CAS 3767-28-0
:p-Nitrofenil α-D-glucopiranoside
Descrizione:
p-Nitrofenil α-D-glucopiranoside è un composto sintetico comunemente utilizzato come substrato in saggi enzimatici, in particolare per la rilevazione dell'attività delle glicosidasi. È caratterizzato dalla sua struttura, che consiste in un moiety di glucopiranosio legato a un gruppo p-nitrofenile. Questo composto è tipicamente un solido cristallino bianco a giallo pallido che è solubile in acqua e solventi organici, rendendolo versatile per applicazioni di laboratorio. Dopo l'idrolisi da parte delle glicosidasi, rilascia p-nitrofenolo, che può essere quantificato spettrofotometricamente, fornendo un mezzo per misurare l'attività enzimatica. Il composto è stabile in condizioni normali di laboratorio, ma deve essere conservato lontano dalla luce per prevenire la degradazione. La sua formula molecolare riflette la sua composizione di carbonio, idrogeno, azoto e ossigeno, e ha un peso molecolare specifico. p-Nitrofenil α-D-glucopiranoside è ampiamente utilizzato nella ricerca biochimica, in particolare in studi che coinvolgono il metabolismo dei carboidrati e la cinetica enzimatica.
Formula: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
InChI key: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
Sinonimi:- 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
- Vedi altri sinonimi
Ordinare per
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11 prodotti.
4-Nitrophenyl α-D-Glucopyranoside [Substrate for α-D-Glucosidase]
CAS:Formula:C12H15NO8Purezza:>98.0%(HPLC)Colore e forma:Very Pale Yellow - Pale Yellow SolidPeso molecolare: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>Formula:C12H15NO8Purezza:98+%Colore e forma:Crystalline powder, White to pale creamPeso molecolare:301.25A-D-GLUCOPYRANOSIDE, 4-NITROPHENYL
CAS:Formula:C12H15NO8Purezza:97%Colore e forma:SolidPeso molecolare:301.24944-Nitrophenyl a-D-glucopyranoside
CAS:Formula:C12H15NO8Purezza:≥ 98%Colore e forma:White to off-white crystalline powderPeso molecolare:301.254-Nitrophenyl α-D-glucopyranoside
CAS:<p>4-Nitrophenyl α-D-glucopyranoside</p>Formula:C12H15NO8Purezza:By hplc: 99.6% by area (Typical Value in Batch COA)Colore e forma: white crystalline powderPeso molecolare: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>Formula:C12H15NO8Purezza:Min. 98.0 Area-%Peso molecolare: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>Formula:C12H15NO8Purezza:Min. 99.0 Area-%Peso molecolare:301.26 g/molp-Nitrophenyl-Ä-D-glucopyranoside
CAS:<p>M02745 - p-Nitrophenyl-Ä-D-glucopyranoside</p>Formula:C12H15NO8Purezza:95%Colore e forma:SolidPeso molecolare:301.251p-Nitrophenyl-a-D-Glucopyranoside extrapure, 98%
CAS:Formula:C12H15NO8Purezza:min. 98%Colore e forma:White to off-white, Crystalline powderPeso molecolare: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>Formula:C12H15NO8Colore e forma:White To Off-WhitePeso molecolare:301.254-Nitrophenyl a-D-glucopyranoside
CAS:<p>Chromogenic substrate for alpha-glucosidase</p>Formula:C12H15NO8Purezza:Min. 98 Area-%Colore e forma:White PowderPeso molecolare:301.25 g/mol
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