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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%
质量水平
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
Study of subcellular localization and proteolysis of ataxin-3
Pozzi C, et al.
Neurobiology of Disease, 30(2), 190-200 (2008)
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)
Jin-Jin Xie et al.
International journal of biological macromolecules, 39(4-5), 159-164 (2006-07-04)
Chemical modification of p-chloromercuribenzoate (PCMB) on beta-N-acetyl-d-glucosaminidase (NAGase, EC 3.2.1.52) from green crab (Scylla serrata) has been studied. The results show that sulfhydryl group is essential for the activity of the enzyme. Inhibitory kinetics of the enzyme by mercuric chloride
N O Keyhani et al.
The Journal of biological chemistry, 271(52), 33414-33424 (1996-12-27)
Chitin catabolism in Vibrio furnissii comprises several signal transducing systems and many proteins. Two of these enzymes are periplasmic and convert chitin oligosaccharides to GlcNAc and (GlcNAc)2. One of these unique enzymes, a chitodextrinase, designated EndoI, is described here. The
S Drouillard et al.
The Biochemical journal, 328 ( Pt 3), 945-949 (1998-02-07)
The stereochemistry of the reaction catalysed by Serratia marcescens chitobiase was determined by HPLC separation of the anomers of N-acetylglucosamine produced during the hydrolysis of p-nitrophenyl N-acetyl-beta-d-glucosaminide (PNP-GlcNAc). In the early stages of the reaction, the beta-anomer was found to
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