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

N4,N4-DIMETHYL-N6-(3-METHYLPHENYL)-N2-(4-METHYLPHENYL)-2,4,6-PYRIMIDINETRIAMINE | 445453-07-6

中文名称
——
中文别名
——
英文名称
N4,N4-DIMETHYL-N6-(3-METHYLPHENYL)-N2-(4-METHYLPHENYL)-2,4,6-PYRIMIDINETRIAMINE
英文别名
4-N,4-N-dimethyl-6-N-(3-methylphenyl)-2-N-(4-methylphenyl)pyrimidine-2,4,6-triamine
N4,N4-DIMETHYL-N6-(3-METHYLPHENYL)-N2-(4-METHYLPHENYL)-2,4,6-PYRIMIDINETRIAMINE化学式
CAS
445453-07-6
化学式
C20H23N5
mdl
——
分子量
333.436
InChiKey
CJYVIMBZCVTPFA-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):
    5.1
  • 重原子数:
    25
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    53.1
  • 氢给体数:
    2
  • 氢受体数:
    5

文献信息

  • Use of GAL3 receptor antagonists for the treatment of depression and/or anxiety and compounds useful in such methods
    申请人:——
    公开号:US20030078271A1
    公开(公告)日:2003-04-24
    This invention is directed to pyrimidine and indolone derivatives which are selective antagonists for the GAL3 receptor. The invention provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention also provides a pharmaceutical composition made by combining a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention further provides a process for making a pharmaceutical composition comprising combining a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention also provides a method of treating a subject suffering from depression and/or anxiety which comprises administering to the subject an amount of a compound of the invention effective to treat the subject's depression and/or anxiety. This invention also provides a method of treating depression and/or anxiety in a subject which comprises administering to the subject a composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a GAL3 receptor antagonist.
    这项发明涉及嘧啶吲哚酮衍生物,它们是选择性GAL3受体拮抗剂。该发明提供了一种包含该发明化合物的治疗有效量和药用载体的药物组合物。该发明还提供了通过结合该发明化合物的治疗有效量和药用载体制备的药物组合物。该发明进一步提供了一种制备药物组合物的方法,包括结合该发明化合物的治疗有效量和药用载体。该发明还提供了一种治疗患有抑郁症和/或焦虑症的受试者的方法,包括向受试者施用足以治疗受试者抑郁症和/或焦虑症的该发明化合物的量。该发明还提供了一种治疗受试者抑郁症和/或焦虑症的方法,包括向受试者施用包含药用载体和治疗有效量GAL3受体拮抗剂的组合物。
  • GAL3 antagonists for the treatment of neuropathic pain
    申请人:——
    公开号:US20040092570A1
    公开(公告)日:2004-05-13
    This invention is directed to pyrimidine and indolone derivatives which are selective antagonists for the GAL3 receptor and are useful for the treatment of neuropathic pain and other abnormalities. This invention also provides a method of treating a subject suffering from an abnormality which comprises administering to the subject an amount of a compound of the invention effective to treat the subject's abnormality. This invention also provides a method of treating an abnormality in a subject which comprises administering to the subject a composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a GAL3 receptor antagonist.
    这项发明涉及嘧啶吲哚酮衍生物,它们是选择性的GAL3受体拮抗剂,可用于治疗神经病痛和其他异常。这项发明还提供了一种治疗患有异常的受试者的方法,包括向受试者投予本发明中的化合物的有效剂量以治疗受试者的异常。这项发明还提供了一种治疗受试者异常的方法,包括向受试者投予包含药用载体和治疗有效量的GAL3受体拮抗剂的组合物。
  • GAL3 receptor antagonists for the treatment of affective disorders
    申请人:——
    公开号:US20040110821A1
    公开(公告)日:2004-06-10
    This invention is directed to pyrimidine and indolone derivatives which are selective antagonists for the GAL3 receptor. This invention provides a method of treating a subject suffering from an affective disorder which comprises administering to the subject an amount of a compound of the invention effective to treat the subject's affective disorder. This invention also provides a method of treating an affective disorder in a subject which comprises administering to the subject a composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a GAL3 receptor antagonist. This invention further provides a process for making a pharmaceutical composition comprising combining a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier.
    这项发明涉及选择性拮抗剂对GAL3受体的嘧啶吲哚酮衍生物。该发明提供了一种治疗患有情感障碍的受试者的方法,包括向受试者施用一定量的该发明化合物,以有效治疗受试者的情感障碍。该发明还提供了一种治疗受试者情感障碍的方法,包括向受试者施用包含药用可接受载体和治疗有效量GAL3受体拮抗剂的组合物。该发明进一步提供了一种制备药物组合物的方法,包括结合该发明化合物的治疗有效量和药用可接受载体。
  • Use of GAL3 antagonist for treatment of depression and/or anxiety and compounds useful in such methods
    申请人:Blackburn P. Thomas
    公开号:US20070259942A1
    公开(公告)日:2007-11-08
    This invention is directed to pyrimidine and indolone derivatives which are selective antagonists for the GAL3 receptor. The invention provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention also provides a pharmaceutical composition made by combining a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention further provides a process for making a pharmaceutical composition comprising combining a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention also provides a method of treating a subject suffering from depression and/or anxiety which comprises administering to the subject an amount of a compound of the invention effective to treat the subject's depression and/or anxiety. This invention also provides a method of treating depression and/or anxiety in a subject which comprises administering to the subject a composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a GAL3 receptor antagonist.
    这项发明涉及选择性拮抗GAL3受体的嘧啶吲哚酮衍生物。该发明提供了一种药物组合物,包括本发明化合物的治疗有效量和药学上可接受的载体。该发明还提供了一种由本发明化合物的治疗有效量和药学上可接受的载体组合而成的药物组合物。该发明进一步提供了一种制备药物组合物的方法,包括将本发明化合物的治疗有效量和药学上可接受的载体组合。该发明还提供了一种治疗患有抑郁和/或焦虑的受试者的方法,包括向受试者投予本发明化合物的治疗有效量。该发明还提供了一种治疗受试者抑郁和/或焦虑的方法,包括向受试者投予一种药学上可接受的载体和治疗有效量的GAL3受体拮抗剂的组合物。
  • Use of GAL 3 receptor antagonists for the treatment of depression and /or anxiety and compounds useful in such methods
    申请人:H. Lundbeck A/S
    公开号:EP2140862A2
    公开(公告)日:2010-01-06
    This invention is directed to pyrimidine and indolone derivatives which are selective antagonists for the GAL3 receptor. The invention provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention also provides a pharmaceutical composition made by combining a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention further provides a process for making a pharmaceutical composition comprising combining a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention also provides a method of treating a subject suffering from depression and/or anxiety which comprises administering to the subject an amount of a compound of the invention effective to treat the subject's depression and/or anxiety. This invention also provides a method of treating depression and/or anxiety in a subject which comprises administering to the subject a composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a GAL3 receptor antagonist.
    本发明涉及嘧啶吲哚酮衍生物,它们是 GAL3 受体的选择性拮抗剂。本发明提供了一种药物组合物,它包含治疗有效量的本发明化合物和药学上可接受的载体。本发明还提供了一种由治疗有效量的本发明化合物和药学上可接受的载体组合而成的药物组合物。本发明进一步提供了一种药物组合物的制造工艺,该工艺包括将治疗有效量的本发明化合物与药学上可接受的载体相结合。本发明还提供了一种治疗抑郁症和/或焦虑症患者的方法,该方法包括向患者施用有效量的本发明化合物,以治疗患者的抑郁症和/或焦虑症。本发明还提供了一种治疗受试者抑郁症和/或焦虑症的方法,该方法包括向受试者施用一种组合物,该组合物包含药学上可接受的载体和治疗有效量的GAL3受体拮抗剂。
查看更多

同类化合物

(乙腈)二氯镍(II) (R)-(-)-α-甲基组胺二氢溴化物 (N-(2-甲基丙-2-烯-1-基)乙烷-1,2-二胺) (4-(苄氧基)-2-(哌啶-1-基)吡啶咪丁-5-基)硼酸 (11-巯基十一烷基)-,,-三甲基溴化铵 鼠立死 鹿花菌素 鲸蜡醇硫酸酯DEA盐 鲸蜡硬脂基二甲基氯化铵 鲸蜡基胺氢氟酸盐 鲸蜡基二甲胺盐酸盐 高苯丙氨醇 高箱鲀毒素 高氯酸5-(二甲氨基)-1-({(E)-[4-(二甲氨基)苯基]甲亚基}氨基)-2-甲基吡啶正离子 高氯酸2-氯-1-({(E)-[4-(二甲氨基)苯基]甲亚基}氨基)-6-甲基吡啶正离子 高氯酸2-(丙烯酰基氧基)-N,N,N-三甲基乙铵 马诺地尔 马来酸氢十八烷酯 马来酸噻吗洛尔EP杂质C 马来酸噻吗洛尔 马来酸倍他司汀 顺式环己烷-1,3-二胺盐酸盐 顺式氯化锆二乙腈 顺式吡咯烷-3,4-二醇盐酸盐 顺式双(3-甲氧基丙腈)二氯铂(II) 顺式3,4-二氟吡咯烷盐酸盐 顺式1-甲基环丙烷1,2-二腈 顺式-二氯-反式-二乙酸-氨-环己胺合铂 顺式-二抗坏血酸(外消旋-1,2-二氨基环己烷)铂(II)水合物 顺式-N,2-二甲基环己胺 顺式-4-甲氧基-环己胺盐酸盐 顺式-4-环己烯-1.2-二胺 顺式-4-氨基-2,2,2-三氟乙酸环己酯 顺式-3-氨基环丁烷甲腈盐酸盐 顺式-2-羟基甲基-1-甲基-1-环己胺 顺式-2-甲基环己胺 顺式-2-(苯基氨基)环己醇 顺式-2-(苯基氨基)环己醇 顺式-2-(氨基甲基)-1-苯基环丙烷羧酸盐酸盐 顺式-1,3-二氨基环戊烷 顺式-1,2-环戊烷二胺二盐酸盐 顺式-1,2-环戊烷二胺 顺式-1,2-环丁腈 顺式-1,2-双氨甲基环己烷 顺式--N,N'-二甲基-1,2-环己二胺 顺式-(R,S)-1,2-二氨基环己烷铂硫酸盐 顺式-(2-氨基-环戊基)-甲醇 顺-2-戊烯腈 顺-1,3-环己烷二胺 顺-1,3-双(氨甲基)环己烷