As with many compounds containing heterocycles, the structural diversity and potential applications of 1-(4-bromophenyl)-2-(6-methyl-4-oxo-1H-pyrimidin-2-yl)guanidine make it an intriguing subject of study among chemists and pharmacologists alike. Its unique characteristics emphasize the importance of molecular design in the context of pharmacotherapy.

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