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N3378

Sigma-Aldrich

4-Nitrophenyl β-D-fuco­pyran­oside

≥98% (TLC), powder

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About This Item

經驗公式(希爾表示法):
C12H15NO7
CAS號碼:
分子量::
285.25
Beilstein:
1291394
MDL號碼:
分類程式碼代碼:
12352204
PubChem物質ID:
NACRES:
NA.32

product name

4-Nitrophenyl β-D-fuco­pyran­oside, ≥98% (TLC)

化驗

≥98% (TLC)

形狀

powder

溶解度

ethanol: soluble 25 mg/mL, clear, colorless to faintly yellow

儲存溫度

−20°C

SMILES 字串

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

InChI

1S/C12H15NO7/c1-6-9(14)10(15)11(16)12(19-6)20-8-4-2-7(3-5-8)13(17)18/h2-6,9-12,14-16H,1H3/t6-,9+,10+,11-,12+/m1/s1

InChI 密鑰

YILIDCGSXCGACV-BVWHHUJWSA-N

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相關類別

應用

4-Nitrophenyl β-D-fucopyranoside has been used as a chromogenic substrate to study substrate specificity and kinetic parameters of β-galactosidase.

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


分析證明 (COA)

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New alkalophilic beta-galactosidase with high activity in alkaline pH region from Teratosphaeria acidotherma AIU BGA-1
Yamada M, et al.
Journal of Bioscience and Bioengineering, 123(1), 15-19 (2017)
Purification and analysis of an extremely halophilic beta-galactosidase from Haloferax alicantei
Holmes M L, et al.
Biochimica et Biophysica Acta, Protein Structure and Molecular Enzymology, 1337(2), 276-286 (1997)
Identification, purification and characterization of a novel glycosidase (BgLm1) from Leuconostoc mesenteroides
del Pino-Garcia R, et al.
Food Sci. Technol., 122, 108829-108829 (2020)
Beatrice Cobucci-Ponzano et al.
Biochemistry, 42(32), 9525-9531 (2003-08-13)
We have recently reported that a functional alpha-L-fucosidase could be expressed by a single insertional mutation in the region of overlap between the ORFs SSO11867 and SSO3060 of the hyperthermophilic Archaeon Sulfolobus solfataricus [Cobucci-Ponzano et al. J. Biol. Chem. (2003)
M A Cohenford et al.
Analytical biochemistry, 177(1), 172-177 (1989-02-15)
A novel, rapid, and reliable colorimetric method for measuring L-fucose has been developed. This method utilizes NADH formed from the interaction of L-fucose with fucose dehydrogenase and NAD to generate color in a reaction involving CuSO4 and neocuproine. NADH reduces

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