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O-α-L-Fucopyranosyl-(1->2)-O-β-D-galactopyranosyl-(1->4)-O-<α-L-fucopyranosyl-(1->3)>-D-glucose | 34852-43-2

中文名称
——
中文别名
——
英文名称
O-α-L-Fucopyranosyl-(1->2)-O-β-D-galactopyranosyl-(1->4)-O-<α-L-fucopyranosyl-(1->3)>-D-glucose
英文别名
α-L-Fuc-(1->2)-β-D-Gal-(1->4)-D-Glc-(3->1)-α-L-Fuc;2',3-difucosyllactose;lactodifucotetraose;difucosyllactose;Fuc(α1-2)Gal(β1-4)[Fuc(α1-3)]Glc;O-α-L-Fucopyranosyl-(1->2)-O-β-D-galactopyranosyl-(1->4)-O-[α-L-fucopyranosyl-(1->3)]-D-glucose;Fuc(a1-2)Gal(b1-4)[Fuc(a1-3)]Glc;(2S,3S,4R,5S,6S)-2-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4R,5R)-5,6-dihydroxy-2-(hydroxymethyl)-4-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol
O-α-L-Fucopyranosyl-(1->2)-O-β-D-galactopyranosyl-(1->4)-O-<α-L-fucopyranosyl-(1->3)>-D-glucose化学式
CAS
34852-43-2;109959-08-2
化学式
C24H42O19
mdl
——
分子量
634.586
InChiKey
LKOHREGGXUJGKC-NTQZDHPLSA-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

物化性质

  • 沸点:
    930.8±65.0 °C(Predicted)
  • 密度:
    1.72±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -6.9
  • 重原子数:
    43
  • 可旋转键数:
    8
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    307
  • 氢给体数:
    12
  • 氢受体数:
    19

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:
    Benzyl O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->2)-O-(3-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-(1->4)-O-<2,3,4-tri-O-benzyl-α-L-fucopyranosyl-(1->3)>-2-O-benzyl-β-D-glucopyranoside 在 palladium on activated charcoal 氢气 作用下, 以 溶剂黄146 为溶剂, 反应 72.0h, 以86%的产率得到O-α-L-Fucopyranosyl-(1->2)-O-β-D-galactopyranosyl-(1->4)-O-<α-L-fucopyranosyl-(1->3)>-D-glucose
    参考文献:
    名称:
    Synthesis of lactodifucotetraose
    摘要:
    DOI:
    10.1016/s0008-6215(00)90765-1
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文献信息

  • [EN] CRYSTALLINE DIFUCOSYLLACTOSE<br/>[FR] DIFUCOSYLLACTOSE CRISTALLIN
    申请人:GLYCOM AS
    公开号:WO2016086947A1
    公开(公告)日:2016-06-09
    Crystalline difucosyllactose, useful in a pharmaceutical composition and a nutritional composition is disclosed. Also disclosed is a method of obtaining crystalline difucosyllactose by crystallisation from a mixture of water and one or more C1 - C4 alcohols and a method of synthesising difucosyllactose from suitably protected lactose and a glycosyl donor.
    本发明揭示了结晶二岐糖乳酸,其在制药组合物和营养组合物中有用。还揭示了一种从水和一种或多种C1-C4醇的混合物中通过结晶获得结晶二岐糖乳酸的方法,以及从适当保护的乳糖和糖基供体合成二岐糖乳酸的方法。
  • Acceptor Specificity of Different Length Constructs of Human Recombinant α1,3/4-Fucosyltransferases
    作者:Theodora de Vries、Cheryl A. Srnka、Monica M. Palcic、Stuart J. Swiedler、Dirk H. van den Eijnden、Bruce A. Macher
    DOI:10.1074/jbc.270.15.8712
    日期:1995.4
    activity toward glycoproteins, whereas chimeric Fuc-TIII and Fuc-TV had a decreased activity with glycosphingolipids, compared to the full-length enzymes. Unexpectedly, chimeric Fuc-TV exhibited a GDP-fucose hydrolyzing activity. In substrates with multiple acceptor sites, the preferred site of fucosylation was identified. Fuc-TIII and Fuc-TV catalyzed fucose transfer exclusively to OH-3 of glucose in
    在COS-7细胞中表达的重组全长,与膜结合的岩藻糖基转移酶的受体特异性以及α1,3-岩藻糖基转移酶(Fuc-T)III,Fuc-TIV和Fuc-的可溶性蛋白A嵌合形式电视被分析为各种寡糖,糖脂和糖蛋白底物。我们对全长酶的研究结果证实并扩展了先前的研究。然而,与全长酶相比,嵌合Fuc-Ts对糖蛋白的活性增加,而嵌合Fuc-TIII和Fuc-TV对糖鞘脂的活性却降低。出乎意料的是,嵌合的Fuc-TV表现出GDP-岩藻糖的水解活性。在具有多个受体位点的底物中,鉴定了岩藻糖基化的优选位点。1 H NMR光谱证实,Fuc-TIII和Fuc-TV分别催化将岩藻糖仅转移至乳糖N-新四糖和乳糖N-四糖中葡萄糖的OH-3上。薄层色谱免疫染色显示,FucT-IV首选nLc6Cer中的远端GlcNAc残基,而Fuc-TV则首选近端G1-cNAc残基。将Fuc-TIV或Fuc-TV与VI3NeuAcnLc6Cer
  • The cloning and expression of a human α-1,3 fucosyltransferase capable of forming the E-selectin ligand
    作者:Kari L. Koszdin、Benjamin R. Bowen
    DOI:10.1016/s0006-291x(05)81472-x
    日期:1992.8
    The polymerase chain reaction was used to amplify a novel fucosyltransferase cDNA (FucT-VI) from A431 and from HL60 cells. The amplified cDNA has a high degree of sequence identity to FucT-V and to FucT-III, and a much lower level of similarity to FucT-IV. Transfection of the FucT-VI gene into mammalian cells confers alpha-1,3 fucosyltransferase activity to the cells, resulting in cell surface expression of Lewis x and sialyl-Lewis x carbohydrates. In contrast to FucT-IV activity, FucT-VI catalyzes the transfer of fucose from GDP-beta-fucose to alpha-2,3 sialylated substrates. The substrate specificity of the FucT-VI gene product suggests that FucT-VI may be an enzyme involved in the biosynthesis of the E-Selectin ligand, sialyl-Lewis x, in myeloid cells.
  • Synthesis of lactodifucotetraose
    作者:Ken'ichi Takeo、Saimei Tei
    DOI:10.1016/s0008-6215(00)90765-1
    日期:1985.8
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