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1-(1H-Imidazol-1-yl)ethyl tetradecanoate | 562069-47-0

中文名称
——
中文别名
——
英文名称
1-(1H-Imidazol-1-yl)ethyl tetradecanoate
英文别名
1-imidazol-1-ylethyl tetradecanoate
1-(1H-Imidazol-1-yl)ethyl tetradecanoate化学式
CAS
562069-47-0
化学式
C19H34N2O2
mdl
——
分子量
322.5
InChiKey
LINNUSCVVYVOLU-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):
    6.6
  • 重原子数:
    23
  • 可旋转键数:
    15
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.79
  • 拓扑面积:
    44.1
  • 氢给体数:
    0
  • 氢受体数:
    3

文献信息

  • Method and composition for preventing pain in sickle cell patients
    申请人:——
    公开号:US20040072796A1
    公开(公告)日:2004-04-15
    A method of preventing pain in a sickle cell patient is disclosed. The method includes orally administering to the patient, an amount of an active agent effective on oral administration to inhibit binding of the patient's sickle erythrocytes to P-selectin on the patient's vascular endothelium. The inhibition may be evidenced in a number of ways. The active agent administration inhibits the adhesion of sickle erythrocytes to vascular endothelium in the patient, thereby preventing patient pain associated with vascular occlusion. Also disclosed are compositions useful in practicing the method.
    本发明公开了一种预防镰状细胞患者疼痛的方法。该方法包括向患者口服一定量的活性剂,口服后可有效抑制患者镰状红细胞与患者血管内皮上的 P-选择素结合。抑制作用可通过多种方式体现。活性剂给药可抑制镰状红细胞与患者血管内皮的粘附,从而防止患者因血管闭塞而产生疼痛。还公开了用于实施本方法的组合物。
  • METHOD AND COMPOSITION FOR PREVENTING PAIN IN SICKLE CELL PATIENTS
    申请人:Embury, Stephen H.
    公开号:EP1542704A1
    公开(公告)日:2005-06-22
  • HEPARIN COMPOSTIONS AND SELECTIN INHIBITION
    申请人:The Regents of the University of California, Office of Technology Transfer, University of California
    公开号:EP1906974A2
    公开(公告)日:2008-04-09
  • Heparin compositions and selectin inhibition
    申请人:Varki Ajit
    公开号:US20070021378A1
    公开(公告)日:2007-01-25
    The disclosure provides in vitro and in vivo methods for identifying Heparins and Heparinoids that modulate the activity of selecting. The disclosure also provides Heparins and Heparinoids that modulate the activity of selecting. The identification and isolation of these heparin formulations has the potential to mediate a wide variety of pathologies mediated by P- and/or L-selectin, including hematogenous metastasis, diseases associated with inflammation (e.g., asthma, arthritis, allergic dermatitis), ischemia-reperfusion injury, or other pathologies such as sickle cell anemia. Selectin inhibition can be achieved at plasma concentrations lower than those that cause excessive anticoagulation or unwanted bleeding in a human subject.
  • Heparin Compositions and Selectin Inhibition
    申请人:Varki Ajit
    公开号:US20100081630A1
    公开(公告)日:2010-04-01
    The disclosure provides in vitro and in vivo methods for identifying Heparins and Heparinoids that modulate the activity of selectins. The disclosure also provides Heparins and Heparinoids that modulate the activity of selectins. The identification and isolation of these heparin formulations has the potential to mediate a wide variety of pathologies mediated by P- and/or L-selectin, including hematogenous metastasis, diseases associated with inflammation (e.g., asthma, arthritis, allergic dermatitis), ischemia-reperfusion injury, or other pathologies such as sickle cell anemia. Selectin inhibition can be achieved at plasma concentrations lower than those that cause excessive anticoagulation or unwanted bleeding in a human subject.
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