loading...| Preferred Name |
Valacyclovir |
|
| Synonyms |
valacyclovir L-Valine ester with 9-((2-hydroxyethoxy)methyl)guanine Valaciclovir Valacyclovir VALACYCLOVIR ValACV Zelitrex |
|
| Definitions |
The hydrochloride salt of the L-valyl ester of the antiviral drug acyclovir. Orally administered, valacyclovir is rapidly converted to acyclovir which inhibits viral DNA replication after further conversion to the nucleotide analog acyclovir triphosphate by viral thymidine kinase, cellular guanyl cyclase, and a number of other cellular enzymes. Acyclovir triphosphate competitively inhibits viral DNA polymerase; incorporates into and terminates the growing viral DNA chain; and inactivates viral DNA polymerase. The greater antiviral activity of acyclovir against herpes simplex virus (HSV) compared with varicella-zoster virus (VZV) is due to its more efficient phosphorylation by HSV thymidine kinase. |
|
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C28235 |
|
| ALT_DEFINITION |
A substance that is being studied in the prevention of fungal, bacterial, and viral infections in patients undergoing donor stem cell transplantation with cells that are infected with cytomegalovirus. It belongs to the family of drugs called antivirals. |
|
| CAS_Registry |
124832-26-4 |
|
| CHEBI_ID |
CHEBI:35854 |
|
| Chemical_Formula |
C13H20N6O4 |
|
| code |
C28235 |
|
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C176424 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116978 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C201600 |
|
| Contributing_Source |
CTRP FDA HemOnc |
|
| DEFINITION |
The hydrochloride salt of the L-valyl ester of the antiviral drug acyclovir. Orally administered, valacyclovir is rapidly converted to acyclovir which inhibits viral DNA replication after further conversion to the nucleotide analog acyclovir triphosphate by viral thymidine kinase, cellular guanyl cyclase, and a number of other cellular enzymes. Acyclovir triphosphate competitively inhibits viral DNA polymerase; incorporates into and terminates the growing viral DNA chain; and inactivates viral DNA polymerase. The greater antiviral activity of acyclovir against herpes simplex virus (HSV) compared with varicella-zoster virus (VZV) is due to its more efficient phosphorylation by HSV thymidine kinase. |
|
| Display_Name |
Valacyclovir |
|
| FDA_UNII_Code |
MZ1IW7Q79D |
|
| FULL_SYN |
valacyclovir L-Valine ester with 9-((2-hydroxyethoxy)methyl)guanine Valaciclovir Valacyclovir VALACYCLOVIR ValACV Zelitrex |
|
| Has_Salt_Form | ||
| label |
Valacyclovir |
|
| Legacy Concept Name |
Valacyclovir |
|
| NCI_Drug_Dictionary_ID |
257236 |
|
| PDQ_Closed_Trial_Search_ID |
257236 |
|
| PDQ_Open_Trial_Search_ID |
257236 |
|
| Preferred_Name |
Valacyclovir |
|
| prefixIRI |
Thesaurus:C28235 |
|
| Semantic_Type |
Organic Chemical Pharmacologic Substance |
|
| UMLS_CUI |
C0249458 |
|
| subClassOf |