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5-Methyl-2,3-pyridoimidazol | 24638-30-0

中文名称
——
中文别名
——
英文名称
5-Methyl-2,3-pyridoimidazol
英文别名
6-methyl-1(3)H-imidazo[4,5-b]pyridine;6-Methyl-1H-imidazo[4,5-b]pyridine
5-Methyl-2,3-pyridoimidazol化学式
CAS
24638-30-0
化学式
C7H7N3
mdl
——
分子量
133.153
InChiKey
WWLVCLBPTIGNLA-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):
    1.1
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    41.6
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • FLAP MODULATORS
    申请人:JANSSEN PHARMACEUTICA NV
    公开号:US20140221310A1
    公开(公告)日:2014-08-07
    The present invention relates to compounds of Formula (I), or a form thereof, wherein ring A, R 1 , L and R 2 are as defined herein, useful as FLAP modulators. The invention also relates to pharmaceutical compositions comprising compounds of Formula (I). Methods of making and using the compounds of Formula (I) are also within the scope of the invention.
    本发明涉及式(I)化合物,或其形式,其中环A,R1,L和R2如本文所定义,作为FLAP调节剂有用。该发明还涉及包含式(I)化合物的药物组合物。制备和使用式(I)化合物的方法也属于本发明的范围。
  • OXO-HETEROCYCLE FUSED PYRIMIDINE COMPOUNDS, COMPOSITIONS AND METHODS OF USE
    申请人:Bergeron Philippe
    公开号:US20100331305A1
    公开(公告)日:2010-12-30
    Disclosed are compounds of Formula I, including steroisomers, geometric isomers, tautomers, solvates, metabolites and pharmaceutically acceptable salts thereof, that are useful in modulating PIKK related kinase signaling, e.g., mTOR, and for the treatment of diseases (e.g., cancer) that are mediated at least in part by the dysregulation of the PIKK signaling pathway (e.g., mTOR).
    公开的是Formula I的化合物,包括立体异构体、几何异构体、互变异构体、溶剂合物、代谢物及其药学上可接受的盐,这些化合物在调节PIKK相关激酶信号传导方面很有用,例如mTOR,并用于治疗至少部分由PIKK信号传导途径失调引起的疾病(例如癌症)。
  • [EN] QUINOLONE COMPOUND<br/>[FR] COMPOSÉ QUINOLONE
    申请人:OTSUKA PHARMA CO LTD
    公开号:WO2013029548A1
    公开(公告)日:2013-03-07
    The present invention provides a compound represented by the formula (I) wherein X is a hydrogen atom or a fluorine atom; R is a hydrogen atom or alkyl; R1 is (1) cyclopropyl optionally substituted by to 3 halogen atoms or (2) phenyl optionally substituted by 1 to 3 halogen atoms; R2 is alkyl, alkoxy, haloalkoxy, a halogen atom, cyano, etc.; and R3 is 7-oxo-7,8-dihydro-1,8-naphthyridinyl, 3-pyridyl, etc., or a salt thereof. The compound of the present invention has excellent antimicrobial activity against Clostridium difficile and is useful for the prevention or treatment of intestinal infection such as Clostridium difficile- associated diarrhea.
    本发明提供了一种化合物,其表示为式(I),其中X为氢原子或氟原子;R为氢原子或烷基;R1为(1)环丙基,可选择地被1至3个卤原子取代,或(2)苯基,可选择地被1至3个卤原子取代;R2为烷基、烷氧基、卤代烷氧基、卤原子、氰基等;R3为7-氧代-7,8-二氢-1,8-萘啶基,3-吡啶基等,或其盐。本发明的化合物对厌氧菌艰难梭菌具有优异的抗菌活性,并可用于预防或治疗肠道感染,如厌氧菌艰难梭菌相关性腹泻。
  • NEW COMPOUNDS
    申请人:HAUEL Norbert
    公开号:US20100240669A1
    公开(公告)日:2010-09-23
    The present invention relates to the compounds of general formula I wherein n, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 and X are defined as described hereinafter, the enantiomers, the diastereomers, the mixtures and the salts thereof, particularly the physiologically acceptable salts thereof with organic or inorganic acids or bases, which have valuable properties, the preparation thereof, the medicaments containing the pharmacologically effective compounds, the preparation thereof and the use thereof.
    本发明涉及一般式I的化合物,其中n、R1、R2、R3、R4、R5、R6、R7、R8、R9、R10、R11和X的定义如下所述,其对映体、非对映体、混合物及其盐,特别是其与有机或无机酸或碱形成的生理上可接受的盐,具有有价值的性质,其制备方法,含有药理学有效化合物的药物,其制备方法和用途。
  • [EN] COMPOUNDS AND COMPOSITIONS FOR THE TREATMENT OF PARASITIC DISEASES<br/>[FR] COMPOSÉS ET COMPOSITIONS POUR LE TRAITEMENT DE MALADIES PARASITAIRES
    申请人:IRM LLC
    公开号:WO2014078813A1
    公开(公告)日:2014-05-22
    The present invention provides compounds of formula I: [INSERT FORMULA HERE] or a pharmaceutically acceptable salt, tautomer, or stereoisomer, thereof, wherein the variables are as defined herein. The present invention further provides pharmaceutical compositions comprising such compounds and methods of using such compounds for treating, preventing, inhibiting, ameliorating, or eradicating the pathology and/or symptomology of a disease, such as malaria, caused by a Plasmodium parasite.
    本发明提供了式I的化合物:[在此插入公式]或其药学上可接受的盐、互变异构体或立体异构体,其中变量如本文所定义。本发明还提供了包含这种化合物的药物组合物以及使用这种化合物治疗、预防、抑制、改善或根除由疟原虫引起的疟疾等疾病的方法。
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