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2-(chloromethyl)-8-fluoroquinazolin-4(3H)-one | 1263413-75-7

中文名称
——
中文别名
——
英文名称
2-(chloromethyl)-8-fluoroquinazolin-4(3H)-one
英文别名
2-(chloromethyl)-8-fluoro-4(3H)-quinazolinone;2-(chloromethyl)-8-fluoro-3H-quinazolin-4-one
2-(chloromethyl)-8-fluoroquinazolin-4(3H)-one化学式
CAS
1263413-75-7
化学式
C9H6ClFN2O
mdl
——
分子量
212.611
InChiKey
NBJCWHJIIUCFJS-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):
    1.4
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    41.5
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • [EN] BENZOXAZINONE DERIVATIVES FOR THE TREATMENT OF GLYTL MEDIATED DISORDERS<br/>[FR] DÉRIVÉS DE BENZOXAZINONE POUR TRAITER DES TROUBLES INDUITS PAR GLYTL
    申请人:GLAXO GROUP LTD
    公开号:WO2011012622A1
    公开(公告)日:2011-02-03
    The present invention relates to benzoxazinone derivatives, processes for their preparation, pharmaceutical compositions and medicaments containing them and to their use in treating disorders mediated by GlyT1, including neurological and neuropsychiatric disorders, in particular psychoses, dementia or attention deficit disorder.
    本发明涉及苯并噁唑酮衍生物,其制备方法,含有它们的药物组合物和药物,以及它们在治疗由GlyT1介导的疾病中的应用,包括神经系统和神经精神疾病,特别是精神病、痴呆或注意力缺陷障碍。
  • Agonists of the apelin receptor and methods of use thereof
    申请人:Sanford Burnham Prebys Medical Discovery Institute
    公开号:US10570128B2
    公开(公告)日:2020-02-25
    Provided herein are small molecule agonists of the apelin receptor for the treatment of disease. The compounds disclosed herein are useful for the treatment of a range of cardiovascular, renal and metabolic conditions. The present invention is based on the seminal discovery of a series of potent small molecule agonists of the apelin receptor, which are useful for the treatment of diseases including heart failure, chronic kidney disease, hypertension, and metabolic disorders such as insulin resistance/diabetes and obesity. The compounds disclosed herein are highly specific for the apelin receptor versus the angiotensin II receptor (ATI).
    本文提供了用于治疗疾病的阿佩林受体小分子激动剂。本文公开的化合物可用于治疗一系列心血管、肾脏和代谢疾病。本发明基于一系列凋亡素受体强效小分子激动剂的开创性发现,这些激动剂可用于治疗包括心力衰竭、慢性肾病、高血压以及胰岛素抵抗/糖尿病和肥胖症等代谢性疾病。与血管紧张素 II 受体(ATI)相比,本文公开的化合物对阿佩林受体具有高度特异性。
  • AGONISTS OF THE APELIN RECEPTOR AND METHODS OF USE THEREOF
    申请人:Sanford-Burnham Medical Research Institute
    公开号:US20170197958A1
    公开(公告)日:2017-07-13
    Provided herein are small molecule agonists of the apelin receptor for the treatment of disease. The compounds disclosed herein are useful for the treatment of a range of cardiovascular, renal and metabolic conditions. The present invention is based on the seminal discovery of a series of potent small molecule agonists of the apelin receptor, which are useful for the treatment of diseases including heart failure, chronic kidney disease, hypertension, and metabolic disorders such as insulin resistance/diabetes and obesity. The compounds disclosed herein are highly specific for the apelin receptor versus the angiotensin II receptor (ATI).
  • [EN] AGONISTS OF THE APELIN RECEPTOR AND METHODS OF USE THEREOF<br/>[FR] AGONISTES DU RÉCEPTEUR DE L'APÉLINE ET LEURS PROCÉDÉS D'UTILISATION
    申请人:SANFORD BURNHAM MED RES INST
    公开号:WO2015184011A2
    公开(公告)日:2015-12-03
    Provided herein are small molecule agonists of the apelin receptor for the treatment of disease. The compounds disclosed herein are useful for the treatment of a range of cardiovascular, renal and metabolic conditions.
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