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(4-benzyloxy-phenyl)-[6-(4-dimethylaminomethyl-phenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-amine | 497839-74-4

中文名称
——
中文别名
——
英文名称
(4-benzyloxy-phenyl)-[6-(4-dimethylaminomethyl-phenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-amine
英文别名
6-[4-[(dimethylamino)methyl]phenyl]-N-(4-phenylmethoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine
(4-benzyloxy-phenyl)-[6-(4-dimethylaminomethyl-phenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-amine化学式
CAS
497839-74-4
化学式
C28H27N5O
mdl
——
分子量
449.555
InChiKey
LMXINPZKDPTNLH-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

物化性质

  • 密度:
    1.245±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.5
  • 重原子数:
    34
  • 可旋转键数:
    8
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    66.1
  • 氢给体数:
    2
  • 氢受体数:
    5

上下游信息

  • 上游原料
    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

  • Cyclic amine compounds and pharmaceutical composition containing the same
    申请人:KOWA CO., LTD.
    公开号:US20040010147A1
    公开(公告)日:2004-01-15
    A cyclic amine compound represented by the following general formula (1): 1 wherein, R 1 , R 2 and R 3 each independently represent a hydrogen atom or an alkoxy group; W 1 and W 2 each independently represent N or CH; X represents O, NR 4 , CONR 4 or NR 4 CO; R 4 represents a hydrogen atom, or an alkyl, aryl, heteroaryl, aralkyl, or heteroaralkyl group; and l, m and n each represents a number of 0 or 1, a salt thereof and a hydrate thereof are provided. These compounds have inhibitory effects on both cell adhesion and cell infiltration and are useful as anti-asthmatic agents, anti-allergic agents, anti-rheumatic agents, anti-arteriosclerotic agents, anti-inflammatory agents, anti-Sjogren's syndrome agents or the like.
    以下是通用公式(1)表示的一个环胺化合物: 其中, R 1 ,R 2 和R 3 分别独立地表示氢原子或烷氧基; W 1 和W 2 分别独立地表示N或CH; X表示O,NR 4 ,CONR 4 或NR 4 CO; R 4 表示氢原子,或烷基,芳基,杂芳基,芳基烷基或杂芳基烷基; l,m和n分别表示0或1的数字, 提供其盐和合物。 这些化合物对细胞粘附和细胞浸润均具有抑制作用,并可用作抗哮喘剂,抗过敏剂,抗风湿剂,抗动脉硬化剂,抗炎剂,抗干燥综合征剂等。
  • 4-amino-6-phenyl-pyrrolo[2,3-d]pyrimidine derivatives
    申请人:——
    公开号:US20040242600A1
    公开(公告)日:2004-12-02
    The invention relates to 7H-pyrrolo[2,3-d]pyrimidine derivatives of formula I wherein the symbols and substituents are as defined in the description, to processes for the preparation thereof, to pharmaceutical compositions comprising such derivatives and to the use of such derivatives-alone or in combination with one or more other pharmaceutically active compounds-for the preparation of pharmaceutical compositions for the treatment especially of a proliferative disease, such as a tumour. 1
    本发明涉及式I的7H-吡咯[2,3-d]嘧啶生物,其中符号和取代基如描述中所定义,以及制备这些衍生物的方法,包括这些衍生物的制药组合物和使用这些衍生物-单独或与一种或多种其他药理活性化合物结合-制备用于治疗增殖性疾病,如肿瘤的制药组合物。1
  • Erythropoietin production accelerator
    申请人:Imagawa Shigehiko
    公开号:US20060040986A1
    公开(公告)日:2006-02-23
    The present invention relates to a preventive or therapeutic agent for pathological conditions caused by reduced production of erythropoietin, or for anemia, or for chronic anemia, renal anemia, aplastic anemia, or pure red cell aplasia, the agent comprising, as an active ingredient, a cyclic amine compound represented by the following formula (1): wherein, R 1 , R 2 and R 3 each independently represent a hydrogen atom, a halogen atom, or hydroxy, alkyl, halogen-substituted alkyl, alkoxy, alkylthio, carboxyl, alkoxycarbonyl or alkanoyl group; W 1 and W 2 each independently represent N or CH; X represents O, NR 4 , CONR 4 or NR 4 CO; R 4 each represents a hydrogen atom, or an alkyl, alkenyl, alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted aralkyl, or substituted or unsubstituted heteroaralkyl group; and l, m and n each represents a number of 0 or 1, or a salt thereof or a solvate thereof.
    本发明涉及一种预防或治疗由于红细胞生成素减少引起的病理状态,或用于贫血,慢性贫血,肾性贫血,再生障碍性贫血或纯红细胞再生障碍的药物,该药物包含以下式(1)所表示的环状胺化合物作为活性成分:其中,R1,R2和R3各自独立地表示氢原子,卤素原子,羟基,烷基,卤代烷基,烷氧基,烷基,羧基,烷氧羰基或烷酰基;W1和W2各自独立地表示N或CH;X表示O,NR4,CONR4或NR4CO;R4表示氢原子,或烷基,烯基,炔基,取代或未取代芳基,取代或未取代杂芳基,取代或未取代芳基甲基,或取代或未取代杂芳基甲基基团;l,m和n各自表示0或1的数字,或其盐或溶剂化物。
  • 4-AMINO-6-PHENYL-PYRROLO[2,3-D]PYRIMIDINE DERIVATIVES
    申请人:Bold Guido
    公开号:US20070161632A1
    公开(公告)日:2007-07-12
    The invention relates to 7H-pyrrolo[2,3-d]pyrimidine derivatives of formula I wherein the symbols and substituents are as defined in the description, to processes for the preparation thereof, to pharmaceutical compositions comprising such derivatives and to the use of such derivatives—alone or in combination with one or more other pharmaceutically active compounds—for the preparation of pharmaceutical compositions for the treatment especially of a proliferative disease, such as a tumour.
    本发明涉及式I的7H-吡咯并[2,3-d]嘧啶生物,其中符号和取代基的定义如描述所述,以及其制备过程,包括这种衍生物的制药组合物以及使用这种衍生物 - 单独或与一个或多个其他药物活性化合物结合 - 制备用于特别治疗增生性疾病(如肿瘤)的制药组合物。
  • UNSYMMETRICAL CYCLIC DIAMINE COMPOUND
    申请人:Kowa Co., Ltd.
    公开号:EP1400513A1
    公开(公告)日:2004-03-24
    A cyclic diamine compound of formula (1): wherein A is (CH2)n, (CH2)n-CH=CH, CO-(CH2)n or CO-(CH2)n-CH=CH, in which n is a number of 0 to 3; Z represents a formula (2) or (3) : in which R1, R2, R4, R5 and R6 are individually a hydrogen atom, alkyl group, and X and Y are individually CH or a nitrogen atom; and m is 1 or 2; an acid-addition salt thereof, or a hydrate thereof, and a medicine containing such a compound, having excellent effects on both adhesion and cell infiltration, as well as being useful for the prevention and treatment of allergy, asthma, inflammation, rhumatism, and orteriosclerosis.
    式(1)的环状二胺化合物: 其中 A 是 (CH2)n、( )n-CH=CH、CO-( )n 或 CO-( )n-CH=CH,其中 n 是 0 至 3 的数字;Z 代表式 (2) 或 (3) : 其中 R1、R2、R4、R5 和 R6 分别为氢原子或烷基,X 和 Y 分别为 CH 或氮原子;且 m 为 1 或 2; 其酸加盐或其合物,以及含有这种化合物的药物,对粘附性和细胞浸润性均有很好的效果,并可用于预防和治疗过敏、哮喘、炎症、风湿病和动脉硬化。
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