Preferred Name | letermovir | |
Synonyms |
AIC246 MK-8228 |
|
Definitions |
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. Check for "https://www.cancer.gov/about-cancer/treatment/clinical-trials/intervention/C115099" active clinical trials using this agent. ("http://ncit.nci.nih.gov/ncitbrowser/ConceptReport.jsp?dictionary=NCI%20Thesaurus&code=C115099" NCI Thesaurus) |
|
ID |
http://purl.bioontology.org/ontology/PDQ/CDR0000759734 |
|
altLabel |
AIC246 MK-8228 |
|
cui |
C4053578 C3852938 C3852463 |
|
DATE FIRST PUBLISHED |
2014-04-08 |
|
Date last modified |
2015-06-30 |
|
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. Check for "https://www.cancer.gov/about-cancer/treatment/clinical-trials/intervention/C115099" active clinical trials using this agent. ("http://ncit.nci.nih.gov/ncitbrowser/ConceptReport.jsp?dictionary=NCI%20Thesaurus&code=C115099" NCI Thesaurus) |
|
NCI ID |
C115099 |
|
notation |
CDR0000759734 |
|
ORIG STY |
Drug/agent |
|
prefLabel |
letermovir |
|
tui |
T109 T121 |