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1-(4-oxo-3,4-dihydro-quinazolin-2-yl)-1H-pyrazole-4-carboxylic acid | 1238692-06-2

中文名称
——
中文别名
——
英文名称
1-(4-oxo-3,4-dihydro-quinazolin-2-yl)-1H-pyrazole-4-carboxylic acid
英文别名
1-(4-oxo-3H-quinazolin-2-yl)pyrazole-4-carboxylic acid
1-(4-oxo-3,4-dihydro-quinazolin-2-yl)-1H-pyrazole-4-carboxylic acid化学式
CAS
1238692-06-2
化学式
C12H8N4O3
mdl
——
分子量
256.221
InChiKey
GNWGHJTVIBPFGI-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):
    0.6
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    96.6
  • 氢给体数:
    2
  • 氢受体数:
    4

文献信息

  • QUINAZOLINONES AS PROLYL HYDROXYLASE INHIBITORS
    申请人:Bembenek Scott D.
    公开号:US20100204226A1
    公开(公告)日:2010-08-12
    Quinazolinone compounds of formula (I) are described, which are useful as prolyl hydroxylase inhibitors. Such compounds may be used in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by prolyl hydroxylase activity. Thus, the compounds may be administered to treat, e.g., anemia, vascular disorders, metabolic disorders, and wound healing.
    公式(I)的喹唑啉酮化合物被描述为脯酸羟化酶抑制剂,这些化合物可用于制药组合物和治疗由脯酸羟化酶活性介导的疾病状态、紊乱和情况的方法。因此,这些化合物可用于治疗贫血、血管紊乱、代谢紊乱和伤口愈合等疾病。
  • PYRAZOLOPYRIMIDINE COMPOUND
    申请人:MITSUBISHI TANABE PHARMA CORPORATION
    公开号:US20150239889A1
    公开(公告)日:2015-08-27
    Provided is a pyrazolopyrimidine compound represented by formula (I) having an HIF-PHD inhibitory effect, or a pharmaceutically acceptable salt thereof. [In the formula, represents an optionally substituted 7-hydroxypyrazolo[4,3-d]pyrimidine-5-yl, X represents a simple bond or an optionally substituted straight-chain alkylene, Z represents hydrogen atom, or formula (i), formula (ii) or formula (iii) and rings A and A′ are independently an optionally substituted aryl, an optionally substituted heteroaryl, an optionally substituted alicyclic hydrocarbon, or an optionally substituted non-aromatic heterocycle.]
    提供的是一种具有HIF-PHD抑制效果的吡唑嘧啶化合物,其由公式(I)表示,或其药用可接受的盐。[在公式中,代表一个可选地取代的7-羟基吡唑并[4,3-d]嘧啶-5-基,X代表一个简单键或一个可选地取代的直链亚烷基,Z代表氢原子,或公式(i),公式(ii)或公式(iii)和环A和A'分别独立地代表一个可选地取代的芳香族,一个可选地取代的杂芳族,一个可选地取代的脂肪环烃,或一个可选地取代的非芳香族杂环]。
  • MOBILIZING AGENTS AND USES THEREFOR
    申请人:MATER MEDICAL RESEARCH INSTITUTE LIMITED
    公开号:US20160015786A1
    公开(公告)日:2016-01-21
    Disclosed is the use of a HIF-α potentiating agent and a mobilizer of hematopoietic stem cells and/or progenitor cells in methods and compositions for mobilizing hematopoietic stem cell and progenitor cells from the bone marrow into the peripheral blood. The compositions and methods are particularly useful for stem cell transplantation and for treating or preventing immune deficiencies.
  • US8937078B2
    申请人:——
    公开号:US8937078B2
    公开(公告)日:2015-01-20
  • [EN] QUINAZOLINONES AS PROLYL HYDROXYLASE INHIBITORS<br/>[FR] QUINAZOLINONES EN TANT QU'INHIBITEURS DE PROLYLE HYDROXYLASE
    申请人:JANSSEN PHARMACEUTICA NV
    公开号:WO2010093727A1
    公开(公告)日:2010-08-19
    Quinazolinone compounds of formula (I) are described, which are useful as prolyl hydroxylase inhibitors. Such compounds may be used in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by prolyl hydroxylase activity. Thus, the compounds may be administered to treat, e.g., anemia, vascular disorders, metabolic disorders, and wound healing.
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