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B6760

Sigma-Aldrich

N-Benzoyl-L-tyrosine p-nitroanilide

≥98.0% (TLC)

Synonym(s):

Benzoyl-L-tyrosine p-nitroanilide

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About This Item

Empirical Formula (Hill Notation):
C22H19N3O5
CAS Number:
6154-45-6
Molecular Weight:
405.40
MDL number:
MFCD00038109
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
24891820
NACRES:
NA.26

product name

N-Benzoyl-L-tyrosine p-nitroanilide,

Assay

≥98.0% (TLC)

form

powder

color

white

mp

235-237 °C

storage temp.

−20°C

SMILES string

Oc1ccc(CC(NC(=O)c2ccccc2)C(=O)Nc3ccc(cc3)[N+]([O-])=O)cc1

InChI

1S/C22H19N3O5/c26-19-12-6-15(7-13-19)14-20(24-21(27)16-4-2-1-3-5-16)22(28)23-17-8-10-18(11-9-17)25(29)30/h1-13,20,26H,14H2,(H,23,28)(H,24,27)

InChI key

CJERUMAUMMIPRF-UHFFFAOYSA-N

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Application

N-Benzoyl-L-tyrosine p-nitroanilide (BTPNA) is used as a substrate to identify, differentiate and characterize serine carboxypeptidase(s) and various proteases.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Protease activity in gut of Daphnia magna: evidence for trypsin and chymotrypsin enzymes.
von Elert E, Agrawal MK, et al.
Comp. Biochem. Physiol., B: Comp. Biochem., 137, 287-296 (2004)
G Colebatch et al.
Insect biochemistry and molecular biology, 31(4-5), 415-423 (2001-02-27)
Protease activities in the secreted saliva, salivary glands and midgut of the green mirid, Creontiades dilutus, were investigated. The saliva and salivary glands had more protease activity than the midgut, but no differences in protease activity levels were detected between
K S LIU et al.
The Analyst, 115(8), 1143-1144 (1990-08-01)
In assaying chymotrypsin inhibition by the soybean Bowman-Birk inhibitor, two sequences of mixing the reactants were tried: adding the substrate last (s-last test) or adding the enzyme last (e-last test). The inhibition values obtained from the s-last test were either
J Suh et al.
Bioorganic & medicinal chemistry letters, 8(11), 1331-1336 (1999-01-01)
Both activity and stability of alpha-Chymotrypsin (ChT) are substantially enhanced in the microdomains of laurylated or benzylated derivatives of poly(ethylenimine). EPR data revealed that the enhancement in activity of ChT is due to increase in the polarity of the microenvironment
A Gervaix et al.
Journal of immunology (Baltimore, Md. : 1950), 147(6), 1912-1919 (1991-09-15)
The effects of carbobenzyloxy-leucine-tyrosine-chloromethylketone (zLYCK), an inhibitor of chymotrypsin, were investigated on the activation pathways of the human neutrophil respiratory burst. At 10 microM zLYCK, a parallel inhibition was observed of superoxide production stimulated with the chemo-attractant FMLP and of
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Chymotrypsin

Analytical Enzyme Chymotrypsin: Chymotrypsin is produced in the acinar cells of the pancreas as the inactive precursor, chymotrypsinogen.

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