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2-(Dicyanomethyl)-2-methylpropanedioic acid

中文名称
——
中文别名
——
英文名称
2-(Dicyanomethyl)-2-methylpropanedioic acid
英文别名
2-(dicyanomethyl)-2-methylpropanedioic acid
2-(Dicyanomethyl)-2-methylpropanedioic acid化学式
CAS
——
化学式
C7H6N2O4
mdl
——
分子量
182.13
InChiKey
WVXWGFCXDVHEME-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):
    -0.4
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    122
  • 氢给体数:
    2
  • 氢受体数:
    6

文献信息

  • [EN] PYRAZOLE DERIVATIVES AS SGC STIMULATORS<br/>[FR] DÉRIVÉS DE PYRAZOLE UTILISÉS COMME STIMULATEURS DE SGC
    申请人:IRONWOOD PHARMACEUTICALS INC
    公开号:WO2016044447A1
    公开(公告)日:2016-03-24
    There are described imidazole and pyrazole derivatives which are useful as stimulators of sGC, particularly NO-independent, heme-dependent stimulators. These compounds are also useful for treating, preventing or managing various disorders that are herein disclosed.
    描述了咪唑吡唑生物,它们可作为sGC的刺激剂,特别是NO独立、依赖血红素的刺激剂。这些化合物还可用于治疗、预防或管理本文中披露的各种疾病。
  • SUBSTITUTED ANNULATED PYRIMIDINES AND TRIAZINES, AND USE THEREOF
    申请人:BAYER INTELLECTUAL PROPERTIES GMBH
    公开号:US20140357637A1
    公开(公告)日:2014-12-04
    The present application relates to novel substituted fused pyrimidines and triazines, to processes for their preparation, to their use alone or in combinations for the treatment and/or prophylaxis of diseases, and to their use for producing medicaments for the treatment and/or prophylaxis of diseases, in particular for the treatment and/or prophylaxis of cardiovascular disorders.
    本申请涉及新颖的取代融合嘧啶和三嗪化合物,以及它们的制备方法,单独或组合用于治疗和/或预防疾病,以及用于生产药物治疗和/或预防疾病,特别是用于治疗和/或预防心血管疾病。
  • FLUOROALKYL-SUBSTITUTED PYRAZOLOPYRIDINES AND USE THEREOF
    申请人:Follmann Markus
    公开号:US20140100229A1
    公开(公告)日:2014-04-10
    The present application relates to novel fluoroalkyl-substituted pyrazolopyridines, to processes for their preparation, to their use, alone or in combinations, for the treatment and/or prophylaxis of diseases and to their use for production of medicaments for the treatment and/or prophylaxis of diseases, especially for the treatment and/or prophylaxis of cardiovascular disorders.
    本申请涉及新颖的氟烷基取代的吡唑吡啶类化合物,以及它们的制备方法,它们的单独或组合使用用于治疗和/或预防疾病,以及它们用于生产用于治疗和/或预防疾病的药物,特别是用于治疗和/或预防心血管疾病。
  • SUBSTITUTED ANNULATED TRIAZINES AND USE THEREOF
    申请人:BAYER INTELLECTUAL PROPERTY GMBH
    公开号:US20150274754A1
    公开(公告)日:2015-10-01
    The present application relates to novel substituted fused pyrimidines and triazines, to processes for their preparation, to their use alone or in combinations for the treatment and/or prophylaxis of diseases, and to their use for producing medicaments for the treatment and/or prophylaxis of diseases, in particular for the treatment and/or prophylaxis of cardiovascular disorders.
    本申请涉及新型取代融合嘧啶和三嗪,其制备方法,它们单独或组合用于治疗和/或预防疾病,以及它们用于制造治疗和/或预防疾病的药物,特别是用于治疗和/或预防心血管疾病。
  • Fused pyrazine derivatives useful as soluble guanylate cyclase stimulators
    申请人:Merck Sharp & Dohme Corp.
    公开号:US10780092B2
    公开(公告)日:2020-09-22
    The invention provides certain fused pyrazine compounds of the Formula (I) or a pharmaceutically acceptable salts thereof, wherein X, Y, R1, R3, R4a, R5a, R5b, R6, and the subscript t are as described herein. The compounds or their pharmaceutically acceptable salts can modulate the body's production of cyclic guanosine monophosphate (“cGMP”), and are generally suitable for the therapy and prophylaxis of diseases or disorders which are associated with a disturbed cGMP balance. The invention also provides pharmaceutical compositions which comprise compounds of Formula (I) or pharmaceutically acceptable salts thereof. The invention also relates to methods for use of the compounds or their pharmaceutically acceptable salts in the therapy and prophylaxis of the abovementioned diseases and disorders and for preparing pharmaceuticals for this purpose.
    本发明提供了某些式(I)的融合吡嗪化合物或其药学上可接受的盐类,其中 X、Y、R1、R3、R4a、R5a、R5b、R6 和下标 t 如本文所述。本发明的化合物或其药学上可接受的盐类可以调节体内环磷酸鸟苷("cGMP")的产生,通常适用于治疗和预防与 cGMP 平衡紊乱有关的疾病或失调。本发明还提供了包含式(I)化合物或其药学上可接受的盐的药物组合物。本发明还涉及将这些化合物或其药学上可接受的盐用于治疗和预防上述疾病和紊乱的方法,以及为此目的制备药物的方法。
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