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1,2,3,5-Tetrafluoro-4-methyl-6-[(2-methylpropan-2-yl)oxy]benzene

中文名称
——
中文别名
——
英文名称
1,2,3,5-Tetrafluoro-4-methyl-6-[(2-methylpropan-2-yl)oxy]benzene
英文别名
1,2,3,5-tetrafluoro-4-methyl-6-[(2-methylpropan-2-yl)oxy]benzene
1,2,3,5-Tetrafluoro-4-methyl-6-[(2-methylpropan-2-yl)oxy]benzene化学式
CAS
——
化学式
C11H12F4O
mdl
——
分子量
236.21
InChiKey
CCYNNMVXRNDOIR-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):
    3.6
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    5

文献信息

  • BIFUNCTIONAL CYTOTOXIC AGENTS CONTAINING THE CTI PHARMACOPHORE
    申请人:Pfizer Inc.
    公开号:US20160271270A1
    公开(公告)日:2016-09-22
    The present invention is directed to novel bifunctional CTI-CTI and CBI-CTI dimers of the formula: F 1 -L 1 -T-L 2 -F 2 where F 1 , L 1 , T, L 2 and F 2 are as defined herein, useful for the treatment for proliferative diseases, where the inventive dimers can function as stand-alone drugs, payloads in antibody-drug-conjugates (ADCs), and linker-payload compounds useful in connection with the production or administration of such ADCs; and to compositions including the aforementioned dimers, linker-payloads and ADCs, and methods for using these dimers, linker-payloads and ADCs, to treat pathological conditions including cancer.
    本发明涉及新颖的具有双重功能的CTI-CTI和CBI-CTI二聚物,其公式为: F1-L1-T-L2-F2 其中F1、L1、T、L2和F2如本文所述定义,用于治疗增殖性疾病,其中发明的二聚物可以作为独立药物、抗体药物偶联物(ADCs)中的有效载荷以及与生产或施用此类ADCs相关的连接器有效载荷化合物;以及包括前述二聚物、连接器有效载荷和ADCs的组合物,以及使用这些二聚物、连接器有效载荷和ADCs治疗包括癌症在内的病理状况的方法。
  • BIFUNCTIONAL CYTOTOXIC AGENTS
    申请人:Pfizer Inc.
    公开号:US20150209445A1
    公开(公告)日:2015-07-30
    Cytotoxic dimers comprising CBI-based and/or CPI-based sub-units, antibody drug conjugates comprising such dimers, and to methods for using the same to treat cancer and other conditions.
    细胞毒性二聚体包括基于CBI和/或CPI的亚单位,包括这种二聚体的抗体药物结合物,以及使用它们治疗癌症和其他疾病的方法。
  • SPLICEOSTATIN ANALOGS AND METHODS FOR THEIR PREPARATION
    申请人:PFIZER INC.
    公开号:US20140134193A1
    公开(公告)日:2014-05-15
    The present invention is directed to novel cytotoxic spliceostatin analogs and derivatives, to antibody drug conjugates thereof, and to methods for using the same to treat medical conditions including cancer.
    本发明涉及新型细胞毒性剪接素类似物和衍生物,其抗体药物偶联物,以及使用它们治疗包括癌症在内的医学状况的方法。
  • SPLICEOSTATIN ANALOGS AND METHOS FOR THEIR PREPARATION
    申请人:PFIZER INC.
    公开号:US20170014523A1
    公开(公告)日:2017-01-19
    The present invention is directed to novel cytotoxic spliceostatin analogs and derivatives, to antibody drug conjugates thereof, and to methods for using the same to treat medical conditions including cancer.
  • Prodrugs Comprising an Aminoalkyl Glycine Linker
    申请人:ASCENDIS PHARMA A/S
    公开号:US20170224829A1
    公开(公告)日:2017-08-10
    The present invention relates to novel prodrugs of primary or secondary amine- or hydroxyl-comprising biologically active moieties and pharmaceutically acceptable salts thereof, prodrug reagents, pharmaceutical compositions comprising said prodrugs and the use of said prodrugs.
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