N2127
4-硝基苯基-α-D-吡喃甘露糖苷
α-mannosidase substrate, chromogenic, ≥98% (TLC), powder
别名:
4-Nitrophenyl a-D-mannopyranoside, 4-Nitrophenyl alpha-D-mannopyranoside, pNP-alpha-D-Man, pNPalphaMan
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所有图片(6)
About This Item
经验公式（希尔记法）:
C12H15NO8
CAS号:
分子量:
301.25
Beilstein:
92210
EC 号:
MDL编号:
UNSPSC代码:
12352204
PubChem化学物质编号:
NACRES:
NA.32
推荐产品
产品名称
4-硝基苯基-α-D-吡喃甘露糖苷, α-mannosidase substrate
质量水平
方案
≥98% (TLC)
表单
powder
溶解性
DMF: 50 mg/mL
储存温度
−20°C
SMILES字符串
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
InChI key
IFBHRQDFSNCLOZ-GCHJQGSQSA-N
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一般描述
4-硝基苯α-D-吡喃半乳糖苷可作为α-甘露糖苷酶的显色底物。
应用
4-硝基苯α-D-吡喃半乳糖苷已在水解酶活性测定中用作α-甘露糖苷酶的检测底物。
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
监管及禁止进口产品
从最新的版本中选择一种：
分析证书(COA)
Lot/Batch Number
I Sielezneff et al.
Chirurgie; memoires de l'Academie de chirurgie, 124(2), 159-164 (1999-06-01)
Peritoneal colonization is a crucial event in the pathogenesis of peritonitis and its local complications. Adherence to the serosal mesothelium is mediated in a number of microorganisms derived from the digestive tract (especially E. coli) by type-1 fimbriae which have
Yanping Zhu et al.
Nature chemical biology, 6(2), 125-132 (2010-01-19)
Colonic bacteria, exemplified by Bacteroides thetaiotaomicron, play a key role in maintaining human health by harnessing large families of glycoside hydrolases (GHs) to exploit dietary polysaccharides and host glycans as nutrients. Such GH family expansion is exemplified by the 23
R Madiyalakan et al.
European journal of cancer & clinical oncology, 23(7), 901-906 (1987-07-01)
A modified procedure was developed for the determination of UDP-galactose: 2-acetamido-2-deoxy-glucopyranoside beta-(1----4)-galactosyltransferase (GT) in human serum which employed the synthetic substrates p-nitrophenyl 6-0-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-beta-D-galactopyranoside and p-nitrophenyl 6-0-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-alpha-D- mannopyranoside as acceptors. The enzyme products were identified by thin layer chromatography with authentic
Synthesis and evaluation of two mannosamine-derived lactone-type inhibitors of snail beta-mannosidase
Terinek M and Vasella A
Tetrahedron Asymmetry, 16, 449-469 (2005)
S Howard et al.
Biochemical and biophysical research communications, 238(3), 896-898 (1997-10-23)
The stereochemical course of the hydrolyses catalysed by two alpha-mannosidases has been determined directly by 1H NMR. Synthetic substrates were incubated with the enzymes and the anomeric configuration of the initially formed product was ascertained in each case by observation
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