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ChemicalBook--->CAS DataBase List--->59721-29-8

59721-29-8

59721-29-8 Structure

59721-29-8 Structure
IdentificationMore
[Name]

Camostat mesilate
[CAS]

59721-29-8
[Synonyms]

CAMOSTAT MESILATE
CAMOSTAT MESYLATE
4-((4-((aminoiminomethyl)amino)benzoyl)oxy)-benzeneaceticaci2-(dimethylam
ino)-2-oxoethylester,monomethanesulfonate
n,n-dimethylcarbamoylmethyl4-(4-guanidinobenzoyloxy)phenylacetatemethanesul
p-(p-guanidinobenzoyloxy)phenylaceticacid,n,n-dimethylcarbamoylmethyleste
Camostatemesylate
2-(Dimethylamino)-2-oxoethyl 4-(4-guanidinobenzoyloxy)phenylacetate methanesulphonate
4-[[4-[(Aminoiminomethyl)amino]benzoyl]oxy]benzeneacetic Acid 2-(Dimethylamino)-2-oxoethyl Ester Methanesulfonate
Foipan
FOY-S 980
4-Guanidinobenzoic acid 4-[[[(dimethylcarbamoyl)methoxy]carbonyl]methyl]phenyl·methanesulfonic acid
Camostate mesilate
[EINECS(EC#)]

694-565-6
[Molecular Formula]

C21H26N4O8S
[MDL Number]

MFCD00941410
[Molecular Weight]

494.52
[MOL File]

59721-29-8.mol
Chemical PropertiesBack Directory
[Appearance]

Crystalline Solid
[Melting point ]

150-1550C
[RTECS ]

CY1571620
[storage temp. ]

2-8°C
[solubility ]

H2O: ≥24mg/mL
[form ]

powder
[color ]

white to tan
[Water Solubility ]

Soluble in water (100 mM), DMSO (100 mM), and ethanol (<1 mg/ml).
[Usage]

Orally active, non-peptide proteolitic enzyme inhibitor with anti-trypsin and anti-plasmin activities, related structurally to gabexate. Protease inhibitor
[Merck ]

14,1728
[Stability:]

Stable for 2 years? from date of purchase as supplied. Solutions in DMSO or distilled water may be stored at -20° for up to 1 month.
[CAS DataBase Reference]

59721-29-8(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi,N
[Risk Statements ]

36/37/38-50
[Safety Statements ]

26-61
[RIDADR ]

UN 3077 9 / PGIII
[WGK Germany ]

3
[HazardClass ]

9
[HS Code ]

2934999090
Hazard InformationBack Directory
[Description]

Camostat mesylate is a broad spectrum protease inhibitor useful in the treatment of chronic pancreatitis.
[Chemical Properties]

Crystalline Solid
[Originator]

Ono (Japan)
[Uses]

Orally active, non-peptide proteolitic enzyme inhibitor with anti-trypsin and anti-plasmin activities, related structurally to gabexate. Protease inhibitor
[Definition]

ChEBI: Camostat mesylate is a methanesulfonate (mesylate) salt prepared from equimolar amounts of camostat and methanesulfonic acid. It is a serine protease inhibitor approved and marketed in Japan in 1985 for the alleviation of acute symptoms associated with chronic pancreatitis. In 1994, it was approved for the treatment of postoperative reflux esophagitis. It has a role as an anticoronaviral agent, an anti-inflammatory agent, an antifibrinolytic drug, an antihypertensive agent, an antineoplastic agent, an antiviral agent and a serine protease inhibitor. It contains a camostat(1+).
[Brand name]

FOIPAN
[Biological Activity]

Orally active protease inhibitor. Known to inhibit trypsin and various inflammatory proteases including plasmin, kallikrein and thrombin. Suppresses pancreatitis-induced pain in rats following oral administration.
[storage]

Desiccate at RT
[References]

1) Gibo?et al.?(2005),?Camostat mesylate attenuates pancreatic fibrosis via inhibition of monocytes and pancreatic stellate cells activity;?Lab Invest.,?85?75 2) Albarazanji?et al.?(2019),?Intestinal serine protease inhibition increases FGF21 and improves metabolism in obese mice.; Am. J. Physiol. Gastrointest. Liver Physiol.,?316?G653 3) Ueda?et al.?(2015),?The serine protease inhibitor camostat mesylate attenuates the progression of chronic kidney disease through its antioxidant effects; Nephron,?129?223 4) Yamaya?et al.?(2015),?The serine protease inhibitor camostat inhibits influenza virus replication and cytokine production in primary cultures of human tracheal epithelial cells; Pulm. Pharmacol. Ther.,?33?66 5) Hoffmann?et al.?(2020),?SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor; Cell, 181 271
Spectrum DetailBack Directory
[Spectrum Detail]

Camostat mesilate(59721-29-8)1HNMR
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