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p-Nitrophenyl 2,3-di-O-benzoyl-α-L-arabinopyranoside | 643758-65-0

中文名称
——
中文别名
——
英文名称
p-Nitrophenyl 2,3-di-O-benzoyl-α-L-arabinopyranoside
英文别名
p-Nitrophenyl 2,3-di-O-benzoyl-alpha-L-arabinopyranoside;[(2S,3R,4S,5S)-3-benzoyloxy-5-hydroxy-2-(4-nitrophenoxy)oxan-4-yl] benzoate
p-Nitrophenyl 2,3-di-O-benzoyl-α-L-arabinopyranoside化学式
CAS
643758-65-0
化学式
C25H21NO9
mdl
——
分子量
479.443
InChiKey
PXODJNRBUIQKGI-FUCAVZNHSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.1
  • 重原子数:
    35
  • 可旋转键数:
    8
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    137
  • 氢给体数:
    1
  • 氢受体数:
    9

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    苯甲酰氯对硝基苯基 alpha-L-阿拉伯吡喃糖苷乙酸乙酯 、 ethyl acetate heptane 作用下, 以 N,N-二甲基甲酰胺吡啶 为溶剂, 反应 16.0h, 以yielded 4 as a white powder (520 mg, 1.11 mmol, 29%)的产率得到p-Nitrophenyl 2,3-di-O-benzoyl-α-L-arabinopyranoside
    参考文献:
    名称:
    Engineered Enzymes and Their Use for Synthesis of Thioglycosides
    摘要:
    突变的糖苷酶中,活性位点中作为酸、碱或酸碱催化剂的氨基酸从羧酸转变为其他氨基酸(例如转变为简单的烷基,如丙氨酸或甘氨酸),可以催化硫代糖受体和活化供体的反应形成硫代糖苷。这些“硫代糖合酶”代表了突变酶的一类新型酶,也代表了本发明的第一个方面。可以根据本方法使用硫代糖受体和活化供体耦合形成硫代糖苷。通过选择供体和受体物种以及具体的酶,可以获得不同结构和立体化学的硫代糖苷。
    公开号:
    US20070004010A1
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文献信息

  • Engineered enzymes and their use for synthesis of thioglycosides
    申请人:Withers G Stephen
    公开号:US20060035342A1
    公开(公告)日:2006-02-16
    Mutant glycosidases in which the amino acid in the active site that serves as the acid, base or acid/base-catalyst is converted from a carboxylic acid to some other amino acid (for example to a simple alkyl, as in alanine or glycine) can catalyze the reaction of a thiosugar acceptor and an activated donor to form a thioglycoside. The “thioglycoligases” represent a novel class of mutant enzymes, and represent a first aspect of the invention. Thioglycoligases can be used in accordance with the method of the invention to couple a thiosugar acceptor and an activated donor to form a thioglycoside. By selection of the donor and acceptor species, as well as the specific enzyme employed, thioglycosides of different structure and stereochemistry can be obtained.
    突变的糖苷酶中,活性位点中作为酸、碱或酸碱催化剂的氨基酸从羧酸转变为其他氨基酸(例如转变为简单的烷基,如丙氨酸或甘氨酸),可以催化硫代糖受体和活化供体的反应,形成硫代糖苷。 "硫代糖聚合酶"代表一类新型突变酶,并代表本发明的第一个方面。可以根据本发明的方法使用硫代糖聚合酶将硫代糖受体和活化供体偶联形成硫代糖苷。通过选择供体和受体物种以及特定的酶,可以获得不同结构和立体化学的硫代糖苷。
  • [EN] ENGINEERED ENZYMES AND THEIR USE FOR SYNTHESIS OF THIOGLYCOSIDES<br/>[FR] ENZYMES MODIFIEES ET LEUR UTILISATION POUR LA SYNTHESE DE THIOGLYCOSIDES
    申请人:UNIV BRITISH COLUMBIA
    公开号:WO2004024908A1
    公开(公告)日:2004-03-25
    Mutant glycosidases in which the amino acid in the active site that serves as the acid, base or acid/base-catalyst is converted from a carboxylic acid to some other amino acid (for example to a simple alkyl, as in alanine or glycine) can catalyze the reaction of a thiosugar acceptor and an activated donor to form a thioglycoside. The 'thioglycoligases' represent a novel class of mutant enzymes, and represent a first aspect of the invention. Thioglycoligases can be used in accordance with the method of the invention to couple a thiosugar acceptor and an activated donor to form a thioglycoside. By selection of the donor and acceptor species, as well as the specific enzyme employed, thioglycosides of different structure and stereochemistry can be obtained.
  • Engineered Enzymes and Their Use for Synthesis of Thioglycosides
    申请人:Withers G. Stephen
    公开号:US20070004010A1
    公开(公告)日:2007-01-04
    Mutant glycosidases in which the amino acid in the active site that serves as the acid, base or acid/base-catalyst is converted from a carboxylic acid to some other amino acid (for example to a simple alkyl, as in alanine or glycine) can catalyze the reaction of a thiosugar acceptor and an activated donor to form a thioglycoside. The “thioglycoligases” represent a novel class of mutant enzymes, and represent a first aspect of the invention. Thioglycoligases can be used in accordance with the method of the invention to couple a thiosugar acceptor and an activated donor to form a thioglycoside. By selection of the donor and acceptor species, as well as the specific enzyme employed, thioglycosides of different structure and stereochemistry can be obtained.
    突变的糖苷酶中,活性位点中作为酸、碱或酸碱催化剂的氨基酸从羧酸转变为其他氨基酸(例如转变为简单的烷基,如丙氨酸或甘氨酸),可以催化硫代糖受体和活化供体的反应形成硫代糖苷。这些“硫代糖合酶”代表了突变酶的一类新型酶,也代表了本发明的第一个方面。可以根据本方法使用硫代糖受体和活化供体耦合形成硫代糖苷。通过选择供体和受体物种以及具体的酶,可以获得不同结构和立体化学的硫代糖苷。
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