CAS: 66068-38-0; P-Nitrophenyl α-Maltopentaoside
该化合物其高纯度和定义明确的结构确保研究和诊断应用的可复制结果.该基质对于研究内应作用的膜特别有用,因为它的内应镜骨骨骨,可模拟天然聚氨基亚底体. 它在标准实验室条件下的稳定性和与自动系统兼容性进一步加强其在高通量筛选和临床诊断中的效用.该试剂被广泛用于酶学和碳水化合物新陈代谢研究.
- 英文名称P-Nitrophenyl α-Maltopentaoside
- 中文名称对硝基苯基α-麦芽五糖苷
- IUPAC名称(2R,3R,4S,5S,6R)-2-(((2R,3S,4R,5R,6R)-6-(((2R,3S,4R,5R,6R)-6-(((2R,3S,4R,5R,6R)-6-(((2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-(4-nitrophenoxy)tetrahydro-2H-pyran-3-yl)oxy)-4,5-dihydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)oxy)-4,5-dihydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)oxy)-4,5-dihydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
- 其它别名4-Nitrophenyl-Alpha-D-Maltopentaoside; 4-Nitrophenyl-Alpha-D-Penta-(1->4)-Glucopyranoside; Pg5; Pnp-Alpha-D-Maltopentaoside; P-Nitrophenyl-Alpha-D-Penta-Glucopyranoside; P-Nitrophenyl-Alpha-D-Maltopentaoside; 4)-Gluco Pyranoside; 4-Nitrophenyl-Alpha-D-Penta-(1->
- CAS编号66068-38-0
- MFCD编号:MFCD00065706
- EINECS号:636-249-2
- 分子式:C36H55NO28分子量:949.82
- 产品CID: 1641654
- 产品分类有机原料→分子砌块→手性化合物→手性砌块
相似化合物
3482-57-3 129411-63-8 129411-66-1物理性质
MSDS等安全信息
- GHS象形图
- GHS符号GHS07;
注释: Exclamation mark - 危险类别急性毒性 类别4(吸入)
急性毒性 类别4(经皮)
急性毒性 类别4(经口)
特定目标器官毒性 - 单次接触 类别3
皮肤腐蚀/刺激 类别2
严重眼刺激 类别2 - 警示词Warning(警告)
- 危险描述H332 |吸入有害.
H312 |皮肤接触有害.
H302 |吞咽有害.
H335 |可能引起呼吸道刺激.
H315 |造成皮肤刺激.
H319 |造成严重眼刺激. - 防范说明P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
- UN编号NONH for all modes of transport
- 危险品标志Xn
- 安全声明26-36-24/25-22
- 危险类别码20/21/22-36/37/38
- WGK Germany3
欧盟法规
C&L通报上下游产品
CAS号1668-09-3 麦芽五糖 | CAS号3767-28-0 4-硝基苯-Α-D-葡吡喃糖苷 | CAS号74173-30-1 4-硝基苯基α-D-麦芽六糖苷 | CAS号3482-57-3 4-硝基苯基-β-D-纤维二糖苷 | CAS号66451-58-9 4-nitrophenyl α... | CAS号3767-28-0 4-硝基苯-Α-D-葡吡喃糖苷 | CAS号66068-37-9 4-硝基苯基aD-麦芽四糖苷 | CAS号14609-74-6 Phenol, 4-nitro...合成工艺路线路线简述
📜Maltopentaose,对硝基苯-α-D-葡萄糖吡喃苷置于phosphate Buffer,G4-Amylase体系中,用 水,二甲基亚砜 作为反应溶剂,化学反应 8.0H,以26 Mg的收率获得产物对硝基苯基麦芽五糖
参考文献:Maltotetraose-Forming,Amylase-Mediated,P-Nitrophenyl α-And β-Maltopentaoside Formation In An Aqueous-organic Solvent System: A Substrate For Human Amylase In Serum
标题:Maltotetraose-Forming,Amylase-Mediated,P-Nitrophenyl α-And β-Maltopentaoside Formation In An Aqueous-organic Solvent System: A Substrate For Human Amylase In Serum
摘要:
DOI:10.1016/0008-6215(91)84068-P
海关参考信息
- 2905122000-异丙醇
2905310000-1,2-乙二醇
2905320000-1,2-丙二醇
2905399001-1,3-丙二醇 - 💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
- 详情请参考：📖 海关编码查询和海关进出口税则
供应商参考报价(招募中)
品牌试剂参考报价(招募中)
📌 第三方产品分析报告
主要参考文献
参考标题:Systematic Synthesis Of Sulfur-ContainingP-Nitrophenyl α-Maltopentaoside Derivatives For A Differential Assay Of Human α-Amylases作者:Kaori Ozawa,Yukako Taki,Hideharu Ishida,Yukari Yamagata,Shinji Satomura,Makoto Kiso,Akira Hasegawa |发布日期:1993.1
摘要:For Use In A Differential Assay Of Human Alpha-Amylases, A Variety Of 6(5)-S-Substituted P-Nitrophenyl Alpha-Maltopentaoside Derivatives (6-54) Were Systematically Synthesized Via The Key Intermediate, P-Nitrophenyl O-(2,3-Di-O-Acetyl-6-S-Acetyl-4-O-Benzoyl-6-Thio-Alpha-D-Glucopyranosyl) - (-->4)-Tris[o-(2,3,6-Tri-O-Acetyl-Alpha-D-Glucopyranosyl)-(1-->4)]-2,3,6 -Tri-O-Acetyl-Alpha-D-Glucopyranoside
合成参考文献
参考文献:10.1016/0003-2697(92)90206-m
摘要:Usui T, Ogawa K, Nagai H, Matsui H. Enzymatic synthesis of p-nitrophenyl 4(5)-O-beta-D-galactosyl-alpha-maltopentaoside as a substrate for human alpha-amylases. Anal Biochem. 1992 Apr;202(1):61–7. doi: 10.1016/0003-2697(92)90206-m.
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