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2,3-diphenoxypropan-1-ol | 6735-31-5

中文名称
——
中文别名
——
英文名称
2,3-diphenoxypropan-1-ol
英文别名
——
2,3-diphenoxypropan-1-ol化学式
CAS
6735-31-5
化学式
C15H16O3
mdl
——
分子量
244.29
InChiKey
XXZWTWDRESTZKU-UHFFFAOYSA-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):
    2.9
  • 重原子数:
    18
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    38.7
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    2,3-diphenoxypropan-1-ol 、 2,3,4,6-四-O-乙酰基-α-D-吡喃甘露糖 三氯乙酰亚胺酯 在 三氟甲磺酸三甲基硅酯 作用下, 以 二氯甲烷 为溶剂, 反应 24.5h, 以20%的产率得到2,3-diphenoxypropan-1-yl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside
    参考文献:
    名称:
    Monovalent mannose-based DC-SIGN antagonists: Targeting the hydrophobic groove of the receptor
    摘要:
    Dendritic cell-specific, intercellular adhesion molecule-3-grabbing non-integrin (DC-SIGN) is a C-type lectin expressed specifically on dendritic cells. It is a primary site for recognition and binding of various pathogens and thus a promising therapeutic target for inhibition of pathogen entry and subsequent prevention of immune defense cell infection. We report the design and synthesis of D-mannose-based DC-SIGN antagonists bearing diaryl substituted 1,3-diaminopropanol or glycerol moieties incorporated to target the hydrophobic groove of the receptor. The designed glycomimetics were evaluated by in vitro assay of the isolated DC-SIGN extracellular domain for their ability to compete with HIV-1 gp120 for binding to the DC-SIGN carbohydrate recognition domain. Compounds 14d and 14e, that display IC50 values of 40 mu M and 50 mu M, are among the most potent monovalent DC-SIGN antagonists reported. The antagonistic effect of all the synthesized compounds was further evaluated by a one-point in vitro assay that measures DC adhesion. Compounds 14d, 14e, 18d and 18e were shown to act as functional antagonists of DC-SIGN-mediated DC adhesion. The binding mode of 14d was also studied by molecular docking and molecular dynamics simulation, which revealed flexibility of 14d in the binding site and provides a basis for further optimization. (C) 2014 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2014.01.047
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文献信息

  • Verwendung von alkoxylierten Verbindungen als nichtionische Emulgatorkomponente in Pflanzenschutzmittelformulierungen
    申请人:BASF Aktiengesellschaft
    公开号:EP0050228B1
    公开(公告)日:1984-01-04
  • US3954690A
    申请人:——
    公开号:US3954690A
    公开(公告)日:1976-05-04
  • US4025479A
    申请人:——
    公开号:US4025479A
    公开(公告)日:1977-05-24
  • US4036862A
    申请人:——
    公开号:US4036862A
    公开(公告)日:1977-07-19
  • US4265745A
    申请人:——
    公开号:US4265745A
    公开(公告)日:1981-05-05
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