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methyl 2-acetamido-2-deoxy-4-O-(3-[4-methoxy-2,3,5 ,6-tetrafluorobenzamido]-3-deoxy-β-D-galactopyranosyl)-β-D-glucopyranoside

中文名称
——
中文别名
——
英文名称
methyl 2-acetamido-2-deoxy-4-O-(3-[4-methoxy-2,3,5 ,6-tetrafluorobenzamido]-3-deoxy-β-D-galactopyranosyl)-β-D-glucopyranoside
英文别名
N-[(2S,3R,4S,5R,6R)-2-[(2R,3S,4R,5R,6R)-5-acetamido-4-hydroxy-2-(hydroxymethyl)-6-methoxyoxan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]-2,3,5,6-tetrafluoro-4-methoxybenzamide
methyl 2-acetamido-2-deoxy-4-O-(3-[4-methoxy-2,3,5 ,6-tetrafluorobenzamido]-3-deoxy-β-D-galactopyranosyl)-β-D-glucopyranoside化学式
CAS
——
化学式
C23H30F4N2O12
mdl
——
分子量
602.491
InChiKey
SGIMAQIHRYNHIZ-HLKZTURFSA-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):
    -2.2
  • 重原子数:
    41
  • 可旋转键数:
    9
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.65
  • 拓扑面积:
    206
  • 氢给体数:
    7
  • 氢受体数:
    16

文献信息

  • Inhibitors against galectins
    申请人:——
    公开号:US20040147730A1
    公开(公告)日:2004-07-29
    The present invention relates to novel compounds, the use of said compounds as a medicament as well as for the manufacture of a medicament for treatment of disorders relating to the binding of galectin to receptors in a mammal. Said galectin is preferably a galectin 3.
    本发明涉及新型化合物,所述化合物的用途为药物,并用于制造治疗哺乳动物中与galectin与受体结合有关的疾病的药物。所述galectin优选为galectin 3。
  • Immunomodulating compositions and uses therefor
    申请人:Ralph, Stephen John
    公开号:EP2591786A1
    公开(公告)日:2013-05-15
    The present invention discloses immunomodulating compositions. More particularly, the present invention discloses compositions comprising an immune-modulating agent and a lectin-interactive agent, which are useful for stimulating and prolonging host immune cell responses. The compositions of the present invention are particularly useful in the treatment and/or prophylaxis of a range of conditions including pathogenic infections, autoimmune diseases, transplant rejection, graft versus host disease, allergies, inflammatory disease, as well as cancers and tumours.
    本发明公开了免疫调节组合物。更具体地说,本发明公开了包含免疫调节剂和凝集素活性剂的组合物,这些组合物有助于刺激和延长宿主免疫细胞反应。本发明的组合物特别适用于治疗和/或预防一系列疾病,包括病原体感染、自身免疫性疾病、移植排斥反应、移植物抗宿主疾病、过敏、炎症性疾病以及癌症和肿瘤。
  • Immunomodulating Compositions and uses Therefor
    申请人:Ralph John Stephen
    公开号:US20070207161A1
    公开(公告)日:2007-09-06
    The present invention discloses immunomodulating compositions. More particularly, the present invention discloses compositions comprising an immune-modulating agent and a lectin-interactive agent, which are useful for stimulating and prolonging host immune cell responses. The compositions of the present invention are particularly useful in the treatment and/or prophylaxis of a range of conditions including pathogenic infections, autoimmune diseases, transplant rejection, graft versus host disease, allergies, inflammatory disease, as well as cancers and tumours.
  • IMMUNOMODULATING COMPOSITIONS AND USES THEREFOR
    申请人:Ralph Stephen John
    公开号:US20150265701A1
    公开(公告)日:2015-09-24
    The present invention discloses immunomodulating compositions. More particularly, the present invention discloses compositions comprising an immune-modulating agent and a lectin-interactive agent, which are useful for stimulating and prolonging host immune cell responses. The compositions of the present invention are particularly useful in the treatment and/or prophylaxis of a range of conditions including pathogenic infections, autoimmune diseases, transplant rejection, graft versus host disease, allergies, inflammatory disease, as well as cancers and tumours.
  • Methods, compositions and kits for treating, modulating, or preventing ocular angiogenesis or fibrosis in a subject using a galectin protein inhibitor
    申请人:TUFTS UNIVERSITY
    公开号:US20150320782A1
    公开(公告)日:2015-11-12
    Methods and kits using a pharmaceutical composition for use in inhibiting ocular angiogenesis or fibrosis are provided herein, such that composition includes a pharmaceutically suitable carrier or diluent and an amount of the inhibitor composition effective to inhibit the angiogenesis or the fibrosis by inhibiting expression and/or activity of a galectin protein or a portion thereof.
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