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(+/-)-N-cyclohexyl-2-(2-(2-methoxy-4-morpholinophenylamino)-7-(4-methoxybenzyl)-5-methyl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-ylamino)benzenesulfonamide | 1312163-90-8

中文名称
——
中文别名
——
英文名称
(+/-)-N-cyclohexyl-2-(2-(2-methoxy-4-morpholinophenylamino)-7-(4-methoxybenzyl)-5-methyl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-ylamino)benzenesulfonamide
英文别名
N-cyclohexyl-2-[[2-(2-methoxy-4-morpholin-4-ylanilino)-7-[(4-methoxyphenyl)methyl]-5-methyl-5,6-dihydropyrrolo[2,3-d]pyrimidin-4-yl]amino]benzenesulfonamide
(+/-)-N-cyclohexyl-2-(2-(2-methoxy-4-morpholinophenylamino)-7-(4-methoxybenzyl)-5-methyl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-ylamino)benzenesulfonamide化学式
CAS
1312163-90-8
化学式
C38H47N7O5S
mdl
——
分子量
713.901
InChiKey
RKJDABDWWFAJCI-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):
    7.3
  • 重原子数:
    51
  • 可旋转键数:
    12
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    139
  • 氢给体数:
    3
  • 氢受体数:
    12

文献信息

  • TREATMENT OF DISEASES BY EPIGENETIC REGULATION
    申请人:McLure Kevin G.
    公开号:US20130281397A1
    公开(公告)日:2013-10-24
    The present disclosure provides non-naturally occurring polyphenol compounds that inhibit the bromodomain and extra terminal domain (BET) proteins. The disclosed compositions and methods can be used for treatment and prevention of cancer, including NUT midline carcinoma, Burkitt's Lymphoma, Acute Myelogenous Leukemia, and Multiple Myeloma; autoimmune or inflammatory diseases or conditions, and sepsis.
    本公开提供了抑制结构域和额外末端结构域(BET)蛋白的非天然存在的多化合物。所公开的组合物和方法可用于治疗和预防癌症,包括NUT中线癌、Burkitt淋巴瘤、急性髓系白血病和多发性骨髓瘤;自身免疫或炎症性疾病或症状,以及败血症。
  • 2,4-DIAMINO-6,7-DIHYDRO-5H-PYRROLO[2,3]PYRIMIDINE DERIVATIVES AS FAK/Pyk2 INHIBITORS
    申请人:Xiao Dengming
    公开号:US20130281438A1
    公开(公告)日:2013-10-24
    The invention relates to a novel class of 2,4-diamino-6,7-dihydro-5H-pyrrolo[2,3]pyrimidine derivatives as a FAK and/or Pyk2 inhibitor, to a process for their preparation, and to a composition thereof, as well as to use of the compounds for the inhibiting FAK and/or Pyk2 and method for the treatment of a FAK and/or Pyk2 mediated disorder or disease.
    本发明涉及一种新型的2,4-二基-6,7-二氢-5H-吡咯[2,3]嘧啶生物,作为FAK和/或Pyk2抑制剂,以及它们的制备方法、组合物和化合物用于抑制FAK和/或Pyk2以及治疗FAK和/或Pyk2介导的疾病或疾病的方法。
  • COMPOSITIONS AND THERAPEUTIC METHODS FOR ACCELERATED PLAQUE REGRESSION
    申请人:LEBIODA Kenneth Eugene
    公开号:US20160346291A1
    公开(公告)日:2016-12-01
    The invention comprises methods for treating and/or preventing cardiovascular, cholesterol, and lipid related disorders, including atherosclerosis, through-co-administration of therapeutically effective amounts of a compound of Formula I or a pharmaceutically acceptable salt thereof and rosuvastatin or pravastatin or a pharmaceutically acceptable salt of rosuvastatin or pitavastatin. The invention further provides compositions comprising a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt thereof and a therapeutically effective amount of or pitavastatin or a pharmaceutically acceptable salt of rosuvastatin or pitavastatin.
  • US9428508B2
    申请人:——
    公开号:US9428508B2
    公开(公告)日:2016-08-30
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