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4-[[(1R,2S,3R,4S)-2-(3-chloro-2-fluorophenyl)-3-(4-chloro-2-fluorophenyl)-3-cyano-4-(2,2-dimethylpropyl)cyclopentanecarbonyl]amino]-3-methoxybenzoic acid

中文名称
——
中文别名
——
英文名称
4-[[(1R,2S,3R,4S)-2-(3-chloro-2-fluorophenyl)-3-(4-chloro-2-fluorophenyl)-3-cyano-4-(2,2-dimethylpropyl)cyclopentanecarbonyl]amino]-3-methoxybenzoic acid
英文别名
——
4-[[(1R,2S,3R,4S)-2-(3-chloro-2-fluorophenyl)-3-(4-chloro-2-fluorophenyl)-3-cyano-4-(2,2-dimethylpropyl)cyclopentanecarbonyl]amino]-3-methoxybenzoic acid化学式
CAS
——
化学式
C32H30Cl2F2N2O4
mdl
——
分子量
615.5
InChiKey
UOCGXEYYBZYWLK-PRIZDDEYSA-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):
    7.6
  • 重原子数:
    42
  • 可旋转键数:
    8
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.34
  • 拓扑面积:
    99.4
  • 氢给体数:
    2
  • 氢受体数:
    7

文献信息

  • Pharmaceutical composition with improved bioavailability
    申请人:Hoffmann-La Roche Inc.
    公开号:US10034854B2
    公开(公告)日:2018-07-31
    The invention relates to solid dispersions of poorly water soluble compounds, in particular Compound A as disclosed herein, formed by solvent co-precipitation or spray drying, resulting in improved bioavailability, safety and tolerability of said compounds.
    本发明涉及通过溶剂共沉淀或喷雾干燥形成的溶性差的化合物,特别是本文所披露的化合物 A 的固体分散体,从而提高了上述化合物的生物利用度、安全性和耐受性。
  • Use of trans-[tetrachlorobis(1H-indazole)ruthenate(III)] for the treatment of cancer
    申请人:Bold Therapeutics, Inc.
    公开号:US10821095B2
    公开(公告)日:2020-11-03
    IT-139, sodium trans-[tetrachlorobis(1H-indazole)ruthenate(III)], is an intravenously administered small molecule compound. In preclinical anti-tumor and mechanism of action studies, IT-139 showed activity against a broad range of tumor types, including those which are resistant to standard anti-cancer agents (e.g., platinums, vinca alkaloids, taxanes, anthracyclines). This activity is believed to arise from IT-139's novel mechanism of action that targets the GRP78 pathway. It was found that up-regulation of GRP78 is a key cancer cell survival pathway. Downregulation of GRP78 using IT-139 removes this resistance pathway allowing for chemotherapy and immuno-oncology agents to be more effective in treating cancer.
    IT-139,反式-[四双(1H-吲唑)(III)],是一种静脉注射小分子化合物。在临床前抗肿瘤和作用机制研究中,IT-139 对多种类型的肿瘤具有活性,包括对标准抗癌药物(如类、长春花生物碱、紫杉类、环类)具有抗药性的肿瘤。据信,这种活性源于 IT-139 针对 GRP78 通路的新作用机制。研究发现,GRP78 的上调是癌细胞生存的关键途径。使用 IT-139 下调 GRP78 可以消除这一抗药性途径,从而使化疗和免疫肿瘤学药物更有效地治疗癌症。
  • BLOCK COPOLYMERS FOR STABLE MICELLES
    申请人:Intezyne Technologies, Inc.
    公开号:US20140113879A1
    公开(公告)日:2014-04-24
    The present invention relates to the field of polymer chemistry and more particularly to multiblock copolymers and micelles comprising the same. Compositions herein are useful for drug-delivery applications.
  • PHARMACEUTICAL COMPOSITION WITH IMPROVED BIOAVAILABILITY
    申请人:Hoffmann-La Roche Inc.
    公开号:US20140206742A1
    公开(公告)日:2014-07-24
    The invention relates to solid dispersions of poorly water soluble compounds, in particular Compound A as disclosed herein, formed by solvent co-precipitation or spray drying, resulting in improved bioavailability, safety and tolerability of said compounds.
  • IRON STABILIZED MICELLES AS MAGNETIC CONTRAST AGENTS
    申请人:Intezyne Technologies
    公开号:US20160346408A1
    公开(公告)日:2016-12-01
    The present invention relates to the field of polymer chemistry and more particularly to multiblock copolymers and iron stabilized micelles comprising the same, as magnetic contrast agents. Compositions herein are useful for diagnostic and drug-delivery applications.
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