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2-((4-amino-3-(4-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)-5-bromo-3-(2-chlorobenzyl)-5-(5-hydroxypent-1-ynyl)quinazolin-4(3H)-one | 1293914-93-8

中文名称
——
中文别名
——
英文名称
2-((4-amino-3-(4-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)-5-bromo-3-(2-chlorobenzyl)-5-(5-hydroxypent-1-ynyl)quinazolin-4(3H)-one
英文别名
2-((4-Amino-3-(4-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)-3-(2-chloro benzyl)-5-(5-hydroxypent-1-ynyl)quinazolin-4(3H)-one;2-((4-amino-3-(4-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)-3-(2-chlorobenzyl)-5-(5-hydroxypent-1-ynyl)quinazolin-4(3H)-one;2-[[4-Amino-3-(4-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-3-[(2-chlorophenyl)methyl]-5-(5-hydroxypent-1-ynyl)quinazolin-4-one
2-((4-amino-3-(4-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)-5-bromo-3-(2-chlorobenzyl)-5-(5-hydroxypent-1-ynyl)quinazolin-4(3H)-one化学式
CAS
1293914-93-8
化学式
C32H26ClN7O3
mdl
——
分子量
592.057
InChiKey
DFYDLTALGVPURS-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

物化性质

  • 沸点:
    891.1±75.0 °C(Predicted)
  • 密度:
    1.43±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.4
  • 重原子数:
    43
  • 可旋转键数:
    8
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.16
  • 拓扑面积:
    143
  • 氢给体数:
    3
  • 氢受体数:
    8

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Dosing regime and formulations for type B adenovirus
    申请人:PSIOXUS THERAPEUTICS LIMITED
    公开号:US11173186B2
    公开(公告)日:2021-11-16
    A method of treating a human patient comprising systemically administering multiple doses of a parenteral formulation of a replication capable oncolytic adenovirus of subgroup B in a single treatment cycle, wherein the total dose given in each dose is in the range of 1×1010 to 1×1014 viral particles, and wherein each dose of virus is administered over a period of 1 to 90 minutes, for example at a rate of viral particle delivery in the range of 2×1010 particles per minute to 2×1012 particles per minute. Also provided are formulations of the oncolytic adenoviruses and combination therapies of the viruses and formulations with other therapeutic agents.
    一种治疗人类患者的方法,包括在一个治疗周期内全身给药多个剂量的B亚群具有复制能力的溶瘤腺病毒的肠外制剂,其中每次给药的总剂量在1×1010至1×1014个病毒颗粒的范围内,每次给药的时间为1至90分钟,例如,病毒颗粒的递送速度在每分钟2×1010个颗粒至每分钟2×1012个颗粒的范围内。还提供了溶瘤腺病毒的制剂以及病毒和制剂与其他治疗剂的组合疗法。
  • QUINAZOLIN-4(3H)-ONE DERIVATIVES USED AS PI3 KINASE INHIBITORS
    申请人:Respivert Limited
    公开号:EP2491037B1
    公开(公告)日:2014-04-30
  • A DOSING REGIME AND FORMULATIONS FOR TYPE B ADENOVIRUSES
    申请人:Psioxus Therapeutics Limited
    公开号:EP3007711B1
    公开(公告)日:2020-10-21
  • A Dosing Regime and Formulations for Type B Adenovirus
    申请人:PSIOXUS THERAPEUTICS LIMITED
    公开号:US20160120922A1
    公开(公告)日:2016-05-05
    The present disclosure provides a method of treating a human patient comprising the steps of: systemically administering multiple doses of a parenteral formulation of a replication capable oncolytic adenovirus of subgroup B in a single treatment cycle, wherein the total dose given in each dose is in the range of 1×10 10 to 1×10 14 viral particles, and wherein each dose of virus is administered over a period of 1 to 90 minutes, for example at a rate of viral particle delivery in the range of 2×10 10 particles per minute to 2×10 12 particles per minute. The disclosure further extends to formulations of the said oncolytic adenoviruses and combination therapies of the viruses and formulations with other therapeutic agents.
  • DOSING REGIME AND FORMULATIONS FOR TYPE B ADENOVIRUSES
    申请人:PSIOXUS THERAPEUTICS LIMITED
    公开号:US20220054563A1
    公开(公告)日:2022-02-24
    The present disclosure provides a method of treating a human patient comprising the steps of: systemically administering multiple doses of a parenteral formulation of a replication capable oncolytic adenovirus of subgroup B in a single treatment cycle, wherein the total dose given in each dose is in the range of 1×10 10 to 1×10 14 viral particles, and wherein each dose of virus is administered over a period of 1 to 90 minutes, for example at a rate of viral particle delivery in the range of 2×10 10 particles per minute to 2×10 12 particles per minute. The disclosure further extends to formulations of the said oncolytic adenoviruses and combination therapies of the viruses and formulations with other therapeutic agents.
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