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

1-<4-(2-Diaethylamino-aethoxy)-phenyl>-1-<4-chlor-phenyl>-2-phenyl>-aethanol | 115208-53-2

中文名称
——
中文别名
——
英文名称
1-<4-(2-Diaethylamino-aethoxy)-phenyl>-1-<4-chlor-phenyl>-2-phenyl>-aethanol
英文别名
1-<4-Chlor-phenyl>-1-<4-(2-diaethylamino-aethoxy)-phenyl>-2-phenyl-aethanol;1-(4-Chlorophenyl)-1-[4-[2-(diethylamino)ethoxy]phenyl]-2-phenylethanol
1-<4-(2-Diaethylamino-aethoxy)-phenyl>-1-<4-chlor-phenyl>-2-phenyl>-aethanol化学式
CAS
115208-53-2
化学式
C26H30ClNO2
mdl
——
分子量
423.983
InChiKey
NWZZKKWBEXLTLD-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):
    5.9
  • 重原子数:
    30
  • 可旋转键数:
    10
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    32.7
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • Prevention and treatment of cardiovascular pathologies with tamoxifen analogues
    申请人:NeoRx Corporation
    公开号:US20020068731A1
    公开(公告)日:2002-06-06
    A method for treating or preventing cardiovascular pathologies by administering a compound of the formula (I): 1 wherein Z is C═O or a covalent bond; Y is H or O(C 1 -C 4 )alkyl, R 1 and R 2 are individually (C 1 -C 4 )allyl or together with N are a saturated heterocyclic group, R 3 is ethyl or chloroethyl, R 4 is H, R 5 is I, O(C 1 -C 4 )alkyl or H and R 6 is I, O(C 1 -C 4 )alkyl or H with the proviso that when R 4 , R 5 , and R 6 are H, R 3 is not ethyl; or a pharmaceutically acceptable salt thereof, effective to elevate the level of TGF-beta to treat and/or prevent conditions such as atherosclerosis, thrombosis, myocardial infarction, and stroke is provided. Useful compounds include idoxifene, toremifene or salts thereof. Further provided is a method for identifying an agent that elevates the level of TGF-beta. Another embodiment of the invention is an assay or kit to determine TGF-beta in vitro. Also provided is a therapeutic method comprising inhibiting smooth muscle cell proliferation associated with procedural vascular trauma employing the administration of tamoxifen or structural analogs thereof, including compounds of formula (I).
    一种通过施用式(I)化合物治疗或预防心血管疾病的方法: 1 其中 Z 是 C&boxH;O 或共价键;Y 是 H 或 O(C 1 -C 4 烷基,R 1 和 R 2 分别是(C 1 -C 4 )烯丙基或与 N 一起为饱和杂环基团,R 3 是乙基或乙基,R 4 是 H,R 5 是 I、O(C 1 -C 4 烷基或 H,而 R 6 是 I、O(C 1 -C 4 烷基或 H,但当 R 4 , R 5 和 R 6 为 H,R 3 不是乙基;或其药学上可接受的盐,可有效提高 TGF-beta 的平,从而治疗和/或预防动脉粥样硬化、血栓形成、心肌梗塞和中风等疾病。有用的化合物包括依多昔芬、托瑞米芬或其盐类。本发明还提供了一种鉴定可提高 TGF-beta 平的制剂的方法。本发明的另一个实施方案是一种测定体外 TGF-beta 的检测方法或试剂盒。本发明还提供了一种治疗方法,包括通过施用他莫昔芬或其结构类似物(包括式(I)化合物)来抑制与程序性血管创伤相关的平滑肌细胞增殖。
  • Method to determine TGF-beta
    申请人:NeoRx Corporation
    公开号:US20020182659A1
    公开(公告)日:2002-12-05
    A method for treating or preventing cardiovascular pathologies by administering a compound of the formula (1): 1 wherein Z is C═O or a covalent bond; Y is H or O(C 1 -C 4 )alkyl, R 1 and R 2 are individually (C 1 -C 4 )alkyl or together with N are a saturated heterocyclic group, R 3 is ethyl or chloroethyl, R 4 is H or together with R 3 is —CH 2 CH 2 — or —S—, R 5 is I, O(C 1 -C 4 )alkyl or H, and R 6 is I, O(C 1 -C 4 )alkyl or H with the proviso that when R 4 , R 5 , and R 6 are H, R 3 is not ethyl; or a pharmaceutically acceptable salt thereof, effective to activate or stimulate production of TGF-beta to treat and/or prevent conditions such as atherosclerosis, thrombosis, myocardial infarction, and stroke is provided. Useful compounds include idoxifene and salts thereof. Further provided is a method for identifying a compound that is a TGF-beta activator or production stimulator is provided. Another embodiment of the invention is an assay or kit to determine TGF-beta in vitro. Also provided is a therapeutic method comprising inhibiting smooth muscle cell proliferation associated with procedural vascular trauma employing the administration of tamoxifen or structural analogs thereof, including compounds of formula (I).
    一种通过施用式(1)化合物治疗或预防心血管疾病的方法: 1 其中 Z 是 C&boxH;O 或共价键;Y 是 H 或 O(C 1 -C 4 )烷基,R 1 和 R 2 分别是(C 1 -C 4 )烷基或与 N 一起为饱和杂环基团,R 3 是乙基或乙基,R 4 是 H 或与 R 3 是-CH 2 CH 2 - 或-S-,R 5 是 I、O(C 1 -C 4 烷基或 H,而 R 6 是 I、O(C 1 -C 4 烷基或 H,但当 R 4 , R 5 和 R 6 为 H,R 3 不是乙基;或其药学上可接受的盐,可有效激活或刺激 TGF-beta 的产生,从而治疗和/或预防动脉粥样硬化、血栓形成、心肌梗塞和中风等疾病。有用的化合物包括艾多昔芬及其盐类。本发明还提供了一种用于鉴定 TGF-beta 激活剂或生成刺激剂的化合物的方法。本发明的另一个实施方案是一种测定体外 TGF-beta 的检测方法或试剂盒。本发明还提供了一种治疗方法,包括通过施用他莫昔芬或其结构类似物(包括式 (I) 化合物)来抑制与程序性血管创伤相关的平滑肌细胞增殖。
  • Compounds and therapies for the prevention of vascular and non-vascular pathologies
    申请人:NeoRx Corporation
    公开号:US20030064970A1
    公开(公告)日:2003-04-03
    The invention provides a method of treating a mammal having, or at risk of, an indication associated with a TGF-beta deficiency comprising administering one or more agents that is effective to elevate the level of TGF-beta. The invention also provides novel compounds that elevate TGF-beta levels, as well as pharmaceutical compositions comprising compounds that elevate TGF-beta levels, and methods for detecting diseases associated with endothelial cell activation.
    本发明提供了一种治疗哺乳动物的方法,该哺乳动物具有或有可能具有与 TGF-beta 缺乏有关的适应症,该方法包括施用一种或多种能有效提高 TGF-beta 平的制剂。本发明还提供了能提高TGF-beta平的新型化合物、包含能提高TGF-beta平的化合物的药物组合物,以及检测与内皮细胞活化相关的疾病的方法。
  • Prevention and treatment of cardiovascular pathologies
    申请人:Grainger J. David
    公开号:US20060029986A1
    公开(公告)日:2006-02-09
    A method for treating or preventing cardiovascular pathologies by administering a compound of the formula (I): wherein Z is C═O or a covalent bond; Y is H or O(C 1 -C 4 )alkyl, R 1 and R 2 are individually (C 1 -C 4 )alkyl or together with N are a saturated heterocyclic group, R 3 is ethyl or chloroethyl, R 4 is H or together with R 3 is —CH 2 —CH 2 — or —S—, R 5 is I, O(C 1 -C 4 )alkyl or H and R 6 is 1, O(C 1 -C 4 )alkyl or H with the proviso that when R 4 , R 5 , and R 6 are H, R 3 is not ethyl; or a pharmaceutically acceptable salt thereof, effective to activate or stimulate production of TGF-beta to treat and/or prevent conditions such as atherosclerosis, thrombosis, myocardial infarction, and stroke is provided. Useful compounds include idoxifene and salts thereof. Further provided is a method for identifying a compound that is a TGF-beta activator or production stimulator is provided. Another embodiment of the invention is an assay or kit to determine TGF-beta in vitro. Also provided is a therapeutic method comprising inhibiting smooth muscle cell proliferation associated with procedural vascular trauma employing the administration of tamoxifen or structural analogs thereof, including compounds of formula (I).
    一种通过施用式(I)化合物治疗或预防心血管疾病的方法: 其中 Z 是 C═O 或共价键;Y 是 H 或 O(C 1 -C 4 )烷基,R 1 和 R 2 分别是(C 1 -C 4 )烷基或与 N 一起为饱和杂环基团,R 3 是乙基或乙基,R 4 是 H 或与 R 3 是-CH 2 -CH 2 - 或-S-,R 5 是 I、O(C 1 -C 4 烷基或 H,而 R 6 是 1、O(C 1 -C 4 烷基或 H,但当 R 4 , R 5 和 R 6 为 H,R 3 不是乙基;或其药学上可接受的盐,可有效激活或刺激 TGF-beta 的产生,从而治疗和/或预防动脉粥样硬化、血栓形成、心肌梗塞和中风等疾病。有用的化合物包括艾多昔芬及其盐类。本发明还提供了一种用于鉴定 TGF-beta 激活剂或生成刺激剂的化合物的方法。本发明的另一个实施方案是一种测定体外 TGF-beta 的检测方法或试剂盒。本发明还提供了一种治疗方法,包括通过施用他莫昔芬或其结构类似物(包括式 (I) 化合物)来抑制与程序性血管创伤相关的平滑肌细胞增殖。
  • PREVENTION AND TREATMENT OF CARDIOVASCULAR PATHOLOGIES WITH TAMOXIFEN ANALOGUES
    申请人:NEORX CORPORATION
    公开号:EP0833624A2
    公开(公告)日:1998-04-08
查看更多

同类化合物

(E,Z)-他莫昔芬N-β-D-葡糖醛酸 (E/Z)-他莫昔芬-d5 (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] (1R,2R)-2-(二苯基膦基)-1,2-二苯基乙胺 鼓槌石斛素 黄子囊素 高黄绿酸 顺式白藜芦醇三甲醚 顺式白藜芦醇 顺式己烯雌酚 顺式-白藜芦醇3-O-beta-D-葡糖苷酸 顺式-桑皮苷A 顺式-曲札芪苷 顺式-二苯乙烯 顺式-beta-羟基他莫昔芬 顺式-a-羟基他莫昔芬 顺式-3,4',5-三甲氧基-3'-羟基二苯乙烯 顺式-1-(3-甲基-2-萘基)-2-(2-萘基)乙烯 顺式-1,2-双(三甲基硅氧基)-1,2-双(4-溴苯基)环丙烷 顺式-1,2-二苯基环丁烷 顺-均二苯乙烯硼酸二乙醇胺酯 顺-4-硝基二苯乙烯 顺-1-异丙基-2,3-二苯基氮丙啶 非洲李(PRUNUSAFRICANA)树皮提取物 阿非昔芬 阿里可拉唑 阿那曲唑二聚体 阿托伐他汀环氧四氢呋喃 阿托伐他汀环氧乙烷杂质 阿托伐他汀环(氟苯基)钠盐杂质 阿托伐他汀环(氟苯基)烯丙基酯 阿托伐他汀杂质D 阿托伐他汀杂质94 阿托伐他汀杂质7 阿托伐他汀杂质5 阿托伐他汀内酰胺钠盐杂质 阿托伐他汀中间体M4 阿奈库碘铵 锌(II)(苯甲醛)(四苯基卟啉) 银松素 铜酸盐(5-),[m-[2-[2-[1-[4-[2-[4-[[4-[[4-[2-[4-[4-[2-[2-(羧基-kO)苯基]二氮烯基-kN1]-4,5-二氢-3-甲基-5-(羰基-kO)-1H-吡唑-1-基]-2-硫代苯基]乙烯基]-3-硫代苯基]氨基]-6-(苯基氨基)-1,3,5-三嗪-2-基]氨基]-2-硫代苯基]乙烯基]-3-硫代 铒(III) 离子载体 I 铀,二(二苯基甲酮)四碘- 钾钠2,2'-[(E)-1,2-乙烯二基]二[5-({4-苯胺基-6-[(2-羟基乙基)氨基]-1,3,5-三嗪-2-基}氨基)苯磺酸酯](1:1:1) 钠{4-[氧代(苯基)乙酰基]苯基}甲烷磺酸酯 钠;[2-甲氧基-5-[2-(3,4,5-三甲氧基苯基)乙基]苯基]硫酸盐 钠4-氨基二苯乙烯-2-磺酸酯