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Merck

G2505

N-Glutaryl-L-phenylalanine p-nitroanilide

protease substrate

Synonym(s):

Glutaryl-L-phenylalanine 4-nitroanilide

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G2505-1G

CHF 278.00

G2505-5G

CHF 951.00

CHF 278.00

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About This Item

Empirical Formula (Hill Notation):
C20H21N3O6
CAS Number:
5800-34-0
Molecular Weight:
399.40
Beilstein:
2919832
EC Number:
227-351-4
MDL number:
MFCD00038362
UNSPSC Code:
12352204
PubChem Substance ID:
24895096
NACRES:
NA.83

Key Documents

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Assay

≥98% (HPLC)

form

powder

solubility

methanol with 1 M NH4OH: 50 mg/mL, clear to slightly hazy

storage temp.

−20°C

SMILES string

OC(=O)CCCC(=O)N[C@@H](Cc1ccccc1)C(=O)Nc2ccc(cc2)[N+]([O-])=O

InChI

1S/C20H21N3O6/c24-18(7-4-8-19(25)26)22-17(13-14-5-2-1-3-6-14)20(27)21-15-9-11-16(12-10-15)23(28)29/h1-3,5-6,9-12,17H,4,7-8,13H2,(H,21,27)(H,22,24)(H,25,26)/t17-/m0/s1

InChI key

LFZGBNATHRHOKZ-KRWDZBQOSA-N

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1 of 4

This Item
M4765G6133T6140
N-Glutaryl-L-phenylalanine p-nitroanilide protease substrate

Sigma-Aldrich

G2505

N-Glutaryl-L-phenylalanine p-nitroanilide

N-Methoxysuccinyl-Ala-Ala-Pro-Val p-nitroanilide elastase substrate

Sigma-Aldrich

M4765

N-Methoxysuccinyl-Ala-Ala-Pro-Val p-nitroanilide

L-Glutamic acid γ-(p-nitroanilide) hydrochloride γ-glutamyl transpeptidase substrate

Sigma-Aldrich

G6133

L-Glutamic acid γ-(p-nitroanilide) hydrochloride

N-(p-Tosyl)-Gly-Pro-Lys 4-nitroanilide acetate salt plasmin substrate

Sigma-Aldrich

T6140

N-(p-Tosyl)-Gly-Pro-Lys 4-nitroanilide acetate salt

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (TLC)

solubility

methanol with 1 M NH4OH: 50 mg/mL, clear to slightly hazy

solubility

DMF: soluble 25 mg/mL, clear, colorless to light yellow

solubility

water: 5 mg/mL, clear, yellow

solubility

ethanol: 50 mg/mL, colorless to yellow

Quality Level

100

Quality Level

300

Quality Level

300

Quality Level

200

form

powder

form

powder

form

powder

form

powder

storage temp.

−20°C

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

−20°C

Application

N-Glutaryl-L-phenylalanine p-nitroanilide has been used as a substrate to determine chymotrypsin activity.[1][2]

Biochem/physiol Actions

N-Glutaryl-L-phenylalanine p-nitroanilide is useful in testing α-chymotrypsin activity.[3][4]

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ4284
MKCX5416
MKCX0556
MKCR1562
MKCR0464

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New properties of chymotrypsin modified by fixation with a hydrophobic molecule: hexanal.
M H Remy et al.
Annals of the New York Academy of Sciences, 434, 343-346 (1984-01-01)
S Blais et al.
The Journal of biological chemistry, 268(25), 18637-18639 (1993-09-05)
The Michaelis constant of alpha-chymotrypsin, immobilized on a glutaraldehyde-activated silicate support, for N-glutaryl-L-phenylalanine-p-nitroanilide was determined and was found to be identical with that of the enzyme in solution. The influence of intraparticular diffusion was taken into account by immobilizing different
S V Verevka
Ukrainskii biokhimicheskii zhurnal (1978), 68(3), 36-41 (1996-05-01)
Data on the kinetics of S2'-stimulated alpha-chymotrypsin action have been presented. It is supposed that the increase of the catalytic action of S2'-stimulated chymotrypsin occurs at all three stages of the hydrolytic process-at the enzyme-substrate complex formation, its transformation to
Daniel Brugger et al.
The British journal of nutrition, 116(3), 425-433 (2016-05-28)
This study investigated the effects of short-term subclinical Zn deficiency on exocrine pancreatic activity and changes in digestive capacity. A total of forty-eight weaned piglets were fed ad libitum a basal diet (maize and soyabean meal) with adequate Zn supply
N Spreti et al.
European journal of biochemistry, 268(24), 6491-6497 (2001-12-12)
alpha-Chymotrypsin activity was tested with N-glutaryl-l-phenylalanine p-nitroanilide (GPNA) in aqueous media in the presence of synthetic surfactants, which differ in the flexibility of their bulky head groups. Superactivity can be ascribed to the presence of the tributylammonium residue on the
View All Related Papers

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