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About This Item
经验公式（希尔记法）:
C14H18N2O8
CAS号:
分子量:
342.30
EC號碼:
MDL號碼:
分類程式碼代碼:
12352204
PubChem物質ID:
NACRES:
NA.32
推荐产品
product name
4-硝基苯基N-乙酰基-α-D-氨基葡萄糖, ≥98%
化驗
≥98%
形狀
powder
溶解度
warm ethanol: acetic acid (1:1): 20 mg/mL, clear, colorless to faintly yellow
儲存溫度
−20°C
SMILES 字串
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 密鑰
OMRLTNCLYHKQCK-KSTCHIGDSA-N
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應用
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。
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
其他客户在看
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)
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
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
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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