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4-(4-{[2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-en-1-yl]methyl}piperazin-1-yl)-2-[(6-fluoro-1H-indol-5-yl)oxy]-N-({4-[(4-fluorotetrahydro-2H-pyran-4-yl)methoxy]-3-nitrophenyl}sulfonyl)benzamide | 1228941-31-8

中文名称
——
中文别名
——
英文名称
4-(4-{[2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-en-1-yl]methyl}piperazin-1-yl)-2-[(6-fluoro-1H-indol-5-yl)oxy]-N-({4-[(4-fluorotetrahydro-2H-pyran-4-yl)methoxy]-3-nitrophenyl}sulfonyl)benzamide
英文别名
4-[4-[[2-(4-chlorophenyl)-4,4-dimethylcyclohexen-1-yl]methyl]piperazin-1-yl]-2-[(6-fluoro-1H-indol-5-yl)oxy]-N-[4-[(4-fluorooxan-4-yl)methoxy]-3-nitrophenyl]sulfonylbenzamide
4-(4-{[2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-en-1-yl]methyl}piperazin-1-yl)-2-[(6-fluoro-1H-indol-5-yl)oxy]-N-({4-[(4-fluorotetrahydro-2H-pyran-4-yl)methoxy]-3-nitrophenyl}sulfonyl)benzamide化学式
CAS
1228941-31-8
化学式
C46H48ClF2N5O8S
mdl
——
分子量
904.432
InChiKey
KZJRZPZPYVJWBI-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):
    8.4
  • 重原子数:
    63
  • 可旋转键数:
    12
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.37
  • 拓扑面积:
    167
  • 氢给体数:
    2
  • 氢受体数:
    12

文献信息

  • APOPTOSIS-INDUCING AGENTS FOR THE TREATMENT OF CANCER AND IMMUNE AND AUTOIMMUNE DISEASES
    申请人:Bruncko Milan
    公开号:US20100160322A1
    公开(公告)日:2010-06-24
    Disclosed are compounds which inhibit the activity of anti-apoptotic Bcl-2 proteins, compositions containing the compounds and methods of treating diseases during which is expressed anti-apoptotic Bcl-2 protein.
    揭示了抑制抗凋亡Bcl-2蛋白活性的化合物,含有这些化合物的组合物以及治疗在其中表达抗凋亡Bcl-2蛋白的疾病的方法。
  • METHODS OF TREATMENT USING SELECTIVE BCL-2 INHIBITORS
    申请人:Elmore Steven
    公开号:US20120129853A1
    公开(公告)日:2012-05-24
    This invention pertains to methods of treating systemic lupus erythematosus, lupus nephritis or Sjogren's Syndrome with compounds that selectively inhibit the activity of Bcl-2 anti-apoptotic proteins. Specifically, the current invention is directed to treatment with compounds that selectively inhibit the activity of Bcl-2 proteins, with a lesser affinity for inhibiting the activity of other BCL-2 family proteins, including Bcl-x L .
    本发明涉及使用有选择性地抑制BcL-2抗凋亡蛋白活性的化合物来治疗系统性红斑狼疮、狼疮性肾炎或干燥综合症的方法。具体而言,本发明涉及使用有选择性地抑制BcL-2蛋白活性的化合物进行治疗,这些化合物对于抑制其他BCL-2家族蛋白,包括Bcl-xL的活性具有较小的亲和力。
  • Chemical entities that kill senescent cells for use in treating age-related disease
    申请人:Unity Biotechnology, Inc.
    公开号:US10195213B2
    公开(公告)日:2019-02-05
    Disclosed herein are compounds that are effective for treatment of various disease states associated with senescence. The disclosed compounds can be used to eliminate senescent cells for disease treatment. The dosing of the compounds includes both single administration and regimens of cycling dosages.
    本文公开的化合物可有效治疗与衰老有关的各种疾病状态。所公开的化合物可用于消除衰老细胞以治疗疾病。化合物的给药方式包括单次给药和循环给药。
  • Methods and compositions for treating cancer
    申请人:THE UNIVERSITY OF CHICAGO
    公开号:US10888569B1
    公开(公告)日:2021-01-12
    The disclosure relates to improved therapeutic methods for treating cancer patients. The methods include a method for treating cancer in a subject comprising administering an effective amount of a BACH1 inhibitor and an ETC inhibitor to the subject. Further aspects of the disclosure relate to a method for treating cancer in a subject comprising: administering a first therapeutic regimen comprising an ETC inhibitor to the subject after a biological sample from the subject was determined to have a decreased or substantially the same level of expression of BACH1 relative to a control sample or to a cut-off value; wherein the first therapeutic regimen excludes a BACH1 inhibitor; or administering a second therapeutic regimen comprising a BACH1 inhibitor and an ETC inhibitor to the subject after a biological sample from the subject was determined to have an increased level of expression of BACH1 relative to a control sample or a cut-off value.
    本公开涉及治疗癌症患者的改进治疗方法。这些方法包括治疗受试者癌症的方法,该方法包括向受试者施用有效量的 BACH1 抑制剂和 ETC 抑制剂。本公开的其他方面涉及一种治疗受试者癌症的方法,包括在确定受试者的生物样本相对于对照样本或临界值具有降低或基本相同的BACH1表达平之后,向受试者施用包含ETC抑制剂的第一治疗方案;其中第一治疗方案不包括BACH1抑制剂;或 在确定受试者的生物样本相对于对照样本或临界值具有升高的BACH1表达平之后,向受试者施用包含BACH1抑制剂和ETC抑制剂的第二治疗方案。
  • COMPOUNDS AND THERAPEUTIC USES
    申请人:Unity Biotechnology, Inc.
    公开号:US20170281649A1
    公开(公告)日:2017-10-05
    Disclosed herein are compounds that are effective for treatment of various disease states associated with senescence. The disclosed compounds can be used to eliminate senescent cells for disease treatment. The dosing of the compounds includes both single administration and regimens of cycling dosages.
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