Letermovir
Letermovir
Definition
An orally bioavailable, non-nucleoside, 3,4-dihydroquinazolinyl acetic acid and inhibitor of the pUL56 subunit of the viral terminase complex of cytomegalovirus (CMV), with potential CMV-specific antiviral activity. Upon oral administration, letermovir binds to the pUL56 subunit of the viral terminase complex of CMV and prevents the cleavage of concatemeric DNA into monomeric genome length DNA. As this agent interferes with viral DNA processing and subsequent viral DNA packaging into procapsids, CMV replication is blocked and CMV infection is prevented.
Also known as 2-((4S)-8-Fluoro-2-(4-(3-methoxyphenyl)piperazin-1-yl)-3-(2-methoxy-5-(trifluoromethyl)phenyl)-4H-quinazolin-4-yl)acetic Acid, AIC246, LETERMOVIR, MK-8228, Prevymis — per NCIT
Also identified as
- ATC J05AX18 per RXNORM
- NCIT NCIT:C115099 per NCIT
- SCTID 763033005 per RXNORM
- SCTID 763568003 per RXNORM
- UNII 1H09Y5WO1F per RXNORM
Indications
| Disease | Relation | Source |
|---|---|---|
| Cytomegalovirus infection | may prevent | MEDRT · Public domain (U.S. Government work) |