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Pevonedistat
Pevonedistat is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
Therapeutic Areas
No data
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
No data
Labels
FDA
EMA
No data
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
No data
HCPCS
No data
Clinical
Clinical Trials
41 clinical trials
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Indications Phases 4
No data
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Myeloid leukemia acuteD015470C92.0128219
Myelodysplastic syndromesD009190D46861114
Myelomonocytic leukemia chronicD015477C93.12214
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Primary myelofibrosisD055728D47.4212
Non-small-cell lung carcinomaD00228922
Large b-cell lymphoma diffuseD016403C83.3212
Residual neoplasmD01836511
Essential thrombocythemiaD013920D47.3111
Polycythemia veraD011087D45111
Leukemia myeloid chronic atypical bcr-abl negativeD054438C92.2111
Neutrophilic leukemia chronicD015467D47.1111
Eyelid neoplasmsD005142EFO_1000934111
ThrombocytosisD013922D75.83111
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369C8044
Precursor cell lymphoblastic leukemia-lymphomaD054198C91.022
Multiple myelomaD009101C90.022
LymphomaD008223C85.922
Liver diseasesD008107EFO_0001421K70-K7711
Renal insufficiencyD051437HP_0000083N1911
Central nervous system neoplasmsD01654311
Non-hodgkin lymphomaD008228C85.911
B-cell chronic lymphocytic leukemiaD015451C91.111
Follicular lymphomaD008224C8211
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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 namePEVONEDISTAT
INNpevonedistat
Description
Pevonedistat is a pyrrolopyrimidine that is 7H-pyrrolo[2,3-d]pyrimidine which is substituted by a (1S)-2,3-dihydro-1H-inden-1-ylnitrilo group at position 4 and by a (1S,3S,4S)-3-hydroxy-4-[(sulfamoyloxy)methyl]cyclopentyl group at position 7. It is a potent and selective NEDD8-activating enzyme inhibitor with an IC50 of 4.7 nM, and currently under clinical investigation for the treatment of acute myeloid leukemia (AML) and myelodysplastic syndromes. It has a role as an apoptosis inducer and an antineoplastic agent. It is a pyrrolopyrimidine, a secondary amino compound, a member of cyclopentanols, a sulfamidate and a member of indanes.
Classification
Small molecule
Drug classenzyme inhibitors
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
NS(=O)(=O)OC[C@@H]1C[C@@H](n2ccc3c(N[C@H]4CCc5ccccc54)ncnc32)C[C@@H]1O
Identifiers
PDB
CAS-ID905579-51-3
RxCUI
ChEMBL IDCHEMBL1231160
ChEBI ID
PubChem CID16720766
DrugBankDB11759
UNII IDS3AZD8D215 (ChemIDplus, GSRS)
Target
Agency Approved
No data
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 835 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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227 adverse events reported
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