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N-isopropyl-5-(trifluoromethyl)pyridin-2-amine | 847240-94-2

中文名称
——
中文别名
——
英文名称
N-isopropyl-5-(trifluoromethyl)pyridin-2-amine
英文别名
N-propan-2-yl-5-(trifluoromethyl)pyridin-2-amine
N-isopropyl-5-(trifluoromethyl)pyridin-2-amine化学式
CAS
847240-94-2
化学式
C9H11F3N2
mdl
MFCD06635262
分子量
204.195
InChiKey
XREHFRWADMHXHK-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:
    238.0±40.0 °C(Predicted)
  • 密度:
    1.208±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.9
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.444
  • 拓扑面积:
    24.9
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

点击查看最新优质反应信息

文献信息

  • HETEROCYCLIC TRPV1 RECEPTOR LIGANDS
    申请人:Tafesse Laykea
    公开号:US20100137306A1
    公开(公告)日:2010-06-03
    The invention relates to compounds of formulae I(a)-I(d): and pharmaceutically acceptable derivatives thereof, compositions comprising an effective amount of a compound of formulae I(a)-I(d) or a pharmaceutically acceptable derivative thereof, and methods for treating or preventing a condition such as pain, UI, an ulcer, IBD and IBS, comprising administering to an animal in need thereof an effective amount of a compound of formulae I(a)-I(d) or a pharmaceutically acceptable derivative thereof.
    该发明涉及以下化合物的化学式:I(a)-I(d),及其药学上可接受的衍生物,包括含有化合物I(a)-I(d)或其药学上可接受的衍生物的有效量的组合物,以及用于治疗或预防疼痛、尿失禁、溃疡、炎症性肠病和肠易激综合征等疾病的方法,包括向需要的动物施用化合物I(a)-I(d)或其药学上可接受的衍生物的有效量。
  • [EN] MEMBRANE-ACTIVE ANTI-BACTERIAL COMPOUNDS AND USES THEREOF<br/>[FR] COMPOSÉS ANTIBACTÉRIENS À MEMBRANE ACTIVE ET LEURS UTILISATIONS
    申请人:DARTMOUTH COLLEGE
    公开号:WO2021042046A1
    公开(公告)日:2021-03-04
    In an embodiment, the present disclosure pertains to methods of inhibiting bacterial growth. Generally, the methods include exposing bacteria to an anti-bacterial compound as disclosed herein. In some embodiments, the exposing occurs in vivo in a subject in order to treat or prevent a bacterial infection. In additional embodiments, the present disclosure pertains to anti- bacterial compounds that are suitable for inhibiting bacterial growth.
    在一种实施例中,本公开涉及抑制细菌生长的方法。一般来说,这些方法包括将细菌暴露于本公开披露的抗细菌化合物中。在某些实施例中,这种暴露发生在体内的受试者中,以治疗或预防细菌感染。在其他实施例中,本公开涉及适用于抑制细菌生长的抗细菌化合物。
  • [EN] OXALAMIDE HETEROBYCYCLIC COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH STING ACTIVITY<br/>[FR] COMPOSÉS OXALAMIDE HÉTÉROBYCYCLIQUES ET COMPOSITIONS POUR LE TRAITEMENT D'AFFECTIONS ASSOCIÉES À UNE ACTIVITÉ DE STING
    申请人:IFM DUE INC
    公开号:WO2021067805A1
    公开(公告)日:2021-04-08
    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/或水合物,和/或共晶,和/或化合物的药物组合),其抑制(例如,拮抗)干扰素基因激活器(STING)。所述化学实体可用于治疗条件、疾病或障碍,其中增加(例如,过度)STING激活(例如,STING信号传导)对主体(例如,人类)的病理和/或症状和/或疾病或障碍的进展有贡献。本公开还涉及含有相同化学实体的组合物,以及使用和制备这些组合物的方法。
  • METHODS AND COMPOSITIONS OF TARGETED DRUG DEVELOPMENT
    申请人:Errico Joseph P.
    公开号:US20110301193A1
    公开(公告)日:2011-12-08
    Provided herein are compounds having anti-proliferative effect. Also provided are compounds that can modulate the activity of multi-domain proteins comprising a dimerization arm and interdomain tether, such as EGFR, where an untethered, extended conformation is the active state and a tethered conformation is the inactive state, resulting in an autoinhibited configuration. Also provided are methods and pharmacophores for identifying such compounds. Other aspects provide methods or therapeutic treatment for proliferative diseases, disorders, or conditions, such as those associated with EGFR.
    本文提供具有抗增殖作用的化合物。还提供一些化合物,可以调节由二聚化臂和域间系带组成的多域蛋白的活性,例如EGFR,其中未系带的延伸构象是活性状态,而系带的构象是非活性状态,导致自抑制构型。还提供了用于识别此类化合物的方法和药效团。其他方面提供了治疗增殖性疾病、疾病或病状的方法或治疗。例如与EGFR相关的疾病。
  • COMPOSITIONS OF TARGETED DRUG DEVELOPMENT
    申请人:Errico Joseph P.
    公开号:US20140163069A1
    公开(公告)日:2014-06-12
    Provided herein are compounds having anti-proliferative effect. Also provided are compounds that can modulate the activity of multi-domain proteins comprising a dimerization arm and interdomain tether, such as EGFR, where an untethered, extended conformation is the active state and a tethered conformation is the inactive state, resulting in an autoinhibited configuration. Also provided are methods and pharmacophores for identifying such compounds. Other aspects provide methods or therapeutic treatment for proliferative diseases, disorders, or conditions, such as those associated with EGFR.
    本文提供具有抗增殖效应的化合物。还提供了可以调节多域蛋白质活性的化合物,包括具有二聚化臂和域间系索的EGFR,其中无系索的伸展构象是活性状态,而系索的构象是非活性状态,导致自抑制构型。还提供了用于识别此类化合物的方法和药效团。其他方面提供了治疗增殖性疾病、疾病或病情的方法或治疗。例如与EGFR相关的疾病。
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