CAS 3767-28-0
:p-Nitrofenil α-D-glucopiranósido
Descripción:
p-Nitrofenil α-D-glucopiranósido es un compuesto sintético comúnmente utilizado como sustrato en ensayos enzimáticos, particularmente para la detección de la actividad de glicosidasas. Se caracteriza por su estructura, que consiste en un moiety de glucopiranósido unido a un grupo p-nitrofenilo. Este compuesto es típicamente un sólido cristalino blanco a amarillo pálido que es soluble en agua y disolventes orgánicos, lo que lo hace versátil para aplicaciones de laboratorio. Tras la hidrólisis por glicosidasas, libera p-nitrofenol, que puede cuantificarse espectrofotométricamente, proporcionando un medio para medir la actividad enzimática. El compuesto es estable bajo condiciones normales de laboratorio, pero debe almacenarse alejado de la luz para prevenir la degradación. Su fórmula molecular refleja su composición de carbono, hidrógeno, nitrógeno y oxígeno, y tiene un peso molecular específico. p-Nitrofenil α-D-glucopiranósido se utiliza ampliamente en la investigación bioquímica, particularmente en estudios que involucran el metabolismo de carbohidratos y la cinética enzimática.
Fórmula:C12H15NO8
InChI:InChI=1/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
Clave InChI:InChIKey=IFBHRQDFSNCLOZ-ZIQFBCGOSA-N
SMILES:O([C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1)C2=CC=C(N(=O)=O)C=C2
Sinónimos:- 4-Nitrophenyl alpha-D-glucopyranoside
- 4-Nitrophenyl alpha-glucoside
- 4-Nitrophenyl α-<span class="text-smallcaps">D</span>-glucopyranoside
- 4-Nitrophenyl α-<span class="text-smallcaps">D</span>-glucoside
- Glucopyranoside, p-nitrophenyl, α-<span class="text-smallcaps">D</span>-
- p-Nitrophenol α-<span class="text-smallcaps">D</span>-glucoside
- p-Nitrophenyl α-<span class="text-smallcaps">D</span>-glucopyranoside
- p-Nitrophenyl α-<span class="text-smallcaps">D</span>-glucoside
- α-<span class="text-smallcaps">D</span>-Glucopyranoside, 4-nitrophenyl
- α-<span class="text-smallcaps">D</span>-Glucopyranoside, p-nitrophenyl
- α-<span class="text-smallcaps">D</span>-Glucoside, p-nitrophenyl
- α-D-Glucoside, p-nitrophenyl
- 4-Nitrophenyl α-D-glucopyranoside
- Glucopyranoside, p-nitrophenyl, α-D-
- α-D-Glucopyranoside, 4-nitrophenyl
- α-D-Glucopyranoside, p-nitrophenyl
- 4-Nitrophenyl alpha-D-Glucopyranoside [Substrate for alpha-D-Glucosidase]
- 4-Nitrophenyl α-D-Glucoside
- .alpha.-D-Glucopyranoside, 4-nitrophenyl
- p-Nitrophenol a-D-Glucoside
- 4-Nitrophenyl-ɑ-D-glucopyranoside, 98+%
- PNP-ALPHA-GLU
- 4-Nitrophenyla-D-glucopyranoside
- PNP ALPHA-D-GLUCOPYRANOSIDE
- p-Nitrophenol α-D-Glucoside
- 4-nitrophenylalpha-glucoside
- P-NITROPHENYL-ALPHA-D-GLUCOSIDE
- P-NITROPHENYL A-D-GLUCOPYRANOSIDE
- P-Nitrophenyl-Alpha-D-GlucopyranosideA.R.
- 4-Nitrophenyl a-D-Glucoside
- PNP-ALPHA-D-GLC
- Ver más sinónimos
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Encontrado 11 productos.
4-Nitrophenyl α-D-Glucopyranoside [Substrate for α-D-Glucosidase]
CAS:Fórmula:C12H15NO8Pureza:>98.0%(HPLC)Forma y color:Very Pale Yellow - Pale Yellow SolidPeso molecular:301.254-Nitrophenyl-α-D-glucopyranoside, 98+%
CAS:<p>4-Nitrophenyl--D-glucopyranoside acts as a chromogenic substrate for alfa-D-glucosidase inhibitor. It is also used in the detection of glucansucrases and for yeast alfa-D-glucosidase. Further, it is a substrate for lysosomal alfa-glucosidase and maltase-glucoamylase. This Thermo Scientific Chemicals</p>Fórmula:C12H15NO8Pureza:98+%Forma y color:Crystalline powder, White to pale creamPeso molecular:301.25A-D-GLUCOPYRANOSIDE, 4-NITROPHENYL
CAS:Fórmula:C12H15NO8Pureza:97%Forma y color:SolidPeso molecular:301.24944-Nitrophenyl a-D-glucopyranoside
CAS:Fórmula:C12H15NO8Pureza:≥ 98%Forma y color:White to off-white crystalline powderPeso molecular:301.254-Nitrophenyl α-D-glucopyranoside
CAS:<p>4-Nitrophenyl α-D-glucopyranoside</p>Fórmula:C12H15NO8Pureza:By hplc: 99.6% by area (Typical Value in Batch COA)Forma y color: white crystalline powderPeso molecular:301.24939g/mol4-Nitrophenyl-α-D-glucopyranoside
CAS:<p>Chromogenic substrate for α-D-glucosidase yielding a yellow solution upon cleavage. Also used for the detection of glucansucrases and for yeast α-D-glucosidase and for studies of the crystal structure of the complexes of concanavalin A.</p>Fórmula:C12H15NO8Pureza:Min. 98.0 Area-%Peso molecular:301.26 g/mol4-Nitrophenyl-α-D-glucopyranoside, β-Anomer < 0.1%
CAS:<p>4-Nitrophenyl-alpha-D-glucopyranoside, beta-Anomer is a chromogenic sugar that can be used as an indicator for the presence of 4-nitrophenol. It is a highly reactive compound that spontaneously reacts with nitrobenzene to form a dinitroaniline. This anomeric structure is easily oxidized by air and light to form the corresponding o-dinitroaniline. When this reaction occurs, this substance changes color from yellow to red.</p>Fórmula:C12H15NO8Pureza:Min. 99.0 Area-%Peso molecular:301.26 g/molp-Nitrophenyl-Ä-D-glucopyranoside
CAS:<p>M02745 - p-Nitrophenyl-Ä-D-glucopyranoside</p>Fórmula:C12H15NO8Pureza:95%Forma y color:SolidPeso molecular:301.251p-Nitrophenyl-a-D-Glucopyranoside extrapure, 98%
CAS:Fórmula:C12H15NO8Pureza:min. 98%Forma y color:White to off-white, Crystalline powderPeso molecular:301.25p-Nitrophenyl α-D-Glucopyranoside
CAS:<p>Applications p-Nitrophenyl α-D-Glucopyranoside is a substrate for α-glucosidase inhibitor.<br>References O'Neill, R., et al.: J. Biol. Chem., 264, 20430 (1989), Carpita, N., et al.: Plant J., 3, 1 (1993), Henrissat, B., et al.: Biochem. J., 293, 781 (1993), Nakai, H., et al.: Biochimie, 89, 49 (2007) ,<br></p>Fórmula:C12H15NO8Forma y color:White To Off-WhitePeso molecular:301.254-Nitrophenyl a-D-glucopyranoside
CAS:<p>Chromogenic substrate for alpha-glucosidase</p>Fórmula:C12H15NO8Pureza:Min. 98 Area-%Forma y color:White PowderPeso molecular:301.25 g/mol
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