M7008
4-Methylumbelliferyl-β-D-xylopyranoside
β-xylosidase substrate, fluorogenic, ≥98% (HPLC), powder
동의어(들):
4-Methylumbelliferyl β-D-xyloside
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모든 사진(4)
About This Item
실험식(Hill 표기법):
C15H16O7
CAS Number:
Molecular Weight:
308.28
Beilstein:
39934
EC Number:
MDL number:
UNSPSC 코드:
12352204
PubChem Substance ID:
NACRES:
NA.32
추천 제품
product name
4-Methylumbelliferyl-β-D-xylopyranoside, β-xylosidase substrate
Quality Level
분석
≥98% (HPLC)
형태
powder
solubility
pyridine: 50 mg/mL, clear, colorless to faintly yellow
저장 온도
−20°C
SMILES string
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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기질
A substrate for β-xylosidase
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
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
Loontiens, F.G. and DeBruyne, C.K.
Naturwissenschaften, 52, 661-661 (1965)
K Takagaki et al.
Journal of biochemistry, 119(4), 697-702 (1996-04-01)
Human skin fibroblasts were incubated in the presence of a fluorogenic xyloside, 4-methyl-umbelliferyl-beta-D-xyloside (Xyl-MU), then the cultured medium was recovered, concentrated with a lyophilizer, and dialyzed against distilled water. The structures of the Xyl-MU derivatives purified from the dialyzable fraction
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
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
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