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1,2,3,4-tetrazine | 290-42-6

中文名称
——
中文别名
——
英文名称
1,2,3,4-tetrazine
英文别名
tetrazine;[1,2,3,4]tetrazine;tetrazine radical;1,2,3,4-tetrazin
1,2,3,4-tetrazine化学式
CAS
290-42-6;70816-59-0
化学式
C2H2N4
mdl
——
分子量
82.0647
InChiKey
DPOPAJRDYZGTIR-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):
    -1.2
  • 重原子数:
    6
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    51.6
  • 氢给体数:
    0
  • 氢受体数:
    4

SDS

SDS:cf34f983fbc631a04d49833ba7ea452f
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反应信息

  • 作为反应物:
    描述:
    1,2,3,4-tetrazine四氢呋喃 为溶剂, 以43%的产率得到哒嗪
    参考文献:
    名称:
    ALPHA-HELIX MIMETIC WITH FUNCTIONALIZED PYRIDAZINE
    摘要:
    合成了模拟i、i+3或i+4、i+7残基的新α-螺旋支架。常见的吡啶嗪杂环来自易得的二甲基吡啶嗪-3,6-二甲酸二酯基块。这些支架可以被视为具有一个疏水面和一个疏水面的两侧的两性α-螺旋的合成对应物。
    公开号:
    US20100022549A1
  • 作为产物:
    描述:
    参考文献:
    名称:
    METHODS OF INCORPORATING AN AMINO ACID COMPRISING A BCN GROUP INTO A POLYPEPTIDE USING AN ORTHOGONAL CODON ENCODING IT AND AN ORTHORGONAL PYLRS SYNTHASE
    摘要:
    该发明涉及一种多肽,其中包含一种具有双环[6.1.0]非-4-炔-9-基甲醇(BCN)基团的氨基酸,特别是当该BCN基团存在为:赖氨酸氨基酸的残基。该发明还涉及一种生产包含BCN基团的多肽的方法,该方法包括将含有BCN基团的氨基酸基因地合并到多肽中。该发明还涉及一种含有双环[6.1.0]非-4-炔-9-基甲醇(BCN)的氨基酸,特别是一种双环[6.1.0]非-4-炔-9-基甲醇(BCN)赖氨酸。此外,该发明涉及一种含有突变Y271M、L274G和C313A的PylRS tRNA合成酶。
    公开号:
    US20150148525A1
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文献信息

  • Alkoxycarbonylamino benzoic acid or alkoxycarbonylamino tetrazolyl phenyl derivatives as IP antagonists
    申请人:——
    公开号:US20020165235A1
    公开(公告)日:2002-11-07
    This invention relates to compounds which are generally IP receptor antagonists and which are represented by Formula I: 1 wherein G 1 is selected from the group consisting of a, b 1 , and b 2 2 and A and G 2 are as defined in the specification; or individual isomers, racemic or non-racemic mixtures of isomers, or pharmaceutically acceptable salts or solvates thereof. The invention further relates to pharmaceutical compositions containing such compounds, methods for their use as therapeutic agents, and methods of preparation thereof.
    这项发明涉及一般为IP受体拮抗剂的化合物,其由以下式I表示: 其中G1选自a、b1和b2组成的群;A和G2如规范中定义;或其个别异构体、消旋或非消旋异构体混合物,或其药用可接受盐或溶剂。该发明还涉及含有这种化合物的药物组合物,以及它们作为治疗剂的使用方法和其制备方法。
  • 1H-QUINAZOLINE-2,4-DIONES
    申请人:NOVARTIS AG
    公开号:US20130296332A1
    公开(公告)日:2013-11-07
    The present invention relates to 1H-Quinazoline-2,4-diones of formula (I) wherein R 1 and R 2 are as defined in the specification, their preparation, their use as pharmaceuticals, and pharmaceutical compositions containing them. Further, intermediates for the manufacture of compounds of formula (I) are and combinations comprising compounds of formula (I) are disclosed.
    本发明涉及公式(I)的1H-喹唑啉-2,4-二酮,其中R1和R2如规范所定义,它们的制备,它们作为药物的用途,以及含有它们的药物组合物。此外,还公开了制造公式(I)化合物的中间体和包含公式(I)化合物的组合物。
  • 1H-Quinazoline-2,4-Diones
    申请人:Allgeier Hans
    公开号:US20080153836A1
    公开(公告)日:2008-06-26
    The present invention relates to 1H-Quinazoline-2,4-diones of formula (I) wherein R 1 and R 2 are as defined in the specification, their preparation, their use as pharmaceuticals, and pharmaceutical compositions containing them. Further, intermediates for the manufacture of compounds of formula (I) are and combinations comprising compounds of formula (I) are disclosed.
    本发明涉及公式(I)的1H-喹唑啉-2,4-二酮,其中R1和R2如规范中所定义,它们的制备,它们作为药物的用途以及含有它们的药物组合物。此外,还揭示了制造公式(I)化合物的中间体和包含公式(I)化合物的组合物。
  • 1H-QUINAZ0LINE-2,4-DIONES
    申请人:ALLGEIER Hans
    公开号:US20100144747A1
    公开(公告)日:2010-06-10
    The present invention relates to 1H-Quinazoline-2,4-diones of formula (I) wherein R 1 and R 2 are as defined in the specification, their preparation, their use as pharmaceuticals, and pharmaceutical compositions containing them. Further, intermediates for the manufacture of compounds of formula (I) are and combinations comprising compounds of formula (I) are disclosed.
    本发明涉及式(I)的1H-喹唑啉-2,4-二酮,其中R1和R2如规范中所定义,它们的制备,它们作为药物的用途以及包含它们的制药组合物。此外,还披露了制备式(I)化合物的中间体和包含式(I)化合物的组合物。
  • N-(2,4-dioxo-6-(tetrahydrofuran-2-yl)-7-(trifluoromethyl)-1,4-dihydro-2H-quinazolin-3-yl)methanesulfonamide
    申请人:Novartis AG
    公开号:US08012988B2
    公开(公告)日:2011-09-06
    The present invention relates to 1H-Quinazoline-2,4-diones of formula (I) wherein R1 and R2 are as defined in the specification, their preparation, their use as pharmaceuticals, and pharmaceutical compositions containing them. Further, intermediates for the manufacture of compounds of formula (I) are and combinations comprising compounds of formula (I) are disclosed.
    本发明涉及公式(I)中的1H-喹唑啉-2,4-二酮,其中R1和R2如规范中所定义,其制备方法,其作为药物的用途以及含有它们的药物组合物。此外,还公开了制备公式(I)化合物的中间体和包含公式(I)化合物的组合物。
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同类化合物

酸四嗪 甲四嗪-氨基叔丁酯 四嗪-氨基叔丁酯 嘧啶并[4,5-e]-1,2,3,4-四嗪 二甲基-1,2,4,5-四嗪 二氯均四嗪 METHYLTETRAZINE-ACID,甲基四嗪-羧基 6-苯基-1,2,4,5-四嗪-3-胺 6-乙基-1,2,4,5-四嗪-3-胺 6-丁基氨基-3-(3,5-二甲基吡唑-1-基)四嗪 6-(3,5-二甲基吡唑-1-基)-1,2,4,5-四嗪-3-胺 3,6-二苯基-1,2,4,5-四嗪 3,6-二氨基-1,2-二氢-1,2,4,5-四嗪盐酸盐 3,6-二-4-吡啶基-1,2,4,5-四嗪 3,6-二-2-吡啶基-1,2,4,5-四嗪 3,6-二(噻吩-2-基)-1,2,4,5-四嗪 3,6-二(3-吡啶基)-1,2,4,5-四氮杂苯 3,6-二(3,5-二甲基-1H-吡唑-1-基)-1,2,4,5-四嗪 1-[6-(3,5-二甲基吡唑-1-基)-1,2,4,5-四嗪-3-基]-2-(丙-2-亚基)肼 1,2-二氢-1,2,4,5-四嗪-3,6-二酮 1,2,4,5]四嗪-3,6-二羧酸 1,2,4,5-四嗪-3-胺 1,2,4,5-四嗪-3,6-二羧酸二甲酯 1,2,4,5-四嗪 (9CI)-吡咯并[2,1-d]-1,2,3,5-四嗪 (6-肼基-1,2,4,5-四嗪-3-基)肼 3-(3,5-Dimethyl-1-pyrazolyl)-6-(2-trifluoroacetylhydrazino)-1,2,4,5-tetrazine 3-cyclohexyl-6-(3,5-dimethyl-1H-pyrazol-1-yl)[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazine 3-ethyl-6-(3,5-dimethyl-1H-pyrazol-1-yl)[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazine 6-pentyl-6-(3,5-dimethyl-1H-pyrazol-1-yl)[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazine 3-benzyl-6-(3,5-dimethyl-1H-pyrazol-1-yl)[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazine 3-methyl-6-(3,5-dimethyl-1H-pyrazol-1-yl)[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazine N'-(6-(3,5-dimethyl-1H-pyrazol-1-yl)-1,2,4,5-tetrazin-3-yl)propionohydrazide 3-(2-ethylidenehydrazinyl)-6-(3,5-dimethyl-1H-pyrazol-1-yl)-1,2,4,5-tetrazine (1,2,4,5-tetrazine-3,6-diyl)dimethanol 3-amino-6-chloro-1,2,4,5-tetrazine 6-(3,5-dimethyl-1H-pyrazol-1-yl)-N-methyl-1,2,4,5-tetrazin-3-amine N-(tert-butyl)-6-(3,5-dimethyl-1H-pyrazol-1-yl)-1,2,4,5-tetrazin-3-amine 6-(3,5-dimethyl-1H-pyrazol-1-yl)-N-(prop-2-en-1-yl)-1,2,4,5-tetrazin-3-amine 3-(2-pyrimidyl)-6-(2-hydroxy)ethyl-1,2,4,5-tetrazine 3-isopropyl-6-phenyl-1,2,4,5-tetrazine 6-butylamino-3-chlorotetrazine 3,6-di(1H-pyrazol-4-yl)-1,2,4,5-tetrazine N-(1H-tetrazol-5-yl)-1,2,4,5-tetrazin-3-amine 3-(3,5-dimethylpyrazolyl)-6-[tris(hydroxylmethyl)aminomethane]-1,2,4,5-tetrazine 2-([1,2,4]triazolo[4,3-b][1,2,4,5]tetrazin-3-ylamino)-2-(hydroxymethyl)propane-1,3-diol 6-amino-1,2,4-triazolo<4,3-b><1,2,4,5>tetrazine N-phenethyl-[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazin-3-amine 2,5-dioxopyrrolidin-1-yl 2-(4-(6-methyl-1,2,4,5-tetrazin-3-yl)phenyl)acetate furazano-1,2,3,4-tetrazine 1,3-dioxide