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Seclidemstat
Seclidemstat 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
5 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
Clear cell sarcomaD018227212
Myxoid liposarcomaD018208212
Ewing sarcomaD012512EFO_0000173212
Desmoplastic small round cell tumorD058405212
MyoepitheliomaD009208212
Myelodysplastic syndromesD009190D46111
Myelomonocytic leukemia chronicD015477C93.1111
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Endometrial neoplasmsD016889EFO_000423011
Endometrioid carcinomaD01826911
SarcomaD01250911
NeoplasmsD009369C8011
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameSECLIDEMSTAT
INNseclidemstat
Description
Seclidemstat is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
Classification
Small molecule
Drug classenzyme inhibitors
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
C/C(=N\NC(=O)c1cccc(S(=O)(=O)N2CCN(C)CC2)c1)c1cc(Cl)ccc1O
Identifiers
PDB
CAS-ID1423715-37-0
RxCUI
ChEMBL IDCHEMBL4297641
ChEBI ID
PubChem CID
DrugBank
UNII IDTYH386V3WJ (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:
Mock data
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Additional graphs summarizing 48 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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