N8759
4-硝基苯基N-乙酰基-α-D-氨基葡萄糖
≥98%, powder
别名:
p-硝基苯基2-乙酰氨基-2-脱氧-α-D-吡喃葡萄糖苷
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关于此项目
经验公式（希尔记法）:
C14H18N2O8
化学文摘社编号:
分子量:
342.30
EC 号:
MDL编号:
UNSPSC代码:
12352204
PubChem化学物质编号:
NACRES:
NA.32
产品名称
4-硝基苯基N-乙酰基-α-D-氨基葡萄糖, ≥98%
方案
≥98%
表单
powder
溶解性
warm ethanol: acetic acid (1:1): 20 mg/mL, clear, colorless to faintly yellow
储存温度
−20°C
SMILES字符串
CC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1Oc2ccc(cc2)[N+]([O-])=O
InChI
1S/C14H18N2O8/c1-7(18)15-11-13(20)12(19)10(6-17)24-14(11)23-9-4-2-8(3-5-9)16(21)22/h2-5,10-14,17,19-20H,6H2,1H3,(H,15,18)/t10-,11-,12-,13-,14+/m1/s1
InChI key
OMRLTNCLYHKQCK-KSTCHIGDSA-N
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应用
4-硝基苯基N-乙酰基-α-D-氨基葡萄糖苷被用作测定黄星天牛（Psacothea hilaris）幼虫和成虫肠道中pnp-吡喃葡糖苷水解活性的底物。
生化/生理作用
4-硝基苯基N-乙酰基-α-D-氨基葡萄糖苷被用作在37°C和 405 nm处分析β-己糖胺酶活性的底物。
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Diet and carbohydrate digestion in the yellow-spotted longicorn beetle Psacothea hilaris
Scrivener AM, et al.
Journal of Insect Physiology, 43(11), 1039-1052 (1997)
Study of subcellular localization and proteolysis of ataxin-3
Pozzi C, et al.
Neurobiology of Disease, 30(2), 190-200 (2008)
E Chitlaru et al.
The Journal of biological chemistry, 271(52), 33433-33439 (1996-12-27)
The accompanying papers (Keyhani, N. O., and Roseman, S. (1996) J. Biol. Chem. 271, 33414-33424; Keyhani, N. O., and Roseman, S. (1996) J. Biol. Chem. 271, 33425-33432) describe two unique beta-N-acetylglucosaminidases from Vibrio furnissii. A third, ExoII, is reported here.
T Usui et al.
Biochimica et biophysica acta, 953(2), 179-184 (1988-03-23)
Transchitooligosylation from (GlcNAc)5 to the 4-position of PNP-GlcNAc was efficiently induced through lysozyme catalysis in an aqueous solution containing methanol with a high concentration. Use of the aqueous methanol system in this reaction not only guaranteed solubility of PNP-GlcNAc substrate
E Frändberg et al.
The Journal of applied bacteriology, 76(3), 259-263 (1994-03-01)
Three methods of quantifying chitinase activity were compared. The activities of crude chitinases of 10 bacterial isolates from different environments were estimated in terms of (1) the release of p-nitrophenol from the chromogenic chito-oligosaccharide analogues, p-nitrophenyl-beta-D-N,N'-diacetylchitobiose, p-nitrophenyl-N-acetyl-beta-D-glucosamine and p-nitrophenyl-beta-D-N,N',N"-triacetylchitotriose, (2)
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