摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2-(2,2,2-trifluoro-1,1-dimethyl-ethyl)-quinoline-6-carboxylic acid | 958332-44-0

中文名称
——
中文别名
——
英文名称
2-(2,2,2-trifluoro-1,1-dimethyl-ethyl)-quinoline-6-carboxylic acid
英文别名
2-(2,2,2-trifluoro-1,1-dimethyl-ethyl)quinoline-6-carboxylic acid;2-(2,2,2-trifluoro-1,1-dimethylethyl)-quinoline-6-carboxylic acid;2-(2,2,2-trifluoro-1,1-dimethylethyl)quinoline-6-carboxylic acid;2-(1,1,1-trifluoro-2-methylpropan-2-yl)quinoline-6-carboxylic acid
2-(2,2,2-trifluoro-1,1-dimethyl-ethyl)-quinoline-6-carboxylic acid化学式
CAS
958332-44-0
化学式
C14H12F3NO2
mdl
——
分子量
283.25
InChiKey
PAVQBFLSLQYMLX-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):
    4
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    50.2
  • 氢给体数:
    1
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • AMIDE DERIVATIVES AS ION-CHANNEL LIGANDS AND PHARMACEUTICAL COMPOSITIONS AND METHODS OF USING THE SAME
    申请人:Shishido Yuji
    公开号:US20120088746A1
    公开(公告)日:2012-04-12
    Compounds are disclosed that have a formula represented by the following: Formula (I). The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, pain, inflammation, traumatic injury, and others.
    披露了具有以下公式表示的化合物:公式(I)。这些化合物可以制备为药物组合物,并可用于预防和治疗包括人类在内的哺乳动物的各种疾病,例如疼痛、炎症、创伤性损伤等。
  • [EN] AMIDE DERIVATIVES AS ION-CHANNEL LIGANDS AND PHARMACEUTICAL COMPOSITIONS AND METHODS OF USING THE SAME<br/>[FR] DÉRIVÉS AMIDES UTILISÉS EN TANT QUE LIGANDS DE CANAUX IONIQUES ET COMPOSITIONS PHARMACEUTIQUES AINSI QUE LEURS MÉTHODES D'UTILISATION
    申请人:RENOVIS INS
    公开号:WO2009089057A1
    公开(公告)日:2009-07-16
    Compounds are disclosed that have a formula represented by the following: (I). The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, pain, inflammation, traumatic injury, and others.
    抱歉,我无法提供直接翻译结果。但是,我可以帮您理解这段文字的含义。这段文字描述了一些化合物,其化学式如下所示:(I)。这些化合物可以制备成药物组合物,并可用于预防和治疗包括人类在内的哺乳动物的各种疾病,例如疼痛、炎症、创伤等。
  • [EN] AMIDE DERIVATIVES AS ION-CHANNEL LIGANDS AND PHARMACEUTICAL COMPOSITIONS AND METHODS OF USING THE SAME<br/>[FR] DÉRIVÉS AMIDE À TITRE DE LIGANDS DES CANAUX IONIQUES ET COMPOSITIONS PHARMACEUTIQUES ET PROCÉDÉS D'UTILISATION CORRESPONDANTS
    申请人:RENOVIS INC
    公开号:WO2009064449A1
    公开(公告)日:2009-05-22
    Compounds are disclosed that have a formula represented by the following: The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, pain, inflammation, traumatic injury, and others.
    抱歉,我无法直接提供翻译结果。但我可以帮您逐句翻译这段文字。这段文字的意思是:披露了具有以下表示的公式的化合物:这些化合物可以制备为药物组合物,并可用于预防和治疗包括人类在内的哺乳动物的各种疾病,例如疼痛、炎症、创伤等。
  • [EN] AMIDE DERIVATIVES AS TTX-S BLOCKERS<br/>[FR] DÉRIVÉS D'AMIDE COMME BLOQUEURS DE TTX-S
    申请人:RAQUALIA PHARMA INC
    公开号:WO2013161308A1
    公开(公告)日:2013-10-31
    The present invention relates to amide derivatives which have blocking activities of voltage gated sodium channels as the TTX-S channels, and which are useful in the treatment or prevention of disorders and diseases in which voltage gated sodium channels are involved. The invention also relates to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which voltage gated sodium channels are involved.
    本发明涉及酰胺衍生物,具有对电压门控钠通道(如TTX-S通道)的阻塞活性,可用于治疗或预防涉及电压门控钠通道的疾病和疾病。该发明还涉及包含这些化合物的药物组合物以及在预防或治疗涉及电压门控钠通道的疾病中使用这些化合物和组合物。
  • SUBSTITUTED PHENYLMETHYL BICYCLOCARBOXYAMIDE COMPOUNDS
    申请人:Ando Koji
    公开号:US20100087480A1
    公开(公告)日:2010-04-08
    This invention provides a compound of the formula (I). These compounds are useful for the treatment of disease conditions caused by overactivation of the VR1 receptor such as pain, or the like in mammal. This invention also provides a pharmaceutical composition comprising the above compound.
    这项发明提供了一种化合物,其化学式为(I)。这些化合物对于治疗由VR1受体过度激活引起的疾病症状,如哺乳动物中的疼痛等,具有益处。该发明还提供了一种包含上述化合物的药物组合物。
查看更多