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Glyceryl diacetate has the molecular formula C7H14O5, indicating that it contains two acetyl groups esterified to a glycerol backbone. This unique structure imparts several distinctive properties, including its hydrophilic nature due to the glycerol moiety and its lipophilic characteristics attributed to the acetyl groups. This dual affinity allows glyceryl diacetate to function effectively as an emulsifier, solubilizer, and skin-conditioning agent.


One of the most significant aspects of 6-chloro-1,3-dimethyluracil is its potential role as an antiviral agent. Viruses often rely on host cellular machinery for their replication and transcription, which poses a challenge for developing effective antiviral therapies. In this context, compounds that can inhibit viral polymerases are particularly valuable. Research has shown that 6-chloro-1,3-dimethyluracil exhibits the ability to inhibit RNA polymerases, which could impede viral replication. This mechanism places it in a promising position for further exploration and optimization in developing antiviral drugs.


6-chloro-1,3-dimethyluracil

6-chloro-1,3-dimethyluracil

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