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N2127

Sigma-Aldrich

4-Nitrophenyl α-D-Mannopyranosid

α-mannosidase substrate, chromogenic, ≥98% (TLC), powder

Synonym(e):

4-Nitrophenyl a-D-mannopyranoside, 4-Nitrophenyl alpha-D-mannopyranoside, pNP-alpha-D-Man, pNPalphaMan

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25 MG
CHF 75.10
100 MG
CHF 115.00
250 MG
CHF 222.00
500 MG
CHF 473.00
1 G
CHF 694.00
5 G
CHF 2’810.00

CHF 75.10

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25 MG
CHF 75.10
100 MG
CHF 115.00
250 MG
CHF 222.00
500 MG
CHF 473.00
1 G
CHF 694.00
5 G
CHF 2’810.00

About This Item

Empirische Formel (Hill-System):
C12H15NO8
CAS-Nummer:
10357-27-4
Molekulargewicht:
301.25
Beilstein:
92210
EG-Nummer:
233-776-6
MDL-Nummer:
MFCD00066002
UNSPSC-Code:
12352204
PubChem Substanz-ID:
24897554
NACRES:
NA.32

CHF 75.10

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Produktbezeichnung

4-Nitrophenyl α-D-Mannopyranosid, α-mannosidase substrate

Assay

≥98% (TLC)

Form

powder

Löslichkeit

DMF: 50 mg/mL

Lagertemp.

−20°C

SMILES String

OC[C@H]1O[C@H](Oc2ccc(cc2)[N+]([O-])=O)[C@@H](O)[C@@H](O)[C@@H]1O

InChI

1S/C12H15NO8/c14-5-8-9(15)10(16)11(17)12(21-8)20-7-3-1-6(2-4-7)13(18)19/h1-4,8-12,14-17H,5H2/t8-,9-,10+,11+,12+/m1/s1

InChIKey

IFBHRQDFSNCLOZ-GCHJQGSQSA-N

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Allgemeine Beschreibung

4-Nitrophenyl α-D-mannopyranoside is a chromogenic substrate for α-mannosidase.[1]

Anwendung

4-Nitrophenyl α-D-mannopyranoside has been used as a substrate for α-mannosidase[2] in hydrolase activity assay.[3]

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
0000423317
0000423316
0000423313
0000423316
0000423317

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Daniel J Coleman et al.
Analytical biochemistry, 399(1), 7-12 (2009-12-23)
A simple and reliable continuous assay for measurement of alpha-mannosidase activity is described and demonstrated for analysis with two recombinant human enzymes using the new substrate resorufin alpha-d-mannopyranoside (Res-Man). The product of enzyme reaction, resorufin, exhibits fluorescence emission at 585
P N Kanellopoulos et al.
Journal of structural biology, 116(3), 345-355 (1996-05-01)
Concanavalin A (Con A) is the best-known plant lectin and has important in vitro biological activities arising from its specific saccharide-binding ability. Its exact biological role still remains unknown. The complexes of Con A with 4'-nitrophenyl-alpha-D-mannopyranoside (alpha-PNM) and 4'-nitrophenyl-alpha-D-glucopyranoside (alpha-PNG)
Yoshito Ihara et al.
Methods in molecular biology (Clifton, N.J.), 2132, 295-308 (2020-04-20)
Calnexin (CNX) and calreticulin (CRT) are ER-resident lectin-like molecular chaperones involved in the quality control of secretory or membrane glycoproteins. They can exert molecular chaperone functions via specific binding to the early processing intermediates of Glc1Man9GlcNAc2 oligosaccharides of N-glycoproteins. CNX
Yanping Zhu et al.
Nature chemical biology, 6(2), 125-132 (2010-01-19)
Colonic bacteria, exemplified by Bacteroides thetaiotaomicron, play a key role in maintaining human health by harnessing large families of glycoside hydrolases (GHs) to exploit dietary polysaccharides and host glycans as nutrients. Such GH family expansion is exemplified by the 23
R Madiyalakan et al.
European journal of cancer & clinical oncology, 23(7), 901-906 (1987-07-01)
A modified procedure was developed for the determination of UDP-galactose: 2-acetamido-2-deoxy-glucopyranoside beta-(1----4)-galactosyltransferase (GT) in human serum which employed the synthetic substrates p-nitrophenyl 6-0-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-beta-D-galactopyranoside and p-nitrophenyl 6-0-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-alpha-D- mannopyranoside as acceptors. The enzyme products were identified by thin layer chromatography with authentic
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