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N1377

Sigma-Aldrich

4-Nitrophenyl α-D-glucopyranoside

chromogenic, ≥99%, powder or crystals

Synonyme(s) :

p-Nitrophenyl α-D-glucopyranoside

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About This Item

Formule empirique (notation de Hill):
C12H15NO8
Numéro CAS:
3767-28-0
Poids moléculaire :
301.25
Numéro Beilstein :
92212
Numéro CE :
223-189-3
Numéro MDL:
MFCD00064088
Code UNSPSC :
12352204
ID de substance PubChem :
24897484
Nomenclature NACRES :
NA.32

product name

4-Nitrophenyl α-D-glucopyranoside, ≥99%

Pureté

≥99%

Forme

powder or crystals

Solubilité

methanol: 20 mg/mL, clear to very slightly hazy, colorless to greenish-yellow

Température de stockage

−20°C

Chaîne SMILES 

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

Clé InChI

IFBHRQDFSNCLOZ-ZIQFBCGOSA-N

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Application

4-Nitrophenyl ǥ-D-glucopyranoside has been used as a substrate in an ǥ-glucosidase inhibition assay.

Actions biochimiques/physiologiques

4-Nitrophenyl ǥ-D-glucopyranoside serves as a substrate for glycosidases. Upon cleavage, the substrate is converted to a yellow-colored product.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

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Insight into anti-diabetic potential of Clematis apiifolia: glucose control in diabetes.
Zehra SA, et al.
Pakistan Journal of Agricultural Sciences null
Faryal Chaudhry et al.
Bioorganic chemistry, 82, 267-273 (2018-11-06)
Herein, substituted imidazole-pyrazole hybrids (2a-2n) were prepared via a multi component reaction employing pyrazole-4-carbaldehydes (1a-1d), ammonium acetate, benzil and arylamines as reactants. All the new compounds were characterized through their spectral and elemental analyses. Further these compounds were tested against
Jaegoo Kim et al.
World journal of microbiology & biotechnology, 34(11), 167-167 (2018-11-02)
Candida albicans is a major invasive pathogen, and the development of strains resistant to conventional antifungal agents has been reported in recent years. We evaluated the antifungal activity of 44 compounds against Candida strains. Magnoflorine showed the highest growth inhibitory
Celia Bustos-Brito et al.
Molecules (Basel, Switzerland), 25(8) (2020-04-25)
The aerial parts of Salvia cinnabarina afforded two undescribed labdane diterpenoids 1 and 2 (malonylcommunol and 6β-hydroxy-trans-communic acid) along with two known labdane diterpenoids, trans-communic acid (3) and trans-communol (4). Additionally, seven known metabolites were also isolated; two isopimarane diterpenoids
Hyeong-U Son et al.
Biomolecules, 9(12) (2019-12-11)
To determine the mechanism of action of the effects of phytoalexins in soybeans, we analyzed α-glucosidase inhibition kinetics using Michaelis-Menten plots and Lineweaver-Burk plots. The results showed that the type of inhibition with glyceollin was competitive, that of genistein was
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