(5S)-5-(1H-imidazol-5-ylmethyl)-3-phenyl-2-thioxoimidazolidin-4-one

95%

  • Product Code: 82081
  CAS:    29635-98-1
Molecular Weight: 272.3256 g./mol Molecular Formula: C₁₃H₁₂N₄OS
EC Number: MDL Number: MFCD03703443
Melting Point: Boiling Point: 499.7 °C at 760 mmHg
Density: Storage Condition: 2-8°C
Product Description: This compound is primarily utilized in the field of medicinal chemistry due to its structural properties, which make it a potential candidate for drug development. Its imidazole and thioxoimidazolidinone moieties are particularly significant, as they are often associated with biological activity. In pharmaceutical research, it is explored for its potential as an enzyme inhibitor, particularly targeting enzymes involved in inflammatory or metabolic pathways. The presence of the phenyl group enhances its ability to interact with hydrophobic regions of target proteins, improving binding affinity. Additionally, its structure suggests potential applications in the synthesis of more complex molecules, serving as a building block for compounds with enhanced therapeutic properties. Researchers are also investigating its role in the development of antimicrobial or anticancer agents, leveraging its unique chemical framework to disrupt cellular processes in pathogens or tumor cells. Overall, this compound is a promising scaffold for the design of novel bioactive molecules with diverse therapeutic applications.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.050 10-20 days ฿7,362.00
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0.250 10-20 days ฿22,068.00
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(5S)-5-(1H-imidazol-5-ylmethyl)-3-phenyl-2-thioxoimidazolidin-4-one
This compound is primarily utilized in the field of medicinal chemistry due to its structural properties, which make it a potential candidate for drug development. Its imidazole and thioxoimidazolidinone moieties are particularly significant, as they are often associated with biological activity. In pharmaceutical research, it is explored for its potential as an enzyme inhibitor, particularly targeting enzymes involved in inflammatory or metabolic pathways. The presence of the phenyl group enhances its ability to interact with hydrophobic regions of target proteins, improving binding affinity. Additionally, its structure suggests potential applications in the synthesis of more complex molecules, serving as a building block for compounds with enhanced therapeutic properties. Researchers are also investigating its role in the development of antimicrobial or anticancer agents, leveraging its unique chemical framework to disrupt cellular processes in pathogens or tumor cells. Overall, this compound is a promising scaffold for the design of novel bioactive molecules with diverse therapeutic applications.
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