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

2-[[6-methoxy-3-pyridinyl]methyl]amino-N-[4-(1-propynyl)-3-(trifluoromethyl)phenyl]benzamide | 524729-01-9

中文名称
——
中文别名
——
英文名称
2-[[6-methoxy-3-pyridinyl]methyl]amino-N-[4-(1-propynyl)-3-(trifluoromethyl)phenyl]benzamide
英文别名
[6-Methoxy-3-pyridinyl]methylamino-N-[4-(1-propynyl)-3-(trifluoromethyl)phenyl]benzamide;2-[(6-methoxypyridin-3-yl)methylamino]-N-[4-prop-1-ynyl-3-(trifluoromethyl)phenyl]benzamide
2-[[6-methoxy-3-pyridinyl]methyl]amino-N-[4-(1-propynyl)-3-(trifluoromethyl)phenyl]benzamide化学式
CAS
524729-01-9
化学式
C24H20F3N3O2
mdl
——
分子量
439.437
InChiKey
LELTXJWGZLSFGC-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):
    5.7
  • 重原子数:
    32
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    63.2
  • 氢给体数:
    2
  • 氢受体数:
    7

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Anthranilic acid amides and their use as vegf receptor tyrosine kinase inhibitors
    申请人:Bold Guido
    公开号:US20050096356A1
    公开(公告)日:2005-05-05
    The invention relates to anthranilic acid amide derivatives of formula (I), wherein R 1 represents H or lower alkyl, R 2 represents H or lower alkyl, R 3 represents perfluoro lower alkyl, and X is O or S, or an N-oxide or a tautomer thereof, to salts of such anthranilic acid amides, their N-oxides and their tautomers; processes for the preparation thereof, the application thereof for the treatment of the human or animal body, the use thereof—alone or in combination with one or more other pharmaceutically active compounds—for the treatment especially of a neoplastic disease, such as a tumor disease, of retinopathy or age—related macular degeneration; a method for the treatment of such a disease in animals, especially in humans, and the use of such a compound—alone or in combination with one or more other pharmaceutically active compounds—for the manufacture of a pharmaceutical preparation for the treatment of a neoplastic disease, of retinopathy or age-related macular degeneration.
    本发明涉及公式(I)的蒽酰氨衍生物,其中R1代表H或较低的烷基,R2代表H或较低的烷基,R3代表全氟较低的烷基,X为O或S,或其N-氧化物或互变异构体,以及这些蒽酰氨酸酰胺、它们的N-氧化物和它们的互变异构体的盐;其制备方法,用于治疗人体或动物体的应用,单独使用或与一个或多个其他药物活性化合物结合,特别用于治疗肿瘤疾病,如肿瘤疾病、视网膜病变或年龄相关性黄斑变性的治疗;一种用于治疗这种动物疾病,特别是在人类中的方法,以及这种化合物的使用——单独使用或与一个或多个其他药物活性化合物结合——用于制造治疗肿瘤疾病、视网膜病变或年龄相关性黄斑变性的药物制剂。
  • Anthranilic acid amide derivatives and their pharmaceutical use
    申请人:Bold Guido
    公开号:US20060128684A1
    公开(公告)日:2006-06-15
    The present invention relates to new anthranilic acid amide derivatives, processes for the preparation thereof, the application thereof in a process for the treatment of the human or animal body, the use thereof—alone or in combination with one or more other pharmaceutically active compounds.
    本发明涉及新的蒽酰胺衍生物,其制备方法,其在治疗人体或动物体的过程中的应用,以及其在单独使用或与一个或多个其他药物活性化合物结合使用的用途。
  • Anthranilic acid amides and pharmaceutical use thereof
    申请人:——
    公开号:US20040248947A1
    公开(公告)日:2004-12-09
    The invention relates to anthranilic acid amide derivatives of formula (I), wherein Ar is represented by the subformula (I a ), wherein R a represents II or lower alkyl, and R 1 represents II or perfluoro lower alkyl, R 2 represents II, halogen, C 2 -C 7 alkyl. C 2 -C 7 alkenyl or lower aklynyl: or Ar is represented by the subformula (I b ) and R 1 represents perfluoro lower alkyl, and R 2 represents bromo, iodo, C 2 -C 7 alkyl, C 2 -C 7 alkenyl or lower alkynyl, or R 1 represents H, and R 2 represents fluoro, bromo, iodo, ethyl, C 5 -C 7 alkyl, C 2 -C 7 alkenyl or lower alkynyl; to N-oxides and tautomers thereof, and to salts of such anthranilic acid amides, its N-oxides and tautomers; to processes for their preparation; to their application in the treatment of the human or animal body, to the use thereof—alone or in combination with one or more other pharmaceutically active compounds—for the treatment especially of a neoplastic disease, such as a tumor disease, of retinopathy or age-related macular degeneration; to a method for the treatment of such diseases in animals; and to the use of such a compound-alone or in combination with one or more other pharmaceutically active compounds—for the manufacture of a pharmaceutical preparation for the treatment of a neoplastic disease, of retinopathy or age-related macular degeneration. 1
    本发明涉及公式(I)的蒽酰胺衍生物,其中Ar由亚式公式(Ia)表示,其中R为II或较低的烷基,R1为II或全氟较低烷基,R2为II、卤素、C2-C7烷基、C2-C7烯基或较低的炔基;或Ar由亚式公式(Ib)表示,R1表示全氟较低烷基,R2表示溴、碘、C2-C7烷基、C2-C7烯基或较低的炔基,或R1表示H,R2表示氟、溴、碘、乙基、C5-C7烷基、C2-C7烯基或较低的炔基;以及其N-氧化物和互变异构体,以及这种蒽酰胺酸酰胺、其N-氧化物和互变异构体的盐;其制备方法;其在治疗人体或动物体中的应用,其使用-单独或与一个或多个其他药理活性化合物结合-特别是治疗肿瘤疾病,如肿瘤疾病、视网膜病变或年龄相关性黄斑变性;用于动物治疗此类疾病的方法;以及使用这种化合物-单独或与一个或多个其他药理活性化合物结合-制造用于治疗肿瘤疾病、视网膜病变或年龄相关性黄斑变性的制药制剂。
  • Anthranilic acid amides and their use as VEGF receptor tyrosine kinase inhibitors
    申请人:Bold Guido
    公开号:US20060178409A1
    公开(公告)日:2006-08-10
    The invention relates to anthranilic acid amide derivatives of formula I, wherein R 1 represents H or lower alkyl, R 2 represents H or lower alkyl, R 3 represents perfluoro lower alkyl, and X is O or S, or an N-oxide or a tautomer thereof, to salts of such anthranilic acid amides, their N-oxides and their tautomers; processes for the preparation thereof, the application thereof for the treatment of the human or animal body, the use thereof—alone or in combination with one or more other pharmaceutically active compounds—for the treatment especially of a neoplastic disease, such as a tumor disease, of retinopathy or age-related macular degeneration; a method for the treatment of such a disease in animals, especially in humans, and the use of such a compound—alone or in combination with one or more other pharmaceutically active compounds—for the manufacture of a pharmaceutical preparation for the treatment of a neoplastic disease, of retinopathy or age-related macular degeneration.
    本发明涉及式I的蒽酰胺衍生物,其中R1代表H或较低的烷基,R2代表H或较低的烷基,R3代表全氟较低的烷基,X为O或S,或其N-氧化物或互变异构体,以及这些蒽酰胺及其N-氧化物和互变异构体的盐;制备这些化合物的方法,将其用于治疗人或动物身体的应用,将其单独或与一个或多个其他药物活性化合物结合使用,特别用于治疗肿瘤疾病,如肿瘤疾病、视网膜病变或年龄相关性黄斑变性;一种治疗这种疾病的动物的方法,特别是人类,并且将这种化合物单独或与一个或多个其他药物活性化合物结合使用,用于制造用于治疗肿瘤疾病、视网膜病变或年龄相关性黄斑变性的制药制剂。
  • ANTHRANILIC ACID AMIDES AND PHARMACEUTICAL USE THEREOF
    申请人:Novartis AG
    公开号:EP1446381B1
    公开(公告)日:2011-01-05
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐