5-Acetyl-d3-amino-6-formylamino-3-methyluracil

Product Name 5-Acetyl-d3-amino-6-formylamino-3-methyluracil
CAT No. CS-T-47090
CAS No. 1185082-65-8
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Therapeutic Anti-Migraines
Smileys CC(=O)NC1=C(NC(=O)N(C1=O)C)NC=O
Canonical Smiles CC(=O)NC1=C(NC(=O)N(C1=O)C)NC=O
InchIKey RDZNZFGKEVDNPK-FIBGUPNXSA-N
Inchl InChI=1S/C8H10N4O4/c1-4(14)10-5-6(9-3-13)11-8(16)12(2)7(5)15/h3H,1-2H3,(H,9,13)(H,10,14)(H,11,16)/i1D3
IUPAC 2,2,2-trideuterio-N-(6-formamido-3-methyl-2,4-dioxo-1H-pyrimidin-5-yl)acetamide
Controlled No
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5-Acetyl-d3-amino-6-formylamino-3-methyluracil is a chemical compound that belongs to the class of pyrimidine nucleoside analogues. It is also known as Acyclovir-d3 and is commonly used as an antiviral medication. This compound is structurally similar to the nucleoside thymidine and is used to treat viral infections such as herpes simplex virus and varicella-zoster virus. The chemical formula for 5-Acetyl-d3-amino-6-formylamino-3-methyluracil is C8H7D3N5O3. The compound contains deuterium, which is an isotope of hydrogen, and this makes it useful in studies involving metabolic pathways and pharmacokinetics. The mechanism of action of 5-Acetyl-d3-amino-6-formylamino-3-methyluracil involves its conversion into a triphosphate form by viral thymidine kinase. This triphosphate form then gets incorporated into the viral DNA, leading to chain termination and inhibition of viral replication. 5-Acetyl-d3-amino-6-formylamino-3-methyluracil is available in the form of tablets, capsules, and topical creams. It is generally well-tolerated by most patients, with common side effects including nausea, vomiting, and headache. Patients with renal impairment may require dosage adjustments. In conclusion, 5-Acetyl-d3-amino-6-formylamino-3-methyluracil is a widely used antiviral medication with a unique chemical structure. Its deuterium content makes it useful in research studies, and its mechanism of action involves inhibition of viral DNA replication.

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