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Alvocidib
Alvocidib is a small molecule pharmaceutical. It is currently being investigated in clinical studies. The pharmaceutical is active against cyclin-dependent kinase 2 and cyclin-dependent kinase 4. In addition, it is known to target cyclin-T1.
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Commercial
Therapeutic Areas
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Trade Name
FDA
EMA
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Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Labels
FDA
EMA
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Indications
FDA
EMA
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Agency Specific
FDA
EMA
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Patent Expiration
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ATC Codes
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HCPCS
No data
Clinical
Clinical Trials
64 clinical trials
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Indications Phases 4
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Indications Phases 3
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Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Myeloid leukemia acuteD015470C92.08814
B-cell chronic lymphocytic leukemiaD015451C91.1659
Monocytic leukemia acuteD007948246
Myelomonocytic leukemia acuteD015479C92.5246
Myeloid leukemiaD007951C92246
Erythroblastic leukemia acuteD004915EFO_1001257C94.0246
Megakaryoblastic leukemia acuteD007947C94.2235
Precursor cell lymphoblastic leukemia-lymphomaD054198C91.0515
Waldenstrom macroglobulinemiaD008258C88.0424
LymphomaD008223C85.9234
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369C801818
AnemiaD000740EFO_0004272D64.922
Bcr-abl positive chronic myelogenous leukemiaD015464EFO_000034022
LeukemiaD007938C9511
ThrombocytopeniaD013921HP_0001873D69.611
Male breast neoplasmsD01856711
Hairy cell leukemiaD007943C91.411
Gastrointestinal stromal tumorsD046152EFO_0000505C49.A11
Non-small-cell lung carcinomaD00228911
Small cell carcinomaD01828811
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Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameALVOCIDIB
INNalvocidib
Description
Alvocidib is 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. It has a role as an antineoplastic agent, an EC 2.7.11.22 (cyclin-dependent kinase) inhibitor, an antirheumatic drug and an apoptosis inducer. It is a dihydroxyflavone, a hydroxypiperidine, a member of monochlorobenzenes and a tertiary amino compound. It is a conjugate base of an alvocidib(1+).
Classification
Small molecule
Drug class
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
CN1CC[C@H](c2c(O)cc(O)c3c(=O)cc(-c4ccccc4Cl)oc23)[C@H](O)C1
Identifiers
PDB3BLR
CAS-ID146426-40-6
RxCUI
ChEMBL IDCHEMBL428690
ChEBI ID
PubChem CID5287969
DrugBankDB03496
UNII ID45AD6X575G (ChemIDplus, GSRS)
Target
Agency Approved
CDK2
CDK2
CDK4
CDK4
Organism
Homo sapiens
Gene name
CDK2
Gene synonyms
CDKN2
NCBI Gene ID
Protein name
cyclin-dependent kinase 2
Protein synonyms
cdc2-related protein kinase, Cell division protein kinase 2, p33 protein kinase
Uniprot ID
Mouse ortholog
Cdk2 (12566)
cyclin-dependent kinase 2 (P97377)
Alternate
CCNT1
CCNT1
Organism
Homo sapiens
Gene name
CCNT1
Gene synonyms
NCBI Gene ID
Protein name
cyclin-T1
Protein synonyms
CDK9-associated C-type protein, cyclin C-related protein, human immunodeficiency virus type 1 (HIV-1) expression (elevated) 1, MLLT10/CCNT1 fusion
Uniprot ID
Mouse ortholog
Ccnt1 (12455)
cyclin-T1 (Q9Z0U7)
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 735 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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39 adverse events reported
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