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N-[(2S,5S)-5-[(2S,5S)-3-acetamido-5-[(2S,5R)-3,5-dihydroxy-4-[(2S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[(2S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-2-methyloxan-3-yl]acetamide

中文名称
——
中文别名
——
英文名称
N-[(2S,5S)-5-[(2S,5S)-3-acetamido-5-[(2S,5R)-3,5-dihydroxy-4-[(2S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[(2S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-2-methyloxan-3-yl]acetamide
英文别名
——
N-[(2S,5S)-5-[(2S,5S)-3-acetamido-5-[(2S,5R)-3,5-dihydroxy-4-[(2S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[(2S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-2-methyloxan-3-yl]acetamide化学式
CAS
——
化学式
C35H60N2O25
mdl
——
分子量
908.8
InChiKey
IIQYNFQCNRIEQO-CYJQVKIKSA-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):
    -9.7
  • 重原子数:
    62
  • 可旋转键数:
    15
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.94
  • 拓扑面积:
    425
  • 氢给体数:
    16
  • 氢受体数:
    25

文献信息

  • GLYCOSYLATED POLYPEPTIDE AND PHARMACEUTICAL COMPOSITION CONTAINING SAME
    申请人:Glytech, Inc.
    公开号:EP2762489A1
    公开(公告)日:2014-08-06
    The object of the present invention is to provide a glycosylated polypeptide having uniform sugar chain structure which has interferon β activity. It was found that a glycosylated polypeptide having uniform sugar chain structure as well as having interferon β activity can be prepared by a method comprising a step of synthesizing a glycosylated peptide fragment and at least two peptide fragments and a step of linking the glycosylated peptide fragment and the at least two peptide fragments.
    本发明的目的是提供一种具有均匀糖链结构、具有干扰素β活性的糖基化多肽。研究发现,具有均匀糖链结构并具有干扰素 β 活性的糖基化多肽可通过以下方法制备:合成糖基化多肽片段和至少两个多肽片段的步骤,以及连接糖基化多肽片段和至少两个多肽片段的步骤。
  • Glycosylated polypeptide and pharmaceutical composition containing same
    申请人:GLYTECH, INC.
    公开号:US10358470B2
    公开(公告)日:2019-07-23
    The object of the present invention is to provide a glycosylated polypeptide having uniform sugar chain structure which has interferon β activity. It was found that a glycosylated polypeptide having uniform sugar chain structure as well as having interferon β activity can be prepared by a method comprising a step of synthesizing a glycosylated peptide fragment and at least two peptide fragments and a step of linking the glycosylated peptide fragment and the at least two peptide fragments.
    本发明的目的是提供一种具有均匀糖链结构、具有干扰素β活性的糖基化多肽。研究发现,具有均匀糖链结构并具有干扰素 β 活性的糖基化多肽可通过以下方法制备:合成糖基化多肽片段和至少两个多肽片段的步骤,以及连接糖基化多肽片段和至少两个多肽片段的步骤。
  • HEMOSTATIC PHARMACEUTICAL COMPOSITION
    申请人:OTSUKA CHEMICAL CO., LTD.
    公开号:US20170119844A1
    公开(公告)日:2017-05-04
    The object of the present invention is to provide a hemostatic pharmaceutical composition that has higher usability compared to a hemostatic agent employing conventional biogels and may form a transparent and homogeneous hydrogel in a broad pH. The present invention provides a hemostatic pharmaceutical composition comprising a sugar chain-polypeptide complex characterized in that said polypeptide in said sugar chain-polypeptide complex is a polypeptide comprising an amino acid sequence in which polar and nonpolar amino acid residues are alternately arranged, and one or more sugar chains are bound to said polypeptide.
  • IL-2 VARIANT
    申请人:Kyowa Kirin Co., Ltd.
    公开号:US20210060169A1
    公开(公告)日:2021-03-04
    An object of the present invention is to provide a novel IL-2 variant which has improved selectivity for IL-2R αβγ and selectively activates Tregs. The present invention relates to an IL-2 variant, a method for producing the IL-2 variant, a composition and a therapeutic agent for an immune disease, comprising the IL-2 variant, a method for increasing selectivity of IL-2 for IL-2Rαβγ, a method for improving an affinity of IL-2 for an IL-2Rα subunit, a method of reducing an affinity of IL-2 for at least one of an IL-2Rβ subunit and an IL-2Rγ subunit, and a method for selectively activating regulatory T cells.
  • US9708413B2
    申请人:——
    公开号:US9708413B2
    公开(公告)日:2017-07-18
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