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N4,N4-DIMETHYL-N2-PHENYL-N6-[(2R,3S)-3,6,6-TRIMETHYLBICYCLO[3.1.1]HEPT-2-YL]-2,4,6-PYRIMIDINETRIAMINE

中文名称
——
中文别名
——
英文名称
N4,N4-DIMETHYL-N2-PHENYL-N6-[(2R,3S)-3,6,6-TRIMETHYLBICYCLO[3.1.1]HEPT-2-YL]-2,4,6-PYRIMIDINETRIAMINE
英文别名
4-N,4-N-dimethyl-2-N-phenyl-6-N-[(2R,3S)-3,6,6-trimethyl-2-bicyclo[3.1.1]heptanyl]pyrimidine-2,4,6-triamine
N4,N4-DIMETHYL-N2-PHENYL-N6-[(2R,3S)-3,6,6-TRIMETHYLBICYCLO[3.1.1]HEPT-2-YL]-2,4,6-PYRIMIDINETRIAMINE化学式
CAS
——
化学式
C22H31N5
mdl
——
分子量
365.522
InChiKey
DSSIJUQBIVYXMR-AXGIONNTSA-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:
    27
  • 可旋转键数:
    5
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.55
  • 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.
    这项发明涉及嘧啶和吲哚酮衍生物,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.
    这项发明涉及嘧啶和吲哚酮衍生物,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受体的嘧啶和吲哚酮衍生物。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
    申请人:Synaptic Pharmaceutical Corporation
    公开号:US20040127502A1
    公开(公告)日:2004-07-01
    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.
    本发明涉及嘧啶和吲哚酮衍生物,它们是选择性GAL3受体拮抗剂。本发明提供一种包含本发明化合物的治疗有效量和药学上可接受的载体的制药组合物。本发明还提供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制药组合物。本发明还提供一种制备包括本发明化合物的治疗有效量和药学上可接受的载体的制药组合物的方法。本发明还提供一种治疗患有抑郁症和/或焦虑症的受试者的方法,该方法包括向受试者施用本发明化合物的治疗有效量以治疗受试者的抑郁症和/或焦虑症。本发明还提供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包含药学上可接受的载体和GAL3受体拮抗剂的治疗有效量的组合物。
  • 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受体的嘧啶和吲哚酮衍生物。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。
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同类化合物

(5β,6α,8α,10α,13α)-6-羟基-15-氧代黄-9(11),16-二烯-18-油酸 (3S,3aR,8aR)-3,8a-二羟基-5-异丙基-3,8-二甲基-2,3,3a,4,5,8a-六氢-1H-天青-6-酮 (2Z)-2-(羟甲基)丁-2-烯酸乙酯 (2S,4aR,6aR,7R,9S,10aS,10bR)-甲基9-(苯甲酰氧基)-2-(呋喃-3-基)-十二烷基-6a,10b-二甲基-4,10-dioxo-1H-苯并[f]异亚甲基-7-羧酸盐 (+)顺式,反式-脱落酸-d6 龙舌兰皂苷乙酯 龙脑香醇酮 龙脑烯醛 龙脑7-O-[Β-D-呋喃芹菜糖基-(1→6)]-Β-D-吡喃葡萄糖苷 龙牙楤木皂甙VII 龙吉甙元 齿孔醇 齐墩果醛 齐墩果酸苄酯 齐墩果酸甲酯 齐墩果酸乙酯 齐墩果酸3-O-alpha-L-吡喃鼠李糖基(1-3)-beta-D-吡喃木糖基(1-3)-alpha-L-吡喃鼠李糖基(1-2)-alpha-L-阿拉伯糖吡喃糖苷 齐墩果酸 beta-D-葡萄糖酯 齐墩果酸 beta-D-吡喃葡萄糖基酯 齐墩果酸 3-乙酸酯 齐墩果酸 3-O-beta-D-葡吡喃糖基 (1→2)-alpha-L-吡喃阿拉伯糖苷 齐墩果酸 齐墩果-12-烯-3b,6b-二醇 齐墩果-12-烯-3,24-二醇 齐墩果-12-烯-3,21,23-三醇,(3b,4b,21a)-(9CI) 齐墩果-12-烯-3,11-二酮 齐墩果-12-烯-2α,3β,28-三醇 齐墩果-12-烯-29-酸,3,22-二羟基-11-羰基-,g-内酯,(3b,20b,22b)- 齐墩果-12-烯-28-酸,3-[(6-脱氧-4-O-b-D-吡喃木糖基-a-L-吡喃鼠李糖基)氧代]-,(3b)-(9CI) 鼠特灵 鼠尾草酸醌 鼠尾草酸 鼠尾草酚酮 鼠尾草苦内脂 黑蚁素 黑蔓醇酯B 黑蔓醇酯A 黑蔓酮酯D 黑海常春藤皂苷A1 黑檀醇 黑果茜草萜 B 黑五味子酸 黏黴酮 黏帚霉酸 黄黄质 黄钟花醌 黄质醛 黄褐毛忍冬皂苷A 黄蝉花素 黄蝉花定