| Identification | Back Directory | [Name]
Camostat | [CAS]
59721-28-7 | [Synonyms]
FOY 305
CAMOSTAT
Camostatum
Ccris 7219
FOY-305：Foipan
Unii-0fd207wkdu
Camostatum [inn-latin]
Camostat Monomethanesulfonate
59721-29-8 (Monomethanesulfonate)
Camostat (base and/or unspecified salts)
Dimethylcarbamoylmethyl 4-(4-guqnidinobenzoyloxy)phenylacetat
N，N-Dimethylcarbamoylmethyl-p(p-guanidinobenzoyloxy)phenylacetate
2-(Dimethylamino)-2-oxoethyl 4-(4-guanidinobenzoyloxy)phenylacetate
p-(p-Guanidinobenzoyloxy)phenylacetic acid=dimethylcarbamoylmethyl ester
4-Guanidinobenzoic acid-4-(dimethylcarbamoylmethoxycarbonylmethyl)phenyl ester
2-{4-[(4-carbaMiMidaMidophenyl)carbonyloxy]phenyl}-3-(diMethylcarbaMoyl)propanoate
4-Guanidinobenzoic acid 4-[[[(dimethylcarbamoyl)methoxy]carbonyl]methyl]phenyl ester
4-[[4-[(Aminoiminomethyl)amino]benzoyl]oxy]benzeneaxetic acid 2-(dimethylamino)-oxoethyl ester
4-[[4-[(Aminoiminomethyl)amino]benzoyl]oxy]benzeneacetic acid 2-(dimethylamino)-2-oxoethyl ester
Benzeneacetic acid, 4-[[4-[(aMinoiMinoMethyl)aMino]benzoyl]oxy]-, 2-(diMethylaMino)-2-oxoethyl ester
4-[[4-[(aMinoiMinoMethyl)aMino]benzoyl]oxy]-, 2-(diMethylaMino)-2-oxoethyl ester, MonoMethanesulfonate | [Molecular Formula]
C20H22N4O5 | [MDL Number]
MFCD00867896 | [MOL File]
59721-28-7.mol | [Molecular Weight]
398.41 |
| Hazard Information | Back Directory | [Definition]
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+). |
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