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2,3-dihydrothieno[3,4-d]pyridazine-1,4-dione | 412338-39-7

中文名称
——
中文别名
——
英文名称
2,3-dihydrothieno[3,4-d]pyridazine-1,4-dione
英文别名
——
2,3-dihydrothieno[3,4-d]pyridazine-1,4-dione化学式
CAS
412338-39-7
化学式
C6H4N2O2S
mdl
MFCD22493452
分子量
168.176
InChiKey
XUVKYPYBNMOIJI-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:
    11
  • 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:
    86.4
  • 氢给体数:
    2
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2934999090

反应信息

  • 作为反应物:
    参考文献:
    名称:
    AZOLO COMPOUNDS FOR TREATMENT OF FIBROTIC DISEASES
    摘要:
    本发明涉及一种式 I 的偶氮化合物 其中,该唑基化合物可使 TGFβ 激活的成纤维细胞的胶原蛋白 I mRNA 水平恢复正常,并将胶原蛋白的产生逆转至未受刺激的成纤维细胞的正常水平。
    公开号:
    EP4279074A1
  • 作为产物:
    参考文献:
    名称:
    Emotional Change Processes in Music-Assisted Reframing
    摘要:
    情感过程对理解和促进持久的治疗变化至关重要。研究人员使用40名焦虑成年人的样本,考察了音乐在认知重构干预中提高情感修正和情绪重组的作用。受试者被分配到典型的重构干预或音乐辅助重构干预组。使用状态-特质焦虑量表、主观痛苦单位量表、抑郁形容词清单和思维大声测量,对两组在焦虑减少、情感修正和意象生动性方面进行了比较。结果表明,音乐辅助重构干预在减少焦虑、修正情感和促进意象生动性方面比典型的重构干预更有效。
    DOI:
    10.1093/jmt/38.3.193
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文献信息

  • [EN] NLRP3 INFLAMMASOME INHIBITOR AND APPLICATION THEREOF<br/>[FR] INHIBITEUR DE L'INFLAMMASOME NLRP3 ET SON UTILISATION<br/>[ZH] NLRP3炎症小体抑制剂及其应用
    申请人:TRANSTHERA SCIENCES NANJING INC
    公开号:WO2022253326A1
    公开(公告)日:2022-12-08
    本发明属于医药技术领域,涉及NLRP3炎症小体抑制剂及其应用。具体涉及通式(I)表示的化合物或其药学上可接受的盐、立体异构体、互变异构体,各基团的定义如说明书中所定义。研究表明,通式(I)表示的化合物或其药学上可接受的盐、立体异构体、互变异构体,对NLRP3炎症小体具有较高的生物活性,对于治疗NLRP3相关疾病具有重要的临床开发价值。
  • 一类取代杂芳酞嗪衍生物的药学用途及其制备方法
    申请人:成都奥睿药业有限公司
    公开号:CN115417856A
    公开(公告)日:2022-12-02
    本公开涉及一种如式(I‑0)所示的取代杂芳酞嗪衍生物,其作为NLRP3抑制剂的用途及制备方法,其具有较好的NLRP3抑制活性。
  • AZOLO COMPOUNDS FOR TREATMENT OF FIBROTIC DISEASES
    申请人:Georg-August-Universität Göttingen Stiftung Öffentlichen Rechts, Universitätsmedizin
    公开号:EP4279074A1
    公开(公告)日:2023-11-22
    The present invention relates to an azolo compound of Formula I for use in the treatment of fibrosis, wherein the azolo compounds normalizes collagen I mRNA-levels of TGFβ-activated fibroblasts and reverses collagen production to the normal levels that are seen in fibroblasts that are not stimulated.
    本发明涉及一种式 I 的偶氮化合物 其中,该唑基化合物可使 TGFβ 激活的成纤维细胞的胶原蛋白 I mRNA 水平恢复正常,并将胶原蛋白的产生逆转至未受刺激的成纤维细胞的正常水平。
  • Robba,M. et al., Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1964, vol. 259, p. 3783 - 3785
    作者:Robba,M. et al.
    DOI:——
    日期:——
  • [EN] NLRP3 MODULATORS<br/>[FR] MODULATEURS DE NLRP3
    申请人:[en]ZOMAGEN BIOSCIENCES LTD
    公开号:WO2023278438A1
    公开(公告)日:2023-01-05
    Described herein are NLRP3 modulators and methods of utilizing NLRP3 modulators in the treatment of diseases, disorders or conditions. Also described herein are pharmaceutical compositions containing such compounds.
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同类化合物

噻吩并[3,4-d]哒嗪-1-羧酸,5-氨基-3,4-二氢-3-(4-甲基苯基)-4-羰基-,乙基酯 1,4-二氯噻吩并[3,4-d]哒嗪 ethyl 5-[(4,4-dimethyl-2,6-dioxocyclohexylidenemethyl)amino]-4-oxo-3-phenyl-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate 5,7-Dimethyl-thieno<3,4-d>pyridazin ethyl 5-amino-3-(4-bromophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate ethyl 3-(3-chlorophenyl)-5-(N-methylacetamido)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate ethyl 5-amino-4-oxo-3-(4-(trifluoromethoxy)phenyl)-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate 5-amino-N-isopropyl-4-oxo-3-(4-(trifluoromethoxy)-phenyl)-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxamide 5-amino-4-oxo-3-(4-(trifluoromethoxy)phenyl)-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylic acid 5-amino-3-(4-chlorophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carbohydrazide ethyl 5-amino-3-(2-chlorophenyl)-4-oxo-3,4-dihydrothieno-[3,4-d]pyridazine-1-carboxylate 7-amino-2-(4-chlorophenyl)-4-methylthieno[3,4-d]pyridazin-1(2H)-one 7-amino-4-methylthieno[3,4-d]pyridazin-1(2H)-one ethyl 5-amino-3-(4-fluorophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate 7-amino-4-methyl-2-(pyridin-3-yl)thieno[3,4-d]pyridazin-1(2H)-one 7-amino-2-benzyl-4-methylthieno[3,4-d]pyridazin-1(2H)-one 7-amino-4-methyl-2-(2,2,2-trifluoroethyl)thieno[3,4-d]pyridazin-1(2H)-one 7-amino-4-methyl-2-(pyridin-2-yl)thieno[3,4-d]pyridazin-1(2H)-one N,N-dimethyl-N'-(7-methyl-4-oxo-3-p-tolyl-1-p-tolylazo-3,4-dihydrothieno[3,4-d]pyridazin-5-yl)-formamidine ethyl 5-amino-4-oxo-3-(o-tolyl)-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate 7-amino-2-isopropyl-4-methylthieno[3,4-d]pyridazin-1(2H)-one ethyl 5-amino-4-oxo-3-(4-(trifluoromethylsulfonyloxy)phenyl)-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate ethyl 5-amino-3-(4-bromophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate 5-amino-3-(4-chlorophenyl)-N-methyl-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxamide 5-amino-3-(4-chlorophenyl)-N,N-dimethyl-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxamide 5-amino-3,4-dihydro-3-p-tolylthieno<3,4-d>-pyridazin-1-carboxylic acid hydrazide 7-amino-2-cyclohexyl-4-methylthieno[3,4-d]pyridazin-1(2H)-one 5-amino-3-(4-hydroxyphenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylic acid ethyl 5-amino-3-(4-hydroxyphenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate 7-amino-2-p-tolyl-2H-thieno[3,4-d]pyridazin-1-one <3,4-d>-Thienopyridazin 5-amino-3-(3-chlorophenyl)-N-isopropyl-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxamide ethyl 5-amino-3-(3-chlorophenyl)-4-oxo-3,4-dihydrothieno-[3,4-d]pyridazine-1-carboxylate 5-amino-3-(3-chlorophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylic acid ethyl 5-(butylamino)-3-(3-chlorophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate butyl 5-(butylamino)-3-(3-chlorophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate ethyl 3-(3-chlorophenyl)-4-oxo-5-(2,2,2-trifluoroacetamido)-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate ethyl 5-((tert-butoxycarbonyl)amino)-3-(3-chlorophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate ethyl 5-(benzylamino)-3-(3-chlorophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate ethyl 3-(3-chlorophenyl)-5-(methylamino)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate 5-amino-3-(4-bromophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylic acid 5-amino-3-(4-bromophenyl)-N-isopropyl-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxamide 5-amino-3-[4-(3-(18F)fluoranylpropoxy)phenyl]-4-oxo-N-propan-2-ylthieno[3,4-d]pyridazine-1-carboxamide tert-butyl N-[3-[4-(2-fluoroethoxy)phenyl]-4-oxo-1-(propan-2-ylcarbamoyl)thieno[3,4-d]pyridazin-5-yl]carbamate tert-butyl N-[3-(4-hydroxyphenyl)-4-oxo-1-(propan-2-ylcarbamoyl)thieno[3,4-d]pyridazin-5-yl]carbamate 5-amino-3-[4-(3-fluoro-2-hydroxypropoxy)phenyl]-4-oxo-N-propan-2-ylthieno[3,4-d]pyridazine-1-carboxamide Tert-butyl 5-amino-3-[4-(2-fluoroethoxy)phenyl]-4-oxothieno[3,4-d]pyridazine-1-carboxylate 5-amino-3-[4-(3-fluoropropoxy)phenyl]-4-oxo-N-propan-2-ylthieno[3,4-d]pyridazine-1-carboxamide 5-amino-3-[4-(2-(18F)fluoranylethoxy)phenyl]-4-oxo-N-propan-2-ylthieno[3,4-d]pyridazine-1-carboxamide 5-amino-3-(4-chlorophenyl)-N-cyclopropyl-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxamide