摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

4-(4-{[2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-en-1-yl]methyl}piperazin-1-yl)-N-[(4-{[(4-cyano-4-methylcyclohexyl)methyl]amino}-3-nitrophenyl)sulfonyl]-2-(1H-pyrrolo[2,3-b]pyridin-5-yloxy)benzamide | 1257050-98-8

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)-N-[(4-{[(4-cyano-4-methylcyclohexyl)methyl]amino}-3-nitrophenyl)sulfonyl]-2-(1H-pyrrolo[2,3-b]pyridin-5-yloxy)benzamide
英文别名
4-[4-[[2-(4-chlorophenyl)-4,4-dimethylcyclohexen-1-yl]methyl]piperazin-1-yl]-N-[4-[(4-cyano-4-methylcyclohexyl)methylamino]-3-nitrophenyl]sulfonyl-2-(1H-pyrrolo[2,3-b]pyridin-5-yloxy)benzamide
4-(4-{[2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-en-1-yl]methyl}piperazin-1-yl)-N-[(4-{[(4-cyano-4-methylcyclohexyl)methyl]amino}-3-nitrophenyl)sulfonyl]-2-(1H-pyrrolo[2,3-b]pyridin-5-yloxy)benzamide化学式
CAS
1257050-98-8
化学式
C48H53ClN8O6S
mdl
——
分子量
905.518
InChiKey
QQUDAOFKIUQEOR-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):
    9.1
  • 重原子数:
    64
  • 可旋转键数:
    12
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    198
  • 氢给体数:
    3
  • 氢受体数:
    11

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:US20100305122A1
    公开(公告)日:2010-12-02
    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。
  • MELT-EXTRUDED SOLID DISPERSIONS CONTAINING AN APOPTOSIS-INDUCING AGENT
    申请人:Birtalan Esther
    公开号:US20120108590A1
    公开(公告)日:2012-05-03
    A pro-apoptotic solid dispersion comprises, in essentially non-crystalline form, a Bcl-2 family protein inhibitory compound of Formula I as defined herein, dispersed in a solid matrix that comprises (a) a pharmaceutically acceptable water-soluble polymeric carrier and (b) a pharmaceutically acceptable surfactant. A process for preparing such a solid dispersion comprises subjecting to elevated temperature the compound of Formula I, the water-soluble polymeric carrier and the surfactant, to provide an extrudable semi-solid mixture; extruding the semi-solid mixture; and cooling the resulting extrudate to to provide a solid matrix comprising the polymeric carrier and the surfactant and having the compound dispersed in essentially non-crystalline form therein. The solid dispersion is suitable for oral administration to a subject in need thereof for treatment of a disease characterized by overexpression of one or more anti-apoptotic Bcl-2 family proteins, for example cancer or an immune or autoimmune disease.
    一种促凋亡的固态分散物包括本文所定义的化合物I公式的Bcl-2家族蛋白抑制剂,以基本非结晶形式分散在固态基质中,该基质包括(a)药学上可接受的溶性聚合物载体和(b)药学上可接受的表面活性剂。制备这种固态分散物的过程包括将公式I的化合物、溶性聚合物载体和表面活性剂暴露于高温下,以提供可挤出的半固体混合物;挤出半固体混合物;并冷却所得到的挤出物,以提供包含聚合物载体和表面活性剂的固态基质,并在其中分散化合物的基本非结晶形式。这种固态分散物适用于口服给予需要治疗由一个或多个抗凋亡Bcl-2家族蛋白过度表达所特征的疾病的患者,例如癌症或免疫或自身免疫性疾病。
  • APOPTOSIS-INDUCING AGENTS FOR THE TREATMENT OF CANCER AND IMMUNE AND AUTOIMMUNE DISEASES
    申请人:Bruncko Milan
    公开号:US20110124628A1
    公开(公告)日:2011-05-26
    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.
    本发明涉及一种抑制抗凋亡Bcl-2蛋白活性的化合物,含有该化合物的组合物以及治疗表达抗凋亡Bcl-2蛋白的疾病的方法。
  • [EN] SOLID DISPERSIONS CONTAINING AN APOPTOSIS-INDUCING AGENT<br/>[FR] DISPERSIONS SOLIDES CONTENANT UN AGENT INDUISANT L'APOPTOSE
    申请人:ABBOTT LAB
    公开号:WO2012058392A1
    公开(公告)日:2012-05-03
    A pro-apoptotic solid dispersion comprises, in essentially non-crystalline form, a Bcl-2 family protein inhibitory compound of Formula I as defined herein, dispersed in a solid matrix that comprises (a) a pharmaceutically acceptable water-soluble polymeric carrier and (b) a pharmaceutically acceptable surfactant. A process for preparing such a solid dispersion comprises dissolving the compound, the polymeric carrier and the surfactant in a suitable solvent, and removing the solvent to provide a solid matrix comprising the polymeric carrier and the surfactant and having the compound dispersed in essentially non-crystalline form therein. The solid dispersion is suitable for oral administration to a subject in need thereof for treatment of a disease characterized by overexpression of one or more anti-apoptotic Bcl-2 family proteins, for example cancer.
    一种促凋亡的固体分散体包括本文所定义的化合物I的Bcl-2家族蛋白抑制剂,在基本非晶态形式下分散在固体基质中,该固体基质包括(a)一种药用可接受的溶性聚合物载体和(b)一种药用可接受的表面活性剂。制备这种固体分散体的过程包括在适当的溶剂中溶解化合物、聚合物载体和表面活性剂,并去除溶剂,以提供包含聚合物载体和表面活性剂的固体基质,并在其中分散化合物的基本非晶态形式。该固体分散体适用于口服给予需要治疗一种或多种抗凋亡Bcl-2家族蛋白过度表达的疾病的受试者,例如癌症。
  • SOLID DISPERSIONS CONTAINING AN APOPTOSIS-INDUCING AGENT
    申请人:Catron Nathaniel
    公开号:US20120277210A1
    公开(公告)日:2012-11-01
    A pro-apoptotic solid dispersion comprises, in essentially non-crystalline form, a Bcl-2 family protein inhibitory compound of Formula I as defined herein, dispersed in a solid matrix that comprises (a) a pharmaceutically acceptable water-soluble polymeric carrier and (b) a pharmaceutically acceptable surfactant. A process for preparing such a solid dispersion comprises dissolving the compound, the polymeric carrier and the surfactant in a suitable solvent, and removing the solvent to provide a solid matrix comprising the polymeric carrier and the surfactant and having the compound dispersed in essentially non-crystalline form therein. The solid dispersion is suitable for oral administration to a subject in need thereof for treatment of a disease characterized by overexpression of one or more anti-apoptotic Bcl-2 family proteins, for example cancer.
    一种促凋亡的固体分散物,其主要以非晶态形式分散在固体基质中,该基质包括以下成分:(a)一种药用可接受的溶性聚合物载体和(b)一种药用可接受的表面活性剂,其中所述化合物为以下公式I所定义的Bcl-2家族蛋白抑制剂。制备这种固体分散物的方法包括将化合物、聚合物载体和表面活性剂溶解在适宜的溶剂中,并去除溶剂以提供包含聚合物载体和表面活性剂并在其中以基本非晶态形式分散有化合物的固体基质。该固体分散物适用于口服给予需要治疗由一个或多个抗凋亡Bcl-2家族蛋白过度表达引起的疾病,例如癌症的患者。
查看更多

同类化合物

([2-(萘-2-基)-4-氧代-4H-色烯-8-基]乙酸) (R)-斯替戊喷酯-d9 (E,Z)-他莫昔芬N-β-D-葡糖醛酸 (E)-3-(4-(叔丁基)苯基)丙烯酸乙酯 (E)-3-(2-(三氟甲基)苯基)丙烯酸乙酯 (E)-3-(2,4-二甲氧基苯基)丙烯酸乙酯 (E/Z)-他莫昔芬-d5 (5Z)-7-氧杂烯醇 (4S,5R)-4,5-二苯基-1,2,3-恶噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4S,4''S,5R,5''R)-2,2''-(1-甲基亚乙基)双[4,5-二氢-4,5-二苯基恶唑] (4R,5S)-4,5-二苯基-1,2,3-恶噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4R,4''R,5S,5''S)-2,2''-(1-甲基亚乙基)双[4,5-二氢-4,5-二苯基恶唑] (4-甲氧基-6-[(E)-2-(3-甲氧基苯基)乙烯基]-5,6-二氢-2H-吡 (2Z)-1,3-二苯基-2-丙烯-1-酮,2-丙烯-1-酮,1,3-二苯基-,(2Z)- (2E)-N-[2-(3-羟基-2-氧代-2,3-二氢-1H-吲哚-3-基)乙基]-3-苯基丙-2-烯酰胺 (1R,2R)-2-(二苯基膦基)-1,2-二苯基乙胺 (11aR)-3,7-双(3,5-二甲基苯基)-10,11,12,13-四氢-5-羟基-5-氧化物-二茚基[7,1-de:1'',7''-fg][1,3,2]二氧杂膦酸 龙血素D 龙血素C 龙血素A 龙血素 B 龙血树脂红血树脂 鼠李素 鼠李柠檬素3-O-beta-D-鼠李三糖苷 鼠李柠檬素 鼠李亭3-O-beta-吡喃葡萄糖苷 鼓槌石斛素 黄麦格霉素 黄金树苷 黄酮醇-2-磺酸钠盐 黄酮胺 黄酮榕碱 黄酮地洛 黄酮哌酯 黄酮 黄豆黄苷 黄豆黄素 黄豆苷元-D6 黄豆苷元-4,7-二葡糖苷 黄诺马甙 黄苏木素 黄花夹竹桃黄酮 黄芪总皂甙 黄芪异黄烷苷,7,2'-二羟基-3',4'-二甲氧基异黄烷 黄芩黄酮II 黄芩黄酮I 黄芩黄酮 黄芩苷甲酯 黄芩苷 黄芩素磷酸酯