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2-Trifluormethyl-4,6-dimethylpyrimidin | 657-49-8

中文名称
——
中文别名
——
英文名称
2-Trifluormethyl-4,6-dimethylpyrimidin
英文别名
4,6-Dimethyl-2-(trifluoromethyl)pyrimidine
2-Trifluormethyl-4,6-dimethylpyrimidin化学式
CAS
657-49-8
化学式
C7H7F3N2
mdl
——
分子量
176.141
InChiKey
FLNWOHKRVOKPEZ-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):
    1.9
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    25.8
  • 氢给体数:
    0
  • 氢受体数:
    5

文献信息

  • [EN] SULFONYL PYRIDYL TRP INHIBITORS<br/>[FR] INHIBITEURS DE SULFONYLPYRIDYLE TRP
    申请人:HOFFMANN LA ROCHE
    公开号:WO2018029288A1
    公开(公告)日:2018-02-15
    The invention is concerned with the compounds of formula I: (I) and pharmaceutically acceptable salts thereof where R1 is a substituted or unsubstituted phenyl or a fused bicyclic comprising a substituted or unsubstituted phenyl. In addition, the present invention relates to methods of manufacturing and methods of using the compounds of formula I as well as pharmaceutical compositions containing such compounds. The compounds may be useful in treating diseases and conditions mediated by TRPA1, such as pain.
    本发明涉及公式I的化合物:(I)以及其中R1是取代的或未取代的苯基或包含取代的或未取代的苯基的并环双环的 pharmaceutically 可接受的盐。此外,本发明还涉及制造和使用公式I化合物的方法以及包含此类化合物的药物组合物。这些化合物可能对治疗由TRPA1介导的疾病和状况,如疼痛,是有用的。
  • [EN] INHIBITORS OF CBL-B AND METHODS OF USE THEREOF<br/>[FR] INHIBITEURS DE CBL-B ET LEURS PROCÉDÉS D'UTILISATION
    申请人:NURIX THERAPEUTICS INC
    公开号:WO2019148005A1
    公开(公告)日:2019-08-01
    Compounds, compositions, and methods for use in inhibiting the E3 enzyme Cbl-b in the ubiquitin proteasome pathway are disclosed. The compounds, compositions, and methods can be used to modulate the immune system, to treat diseases amenable to immune system modulation, and for treatment of cells in vivo, in vitro, or ex vivo.
    揭示了用于抑制泛素蛋白酶体途径中的E3酶Cbl-b的化合物、组合物和使用方法。这些化合物、组合物和方法可用于调节免疫系统,治疗适合免疫系统调节的疾病,并用于体内、体外或体外细胞的治疗。
  • [EN] 1-(HET)ARYLSULFONYL-(PYRROLIDINE OR PIPERIDINE)-2-CARBOXAMIDE DERIVATIVES AND THEIR USE AS TRPA1 ANTAGONISTS<br/>[FR] DÉRIVÉS DE 1-(HET)ARYLSULFONYLE- (PYRROLIDINE OU PIPÉRIDINE)-2-CARBOXAMIDE ET LEUR UTILISATION COMME ANTAGONISTES DE TRPA1
    申请人:HOFFMANN LA ROCHE
    公开号:WO2016128529A1
    公开(公告)日:2016-08-18
    The invention is concerned with the compounds of formula I and salts thereof and other compounds of formulas II-IX as disclosed herein. In addition, the present invention relates to methods of manufacturing and methods of using the compounds of formulas I-IX as well as pharmaceutical compositions containing such compounds. The compounds may be useful in treating diseases and conditions mediated by TRPA1, such as pain or asthma.
    本发明涉及公式I的化合物及其盐,以及如本文所述的公式II-IX的其他化合物。此外,本发明还涉及制造和使用公式I-IX化合物的方法,以及含有这些化合物的药物组合物。这些化合物可能对治疗由TRPA1介导的疾病和状况,如疼痛或哮喘等有帮助。
  • [EN] THIAZOLOPYRIDINE COMPOUNDS, COMPOSITIONS AND THEIR USE AS TYK2 KINASE INHIBITORS<br/>[FR] COMPOSÉS DE THIAZOLOPYRIDINE, COMPOSITIONS ET LEUR UTILISATION COMME INHIBITEURS DE LA KINASE TYK2
    申请人:HOFFMANN LA ROCHE
    公开号:WO2015091584A1
    公开(公告)日:2015-06-25
    Provided are thiazolopyridine compounds that are inhibitors of TYK2 kinase, compositions containing these compounds and methods for treating diseases mediated by TYK2 kinase. In particular, provided are compounds of Formula (I), (II) or (III), stereoisomers, tautomers, solvates, prodrugs or pharmaceutically acceptable salts thereof, where X, R0, R1, R2, R3, R4 and R5 are defined herein, pharmaceutical compositions comprising the compound and a pharmaceutically acceptable carrier, adjuvant or vehicle, methods of using the compound or composition in therapy, for example, for treating a disease or condition mediated by TYK2 kinase in a patient.
    提供了一些噻唑吡啶化合物,这些化合物是TYK2激酶的抑制剂,包含这些化合物的组合物以及治疗由TYK2激酶介导的疾病的方法。具体来说,提供了符合Formula (I)、(II)或(III)的化合物,其立体异构体、互变异构体、溶剂合物、前药或其药用可接受的盐,其中X、R0、R1、R2、R3、R4和R5在此有定义,包括该化合物和药用可接受的载体、辅料或溶剂的药物组合物,使用该化合物或组合物进行治疗的方法,例如,用于治疗患有TYK2激酶介导的疾病或症状的患者。
  • IMIDAZOPYRIDINE COMPOUNDS, COMPOSITIONS AND METHODS OF USE
    申请人:Genentech, Inc.
    公开号:US20140206702A1
    公开(公告)日:2014-07-24
    The invention provides compounds of Formulas Ia-Ib, stereoisomers or pharmaceutically acceptable salts thereof, wherein A, X, R a , R 1 , R 2 , R 4 , R 5 and R 16 are defined herein, a pharmaceutical composition that includes a compound of Formulas Ia-Ib and a pharmaceutically acceptable carrier, adjuvant or vehicle, and methods of using the compound or composition in therapy.
    本发明提供了公式Ia-Ib的化合物、立体异构体或其药学上可接受的盐,其中A、X、Ra、R1、R2、R4、R5和R16在此定义,以及包括公式Ia-Ib化合物和药学上可接受的载体、佐剂或载体的制药组合物,以及使用该化合物或组合物进行治疗的方法。
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