6-Amino-1-benzyl-3-methyl-5-(N-formyl-N-methyl)uracil is a synthetic compound that belongs to the class of uracil derivatives, which are nucleobase analogs. This substance features a uracil core structure modified with an amino group at the 6-position, a benzyl group at the 1-position, and a methyl group at the 3-position, along with a formyl and methyl substituent at the 5-position. These modifications can influence its biological activity, potentially affecting its interaction with nucleic acids or enzymes. The compound may exhibit properties such as solubility in organic solvents, and its structure suggests potential applications in medicinal chemistry, particularly in the development of antiviral or anticancer agents. The presence of both the formyl and methyl groups may enhance its lipophilicity, impacting its pharmacokinetic profile. As with many uracil derivatives, it may also participate in hydrogen bonding and other interactions that are crucial for its biological function. Further studies would be necessary to elucidate its specific properties and potential applications in research or therapeutics.

6-AMINO-1-BENZYL-3-METHYL-5-(N-FORMYL-N-METHYL)URACIL

72816-91-2: 6-Amino-1-benzyl-3-methyl-5-(N-formyl-N-methyl)uracil is a synthetic compound that belongs to the class of uracil derivatives, which are nucleobase analogs. This substance features a uracil core structure modified with an amino group at the 6-position, a benzyl group at the 1-position, and a methyl group at the 3-position, along with a formyl and methyl substituent at the 5-position. These modifications can influence its biological activity, potentially affecting its interaction with nucleic acids or enzymes. The compound may exhibit properties such as solubility in organic solvents, and its structure suggests potential applications in medicinal chemistry, particularly in the development of antiviral or anticancer agents. The presence of both the formyl and methyl groups may enhance its lipophilicity, impacting its pharmacokinetic profile. As with many uracil derivatives, it may also participate in hydrogen bonding and other interactions that are crucial for its biological function. Further studies would be necessary to elucidate its specific properties and potential applications in research or therapeutics.

CAS 72816-91-2

6-AMINO-1-BENZYL-3-METHYL-5-(N-FORMYL-N-METHYL)URACIL