- Cat. No.
- A10617
Nafamostat mesylate
Synonyms: Futhan; FUT-175
Nafamostat is an anticoagulant. Broad spectrum serine protease inhibitor. Reduces eosinophil infiltration, mast cell activation and airway responsiveness in a murine model of asthma.
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Serine protease inhibitors act on peptidases that cleave proteins with a serine, histidine and aspartate triad. The family spans digestive enzymes such as trypsin and chymotrypsin, coagulation factors, kallikreins and neutrophil elastase. Phenylmethylsulfonyl fluoride (PMSF), 4-(2-aminoethyl)benzenesulfonyl fluoride (AEBSF HCl) and the polypeptide aprotinin are broad inhibitors often added to lysis buffers. Sivelestat sodium salt and alvelestat inhibit neutrophil elastase, which is also covered by the neighboring Elastases category. Camostat mesylate and nafamostat mesylate act on transmembrane serine protease 2 (TMPRSS2) and related trypsin-like enzymes. In 2020, camostat mesylate was reported to block TMPRSS2-dependent cell entry of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
Synonyms: Futhan; FUT-175
Nafamostat is an anticoagulant. Broad spectrum serine protease inhibitor. Reduces eosinophil infiltration, mast cell activation and airway responsiveness in a murine model of asthma.
Synonyms: Benzylsulfonyl fluoride
PMSF is an irreversible serine/cysteine protease inhibitor.
Synonyms: AZD9668
Avelestat, also known as AZD9668, is a novel, oral inhibitor of neutrophil elastase (NE).
Synonyms: ONO-5046
Sivelestat sodium salt is a selective leukocyte elastase inhibitor (IC50 = 44 nM) that displays no activity at a range of other proteases. It inhibits NF-kB activation and LTB4-induced neutrophil transmigration in vitro.
Synonyms: BPTI ,Bovine Pancreatic Trypsin Inhibitor
Aprotinin is a small protein serine protease inhibitor, used to reduce perioperative blood loss and transfusion.
AEBSF HCl is a broad spectrum, irreversible serine protease inhibitor.
Synonyms: BCX 1470
BCX 1470 is serine protease inhibitor. BCX 1470 blocks the esterolytic and hemolytic activities of the complement enzymes Cls and factor D in vitro.
Synonyms: Thrombin inhibitor
BCX 1470 is serine protease inhibitor. BCX 1470 blocks the esterolytic and hemolytic activities of the complement enzymes Cls and factor D in vitro.
Camostat mesylate is an orally active protease inhibitor. Known to inhibit trypsin and various inflammatory proteases including plasmin, kallikrein and thrombin.
Bromhexine hydrochloride is a selective inhibitor of the TMPRSS2 protease, exhibiting an IC50 of 0.75 μM. This compound has demonstrated efficacy in preventing and managing SARS-CoV-2 infections. Additionally, bromhexine hydrochloride acts as an autophagy agonist and serves as a mucolytic cough suppressant, making it suitable for research related to various respiratory conditions.
Synonyms: Tripeptidyl Peptidase Inhibitor II N-Ala-Ala-Phe-CMK
AAF-CMK is a serine protease inhibitor which irreversibly inhibits TPPII (tripeptidyl peptidase II), a giant protease which may substitute for some proteasome functions1, and reversibly inhibits Cln2 (TPPI).
Leupeptin hemisulfate is a reversible inhibitor of trypsin-like and cysteine proteases such as calpain.
Synonyms: Elastase Inhibitor IV
Sivelestat is a cell-permeable sulfanilide compound that acts as a potent, substrate-competitive, and highly specific inhibitor of neutrophil elastase (IC50 = 19-49 nM in rat, rabbit, hamster, human, and mouse leukocyte elastase).
SSR 69071 is a high affinity, potent inhibitor of Neutrophil Elastase (human leukocyte elastase, HLE) (IC50 = 3.9 nM).
Synonyms: Macrofusine; Macrofusin
Fumonisin B1 is a fungal metabolite produced by Fusarium moniliforme, that has been shown to inhibit protein serine/threonine phosphatases (PP1, PP2A, PP2B, PP2C, and PP5/T/K/H), and is most effective with PP5.
Demethylwedelolactone is a naturally occurring coumestan that serves as a potent trypsin inhibitor with an IC50 of 3.0 μM. This compound effectively suppresses cell motility and invasion in breast cancer cells, making it a valuable tool for studying mechanisms of cancer progression and metastasis. Its functional properties may also support research into therapeutic approaches targeting proteolytic enzymes in cancer biology.
Synonyms: Hexa-D-arginine aMide
Hexa-D-arginine is a inhibitor of furin (Ki values are 0.106, 0.58 and 13.2 uM for furin, PACE4 and PC1 respectively).
Synonyms: ONO5046-Na; EI546 sodium; LY544349 sodium
Sivelestat sodium is a competitive inhibitor of human neutrophil elastase, also inhibits leukocyte elastase obtained from rabbit, rat, hamster and mouse.
AA26-9 is a potent and broad-spectrum serine hydrolase inhibitor.
FXIa-IN-1 (compound EP-7041) is a potent β-lactam covalent heparin-derived factor XIa (fXIa) inhibitor.
ZK824859 is an oral available and selective urokinase plasminogen activator (uPA) inhibitor with IC50s of 79 nM, 1580 nM and 1330 nM for human uPA, tPA, and plasmin, respectively.
BMS-962212 is a reversible, direct, and highly selective inhibitor of FXIa.
N-alpha-Tosyl-L-lysine chloromethyl ketone (TLCK), a trypsin like protease inhibitor, sensitizes HeLa cells to Fas-mediated cell death.
SBC-110736 is a proprotein convertase subtilisin kexin type 9 (PCSK9) inhibitor extracted from patent WO2014150395A1, Figure 1.
Synonyms: UKI-1C
UKI-1 is a novel synthetic inhibitor of the urokinase-type plasminogen activator system.