摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1-(1H-Imidazol-1-yl)-3-methylbutan-2-one | 89175-24-6

中文名称
——
中文别名
——
英文名称
1-(1H-Imidazol-1-yl)-3-methylbutan-2-one
英文别名
1-imidazol-1-yl-3-methylbutan-2-one
1-(1H-Imidazol-1-yl)-3-methylbutan-2-one化学式
CAS
89175-24-6
化学式
C8H12N2O
mdl
——
分子量
152.19
InChiKey
SIIUTJNQOCSWNP-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):
    0.9
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    34.9
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • [EN] INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE AND METHODS OF THEIR USE<br/>[FR] INHIBITEURS DE L'INDOLÉAMINE 2,3-DIOXYGÉNASE ET LEURS PROCÉDÉS D'UTILISATION
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2020023355A1
    公开(公告)日:2020-01-30
    The present invention provides compounds of formula (I): wherein all of the variables are as defined herein. These compounds are inhibitors of indoleamine 2,3-dioxygenase (IDO), which may be used as medicaments for the treatment of proliferative disorders, such as cancer, viral infections and/or autoimmune diseases.
    本发明提供了以下化合物(I)的公式:其中所有变量如本文所定义。这些化合物是色酸2,3-二氧化酶(IDO)的抑制剂,可用作治疗增殖性疾病,如癌症、病毒感染和/或自身免疫疾病的药物。
  • Indole and Benzimidazole Derivatives
    申请人:Boyce Rustum S.
    公开号:US20080317744A1
    公开(公告)日:2008-12-25
    The present invention relates to new indole and benzimidazole compounds and pharmaceutically acceptable salts, esters or prodrugs thereof, compositions of the new compounds together with pharmaceutically acceptable carriers, and uses of the new compounds. The compounds of the invention have the following general formula:
    本发明涉及新的吲哚苯并咪唑化合物及其药学上可接受的盐、酯或前药,新化合物与药学上可接受的载体的组合物,以及新化合物的用途。本发明的化合物具有以下一般式:
  • OXAZOLIDINONE DERIVATIVE HAVING 7-MEMBERED HETERO RING
    申请人:Suzuki Hideyuki
    公开号:US20100256355A1
    公开(公告)日:2010-10-07
    The present invention provides a novel oxazolidinone derivative of the formula (I): wherein Ring A is (A-1) a 7-membered monocyclic heterocycle containing three N atoms; (A-2) a 7-membered monocyclic heterocycle containing two N atoms and one O atom; or (A-3) a 7-membered monocyclic heterocycle containing two N atoms and one S atom, SO or SO 2 , wherein said monocyclic heterocycle is optionally substituted, optionally unsaturated and optionally fused with another ring; X 1 is a single bond, or a heteroatom-containing group selected from the group consisting of —O—, —S—, —NR 2 —, —CO—, —CS—, —CONR 3 —, —NR 4 CO—, —SO 2 NR 5 —, and —NR 6 SO 2 —, wherein R 2 , R 3 , R 4 , R 5 and R 6 are independently hydrogen or lower alkyl, or lower alkylene or lower alkenylene each optionally interrupted by said heteroatom-containing group; Ring B is optionally substituted carbocycle or optionally substituted heterocycle; and R 1 is hydrogen, or an organic residue which is able to bind to the 5 -position of the oxazolidinone ring in oxazolidinone antimicrobial agents, pharmaceutically acceptable salts and solvates thereof which are useful as an antibacterial agent.
  • US7342016B2
    申请人:——
    公开号:US7342016B2
    公开(公告)日:2008-03-11
  • US7608723B2
    申请人:——
    公开号:US7608723B2
    公开(公告)日:2009-10-27
查看更多