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N-[(E)-(3,4-dimethoxyphenyl)methylideneamino]-7-methylthieno[3,2-d]pyrimidin-4-amine

中文名称
——
中文别名
——
英文名称
N-[(E)-(3,4-dimethoxyphenyl)methylideneamino]-7-methylthieno[3,2-d]pyrimidin-4-amine
英文别名
——
N-[(E)-(3,4-dimethoxyphenyl)methylideneamino]-7-methylthieno[3,2-d]pyrimidin-4-amine化学式
CAS
——
化学式
C16H16N4O2S
mdl
——
分子量
328.4
InChiKey
VWEJHOAFYMZUKT-FBCYGCLPSA-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:
    23
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    96.9
  • 氢给体数:
    1
  • 氢受体数:
    7

文献信息

  • Thienopyrimidine-based inhibitors of the src family
    申请人:——
    公开号:US20040077663A1
    公开(公告)日:2004-04-22
    Various thienopyrimidine-based analog compounds are able to selectively inhibit the Src family of tyrosine kinases. These compounds are useful in the treatment of various diseases including hyperproliferative diseases, hematologic diseases, osteoporosis, neurological diseases, autoimmune diseases, allergic/immunological diseases, or viral infections.
    各种基于噻唑嘧啶的类似化合物能够选择性地抑制Src家族的酪氨酸激酶。这些化合物在治疗各种疾病方面非常有用,包括增生性疾病、血液学疾病、骨质疏松症、神经系统疾病、自身免疫疾病、过敏/免疫疾病或病毒感染。
  • METHODS FOR TREATING TYROSINE-KINASE-INHIBITOR-RESISTANT MALIGNANCIES IN PATIENTS WITH GENETIC POLYMORPHISMS OR AHI1 DYSREGULATIONS OR MUTATIONS EMPLOYING DIANHYDROGALACTITOL, DIACETYLDIANHYDROGALACTITOL, DIBROMODULCITOL, OR ANALOGS OR DERIVATIVES THEREOF
    申请人:Del Mar Pharmaceuticals
    公开号:EP2872161A2
    公开(公告)日:2015-05-20
  • DIANHYDROGALACTITOL FOR USE IN TREATING TYROSINE-KINASE-INHIBITOR-RESISTANT MALIGNANCIES IN PATIENTS WITH GENETIC POLYMORPHISMS OR AHI1 DYSREGULATIONS OR MUTATIONS
    申请人:Del Mar Pharmaceuticals
    公开号:EP2872161B1
    公开(公告)日:2020-12-16
  • METHODS FOR TREATING A CANCER RESISTANT TO AT LEAST ONE TYROSINE KINASE INHIBITOR
    申请人:Del Mar Pharmaceuticals (BC) Ltd.
    公开号:US20210251944A1
    公开(公告)日:2021-08-19
    Methods and compositions suitable for the treatment of malignancies in subjects with a germline deletion polymorphism that blocks the activity of thymidine kinase inhibitors in triggering apoptosis in tumor cells or in subjects having a mutation in or a dysregulation of the AHI-1 gene are disclosed. These methods employ an alkylating hexitol derivative such as dianhydrogalactitol, a derivative or analog of dianhydrogalactitol, diacetyldianhydrogalactitol, a derivative or analog of diacetyldianhydrogalactitol, dibromodulcitol, and a derivative or analog of dibromodulcitol. The compositions can include such alkylating hexitol derivatives. The methods can further include administration of a BH3 mimetic, and the compositions can further include a BH3 mimetic. In subjects having a dysregulation of the AHI-1 gene, the methods can further include the administration of an agent modulating the expression or activity of the AHI-1 gene or AHI-1 protein, and the compositions can further include such an agent.
  • US6503914B1
    申请人:——
    公开号:US6503914B1
    公开(公告)日:2003-01-07
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