Name | (2S,3R,4S,5S)-2-(4-nitrophenoxy)oxane-3,4,5-triol |
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Synonyms | (2S,3R,4S,5S)-2-(4-nitrophenoxy)tetrahydro-2H-pyran-3,4,5-triol |
Description | p-Nitrophenyl α-L-arabinopyranoside is a biochemical reagent. p-Nitrophenyl α-L-arabinopyranoside can be hydrolyzed by recombinant BgaA (rBgaA, isolated from E. coli BL21 (DE3) strain harboring pEBGA29). p-Nitrophenyl α-L-arabinopyranoside has potential application in enzyme activity detection[1][3]. |
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Related Catalog | |
In Vitro | p-Nitrophenyl α-L-arabinopyranoside 与 rBgaA 的亲和度 Km 值为 6.06 mM[1]。 p-Nitrophenyl α-L-arabinopyranoside 对 xylosidase–arabinosidase (xarB) 基因具有高活性[2]。 p-Nitrophenyl α-L-arabinopyranoside 在酶活性检测中的应用[3] (1) 200 µL 2 mM p-Nitrophenyl α-L-arabinopyranoside、100 µL 酶、300 µL 50 mM 磷酸盐缓冲液 (pH 7.0),在 37℃ 下共孵育 0.5、1 和 5 h。 (2) 加入 400 µL 0.5 M 氢氧化钠,终止反应。 (3) 在 405 nm 处测量混合物的吸光度。 注:在人参皂苷存在的情况下,用丁醇萃取终止反应。 |
References |
Density | 1.597g/cm3 |
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Boiling Point | 523.2ºC at 760mmHg |
Melting Point | 205ºC |
Molecular Formula | C11H13NO7 |
Molecular Weight | 271.22300 |
Flash Point | 270.2ºC |
Exact Mass | 271.06900 |
PSA | 124.97000 |
Vapour Pressure | 8.94E-12mmHg at 25°C |
Index of Refraction | 1.654 |
Storage condition | −20°C |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
~% 1223-07-0 |
Literature: Journal of the American Chemical Society, , vol. 74, p. 1883,1884 |
Precursor 2 | |
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DownStream 0 |