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isopropyl 6-(pyridin-2-yl)pyridazine-3-carboxylate

中文名称
——
中文别名
——
英文名称
isopropyl 6-(pyridin-2-yl)pyridazine-3-carboxylate
英文别名
Propan-2-yl 6-pyridin-2-ylpyridazine-3-carboxylate;propan-2-yl 6-pyridin-2-ylpyridazine-3-carboxylate
isopropyl 6-(pyridin-2-yl)pyridazine-3-carboxylate化学式
CAS
——
化学式
C13H13N3O2
mdl
——
分子量
243.265
InChiKey
VYZJNCJDBLMXCJ-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):
    1.5
  • 重原子数:
    18
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    65
  • 氢给体数:
    0
  • 氢受体数:
    5

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

  • Pyran-2-ones as Synthons for Pyridazine-3-carboxylic Derivatives. Oxidation of Nitrogen-Rich Compounds
    作者:Marijan Kočevar、Franc Požgan、Stanislav Kafka、Slovenko Polanc
    DOI:10.3987/com-06-s(w)11
    日期:——
    The reaction of 6-(pyridin-2-yl)-2H-pyran-2-one (1) with hydrazine hydrate toward pyridazine derivatives was investigated. To elucidate the reaction pathway, an intermediary-formed α,δ-dihydrazonohydrazide derivative (3) was successfully isolated. Oxidations of the above compounds as well as of other pyridazine derivatives containing a carbohydrazido group, using ammonium cerium(IV) nitrate (CAN),
    研究了 6-(pyridin-2-yl)-2H-pyran-2-one (1) 与哒嗪生物的反应。为了阐明反应途径,成功分离出中间体形成的 α,δ-二酰生物 (3)。使用硝酸铈 (IV) (CAN)、硝酸 (III) 三合物 (TTN) 或醋酸铜 (II) 合物 (CuDA) 对上述化合物以及其他含有碳酰基的哒嗪生物进行氧化也提出了。
  • Structure–activity relationship study of pyridazine derivatives as glutamate transporter EAAT2 activators
    作者:Xuechao Xing、Ling-Chu Chang、Qiongman Kong、Craig K. Colton、Liching Lai、Marcie A. Glicksman、Chien-Liang Glenn Lin、Gregory D. Cuny
    DOI:10.1016/j.bmcl.2011.08.009
    日期:2011.10
    Excitatory amino acid transporter 2 (EAAT2) is the major glutamate transporter and functions to remove glutamate from synapses. A thiopyridazine derivative has been found to increase EAAT2 protein levels in astrocytes. A structure-activity relationship study revealed that several components of the molecule were required for activity, such as the thioether and pyridazine. Modification of the benzylthioether resulted in several derivatives (7-13, 7-15 and 7-17) that enhanced EAAT2 levels by >6-fold at concentrations <5 mu M after 24 h. In addition, one of the derivatives (7-22) enhanced EAAT2 levels 3.5-3.9-fold after 24 h with an EC50 of 0.5 mu M. (C) 2011 Elsevier Ltd. All rights reserved.
  • Pyridazine derivatives as EAAT2 Activators
    申请人:Cuny Gregory D.
    公开号:US20140303174A1
    公开(公告)日:2014-10-09
    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.
  • US9447075B2
    申请人:——
    公开号:US9447075B2
    公开(公告)日:2016-09-20
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