FB2026_03 , released September 17, 2026
Chemical: camostat
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General Information
Name
camostat
FlyBase ID
FBch0003035
ChEBI Name
camostat
ChEBI ID
PubChem Name
Camostat
PubChem ID
Chemical Structure
Chemical structure of camostat
camostat
InChIKey

XASIMHXSUQUHLV-UHFFFAOYSA-N

Definition (ChEBI)

A benzoate ester resulting from the formal condensation of the carboxy group of 4-guanidinobenzoic acid with the hydroxy group of 2-(dimethylamino)-2-oxoethyl (4-hydroxyphenyl)acetate. It is a potent inhibitor of the human transmembrane protease serine 2 (TMPRSS2) and its mesylate salt is currently under investigation for its effectiveness in COVID-19 patients. ChEBI: Camostat is a benzoate ester resulting from the formal condensation of the carboxy group of 4-guanidinobenzoic acid with the hydroxy group of 2-(dimethylamino)-2-oxoethyl (4-hydroxyphenyl)acetate. It is a potent inhibitor of the human transmembrane protease serine 2 (TMPRSS2) and its mesylate salt is currently under investigation for its effectiveness in COVID-19 patients. It has a role as an anticoronaviral agent, a serine protease inhibitor, an antifibrinolytic drug, an anti-inflammatory agent, an antiviral agent, an antihypertensive agent and an antineoplastic agent. It is a tertiary carboxamide, a carboxylic ester, a diester, a member of guanidines and a benzoate ester. It is functionally related to a 4-guanidinobenzoic acid. It is a conjugate base of a camostat(1+).

Roles Classification (ChEBI)
Comment
Synonyms and Secondary IDs (16)
Synonyms
0FD207WKDU
4-{2-[(dimethylcarbamoyl)methoxy]-2-oxoethyl}phenyl 4-carbamimidamidobenzoate
4-{2-[2-(dimethylamino)-2-oxoethoxy]-2-oxoethyl}phenyl 4-carbamimidamidobenzoate
59721-28-7
CAMOSTAT [MI]
CCRIS 7219
Camostat
Camostat (INN)
Camostat [INN]
Camostatum
Camostatum [INN-Latin]
N,N-dimethylcarbamoylmethyl 4-(4-guanidinobenzoyloxy)phenylacetate
PubChem:2536
camostate
camostatum
Secondary FlyBase IDs
    References (3)