Nafamostat
Nafamostat is a small molecule pharmaceutical. It is currently being investigated in clinical studies. The pharmaceutical is active against serine protease 1, complement C1r subcomponent, and tryptase alpha/beta-1. In addition, it is known to target transient receptor potential cation channel subfamily M member 7, acid-sensing ion channel 3, acid-sensing ion channel 2, transmembrane protease serine 2, and acid-sensing ion channel 1.
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Commercial
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Clinical
Clinical Trials
24 clinical trials
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Indications Phases 4
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Indications Phases 3
No data
Indications Phases 2
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Indications Phases 1
No data
Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Acute kidney injury | D058186 | — | N17 | — | — | — | — | 1 | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
| Drug common name | Nafamostat |
| INN | nafamostat |
| Description | Nafamostat is a member of benzoic acids and a member of guanidines. |
| Classification | Small molecule |
| Drug class | enzyme inhibitors: proteolytic enzyme inhibitors |
| Image (chem structure or protein) |  |
| Structure (InChI/SMILES or Protein Sequence) | N=C(N)Nc1ccc(C(=O)Oc2ccc3cc(C(=N)N)ccc3c2)cc1 |
Identifiers
| PDB | — |
| CAS-ID | 81525-10-2 |
| RxCUI | — |
| ChEMBL ID | CHEMBL273264 |
| ChEBI ID | — |
| PubChem CID | 4413 |
| DrugBank | — |
| UNII ID | Y25LQ0H97D (ChemIDplus, GSRS) |
Target
Alternate
TRPM7
TRPM7
TMPRSS2
TMPRSS2
PLAU
PLAU
Organism
Homo sapiens
Gene name
TRPM7
Gene synonyms
CHAK1, LTRPC7
NCBI Gene ID
Protein name
transient receptor potential cation channel subfamily M member 7
Protein synonyms
Channel-kinase 1, Long transient receptor potential channel 7, LTRPC ion channel family member 7, LTrpC-7, LTrpC7, transient receptor potential-phospholipase C-interacting kinase
Uniprot ID
Mouse ortholog
Trpm7 (58800)
transient receptor potential cation channel subfamily M member 7 (Q923J1)
Variants
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Financial
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Trends
PubMed Central
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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135 adverse events reported
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