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N-(3-diethylamino-propyl)-3-[3-(3-methoxybenzamido)-phenylamino]-benzamide | 1173002-64-6

中文名称
——
中文别名
——
英文名称
N-(3-diethylamino-propyl)-3-[3-(3-methoxybenzamido)-phenylamino]-benzamide
英文别名
N-[3-(diethylamino)propyl]-3-[3-[(3-methoxybenzoyl)amino]anilino]benzamide
N-(3-diethylamino-propyl)-3-[3-(3-methoxybenzamido)-phenylamino]-benzamide化学式
CAS
1173002-64-6
化学式
C28H34N4O3
mdl
——
分子量
474.603
InChiKey
NOCSCLVSJBOTTB-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):
    4.7
  • 重原子数:
    35
  • 可旋转键数:
    12
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    82.7
  • 氢给体数:
    3
  • 氢受体数:
    5

文献信息

  • Compounds for use as therapeutic agents affecting p53 expression and/or activity
    申请人:Société Splicos
    公开号:EP2505198A1
    公开(公告)日:2012-10-03
    The present invention relates to compound (I) wherein R1 and R2 independently represent a hydrogen atom, a (C1-C4)alkoxy group, a fluoro(C1-C4)alkoxy group, a hydroxyl group, a benzyloxy group, a di(C1-C4)alkylamino group, a pyridyl-vinyl group, a pyrimidinyl-vinyl group, a styryl group, or a -NHCOphenyl group; R3, R4 and R5 independently represent a hydrogen atom, a (C1-C4)alkyl group, a CONHR6 group, a -CONR7R8 group, a -SO2NHR6 group, or a heteroaryl group optionally substituted by a halogen atom, a -(CH2)nNR7R8 group or a hydroxy(C1-C4)alkyl group; R6 represents a hydrogen atom, a -(CHR9)m(CH2)nNR7R8 group or a (C1-C6)alkyl group optionally substituted by a hydroxyl group; or anyone of its pharmaceutically acceptable salt, for use as an agent for preventing, inhibiting or treating a disease in a patient suffering thereof, said disease involving a deregulated p53. Some of said compounds are new and also form part of the invention.
    本发明涉及化合物(I),其中R1和R2分别代表氢原子,(C1-C4)烷氧基,代(C1-C4)烷氧基,羟基,苄氧基,二(C1-C4)烷基基,吡啶乙烯基嘧啶乙烯基苯乙烯基,或-NHCO苯基;R3、R4和R5分别代表氢原子,(C1-C4)烷基,CONHR6基团,-CONR7R8基团,-SO2NHR6基团,或杂环烷基,可选择地被卤原子取代,-(CH2)nNR7R8基团或羟基(C1-C4)烷基;R6代表氢原子,-(CHR9)m( )nNR7R8基团或(C1-C6)烷基,可选择地被羟基取代;或其药学上可接受的盐之一,用作预防、抑制或治疗患有该疾病的患者的药剂,所述疾病涉及到p53蛋白的失调。其中一些化合物是新的,也是本发明的一部分。
  • CHEMICAL MOLECULES THAT INHIBIT THE SLICING MECHANISM FOR TREATING DISEASES RESULTING FROM SPLICING ANOMALIES
    申请人:Tazi Jamal
    公开号:US20110053975A1
    公开(公告)日:2011-03-03
    The present invention relates to a compound of one of the formulas I to XXI; a pharmaceutical composition comprising at least one such compound; and the use of at least one such compound in preparing a drug to treat, in a subject, a genetic disease resulting from at least one splicing anomaly.
    本发明涉及公式I至XXI中的化合物之一;包含至少一种这种化合物的药物组合物;以及使用至少一种这种化合物来制备一种药物,用于治疗主体中由至少一个剪接异常导致的遗传疾病。
  • COMPOUNDS FOR USE AS THERAPEUTIC AGENTS AFFECTING P53 EXPRESSION AND/OR ACTIVITY
    申请人:Scherrer Didier
    公开号:US20140206690A1
    公开(公告)日:2014-07-24
    The present invention relates to compound (I) wherein R1 and R2 independently represent a hydrogen atom, a (C 1 -C 4 )alkoxy group, a fluoro(C 1 -C 4 )alkoxy group, a hydroxyl group, a benzyloxy group, a di(C 1 -C 4 )alkylamino group, a pyridyl-vinyl group, a pyrimidinyl-vinyl group, a styryl group, or a —NHCOphenyl group; R3, R4 and R5 independently represent a hydrogen atom, a (C 1 -C 4 )alkyl group, a CONHR6 group, a —CONR7R8 group, a —SO 2 NHR6 group, or a heteroaryl group optionally substituted by a halogen atom, a —(CH 2 ) n NR7R8 group or a hydroxy(C 1 -C 4 )alkyl group; R6 represents a hydrogen atom, a —(CHR9) m (CH 2 ) n NR7R8 group or a (C 1- C 6 )alkyl group optionally substituted by a hydroxyl group; or anyone of its pharmaceutically acceptable salt, for use in a method for preventing, inhibiting or treating a disease in a patient suffering thereof, said disease involving a deregulated p53. Some of said compounds are new and also form part of the invention.
    本发明涉及化合物(I),其中R1和R2分别表示氢原子,(C1-C4)烷氧基,(C1-C4)烷氧基,羟基,苄氧基,二(C1-C4)烷基基,吡啶乙烯基嘧啶乙烯基苯乙烯基或—NHCO苯基;R3,R4和R5分别表示氢原子,(C1-C4)烷基,CONHR6基,—CONR7R8基,—SO2NHR6基或杂环基,所述杂环基可选地被卤原子,—(CH2)nNR7R8基或羟基(C1-C4)烷基取代;R6表示氢原子,—(CHR9)m( )nNR7R8基或(C1-C6)烷基,可选地被羟基取代;或其药学上可接受的盐之一,用于预防,抑制或治疗患有p53失调的患者的疾病的方法。其中一些化合物是新的,也是本发明的一部分。
  • Foaming composition with wettability modifying and corrosion inhibitory properties for high temperature and ultra-high salinity
    申请人:Instituto Mexicano Del Petróleo
    公开号:EP2740781A1
    公开(公告)日:2014-06-11
    The present invention relates to obtaining and using foaming compositions with wettability-modifying and corrosion inhibitory properties that control the channeling of fluids in naturally fractured carbonate reservoirs, favorably alter the rock wettability in crude oil enhanced recovery processes and control uniform corrosion problems occurring in production rigs under high temperature and ultra-high salinity conditions; by means of the synergistic effect resulting from the supramolecular interaction of alkyl amido propyl hydroxysultaines or alkyl hydroxysultaines with sodium alkyl hydroxysulfonates and sodium alkenyl sulfonates (1). The foaming compositions with wettability-modifying and corrosion inhibitory properties are characterized for being tolerant to high concentrations of divalent ions such as calcium, magnesium, strontium and barium and for the fact that for their application in the reservoir, seawater and/or congenital water characteristic of the reservoir may be used as means of transportation.
    本发明涉及获得和使用具有润湿性改良和腐蚀抑制特性的发泡组合物,该组合物可控制天然裂缝碳酸盐储层中的流体通道,有利地改变原油提高采收率过程中的岩石润湿性,并控制高温和超高盐度条件下生产钻机中出现的均匀腐蚀问题;通过烷基酰胺丙基羟基磺烷或烷基羟基磺烷与烷基羟基磺酸钠和烯基磺酸钠的超分子相互作用产生的协同效应(1)。具有润湿改性和缓蚀特性的发泡组合物的特点是能够耐受高浓度的等二价离子,而且在储层中应用时,可以使用海和/或储层特有的先天性作为运输工具。
  • CHEMICAL MOLECULES THAT INHIBIT THE SPLICING MECHANISM FOR TREATING DISEASES RESULTING FROM SPLICING ANOMALIES
    申请人:CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE - CNRS
    公开号:EP3536691A1
    公开(公告)日:2019-09-11
    The present invention relates to specific compounds; pharmaceutical composition comprising at least one of said compounds; and the use of at least one of said compounds in preparing a drug to treat, in a subject, a genetic disease resulting from at least one splicing anomaly.
    本发明涉及特定化合物;包含至少一种所述化合物的药物组合物;以及使用至少一种所述化合物制备药物,以治疗受试者因至少一种剪接异常导致的遗传疾病。
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