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6-(3'-fluoropropoxy)-2-(4'-hydroxyphenyl)imidazo[1,2-a]pyridine | 956499-80-2

中文名称
——
中文别名
——
英文名称
6-(3'-fluoropropoxy)-2-(4'-hydroxyphenyl)imidazo[1,2-a]pyridine
英文别名
4-[6-(3-fluoropropoxy)imidazo[1,2-a]pyridin-2-yl]phenol
6-(3'-fluoropropoxy)-2-(4'-hydroxyphenyl)imidazo[1,2-a]pyridine化学式
CAS
956499-80-2
化学式
C16H15FN2O2
mdl
——
分子量
286.306
InChiKey
DMVUOKSPXGUFKC-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):
    3.7
  • 重原子数:
    21
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    46.8
  • 氢给体数:
    1
  • 氢受体数:
    4

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

点击查看最新优质反应信息

文献信息

  • USE OF NOVEL COMPOUND HAVING AFFINITY FOR AMYLOID, AND PROCESS FOR PRODUCTION OF THE SAME
    申请人:Nihon Medi-Physics Co., Ltd.
    公开号:EP2216051A1
    公开(公告)日:2010-08-11
    The invention provides a reagent for detecting amyloid in a biological tissue which can detect amyloid in vitro and in vivo with high sensitivity using a compound which has affinity with amyloid and is suppressed in toxicity such as mutagenicity. The reagent for detecting amyloid deposited in a biological tissue comprises the compound represented by the following formula (1) or a salt thereof: wherein A1, A2, A3 and A4 independently represent a carbon or a nitrogen, and R3 is a group represented by the following formula: wherein R1 is a radioactive halogen substituent; m is an integer of 0 to 4; and n is an integer of 0 or 1, provided that at least one of A1, A3, A3 and A4 represents a carbon, and R5 binds to a carbon represented by A1, A2, A3 or A4.
    该发明提供了一种用于检测生物组织中淀粉样物质的试剂,该试剂可以使用一种具有与淀粉样物质亲和力且毒性抑制的化合物在体内和体外高灵敏度地检测淀粉样物质。用于检测生物组织中沉积淀粉样物质的试剂包括以下式(1)所表示的化合物或其盐:其中A1、A2、A3和A4独立地表示碳或氮,R3是由以下式表示的基团:其中R1是放射性卤素取代基;m是0至4的整数;n是0或1的整数,但至少有一个A1、A2、A3和A4表示碳,且R5与A1、A2、A3或A4表示的碳结合。
  • Novel Compound Having Affinity to Amyloid
    申请人:Tanifuji Shigeyuki
    公开号:US20100249407A1
    公开(公告)日:2010-09-30
    The invention relates to a compound which has affinity with amyloid, shows sufficiently rapid clearance from normal tissues and is suppressed in toxicity such as mutagenicity, and also relates to a low-toxic diagnostic agent for Alzheimer's disease containing the compound. The compound is represented by the following formula (1) or a salt thereof: wherein A 1 , A 2 , A 3 and A 4 independently represent a carbon or a nitrogen, and R 3 is a group represented by the following formula: wherein R 1 is a radioactive halogen substituent; m is an integer of 0 to 4; and n is an integer of 0 or 1, provided that at least one of A 1 , A 2 , A 3 and A 4 represents a carbon, and R 3 binds to a carbon represented by A 1 , A 2 , A 3 or A 4 .
    本发明涉及一种与淀粉样物质亲和力强、从正常组织中清除速度足够快且毒性被抑制(例如突变原性),以及一种含有该化合物的低毒性诊断剂,用于阿尔茨海默病。该化合物由以下式(1)或其盐表示:其中,A1、A2、A3和A4独立地表示碳或氮,R3是由以下式表示的基团:其中,R1是放射性卤素取代基;m是0至4的整数;n是0或1的整数,但至少有一个A1、A2、A3和A4表示碳,且R3与A1、A2、A3或A4表示的碳结合。
  • Compound having affinity to amyloid
    申请人:Nihon Medi-Physics Co., Ltd.
    公开号:US08022207B2
    公开(公告)日:2011-09-20
    The invention relates to a compound which has affinity with amyloid, shows sufficiently rapid clearance from normal tissues and is suppressed in toxicity such as mutagenicity, and also relates to a low-toxic diagnostic agent for Alzheimer's disease containing the compound. The compound is represented by the following formula (1) or a salt thereof: wherein A1, A2, A3 and A4 independently represent a carbon or a nitrogen, and R3 is a group represented by the following formula: wherein R1 is a radioactive halogen substituent; m is an integer of 0 to 4; and n is an integer of 0 or 1, provided that at least one of A1, A2, A3 and A4 represents a carbon, and R3 binds to a carbon represented by A1, A2, A3 or A4.
    本发明涉及一种具有与淀粉样物质亲和力、从正常组织中快速清除并且毒性被抑制,如致突变性的化合物,以及一种含有该化合物的低毒性阿尔茨海默病诊断剂。该化合物由以下式(1)或其盐表示:其中A1、A2、A3和A4独立地代表碳或氮,R3是由以下式表示的基团:其中R1是放射性卤素取代基;m为0到4的整数;n为0或1的整数,但至少有一个A1、A2、A3和A4代表碳,并且R3结合到由A1、A2、A3或A4表示的碳上。
  • US8022207B2
    申请人:——
    公开号:US8022207B2
    公开(公告)日:2011-09-20
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