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Pyrido<3,4-c>pyridazin | 6133-98-8

中文名称
——
中文别名
——
英文名称
Pyrido<3,4-c>pyridazin
英文别名
Pyrido[3,4-C]pyridazine
Pyrido<3,4-c>pyridazin化学式
CAS
6133-98-8
化学式
C7H5N3
mdl
——
分子量
131.137
InChiKey
DVXYZLCJSYRIPC-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):
    0.1
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    38.7
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

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文献信息

  • [EN] SMALL MOLECULE DCN1 INHIBITORS AND THERAPEUTIC METHODS USING THE SAME<br/>[FR] INHIBITEURS DE DCN1 À PETITES MOLÉCULES ET PROCÉDÉS THÉRAPEUTIQUES LES UTILISANT
    申请人:UNIV MICHIGAN REGENTS
    公开号:WO2018183411A1
    公开(公告)日:2018-10-04
    Compounds of formula (I) as inhibitors of DCNl and compositions containing the same are disclosed. Methods of using the DCNl inhibitors in the treatment of diseases and conditions wherein inhibition of DCNl provides a benefit, like oxidative stress-related diseases and conditions, neurodegenerative diseases and conditions, metabolic disorders, and muscular nerve degeneration, also are disclosed.
    公式(I)的化合物被披露为DCNl的抑制剂,以及含有这些化合物的组合物。还披露了在治疗疾病和病况中使用DCNl抑制剂的方法,其中DCNl的抑制提供益处,如氧化应激相关的疾病和病况、神经退行性疾病和病况、代谢紊乱以及肌肉神经退化。
  • Covalent Small Molecule DCN1 Inhibitors and Therapeutic Methods Using the Same
    申请人:THE REGENTS OF THE UNIVERSITY OF MICHIGAN
    公开号:US20180289677A1
    公开(公告)日:2018-10-11
    Small molecule covalent inhibitors of DCN1 and compositions containing the same are disclosed. Methods of using the DCN1 covalent inhibitors in the treatment of diseases and conditions wherein inhibition of DCN1 provides a benefit, like oxidative stress-related diseases and conditions, neurodegenerative diseases and conditions, metabolic disorders, and muscular nerve degeneration, also are disclosed.
    揭示了DCN1的小分子共价抑制剂和含有这些抑制剂的组合物。还揭示了在治疗疾病和状况中使用DCN1共价抑制剂的方法,其中DCN1的抑制提供益处,如氧化应激相关的疾病和状况、神经退行性疾病和状况、代谢紊乱以及肌肉神经退化。
  • SUBSTITUTED HETEROARYL ALDEHYDE COMPOUNDS AND METHODS FOR THEIR USE IN INCREASING TISSUE OXYGENATION
    申请人:Global Blood Therapeutics, Inc.
    公开号:US20150344483A1
    公开(公告)日:2015-12-03
    Provided are substituted heteroaryl aldehydes and derivatives thereof that act as allosteric modulators of hemoglobin, methods and intermediates for their preparation, pharmaceutical compositions comprising the modulators, and methods for their use in treating disorders mediate by hemoglobin and disorders that would benefit from increased tissue oxygenation.
    提供了替代杂环芳醛及其衍生物,其作为血红蛋白的变构调节剂,以及其制备的方法和中间体,包括这些调节剂的药物组合物,以及在治疗由血红蛋白介导的疾病和需要增加组织氧合的疾病中使用它们的方法。
  • [EN] SUBSTITUTED BENZALDEHYDE COMPOUNDS AND METHODS FOR THEIR USE IN INCREASING TISSUE OXYGENATION<br/>[FR] COMPOSÉS BENZALDÉHYDE SUBSTITUÉS ET PROCÉDÉS D'UTILISATION DE CEUX-CI DANS L'AUGMENTATION DE L'OXYGÉNATION DES TISSUS
    申请人:GLOBAL BLOOD THERAPEUTICS INC
    公开号:WO2013102142A1
    公开(公告)日:2013-07-04
    Provided are substituted benzaldehydes and derivatives thereof that act as allosteric modulators of hemoglobin, methods and intermediates for their preparation, pharmaceutical compositions comprising the modulators, and methods for their use in treating disorders mediate by hemoglobin and disorders that would benefit from increased tissue oxygenation.
    提供了替代苯甲醛及其衍生物,其作为血红蛋白的变构调节剂,以及其制备的方法和中间体,包括这些调节剂的药物组合物,以及在治疗由血红蛋白介导的疾病和需要增加组织氧合的疾病中使用它们的方法。
  • [EN] SUBSTITUTED HETEROARYL ALDEHYDE COMPOUNDS AND METHODS FOR THEIR USE IN INCREASING TISSUE OXYGENATION<br/>[FR] COMPOSÉS D'ALDÉHYDES HÉTÉROARYLES SUBSTITUÉS ET LEURS PROCÉDÉS D'UTILISATION DANS L'ACCROISSEMENT DE L'OXYGÉNATION TISSULAIRE
    申请人:GLOBAL BLOOD THERAPEUTICS INC
    公开号:WO2013102145A1
    公开(公告)日:2013-07-04
    Provided are substituted heteroaryl aldehydes and derivatives thereof that act as allosteric modulators of hemoglobin, methods and intermediates for their preparation, pharmaceutical compositions comprising the modulators, and methods for their use in treating disorders mediate by hemoglobin and disorders that would benefit from increased tissue oxygenation.
    提供了替代杂环芳醛及其衍生物,其作为血红蛋白的变构调节剂,以及其制备的方法和中间体,包括这些调节剂的药物组合物,以及在治疗由血红蛋白介导的疾病和需要增加组织氧合的疾病中使用它们的方法。
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同类化合物

2-(4-chlorophenyl)-7-(4-methylphenyl)-6,8-dioxo-3-thienyl-2,6,7,8-tetrahydropyrido[3,4-c]pyridazine-5-carbonitrile pyrido[4,3-e]furano[2,3-c]pyridazine 2,3,7,8-tetrahydro-7-amino-3,8-dioxo-2-p-tolylpyrido[3,4-c]pyridazine-4-carbonitrile 2,3,7,8-tetrahydro-3,8-dioxo-2-p-tolylpyrido[3,4-c]pyridazine-4-carbonitrile pyrido[3,4-c]pyridazin-4(1H)-one Pyrido<3,4-c>pyridazin 3,8-dioxo-2-phenyl-7H-pyrido[3,4-c]pyridazine-4-carbonitrile 8-bromopyrido[3,4-c]pyridazine-5-carboxylic acid 2-(4-chlorophenyl)-6-(furan-2-yl)-7-[(E)-furan-2-ylmethylideneamino]-3,8-dioxopyrido[3,4-c]pyridazine-4-carbonitrile 2-(4-chlorophenyl)-6-(furan-2-yl)-7-[(Z)-furan-2-ylmethylideneamino]-3,8-dioxopyrido[3,4-c]pyridazine-4-carbonitrile 2-(4-Chlorophenyl)-6-(furan-2-yl)-7-(furan-2-ylmethylideneamino)-3,8-dioxopyrido[3,4-c]pyridazine-4-carbonitrile 4-[(4-chlorophenyl)methyl]-2-[[(2R)-1-(2-ethylsulfonylethyl)pyrrolidin-2-yl]methyl]pyrido[3,4-c]pyridazin-1-ium 1-oxide 2,5,6,12-Tetrazatricyclo[7.4.0.02,6]trideca-1(9),4,7,10,12-pentaene tert-butyl N-[3-[(2R)-2-[[4-[(4-chlorophenyl)methyl]-1-hydroxypyrido[3,4-c]pyridazin-2-yl]methyl]pyrrolidin-1-yl]propyl]carbamate N-[2-[(2R)-2-[[4-[(4-chlorophenyl)methyl]-1-hydroxypyrido[3,4-c]pyridazin-2-yl]methyl]pyrrolidin-1-yl]ethyl]butanamide N-[(4-chlorophenyl)methyl]-6-(4-hydroxybut-2-ynyl)-4-oxo-1H-pyrido[3,4-c]pyridazine-3-carboxamide N-[3-[(2R)-2-[[4-[(4-chlorophenyl)methyl]-1-hydroxypyrido[3,4-c]pyridazin-2-yl]methyl]pyrrolidin-1-yl]propyl]-2-methylpropanamide N-[3-[(2R)-2-[[4-[(4-chlorophenyl)methyl]-1-hydroxypyrido[3,4-c]pyridazin-2-yl]methyl]pyrrolidin-1-yl]propyl]-2,2-dimethylpropanamide 3-[(2R)-2-[[4-[(4-chlorophenyl)methyl]-1-hydroxypyrido[3,4-c]pyridazin-2-yl]methyl]pyrrolidin-1-yl]propanoic acid N-[2-[(2R)-2-[[4-[(4-chlorophenyl)methyl]-1-hydroxypyrido[3,4-c]pyridazin-2-yl]methyl]pyrrolidin-1-yl]ethyl]-2,2-dimethylpropanamide N-[2-[(2R)-2-[[4-[(4-chlorophenyl)methyl]-1-hydroxypyrido[3,4-c]pyridazin-2-yl]methyl]pyrrolidin-1-yl]ethyl]-2-methylpropanamide 3,3,3-trifluoro-N-[1-(5,7,8,11-tetrazatricyclo[7.4.0.02,6]trideca-1(13),2(6),3,7,9,11-hexaen-13-yl)pyrrolidin-3-yl]propanamide N-cyclopropyl-1-(5,7,8,11-tetrazatricyclo[7.4.0.02,6]trideca-1(13),2(6),3,7,9,11-hexaen-13-yl)piperidine-3-carboxamide Cyano-[3-(5,7,8,11-tetrazatricyclo[7.4.0.02,6]trideca-1,3,6,8,10,12-hexaen-13-yl)piperidin-1-yl]methanesulfinate 2-[3-(5,7,8,11-Tetrazatricyclo[7.4.0.02,6]trideca-1,3,6,8,10,12-hexaen-13-yl)piperidin-1-yl]sulfonylacetonitrile Cyano-[3-(5,7,8,11-tetrazatricyclo[7.4.0.02,6]trideca-1,3,6,8,10,12-hexaen-13-yl)piperidin-1-yl]methanesulfinic acid 2-cyano-N-[1-(5,7,8,11-tetrazatricyclo[7.4.0.02,6]trideca-1(13),2(6),3,7,9,11-hexaen-13-yl)piperidin-3-yl]acetamide 1-(5,7,8,11-Tetrazatricyclo[7.4.0.02,6]trideca-1(13),2(6),3,7,9,11-hexaen-13-yl)pyrrolidin-3-amine 3,3,3-trifluoro-N-[1-(5,7,8,11-tetrazatricyclo[7.4.0.02,6]trideca-1(13),2(6),3,7,9,11-hexaen-13-yl)piperidin-3-yl]propanamide 1-(5,7,8,11-Tetrazatricyclo[7.4.0.02,6]trideca-1(13),2(6),3,7,9,11-hexaen-13-yl)piperidine-3-carboxylic acid 4,4,4-trifluoro-N-[1-(5,7,8,11-tetrazatricyclo[7.4.0.02,6]trideca-1(13),2(6),3,7,9,11-hexaen-13-yl)piperidin-3-yl]butanamide 1-(5,7,8,11-Tetrazatricyclo[7.4.0.02,6]trideca-1(13),2(6),3,7,9,11-hexaen-13-yl)piperidin-3-amine 2-cyano-N-[1-(5,7,8,11-tetrazatricyclo[7.4.0.02,6]trideca-1(13),2(6),3,7,9,11-hexaen-13-yl)pyrrolidin-3-yl]acetamide 1-(5,7,8,11-Tetrazatricyclo[7.4.0.02,6]trideca-1(13),2(6),3,7,9,11-hexaen-13-yl)pyrrolidine-3-carboxylic acid 4,4,4-trifluoro-N-[1-(5,7,8,11-tetrazatricyclo[7.4.0.02,6]trideca-1(13),2(6),3,7,9,11-hexaen-13-yl)pyrrolidin-3-yl]butanamide