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8-(4-fluoro-2,6-dimethylphenylamino)-4-methyl-2H-phthalazin-1-one | 1072157-20-0

中文名称
——
中文别名
——
英文名称
8-(4-fluoro-2,6-dimethylphenylamino)-4-methyl-2H-phthalazin-1-one
英文别名
8-(4-fluoro-2,6-dimethylanilino)-4-methyl-2H-phthalazin-1-one
8-(4-fluoro-2,6-dimethylphenylamino)-4-methyl-2H-phthalazin-1-one化学式
CAS
1072157-20-0
化学式
C17H16FN3O
mdl
——
分子量
297.332
InChiKey
UCJHTOJQFVMALG-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):
    3.9
  • 重原子数:
    22
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    53.5
  • 氢给体数:
    2
  • 氢受体数:
    4

文献信息

  • TREATMENT OF FAMILIAL EXUDATIVE VITREORETINOPATHY THROUGH S1PR2 INHIBITION
    申请人:Dalhousie University
    公开号:EP3148550A1
    公开(公告)日:2017-04-05
  • [EN] BLOCKERS OF THE NOGO-A S1PR PATHWAY FOR THE TREATMENT OF DISEASES CHARACTERIZED BY NEURONAL DAMAGE AND LACK OF SUBSEQUENT REPAIR<br/>[FR] BLOQUEURS DE LA VOIX NOGO-A S1PR POUR LE TRAITEMENT DE MALADIES CARACTÉRISÉES PAR UNE LÉSION NEURONALE ET UN DÉFAUT DE RÉPARATION ULTÉRIEURE
    申请人:UNIV ZUERICH
    公开号:WO2012164103A2
    公开(公告)日:2012-12-06
    The present invention provides inhibitors capable of binding to a member of the S1PR receptor group comprised of S1PR2 and S1PR5 with a dissociation constant of 5x10-7 mol/l or smaller for treating neuronal damage, specifically an antibody, an antibody fragment, an antibody-like molecule, a nucleic acid aptamer or an oligopeptide with 6 to 30 amino acid residues in length. Similarly, an interfering RNA or an antisense modulator of gene expression of G13 or a member of the S1PR receptor group described above are provided for treating of neuronal damage.
  • [EN] TREATMENT OF FAMILIAL EXUDATIVE VITREORETINOPATHY THROUGH S1PR2 INHIBITION<br/>[FR] TRAITEMENT DE LA VITRÉORÉTINOPATHIE EXSUDATIVE FAMILIALE PAR INHIBITION DE S1PR2
    申请人:UNIV DALHOUSIE
    公开号:WO2015184541A1
    公开(公告)日:2015-12-10
    Methods and compositions are provided for the treatment of familial exudative vitreoretinopathy (FEVR) and retinopathy of prematurity (ROP) through the administration of a therapeutically effective amount of a Sphingosine-1-phosphate receptor type 2 (S1PR2) inhibitor.
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