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Merck
CN

69591

Sigma-Aldrich

4-甲基伞形酮 α- D -吡喃葡萄糖苷

≥98% (TLC)

别名:

4-甲基伞形酮 α- D -葡萄糖苷

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关于此项目

经验公式（希尔记法）:
C16H18O8
化学文摘社编号:
17833-43-1
分子量:
338.31
Beilstein:
1690776
EC 号:
241-794-0
MDL编号:
MFCD00067661
UNSPSC代码:
12352204
PubChem化学物质编号:
57652200
NACRES:
NA.25

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描述

α-glucosidase substrate

质量水平

200

方案

≥98% (TLC)

表单

powder

溶解性

DMSO: 50 mg/mL, clear, colorless to faintly yellow

荧光

λex 316 nm; λem 375 nm (Reaction product)
λex 317 nm; λem 374 nm (pH9.0)
λex 360 nm; λem 449 nm
λex 365 nm; λem 445 nm in 0.1 M Tris pH 8.0 (α-glucosidase)

储存温度

−20°C

SMILES字符串

CC1=CC(=O)Oc2cc(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)ccc12

InChI

1S/C16H18O8/c1-7-4-12(18)23-10-5-8(2-3-9(7)10)22-16-15(21)14(20)13(19)11(6-17)24-16/h2-5,11,13-17,19-21H,6H2,1H3/t11-,13-,14+,15-,16+/m1/s1

InChI key

YUDPTGPSBJVHCN-JZYAIQKZSA-N

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相关类别

一般描述

4-甲基伞形酮α-D-吡喃葡萄糖苷是 α -葡萄糖苷酶的荧光底物。 4-甲基伞形酮α-D-吡喃葡萄糖苷，又称 4MU- α-glc，反应后生成产物 4MU，其荧光光谱峰值为 440nm。

应用

4-甲基伞形酮α-D-吡喃葡萄糖苷可作为荧光底物，用于α-D-葡萄糖苷酶的鉴别、表征和动力学分析。4-甲基伞形酮α-D-吡喃葡萄糖苷用于高通量筛选实验。它适用于肾脏及白细胞的庞佩氏症诊断。

包装

无底玻璃瓶。内容物在插入的熔锥内。

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

涉药品监管产品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000496165
0000496165
0000471718
0000471718
0000424185

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4-Methylumbelliferyl-alpha-D-glucoside, the fluorogenic substrate of alpha-glucosidase, was used as a selective marker to develop a differential medium for Enterobacter sakazakii. This bacterium showed strong fluorogenic characteristics clearly distinguishable from other microorganisms. On the basis of reducing background noise, an optimum
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Pompe disease, or glycogen storage disease type II, is a rare autosomal recessive disorder caused by mutations in the gene that encodes for alpha-glucosidase. Presentation in infancy is associated with respiratory failure, cardiomyopathy, and severe muscle weakness. Juvenile- or adult-onset
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The early steps of glycoprotein biosynthesis involve processing of the N-glycan core by endoplasmic reticulum α-glucosidases I and II which sequentially trim the outermost α1,2-linked and the two more internal α1,3-linked glucose units, respectively. We have demonstrated the presence of
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