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11-amino-5,6-dihydronaphtho<1',2':4,5>thieno<2,3-d>pyrimidine | 4994-90-5

中文名称
——
中文别名
——
英文名称
11-amino-5,6-dihydronaphtho<1',2':4,5>thieno<2,3-d>pyrimidine
英文别名
5,6-dihydro-naphtho[1',2':4,5]thieno[2,3-d]pyrimidin-11-ylamine;4-Amino-9,10-dihydro-naphtho<1,2-d>-pyrimido<4.5-b>thiophen;11-Amino-5,6-dihydronaphtho[1',2':4,5]thieno[2,3-d]pyrimidine;11-thia-13,15-diazatetracyclo[8.7.0.02,7.012,17]heptadeca-1(10),2,4,6,12,14,16-heptaen-16-amine
11-amino-5,6-dihydronaphtho<1',2':4,5>thieno<2,3-d>pyrimidine化学式
CAS
4994-90-5
化学式
C14H11N3S
mdl
——
分子量
253.327
InChiKey
ZDSPMRXGMLUWHG-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):
    3.2
  • 重原子数:
    18
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    80
  • 氢给体数:
    1
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Thienopyrimidine Ureas as Novel and Potent Multitargeted Receptor Tyrosine Kinase Inhibitors
    摘要:
    A series of novel thienopyrimidine-based receptor tyrosine kinase inhibitors has been discovered. Investigation of structure-activity relationships at the 5- and 6-positions of the thienopyrimidine nucleus led to a series of N,N '-diaryl ureas that potently inhibit all of the vascular endothelial growth factor (VEGF) and platelet-derived growth factor (PDGF) receptor tyrosine kinases. A kinase insert domain-containing receptor (KDR) homology model suggests that these compounds bind to the "inactive conformation" of the enzyme with the urea portion extending into the back hydrophobic pocket adjacent to the adenosine 5 '-triphosphate (ATP) binding site. A number of compounds have been identified as displaying excellent in vivo potency. In particular, compounds 28 and 76 possess favorable pharmacokinetic (PK) profiles and demonstrate potent antitumor efficacy against the HT1080 human fibrosarcoma xenograft tumor growth model (tumor growth inhibition (TGI) = 75% at 25 mg/kg-day, per os (po)).
    DOI:
    10.1021/jm050458h
  • 作为产物:
    描述:
    11-amino-5,6-dihydronaphtho<1',2':4,5>thieno<2,3-d>pyrimidine-10-oxide三氯化磷 作用下, 以 氯仿 为溶剂, 反应 3.0h, 以78%的产率得到11-amino-5,6-dihydronaphtho<1',2':4,5>thieno<2,3-d>pyrimidine
    参考文献:
    名称:
    Some transformations of 1-(1,2,3,4-tetrahydronaphthylidene)-malononitrile or cyanoacetate
    摘要:
    DOI:
    10.1007/bf00809775
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文献信息

  • Taylor,E.C.; Berger,J.G., Angewandte Chemie, 1966, vol. 78, p. 144
    作者:Taylor,E.C.、Berger,J.G.
    DOI:——
    日期:——
  • RAJCA, ANDRZEJ;TISLER, MIHA, MONATSH. CHEM., 121,(1990) N-9, C. 697-701
    作者:RAJCA, ANDRZEJ、TISLER, MIHA
    DOI:——
    日期:——
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