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5-溴-3-甲基-2-(2,2,2-三氟乙氧基)-吡啶 | 1187930-58-0

中文名称
5-溴-3-甲基-2-(2,2,2-三氟乙氧基)-吡啶
中文别名
——
英文名称
5-Bromo-3-methyl-2-(2,2,2-trifluoroethoxy)pyridine
英文别名
——
5-溴-3-甲基-2-(2,2,2-三氟乙氧基)-吡啶化学式
CAS
1187930-58-0
化学式
C8H7BrF3NO
mdl
MFCD11858508
分子量
270.05
InChiKey
LEFHFXVPBQVHRP-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):
    3.3
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.375
  • 拓扑面积:
    22.1
  • 氢给体数:
    0
  • 氢受体数:
    5

文献信息

  • [EN] PYRAZOLE COMPOUNDS AND THEIR USE AS T-TYPE CALCIUM CHANNEL BLOCKERS<br/>[FR] COMPOSÉS DE PYRAZOLE ET LEUR UTILISATION EN TANT QUE BLOQUEURS DES CANAUX CALCIQUES DE TYPE T
    申请人:ACTELION PHARMACEUTICALS LTD
    公开号:WO2015186056A1
    公开(公告)日:2015-12-10
    The invention relates to compounds of formula (I) Formula (I) wherein X, Y, R1, R2, (R4)n, and (R5)m are as defined in the description, and to pharmaceutically acceptable salts of such compounds. These compounds are useful as calcium T-channel blockers.
    这项发明涉及式(I)的化合物。式(I)中X、Y、R1、R2、(R4)n和(R5)m的定义如描述中所述,并且涉及这些化合物的药用盐。这些化合物可用作T通道阻滞剂。
  • [EN] COMPOUNDS AND THEIR METHODS OF USE<br/>[FR] COMPOSÉS ET PROCÉDÉS D'UTILISATION DESDITS COMPOSÉS
    申请人:PRAXIS PREC MEDICINES INC
    公开号:WO2018098499A1
    公开(公告)日:2018-05-31
    The present invention is directed to, in part, fused heteroaryl compounds and compositions useful for preventing and/or treating a disease or condition relating to aberrant function of a voltage-gated, sodium ion channel, for example, abnormal late/persistent sodium current. Methods of treating a disease or condition relating to aberrant function of a sodium ion channel including Dravet syndrome or epilepsy are also provided herein.
    本发明部分涉及融合的杂环化合物和组合物,用于预防和/或治疗与电压门控钠离子通道异常功能相关的疾病或症状,例如异常的晚期/持续性电流。本文还提供了治疗与钠离子通道异常功能相关的疾病或症状,包括德拉维特综合征或癫痫的方法。
  • [EN] COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH STING ACTIVITY<br/>[FR] COMPOSÉS ET COMPOSITIONS POUR TRAITER DES ÉTATS ASSOCIÉS À UNE ACTIVITÉ DE STING
    申请人:IFM DUE INC
    公开号:WO2022015975A1
    公开(公告)日:2022-01-20
    This disclosure features chemical entities (e.g., a compound or a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination of the compound) that inhibit (e.g., antagonize) Stimulator of Interferon Genes (STING). Said chemical entities are useful, e.g., for treating a condition, disease or disorder in which increased (e.g., excessive) STING activation (e.g., STING signaling) contributes to the pathology and/or symptoms and/or progression of the condition, disease or disorder (e.g., cancer) in a subject (e.g., a human). This disclosure also features compositions containing the same as well as methods of using and making the same.
    本公开涉及化学实体(例如,化合物或药用盐,和/或合物,和/或共晶,和/或该化合物的药物组合),其抑制(例如,拮抗)干扰素基因激活剂(STING)。所述化学实体可用于治疗某种疾病、疾病或疾病,其中增加(例如,过多)STING激活(例如,STING信号传导)导致病理和/或症状和/或该疾病、疾病或疾病的进展(例如,癌症)在受试者(例如,人类)中。本公开还涉及包含相同化学实体的组合物,以及使用和制备相同的方法。
  • Pyrazole compounds and their use as T-type calcium channel blockers
    申请人:IDORSIA PHARMACEUTICALS LTD
    公开号:US10065929B2
    公开(公告)日:2018-09-04
    The invention relates to compounds of formula (I) wherein X, Y, R1, R2, (R4)n, and (R5)m are as defined in the description, and to pharmaceutically acceptable salts of such compounds. These compounds are useful as calcium T-channel blockers.
    本发明涉及式 (I) 的化合物 其中X、Y、R1、R2、(R4)n和(R5)m如描述中所定义,并涉及此类化合物的药学上可接受的盐。这些化合物可用作 T 通道阻滞剂。
  • PYRAZOLE COMPOUNDS AND THEIR USE AS T-TYPE CALCIUM CHANNEL BLOCKERS
    申请人:Actelion Pharmaceuticals Ltd.
    公开号:EP3152199A1
    公开(公告)日:2017-04-12
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