Sorivudine
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Systematic (IUPAC) name | |
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1-β-D-arabinofuranosyl-5-[(E)-2-bromovinyl]pyrimidine-2,4(1H,3H)-dione
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Clinical data | |
Routes of administration |
oral |
Pharmacokinetic data | |
Metabolism | Viral thymidine kinase |
Excretion | kidney |
Identifiers | |
CAS Number | 77181-69-2 ![]() |
ATC code | J05AB15 (WHO) |
PubChem | CID: 5282192 |
ChemSpider | 4445384 |
UNII | C7VOZ162LV ![]() |
KEGG | D01734 ![]() |
ChEMBL | CHEMBL375035 ![]() |
Synonyms | BV-araU, Bromovinyl araU, 5-Bromovinyl-araU, 5-[(E)-2-bromoethenyl]-1-[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione |
Chemical data | |
Formula | C11H13BrN2O6 |
Molecular mass | 349.14 g/mol |
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Sorivudine (INN) chemical name (E)-5-(2-Bromovinyl)- 1β-D-arabinofuranosyluracil, is a thymine analogue antiviral drug, marketed under trade names such as Usevir (Nippon Shoji, Eisai) and Brovavir (BMS).
Pharmacology
Feature
- First-line treatment of herpes drug acyclovir was (Zovirax, Activir) from VZV strong activity of the virus.
- Superior gastrointestinal absorption, absorption from the gastrointestinal tract after the most degrading without being excreted as urine.
Mechanism of action
- Sorivudine is phosphorylated by thymidine kinase activity in the body and is absorbed into the virus's DNA instead of the correct nucleoside. It is a competitive inhibitor of DNA polymerase, so the viral DNA cannot be replicated and the virus cannot grow.
Microbiology
Sorivudine is active against most species in the herpesvirus family.
- Herpes simplex virus type I (HSV-1)
- Varicella zoster virus (VZV)
- Epstein-Barr virus (EBV)
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- Drugs with no legal status
- Pharmacology stubs
- Pyrimidinediones
- Anti-herpes virus drugs
- Arabinosides
- Antiinfective agent stubs