145512-85-2
Chemical Structure
Eprociclovir
Synonym(s): A-5021
- CAS No.: 145512-85-2
- Formula:C11H15N5O3
- Molecular Weight:265.27
IUPAC Name: 2-amino-9-(((1S,2R)-1,2-bis(hydroxymethyl)cyclopropyl)methyl)-3,9-dihydro-6H-purin-6-one
InChIKey: JLYSZBQNRJVPEP-KGFZYKRKSA-N
SMILES: OC[C@@]1([C@@H](C1)CO)CN2C3=C(C(N=C(N3)N)=O)N=C2
Biological Activity: Eprociclovir is an antiviral drug with nucleoside analogues. The triphosphate form of Eprociclovir is converted into the active form within virus-infected cells by the virus and possible cellular enzymes, including the viral thymidine kinase, thereby inhibiting the activity of the viral DNA polymerase. The primary activity of Eprociclovir is against herpes viruses, including but not limited to cytomegalovirus (CMV) and herpes simplex virus (HSV). Eprociclovir can be used in studies interfered with by sensitive viruses[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Eprociclovir | Eprociclovir is an antiviral drug with nucleoside analogues. The triphosphate form of Eprociclovir is converted into the active form within virus-infected cells by the virus and possible cellular enzymes, including the viral thymidine kinase, thereby inhibiting the activity of the viral DNA polymerase. The primary activity of Eprociclovir is against herpes viruses, including but not limited to cytomegalovirus (CMV) and herpes simplex virus (HSV). Eprociclovir can be used in studies interfered with by sensitive viruses. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
Keywords
