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Drug ReportsALVOCIDIB
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.
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Target
Variants
Financial
Trends
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Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
Max
Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
Primary completion date
Completion date
Results first post date
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Commercial
No data
Clinical
Clinical Trials
64 clinical trials
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Indications Phases 4
No data
Indications Phases 3
No data
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Myeloid leukemia acuteD015470—C92.088———14
B-cell chronic lymphocytic leukemiaD015451—C91.165———9
Monocytic leukemia acuteD007948——24———6
Myelomonocytic leukemia acuteD015479—C92.524———6
Myeloid leukemiaD007951—C9224———6
Erythroblastic leukemia acuteD004915EFO_1001257C94.024———6
Megakaryoblastic leukemia acuteD007947—C94.223———5
Precursor cell lymphoblastic leukemia-lymphomaD054198—C91.051———5
Waldenstrom macroglobulinemiaD008258HP_0005508C88.042———4
LymphomaD008223—C85.923———4
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369—C8018————18
AnemiaD000740HP_0001903D64.92————2
Bcr-abl positive chronic myelogenous leukemiaD015464EFO_0000340—2————2
LeukemiaD007938—C951————1
ThrombocytopeniaD013921HP_0001873D69.61————1
Male breast neoplasmsD018567——1————1
Hairy cell leukemiaD007943—C91.41————1
Gastrointestinal stromal tumorsD046152EFO_0000505C49.A1————1
Non-small-cell lung carcinomaD002289——1————1
Small cell carcinomaD018288——1————1
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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)Loading
Structure (InChI/SMILES or Protein Sequence)
CN1CC[C@H](c2c(O)cc(O)c3c(=O)cc(-c4ccccc4Cl)oc23)[C@H](O)C1
Identifiers
PDB—
CAS-ID146426-40-6
RxCUI—
ChEMBL IDCHEMBL428690
ChEBI ID—
PubChem CID5287969
DrugBankDB03496
UNII ID45AD6X575G (ChemIDplus, GSRS)
Target
Agency Approved
No data
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
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 5,011 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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72 adverse events reported
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