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(5S,6R,7E,9E,11Z,13E,15S)-5,6,15-trihydroxy-15-methylicosa-7,9,11,13-tetraenoic acid

中文名称
——
中文别名
——
英文名称
(5S,6R,7E,9E,11Z,13E,15S)-5,6,15-trihydroxy-15-methylicosa-7,9,11,13-tetraenoic acid
英文别名
——
(5S,6R,7E,9E,11Z,13E,15S)-5,6,15-trihydroxy-15-methylicosa-7,9,11,13-tetraenoic acid化学式
CAS
——
化学式
C21H34O5
mdl
——
分子量
366.5
InChiKey
YATRXCCXYFPYPD-IFAWBJONSA-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):
    3.3
  • 重原子数:
    26
  • 可旋转键数:
    14
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    98
  • 氢给体数:
    4
  • 氢受体数:
    5

文献信息

  • Lipoxin compounds
    申请人:The Brigham and Women's Hospital, Inc.
    公开号:EP2107050A1
    公开(公告)日:2009-10-07
    Compounds having the active site of natural lipoxins, but a longer tissue half-life are disclosed. These small molecules are useful for treating vasoconstrictive, inflammatory, myeloid suppressive, cardiovascular, and gastrointestinal diseases.
    本研究公开了具有天然脂毒素活性位点但组织半衰期更长的化合物。这些小分子化合物可用于治疗血管收缩性疾病、炎症性疾病、骨髓抑制性疾病、心血管疾病和胃肠道疾病。
  • Use of lipoxin analogs to promote cell defense against gram-negative infections
    申请人:The Brigham and Women's Hospital
    公开号:EP1941875B1
    公开(公告)日:2012-09-12
  • Modulation of Inflammation Related to Columnar Epithelia
    申请人:Madara L. James
    公开号:US20080064660A1
    公开(公告)日:2008-03-13
    This invention provides pharmaceutical compositions containing lipoxin compounds and therapeutic uses for the compounds in treating or preventing a disease or condition associated with columnar epithelial inflammation. The invention also discloses methods for screening for compounds useful in preventing columnar epithelial inflammation.
  • Lipoxin Analogs as Novel Inhibitors of Angiogenesis
    申请人:Serhan N. Charles
    公开号:US20080064749A1
    公开(公告)日:2008-03-13
    The present invention is directed to methods for the prevention or inhibition of angiogenesis. The method is accomplished by the administration of an effective amount of 15-epi-16-(para-fluoro)-phenoxy-lipoxin A 4 , LXA 4 , 15-epi-LXA 4 or 15-R/S-methyl, LXA 4 and pharmaceutically acceptable salts, esters, amides, carboxylic acids, or prodrugs thereof, to a subject in need thereof. As a consequence of the action of the therapeutic agent, angiogenesis is prevented or inhibited in the subject.
  • Novel Approach to Anti-Microbial Host Defense with Molecular Shields with Lipoxin Compounds
    申请人:Serhan Charles N.
    公开号:US20080214665A1
    公开(公告)日:2008-09-04
    Methods to cause tissue, such as mucosal cells, to express increased amounts of bactericidal permeability increasing protein (BPI) are described. The BPI inducing agents include, for example, lipoxin compounds.
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