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Eprenetapopt
Eprenetapopt 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
13 clinical trials
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Mock data
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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 acuteD015470C92.0233
Myelodysplastic syndromesD009190D46222
Myelomonocytic leukemia chronicD015477C93.1222
Mantle-cell lymphomaD020522C83.1122
MelanomaD008545111
Urologic neoplasmsD014571C64-C68111
NeoplasmsD009369C80111
Non-small-cell lung carcinomaD002289111
Stomach neoplasmsD013274EFO_0003897C16111
Urinary bladder neoplasmsD001749C67111
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Hematologic neoplasmsD01933711
Prostatic neoplasmsD011471C6111
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameEPRENETAPOPT
INNeprenetapopt
Description
Eprenetapopt is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
Classification
Small molecule
Drug class
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
COCC1(CO)C(=O)C2CCN1CC2
Identifiers
PDB
CAS-ID5291-32-7
RxCUI
ChEMBL IDCHEMBL3186011
ChEBI ID
PubChem CID52918385
DrugBank
UNII IDZ41TGB4080 (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 233 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
0 adverse events reported
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