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Merck

B4750

Sigma-Aldrich

Nα-Benzoyl-DL-arginin-2-naphthylamid -hydrochlorid

trypsin substrate

Synonym(e):

Nα-Benzoyl-DL-Arginin β-Naphthylamid -hydrochlorid, BANA

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About This Item

Empirische Formel (Hill-System):
C23H25N5O2 · HCl
CAS-Nummer:
Molekulargewicht:
439.94
Beilstein:
3823291
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352204
PubChem Substanz-ID:
NACRES:
NA.32

Qualitätsniveau

Assay

≥98% (TLC)

Form

powder

Löslichkeit

DMF: 50 mg/mL, clear, colorless to faintly yellow

Lagertemp.

2-8°C

SMILES String

Cl[H].NC(=N)NCCCC(NC(=O)c1ccccc1)C(=O)Nc2ccc3ccccc3c2

InChI

1S/C23H25N5O2.ClH/c24-23(25)26-14-6-11-20(28-21(29)17-8-2-1-3-9-17)22(30)27-19-13-12-16-7-4-5-10-18(16)15-19;/h1-5,7-10,12-13,15,20H,6,11,14H2,(H,27,30)(H,28,29)(H4,24,25,26);1H

InChIKey

BNGRKDJZQIGWQF-UHFFFAOYSA-N

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Anwendung

Nα-Benzoyl-DL-arginine β-naphthylamide hydrochloride has been used as a substrate in the BANA test to evaluate the inhibitory activity of stefin. It has also been used as a substrate for the determination of Ki values of inhibitors toward trypsin.

Biochem./physiol. Wirkung

Nα-Benzoyl-DL-arginine β-naphthylamide hydrochloride (BANA) helps to determine the activities of cathepsin B and papain. BANA test is also useful in identifying the number of periodontal sites with periodontal pathogens. Presence of volatile sulfur compounds (VSCs), synthesized by oral bacteria in dental plaque or tongue coating can be colorimetrically confirmed by their ability to hydrolyze N-benzoyl-DL-arginine-2-naphthylamide.

Substrate

A chromogenic substrate for trypsin.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


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Marie-Hélène Weech et al.
Journal of experimental botany, 59(9), 2437-2448 (2008-05-20)
Arabidopsis thaliana (L.) Heynh. genotypes limited in their ability to mount either octadecanoid-dependent induced resistance (IR(-)) or systemic acquired resistance (SAR(-)) were used to characterize the roles of these pathways in plant-herbivore interactions. Molecular and biochemical markers of IR were
Neera Raghav et al.
Bioorganic chemistry, 75, 38-49 (2017-09-16)
Cathepsins have emerged as promising molecular targets in a number of diseases such as Alzeimer's, inflammation and cancer. Elevated cathepsin's levels and decreased cellular inhibitor concentrations have emphasized the search for novel inhibitors of cathepsins. The present work is focused
Kunitz-type protease inhibitors group B from Solanum palustre
Speransky A S, et al.
Biotechnology Journal, 2(11), 1417-1424 (2007)
Relationship of psychological and oral health statuses with self-perceived halitosis in a Jordanian population: a cross-sectional study
Alzoubi F Q, et al.
BMC Oral Health, 15(1), 89-89 (2015)
Association between atherosclerosis and periodontitis
Lopez N J, et al.
Revista medica de Chile, 139(6), 717-724 (2011)

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