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6-(pyridin-2-yl)pyridazin-3-amine | 1159817-09-0

中文名称
——
中文别名
——
英文名称
6-(pyridin-2-yl)pyridazin-3-amine
英文别名
6-pyridin-2-ylpyridazin-3-amine
6-(pyridin-2-yl)pyridazin-3-amine化学式
CAS
1159817-09-0
化学式
C9H8N4
mdl
——
分子量
172.189
InChiKey
JEKCQEZCDAWMIR-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):
    0.1
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    64.7
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

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文献信息

  • [EN] PYRIDAZINE DERIVATIVES AS EAAT2 ACTIVATORS<br/>[FR] DÉRIVÉS DE PYRIDAZINE EN TANT QU'ACTIVATEURS D'EAAT2
    申请人:BRIGHAM & WOMENS HOSPITAL INC
    公开号:WO2017123991A1
    公开(公告)日:2017-07-20
    Pyridazine derivatives that activate the excitatory amino acid transporter 2 (EAAT2), and methods of use thereof for treating or preventing diseases, disorders, and conditions associated with glutamate excitotoxicity.
    吡啶嗪衍生物可以激活兴奋性氨基酸转运体2(EAAT2),并用于治疗或预防与谷酸兴奋毒性相关的疾病、紊乱和状况的方法。
  • [EN] INHIBITORS OF ANOCTAMIN 6 PROTEIN AND USES THEREOF<br/>[FR] INHIBITEURS DE LA PROTÉINE ANOCTAMINE 6 ET LEURS UTILISATIONS
    申请人:ILDONG PHARMACEUTICAL CO LTD
    公开号:WO2022157686A1
    公开(公告)日:2022-07-28
    The present invention relates to a new compound that can inhibit an anoctamin 6 protein, a composition comprising the compound, a method for preparing the compound, and a method for using the compound or composition.
    本发明涉及一种新化合物,可以抑制anoctamin 6蛋白质,包括该化合物的组合物,制备该化合物的方法,以及使用该化合物或组合物的方法。
  • Pyridazine derivatives as EAAT2 activators
    申请人:THE BRIGHAM AND WOMEN'S HOSPITAL, INC.
    公开号:US10787433B2
    公开(公告)日:2020-09-29
    Pyradizine derivatives that activity the excitatory amino acid transporter 2 (EAAT2) of the formula: and methods of use thereof for treating or preventing diseases, disorders, and conditions with glutamate toxicity.
    能激活兴奋性氨基酸转运体 2 (EAAT2) 的拉地嗪(Pyradizine)衍生物: 及其用于治疗或预防谷酸盐毒性疾病、失调和病症的方法。
  • PYRIDAZINE DERIVATIVES AS EAAT2 ACTIVATORS
    申请人:The Brigham and Women's Hospital, Inc.
    公开号:EP3402793A1
    公开(公告)日:2018-11-21
  • THREE-DIMENSIONAL CAVITIES OF DENDRITIC CELL IMMUNORECEPTOR (DCIR), COMPOUNDS BINDING THERETO AND THERAPEUTIC APPLICATIONS RELATED TO INHIBITION OF HUMAN IMMUNODEFICIENCY VIRUS TYPE-1 (HIV-1)
    申请人:Universite Laval
    公开号:US20150157705A1
    公开(公告)日:2015-06-11
    The invention is concerned with compounds, pharmaceutical compositions, screening methods, and therapeutic methods for preventing or reducing a human immunodeficiency virus type-1 (HIV-1) infection and/or propagation associated with dendritic cell immunoreceptor (DCIR). Described herein are compounds which bind on at least one three-dimensional cavity of the DCIR, the cavity(ies) being involved in the interaction between HIV-1 and DCIR. Also described are screening methods for identifying active inhibitors and method of using such inhibitors for the prevention or treatment of virus infections, and more particularly for reducing human immunodeficiency virus type-1 (HIV-1) binding, entry and/or replication in human cells.
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