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AB141432

Nafamostat Mesylate, Protease inhibitor

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(2 Publications)

MW 539.6 Da, Purity >97%. Broad spectrum, potent protease inhibitor (Ki = 95.3 pM). Inhibits NF-κB activation and complement activation. Selective for human tryptase.
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Chemical Structure - Nafamostat Mesylate, Protease inhibitor (AB141432)
  • Chemical Structure

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Chemical Structure - Nafamostat Mesylate, Protease inhibitor (AB141432)

2D chemical structure image of ab141432, Nafamostat Mesylate, Protease inhibitor

Key facts

CAS number

82956-11-4

Purity

>97%

Form

Solid

form

Molecular weight

539.6 Da

Molecular formula

C<sub>2</sub><sub>1</sub>H<sub>2</sub><sub>5</sub>N<sub>5</sub>O<sub>8</sub>S<sub>2</sub>

PubChem

5311180

Nature

Synthetic

Solubility

Soluble in DMSO to 100 mM

Soluble in water to 100 mM

Biochemical name

Nafamostat mesylate

Biological description

Broad spectrum, potent protease inhibitor (Ki = 95.3 pM). Inhibits NF-κB activation and complement activation. Selective for human tryptase.

Canonical smiles

CS(=O)(=O)O.CS(=O)(=O)O.C1=CC(=CC=C1C(=O)OC2=CC3=C(C=C2)C=C(C=C3)C(=N)N)N=C(N)N

InChi

InChI=1S/C19H17N5O2.2CH4O3S/c20-17(21)14-2-1-13-10-16(8-5-12(13)9-14)26-18(25)11-3-6-15(7-4-11)24-19(22)23;2*1-5(2,3)4/h1-10H,(H3,20,21)(H4,22,23,24);2*1H3,(H,2,3,4)

InChiKey

SRXKIZXIRHMPFW-UHFFFAOYSA-N

IUPAC Name

(6-carbamimidoylnaphthalen-2-yl) 4-(diaminomethylideneamino)benzoate;methanesulfonic acid

Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
Storage information
Store under desiccating conditions|The product can be stored for up to 12 months

Product protocols

Publications (2)

Recent publications for all applications. Explore the full list and refine your search

Frontiers in pharmacology 14:1328950 PubMed38273820

2024

Snakebite drug discovery: high-throughput screening to identify novel snake venom metalloproteinase toxin inhibitors.

Applications

Unspecified application

Species

Unspecified reactive species

Rachel H Clare,Charlotte A Dawson,Adam Westhorpe,Laura-Oana Albulescu,Christopher M Woodley,Nada Mosallam,Daniel J W Chong,Jeroen Kool,Neil G Berry,Paul M O'Neill,Nicholas R Casewell

Nature communications 11:6094 PubMed33323937

2020

A therapeutic combination of two small molecule toxin inhibitors provides broad preclinical efficacy against viper snakebite.

Applications

Unspecified application

Species

Unspecified reactive species

Laura-Oana Albulescu,Chunfang Xie,Stuart Ainsworth,Jaffer Alsolaiss,Edouard Crittenden,Charlotte A Dawson,Rowan Softley,Keirah E Bartlett,Robert A Harrison,Jeroen Kool,Nicholas R Casewell
View all publications

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