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Cambridge id 5341535

中文名称
——
中文别名
——
英文名称
Cambridge id 5341535
英文别名
4-[4-(3,4-dimethoxyphenyl)-6-phenylpyrimidin-2-yl]morpholine
Cambridge id 5341535化学式
CAS
——
化学式
C22H23N3O3
mdl
——
分子量
377.4
InChiKey
KMTWCUXXCYMLNV-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):
    3.6
  • 重原子数:
    28
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    56.7
  • 氢给体数:
    0
  • 氢受体数:
    6

文献信息

  • HEPARAN SULFATE INHIBITORS
    申请人:Zacharon Pharmaceuticals, Inc.
    公开号:EP2307440A2
    公开(公告)日:2011-04-13
  • [EN] HEPARAN SULFATE INHIBITORS<br/>[FR] INHIBITEURS D'HÉPARANE SULFATE
    申请人:ZACHARON PHARMACEUTICALS INC
    公开号:WO2010003023A2
    公开(公告)日:2010-01-07
    Provided herein are heparan sulfate inhibitors, including modulators of heparan sulfate glycosylation, heparan sulfate sulfation, and/or heparan sulfate epimerization.
  • [EN] COMPOSITIONS AND METHODS FOR THE TREATMENT AND PREVENTION OF NEUROLOGICAL DISORDERS<br/>[FR] COMPOSITIONS ET MÉTHODES DE TRAITEMENT ET DE PRÉVENTION DE TROUBLES NEUROLOGIQUES
    申请人:YUMANITY THERAPEUTICS INC
    公开号:WO2021252895A2
    公开(公告)日:2021-12-16
    The invention provides compositions and methods for treating neurological disorders, such as amyotrophic lateral sclerosis, frontotemporal degeneration, and Alzheimer's disease, among others. Using the compositions and methods described herein, a patient having a neurological disorder, such as a neurological disorder associated with TAR-DNA binding protein (TDP)-43 aggregation, may be administered an inhibitor of FYVE-type zinc finger containing phosphoinositide kinase (PIKfyve) so as to treat an underlying etiology of the disorder and/or to alleviate one or more symptoms of the disease. The inhibitor of PIKfyve may be a small molecule, an anti-PIKfyve antibody or antigen-binding fragment thereof, or a compound, such as an interfering RNA molecule, that attenuates PIKfyve expression. Patients that may be treated using the compositions and methods described herein include those that express are susceptible to developing TDP-43- mediated aggregation and toxicity.
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