FB2026_03 , released September 17, 2026
Chemical: alvocidib
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General Information
Name
alvocidib
FlyBase ID
FBch0002085
ChEBI Name
alvocidib
ChEBI ID
PubChem Name
Alvocidib
PubChem ID
Chemical Structure
Chemical structure of alvocidib
alvocidib
InChIKey

BIIVYFLTOXDAOV-YVEFUNNKSA-N

Definition (ChEBI)

A synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is substituted by a 3-hydroxy-1-methylpiperidin-4-yl group at position 8 and by a chlorine at the 2' position (the (-)-3S,4R stereoisomer). A cyclin-dependent kinase 9 (CDK9) inhibitor, it has been studied for the treatment of acute myeloid leukaemia, arthritis and atherosclerotic plaque formation.

Roles Classification (ChEBI)
Comment
Synonyms and Secondary IDs (26)
Synonyms
(-)-cis-5,7-dihydroxy-2-(2-chlorophenyl)-8-(4-(3-hydroxy-1-methyl)piperidinyl)-4H-1-benzopyran-4-one
146426-40-6
2-(2-chlorophenyl)-5,7-dihydroxy-8-[(3S,4R)-3-hydroxy-1-methylpiperidin-4-yl]-4H-chromen-4-one
Alvocidib
Alvocidib freebase
Flavopiridol (Alvocidib)
HMR-1274
HMR-1275
L 86-8275
PubChem:5287969
alvocidib freebase
alvocidibum
flavopiridol (alvocidib)
hmr 1274
hmr-1275
l 868275
l-868275
l86-8275
pubchem:5287969
Secondary FlyBase IDs
    References (4)