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-methyl-piperazin-1-ylmethyl)-N-[4-methyl-3-(4-pyridin-4-yl-pyrimidin-2-ylamino)-phenyl]-benzamide | 881676-19-3

中文名称
——
中文别名
——
英文名称
4-(4-methyl-piperazin-1-ylmethyl)-N-[4-methyl-3-(4-pyridin-4-yl-pyrimidin-2-ylamino)-phenyl]-benzamide
英文别名
4-[(4-methylpiperazin-1-yl)methyl]-N-[4-methyl-3-[(4-pyridin-4-ylpyrimidin-2-yl)amino]phenyl]benzamide
4-(4-methyl-piperazin-1-ylmethyl)-N-[4-methyl-3-(4-pyridin-4-yl-pyrimidin-2-ylamino)-phenyl]-benzamide化学式
CAS
881676-19-3
化学式
C29H31N7O
mdl
——
分子量
493.611
InChiKey
BYMYDYHSVGWQTQ-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):
    3.5
  • 重原子数:
    37
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    86.3
  • 氢给体数:
    2
  • 氢受体数:
    7

文献信息

  • Pyrimidine Derivatives
    申请人:Klebl Bert
    公开号:US20080187575A1
    公开(公告)日:2008-08-07
    The present invention relates to pyrimidine derivatives, methods for their synthesis, and the use of said pyrimidine derivatives as pharmaceutically active agents, especially for the prophylaxis and/or treatment of cell proliferation disorders, cancer, leukemia, erectile dysfunction, cardiovascular diseases and disorders, inflammatory diseases, transplant rejection, immunological diseases, neuroimmunological diseases, autoimmune diseases, infective diseases including opportunistic infections, prion diseases and/or neuro-degeneration. Furthermore, the present invention relates to pharmaceutical compositions containing at least one pyrimidine derivative and/or pharmaceutically acceptable salts thereof as an active ingredient together with at least one pharmaceutically acceptable carrier, excipient or diluents as well as to methods for prophylaxis and/or treatment of the above-mentioned diseases and disorders.
    本发明涉及嘧啶生物,其合成方法,以及所述嘧啶生物作为药用活性剂的用途,特别是用于预防和/或治疗细胞增殖紊乱、癌症、白血病、勃起功能障碍、心血管疾病和紊乱、炎症性疾病、移植排斥、免疫性疾病、神经免疫性疾病、自身免疫性疾病、感染性疾病包括机会性感染、朊病和/或神经退行性疾病。此外,本发明涉及含有至少一种嘧啶生物和/或其药用可接受盐作为活性成分的药物组合物,以及用于预防和/或治疗上述疾病和紊乱的方法。
  • PYRIMIDINE DERIVATIVES
    申请人:GPC Biotech AG
    公开号:EP1786781A2
    公开(公告)日:2007-05-23
  • [EN] PYRIMIDINE DERIVATIVES<br/>[FR] DERIVES DE PYRIMIDINE
    申请人:GPC BIOTECH AG
    公开号:WO2006021458A2
    公开(公告)日:2006-03-02
    The present invention relates to pyrimidine derivatives, methods for their synthesis, and the use of said pyrimidine derivatives as pharmaceutically active agents, especially for the prophylaxis and/or treatment of cell proliferation disorders, cancer, leukemia, erectile dysfunction, cardiovascular diseases and disorders, inflammatory diseases, transplant rejection, immunological diseases, neuroimmunological diseases, autoimmune diseases, infective diseases including opportunistic infections, prion diseases and/or neuro-degeneration. Furthermore, the present invention relates to pharmaceutical compositions containing at least one pyrimidine derivative and/or pharmaceutically acceptable salts thereof as an active ingredient together with at least one pharmaceutically acceptable carrier, excipient or diluents as well as to methods for prophylaxis and/or treatment of the above-mentioned diseases and disorders.
  • [EN] METHOD FOR EXTRACTING SUBSTANCES WITH ANTINEOPLASIC ACTIVITY FROM THE CEROPEGIA FUSCA PLANT, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM<br/>[ES] MÉTODO DE EXTRACCIÓN DE SUSTANCIAS DE LA PLANTA CEROPEGIA FUSCA CON ANTICIDAD ANTINEOPLÁSICA Y COMPOSICIONES FARMACÉUTICAS QUE LAS CONTIENEN.<br/>[FR] PROCÉDÉ D'EXTRACTION DE SUBSTANCES DE LA PLANTECEROPEGIA FUSCA PRÉSENTANT UNE ACTIVITÉ ANTINÉOPLASIQUE ET COMPOSITIONS PHARMACEUTIQUES LES CONTENANT
    申请人:LUCIANO REVERON E HIJOS S L
    公开号:WO2008034920A1
    公开(公告)日:2008-03-27
    [EN] Method for extracting substances with antineoplasic activity from the Ceropegia fusca plant, and pharmaceutical compositions containing them. The method involves macerating the fresh plant with ethanol at 25°C; evaporating the solvent using a vacuum and at a temperature of 40°C; extracting the remaining aqueous extract in countercurrent and at reflux using CH2CI2 and subsequently n-butanol. The component substances of the extract are purified by means of silica gel column chromatography using the n-hexane:CHCI3:acetone system in the ratio 1:1:1 as eluents. The extract obtained from Ceropegia fusca has antineoplasic components and can be used in pharmaceutical compositions containing said extract for these purposes.
    [FR] L'invention concerne un procédé d'extraction de substances de la planta Ceropegia fusca présentant une activité antinéoplasique et des compositions pharmaceutiques les contenant. Ledit procédé consiste à faire macérer la plante à froid avec de l'éthanol à 25°C; à évaporer le dissolvant sous vide et à une température de 40 °C; et à extraire l'extrait aqueux restant à contre-courant et à reflux à l'aide de CH2CI2 et, ultérieurement, de n-butanol. Les substances composant l'extrait sont purifiées par chromatographie sur colonne de gel de silice, en utilisant comme éluants du système n-hexane:CHCI3:acétone selon la proportion 1 :1 :1. L'extrait de Ceropegia fusca obtenu contient des composants antinéoplasiques et peut être utilisé dans des compositions pharmaceutiques contenant ledit extrait à cette fin.
    [ES] Método de extracción de sustancias de la planta Ceropegia fusca con actividad antineoplásica y composiciones farmacéuticas que las contienen. El método comprende la maceración de la planta en fresco con etanol a 25 °C; evaporación del disolvente mediante vacío y a una temperatura de 40 °C; extracción del extracto acuoso restante en contracorriente y a reflujo utilizando CH2CI2 y, posteriomente, n-butanol. Las sustancias componentes del extracto se purifican medante cromatografía en columna de gel de sílice utilizando como eluyentes del sistema n-hexano:CHCI3:acetona en la proporción 1 :1 :1. El extracto obtenido de Ceropegia fusca tiene componentes antineoplásicos y pueden ser utilizado en composiciones farmacéuticas que contienen dicho extracto para estos fines.
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,S)-邻甲苯基-DIPAMP (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)-(-)-4,12-双(二苯基膦基)[2.2]对环芳烷(1,5环辛二烯)铑(I)四氟硼酸盐 (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)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(4-叔丁基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(3-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-4,7-双(3,5-二-叔丁基苯基)膦基-7“-[(吡啶-2-基甲基)氨基]-2,2”,3,3'-四氢1,1'-螺二茚满 (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 (R)-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 (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 (4S,4''S)-2,2''-亚环戊基双[4,5-二氢-4-(苯甲基)恶唑] (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 (3aR,6aS)-5-氧代六氢环戊基[c]吡咯-2(1H)-羧酸酯 (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-[[[[[((1S,2S)-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 (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 (1S,2S,3R,5R)-2-(苄氧基)甲基-6-氧杂双环[3.1.0]己-3-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 (1-(2,6-二氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙蒿油 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫-d6 龙胆紫