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3,6-dimethylpyridazine-4-carboxylic acid | 1017485-56-1

中文名称
——
中文别名
——
英文名称
3,6-dimethylpyridazine-4-carboxylic acid
英文别名
3,6-Dimethyl-pyridazin-4-carbonsaeure
3,6-dimethylpyridazine-4-carboxylic acid化学式
CAS
1017485-56-1
化学式
C7H8N2O2
mdl
MFCD03452781
分子量
152.153
InChiKey
RDTNGZBVMDDUJF-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

物化性质

  • 沸点:
    382.4±37.0 °C(Predicted)
  • 密度:
    1.257±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.2
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.285
  • 拓扑面积:
    63.1
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

点击查看最新优质反应信息

文献信息

  • Substituted Indoles
    申请人:AbbVie Inc.
    公开号:US20170174688A1
    公开(公告)日:2017-06-22
    The invention provides for compounds of formula (I) wherein R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 have any of the values defined in the specification, and pharmaceutically acceptable salts thereof, that are useful as agents in the treatment of diseases and conditions mediated and modulated by SUV420H1. Also provided are pharmaceutical compositions comprised of one or more compounds of formula (I).
    该发明提供了以下式(I)的化合物 其中R 1 ,R 2 ,R 3 ,R 4 ,R 5 和R 6 具有规范中定义的任何值,以及其药学上可接受的盐,这些化合物在治疗由SUV420H1介导和调节的疾病和症状中作为药剂是有用的。还提供了由一个或多个式(I)化合物组成的药物组合物。
  • FUSED IMIDAZOLE DERIVATIVE HAVING TTK INHIBITORY ACTION
    申请人:Kusakabe Ken-ichi
    公开号:US20120059162A1
    公开(公告)日:2012-03-08
    Provided are a compound represented by general formula (1) and having a TTK inhibitory action and a medicine containing the compound. In formula (1), (X, Y, V, W) is (—N═, ═CR 1 —, ═N—, —CR 7 ═), (—CR 2 ═, ═N—, ═N—, —CR 7 ═), etc.; A is an (un)substituted aromatic hydrocarbon ring, etc.; L is a single bond, —C(═O)—NR A —, etc.; Z is a group represented by the formula —NR 3 R 4 or a group represented by the formula —OR 5 ; R 1 to R 3 , R 6 , and R 7 each is a hydrogen atom, etc.; R 4 and R 5 each is an (un)substituted alkyl, etc.; and R 8 is an (un)substituted cycloalkyl, etc.
    提供了一个由一般式(1)表示的化合物,具有TTK抑制作用,以及含有该化合物的药物。在式(1)中,(X,Y,V,W)为(—N═,═CR1—,═N—,—CR7═),(—CR2═,═N—,═N—,—CR7═),等等;A为(非)取代芳香烃环等;L为一个单键,—C(═O)—NRA—等;Z为由式—NR3R4或式—OR5表示的基团;R1至R3,R6和R7分别是氢原子等;R4和R5分别是(非)取代烷基等;R8是(非)取代环烷基等。
  • PYRROLIDINE ARYL-ETHER AS NK3 RECEPTOR ANTAGONISTS
    申请人:Jablonski Philippe
    公开号:US20090042896A1
    公开(公告)日:2009-02-12
    The invention relates to a compound of formula I wherein Ar 1 , Ar 2 , R 1 , R 2 , R 3 , R 4 , n, o, p, and q are as defined herein and to a pharmaceutically active salt thereof, including all stereoisomeric forms, individual diastereoisomers and enantiomers of the compound of formula (I) as well as racemic and non-racemic mixtures thereof. The compounds are high potential NK-3 receptor antagonists for the treatment of depression, pain, psychosis, Parkinson's disease, schizophrenia, anxiety and attention deficit hyperactivity disorder (ADHD).
    该发明涉及一种化合物,其化学式为I,其中Ar1、Ar2、R1、R2、R3、R4、n、o、p和q如本文所定义,并且涉及其药用活性盐,包括化合物(I)的所有立体异构形式、单个对映体异构体和对映体,以及其外消旋和非外消旋混合物。这些化合物是高潜力的NK-3受体拮抗剂,用于治疗抑郁症、疼痛、精神病、帕森病、精神分裂症、焦虑和注意力缺陷多动障碍(ADHD)。
  • PYRROLIDINE DERIVATIVES AS NK3 RECEPTOR ANTAGONISTS
    申请人:Knust Henner
    公开号:US20100210659A1
    公开(公告)日:2010-08-19
    The present invention relates to a compounds of formula I wherein A, Ar, R, R2, R3, R4, p, and o are as defined in the specification and claims or to a pharmaceutically active salt thereof. The present compounds are high potential NK-3 receptor antagonists for the treatment of depression, pain, psychosis, Parkinson's disease, schizophrenia, bipolar disorders, anxiety and attention deficit hyperactivity disorder (ADHD).
    本发明涉及公式I的化合物,其中A、Ar、R、R2、R3、R4、p和o如规范和声明中定义的那样,或其药用活性盐。该化合物是高潜力的NK-3受体拮抗剂,用于治疗抑郁症、疼痛、精神病、帕森病、精神分裂症、躁郁症、焦虑症和注意力缺陷多动障碍(ADHD)。
  • Metalloenzyme inhibitor compounds
    申请人:Viamet Pharmaceuticals (Bermuda), Ltd.
    公开号:US10085984B2
    公开(公告)日:2018-10-02
    Provided are compounds having metalloenzyme modulating activity, and methods of treating diseases, disorders or symptoms thereof mediated by such metalloenzymes.
    本文提供了具有属酶调节活性的化合物,以及治疗由此类属酶介导的疾病、失调或症状的方法。
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