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(6-methoxy-[1,5]naphthyridin-4-yl)-hydrazine | 911485-68-2

中文名称
——
中文别名
——
英文名称
(6-methoxy-[1,5]naphthyridin-4-yl)-hydrazine
英文别名
(6-methoxy-1,5-naphthyridin-4-yl)hydrazine
(6-methoxy-[1,5]naphthyridin-4-yl)-hydrazine化学式
CAS
911485-68-2
化学式
C9H10N4O
mdl
MFCD19201531
分子量
190.205
InChiKey
HXRRAAJXTFCPOL-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):
    0.8
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.111
  • 拓扑面积:
    73.1
  • 氢给体数:
    2
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Tetrahydroindazole inhibitors of bacterial type II topoisomerases. Part 2: SAR development and potency against multidrug-resistant strains
    摘要:
    We have previously reported a novel class of tetrahydroindazoles that display potency against a variety of Gram-positive and Gram-negative bacteria, potentially via interaction with type II bacterial topoisomerases. Herein are reported SAR investigations of this new series. Several compounds possessing broad-spectrum potency were prepared. Further, these compounds exhibit activity against multidrug-resistant Gram-positive microorganisms equivalent to that against susceptible strains. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.03.004
  • 作为产物:
    描述:
    8-溴-2-甲氧基-1,5-萘啶sodium hydroxide 作用下, 以 乙醇二氯甲烷 为溶剂, 反应 144.0h, 以83%的产率得到(6-methoxy-[1,5]naphthyridin-4-yl)-hydrazine
    参考文献:
    名称:
    Bicyclic pyrazole compounds as antibacterial agents
    摘要:
    抗菌化合物、含有它们的组合物以及用于抑制细菌活性以及治疗、预防或抑制细菌感染的方法。
    公开号:
    US20060223810A1
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文献信息

  • BICYCLIC PYRAZOLE COMPOUNDS AS ANTIBACTERIAL AGENTS
    申请人:Allison Brett D.
    公开号:US20100280240A1
    公开(公告)日:2010-11-04
    Antibacterial compounds, compositions containing them, and methods of use for the inhibition of bacterial activity and the treatment, prevention or inhibition of bacterial infection.
    抗菌化合物,含有它们的组合物,以及用于抑制细菌活性和治疗、预防或抑制细菌感染的使用方法。
  • BICYCLIC PIRAZOLE COMPOUNDS AS ANTIBACTERIAL AGENTS
    申请人:Allison Brett D.
    公开号:US20100274004A1
    公开(公告)日:2010-10-28
    Antibacterial compounds, compositions containing them, and methods of use for the inhibition of bacterial activity and the treatment, prevention or inhibition of bacterial infection.
    抗菌化合物,含有它们的组合物以及使用方法,用于抑制细菌活动和治疗、预防或抑制细菌感染。
  • Novel pyrazole derivatives as potent inhibitors of type II topoisomerases. Part 1: Synthesis and preliminary SAR analysis
    作者:Laurent Gomez、Michael D. Hack、Jiejun Wu、John J.M. Wiener、Hari Venkatesan、Alejandro Santillán、Daniel J. Pippel、Neelakandha Mani、Brian J. Morrow、S. Timothy Motley、Karen Joy Shaw、Ronald Wolin、Cheryl A. Grice、Todd K. Jones
    DOI:10.1016/j.bmcl.2007.03.003
    日期:2007.5
    In an attempt to search for a new class of antibacterial agents, we have discovered a series of pyrazole analogs that possess good antibacterial activity for Gram-positive and Gram-negative organisms via inhibition of type II bacterial topoisomerases. We have investigated the structure-activity relationships of this series, with an emphasis on the length and conformation of the linker. This work led to the identification of tetrahydroindazole analogs, such as compound 1, as the most potent class of compounds. (c) 2007 Elsevier Ltd. All rights reserved.
  • US7842810B2
    申请人:——
    公开号:US7842810B2
    公开(公告)日:2010-11-30
  • US8232391B2
    申请人:——
    公开号:US8232391B2
    公开(公告)日:2012-07-31
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