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tert-butyl (2-(2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)ethyl)carbamate | 834881-65-1

中文名称
——
中文别名
——
英文名称
tert-butyl (2-(2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)ethyl)carbamate
英文别名
tert-Butyl 2-(2-oxo-2,3-dihydrobenzo[d]imidazol-1-yl)ethylcarbamate;tert-butyl N-[2-(2-oxo-3H-benzimidazol-1-yl)ethyl]carbamate
tert-butyl (2-(2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)ethyl)carbamate化学式
CAS
834881-65-1
化学式
C14H19N3O3
mdl
——
分子量
277.323
InChiKey
FVVKUJPWVUBHNO-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):
    1.4
  • 重原子数:
    20
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    70.7
  • 氢给体数:
    2
  • 氢受体数:
    3

SDS

SDS:8f6a574c6cd7a235bd6520aa2372789b
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上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • SUBSTITUTED DIAMINOPYRIMIDYL COMPOUNDS, COMPOSITIONS THEREOF, AND METHODS OF TREATMENT THEREWITH
    申请人:Signal Pharmaceuticals, LLC
    公开号:US20150175557A1
    公开(公告)日:2015-06-25
    Provided herein are diaminopyrimidyl Compounds having the following structures: wherein X, L, R 1 , and R 2 are as defined herein, compositions comprising an effective amount of a Diaminopyrimidyl Compound, and methods for treating or preventing PKC-theta-mediated disorders, or a condition treatable or preventable by inhibition of a kinase, for example, PKC-theta.
    本文提供具有以下结构的二氨基嘧啶化合物: 其中X、L、R1和R2如本文所定义,包含有效量二氨基嘧啶化合物的组合物,以及用于治疗或预防PKC-theta介导的疾病或通过抑制激酶(例如PKC-theta)可治疗或预防的疾病的方法。
  • Small-molecule modulators of TRP-P8 activity
    申请人:Moreno Ofir
    公开号:US20070232603A1
    公开(公告)日:2007-10-04
    Provided are small-molecule Trp-p8 modulators, including Trp-p8 agonists and Trp-p8 antagonists, and compositions comprising small-molecule Trp-p8 agonists as well as methods for identifying and characterizing novel small-molecule Trp-p8 modulators and methods for decreasing viability and/or inhibiting growth of Trp-p8 expressing cells, methods for activating Trp-p8-mediated cation influx, methods for stimulating apoptosis and/or necrosis, and related methods for the treatment of diseases, including cancers such as lung, breast, colon, and/or prostate cancers as well as other diseases, such as benign prostatic hyperplasia, that are associated with Trp-p8 expression.
    提供了小分子Trp-p8调节剂,包括Trp-p8激动剂和Trp-p8拮抗剂,以及含有小分子Trp-p8激动剂的组合物,以及用于识别和表征新型小分子Trp-p8调节剂的方法,以及降低Trp-p8表达细胞的存活能力和/或抑制生长的方法,激活Trp-p8介导的阳离子流入的方法,刺激凋亡和/或坏死的方法,以及用于治疗疾病的相关方法,包括肺癌、乳腺癌、结肠癌和/或前列腺癌等癌症,以及与Trp-p8表达相关的其他疾病,如良性前列腺增生。
  • [EN] COMPOUNDS AND METHODS FOR THE MODULATION OF AhR<br/>[FR] COMPOSÉS ET PROCÉDÉS POUR LA MODULATION D'AHR
    申请人:IDEAYA BIOSCIENCES INC
    公开号:WO2019156989A1
    公开(公告)日:2019-08-15
    Provided herein are compounds, compositions and methods of using the compounds and compositions for the treatment of diseases modulated, as least in part, by AhR. The compounds are represented by formula: (I) wherein the letters and symbols a, b, c, d, e, f, A, R1, X1, Ar1 and Ar2 have the meanings provided in the specification.
    本文提供了化合物、组合物及使用这些化合物和组合物治疗部分受AhR调控的疾病的方法。这些化合物用以下式表示:(I),其中字母和符号a、b、c、d、e、f、A、R1、X1、Ar1和Ar2的含义在规范中提供。
  • [EN] BICYCLIC HETEROCYCLES CAPABLE OF MODULATING T-CELL RESPONSES, AND METHODS OF USING SAME<br/>[FR] HÉTÉROCYCLES BICYCLIQUES APTES À MODULER DES RÉPONSES DES LYMPHOCYTES T, ET PROCÉDÉS D'UTILISATION ASSOCIÉS
    申请人:NOGRA PHARMA LTD
    公开号:WO2013178815A1
    公开(公告)日:2013-12-05
    The present disclosure is directed in part to bicyclic heterocycles, such as a compound represented by formula (I) or (II) as disclosed herein, and their use in treating medical disorders, such as immune inflammatory disorders such as Crohn's disease, ulcerative colitis, rheumatic disorders, psoriasis, and allergies. The compounds are contemplated to modulate T-Cell responses.
    本公开涉及部分对于双环杂环化合物,例如本文所披露的由式(I)或(II)表示的化合物,以及它们在治疗医学疾病中的应用,如免疫性炎症性疾病,如克罗恩病、溃疡性结肠炎、风湿性疾病、牛皮癣和过敏症。这些化合物被认为可以调节T细胞反应。
  • Sulfonyldihydrobenzimidazolone compounds as 5-hydroxytryptamine-6 ligands
    申请人:Cole Cecil Derek
    公开号:US20050020575A1
    公开(公告)日:2005-01-27
    The present invention provides a compound of formula I and the use thereof in the therapeutic treatment of a central nervous system disorder related to or affected by the 5-HT6 receptor.
    本发明提供了一种I式化合物及其在治疗与5-HT6受体相关或受其影响的中枢神经系统疾病中的用途。
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