M7008
4-甲基伞形酮基β-D-吡喃吡喃糖苷
β-xylosidase substrate, fluorogenic, ≥98% (HPLC), powder
别名:
4-甲基伞形基-β-D-木糖甙
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关于此项目
经验公式（希尔记法）:
C15H16O7
化学文摘社编号:
分子量:
308.28
Beilstein:
39934
EC 号:
MDL编号:
UNSPSC代码:
12352204
PubChem化学物质编号:
NACRES:
NA.32
产品名称
4-甲基伞形酮基β-D-吡喃吡喃糖苷, β-xylosidase substrate
质量水平
方案
≥98% (HPLC)
表单
powder
溶解性
pyridine: 50 mg/mL, clear, colorless to faintly yellow
储存温度
−20°C
SMILES字符串
CC1=CC(=O)Oc2cc(O[C@@H]3OC[C@@H](O)[C@H](O)[C@H]3O)ccc12
InChI
1S/C15H16O7/c1-7-4-12(17)22-11-5-8(2-3-9(7)11)21-15-14(19)13(18)10(16)6-20-15/h2-5,10,13-16,18-19H,6H2,1H3/t10-,13+,14-,15+/m1/s1
InChI key
JWIYLOHVJDJZOQ-KAOXEZKKSA-N
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一般描述
β 的底物-木糖苷酶
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
此项目有
W G Hill et al.
Biochimica et biophysica acta, 1454(2), 174-182 (1999-06-25)
The ability of cells to decorate glycosaminoglycans (GAGs) with sulphate in highly specific patterns is important to extracellular matrix biogenesis and placing appropriate glycosulphated ligands on the cell surface. We have examined sulphate metabolism in two pancreatic duct epithelial cell
S Shibata et al.
The Journal of biological chemistry, 270(23), 13794-13798 (1995-06-09)
4-Methylumbelliferyl-beta-D-xyloside (Xyl-MU) was added to the medium of cultured human skin fibroblasts. After incubation, the culture medium was pooled, and the Xyl-MU-induced oligosaccharides in the medium were purified by gel filtration chromatography. A novel Xyl-MU derivative was obtained, in addition
J E Silbert et al.
The Biochemical journal, 296 ( Pt 1), 119-126 (1993-11-15)
Mouse mastocytoma cells were cultured in medium containing [3H]GlcN and concentrations of [35S]sulphate varying from 0.01 to 0.5 mM. Intracellular [35S]sulphate incorporation increased severalfold from the lowest concentrations, reaching a maximum at 0.1-0.2 mM, whereas incorporation of [3H]hexosamine remained constant
H H Freeze et al.
The Journal of biological chemistry, 268(3), 1618-1627 (1993-01-25)
beta-D-Xylosides are often used to competitively inhibit proteoglycan synthesis by serving as primers for free glycosaminoglycan (GAG) chain assembly. Quite unexpectedly, we found that when human melanoma cells and Chinese hamster ovary cells are labeled with [3H] galactose in the
A Molténi et al.
Cell and tissue research, 295(3), 523-536 (1999-02-18)
Matrix and cell surface proteoglycans (PGs) may play important roles in the control of cellular actions of heparan-binding growth factors such as fibroblast growth factor (FGF) during chondrogenesis and osteogenesis. In this study, we used 4-methylumbelliferyl-beta-d-xyloside, an inhibitor of PG
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