A9545
4-氨基苯基β-D-吡喃半乳糖苷
≥98% (TLC), β-galactosidase substrate
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关于此项目
经验公式（希尔记法）:
C12H17NO6
化学文摘社编号:
分子量:
271.27
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352201
MDL number:
InChI
1S/C12H17NO6/c13-6-1-3-7(4-2-6)18-12-11(17)10(16)9(15)8(5-14)19-12/h1-4,8-12,14-17H,5,13H2
SMILES string
Nc1ccc(OC2OC(CO)C(O)C(O)C2O)cc1
InChI key
MIAKOEWBCMPCQR-UHFFFAOYSA-N
assay
≥98% (TLC)
form
powder
optical activity
[α]/D -42.00 to -34.00°, c = 9.00-11.00 mg/mL in water
technique(s)
thin layer chromatography (TLC): suitable
color
white to yellow cast
solubility
water: 49.00-51.00 mg/mL, clear, colorless to yellow
storage temp.
−20°C
Quality Level
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
涉药品监管产品
此项目有
Benoît Limoges et al.
Journal of the American Chemical Society, 128(18), 6014-6015 (2006-05-04)
Electrochemical responses (e.g., chronoamperometric) obtained with an immobilized enzyme that produces an electroactive species may be used to quantitate the amount of enzyme or the concentration of its substrate. It is shown, on theoretical and experimental bases, that product-to-substrate coupling
Takatoshi Kaya et al.
Chemical communications (Cambridge, England), (2)(2), 248-249 (2004-01-23)
[small beta]-Galactosidase expression in a small number of Escherichia coli cells has been measured in real time with an electrochemical sensor chip. E. coli cells were embedded using collagen gel within a micropore which was microfabricated onto a chip. The
[p-Aminophenyl-beta-D-galactopyranoside as an antigenic determinant in neoglycoproteins].
D M Belen'kiĭ
Molekuliarnaia biologiia, 17(1), 54-61 (1983-01-01)
D M Belen'kiĭ et al.
Biokhimiia (Moscow, Russia), 47(7), 1141-1146 (1982-07-01)
Chemical modification of the COOH-groups of acid alpha-glucosidase from human liver by 1-ethyl-3 (3'-dimethylaminopropyl) carbodiimide. HCl in the presence of rho-aminophenyl-beta-D-galactopyranoside was carried out. The presence of covalently bound galactose derivative in the enzyme was followed by changes in the
Qijing Chen et al.
Journal of controlled release : official journal of the Controlled Release Society, 323, 179-190 (2020-04-26)
Macrophages are attractive therapeutic targets due to their contributions to many pathological processes including cancers, atherosclerosis, obesity, diabetes and other inflammatory diseases. Macrophage-targeted gene therapy is an effective strategy for regulating macrophage function at the site of inflammation to treat
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