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N,N-diethyl-4-[[4-(2-furanylmethyl)-1-piperazinyl](8-quinolinyl)methyl]benzamide | 346722-30-3

中文名称
——
中文别名
——
英文名称
N,N-diethyl-4-[[4-(2-furanylmethyl)-1-piperazinyl](8-quinolinyl)methyl]benzamide
英文别名
N,N-diethyl-4-[[4-(furan-2-ylmethyl)piperazin-1-yl]-quinolin-8-ylmethyl]benzamide
N,N-diethyl-4-[[4-(2-furanylmethyl)-1-piperazinyl](8-quinolinyl)methyl]benzamide化学式
CAS
346722-30-3
化学式
C30H34N4O2
mdl
——
分子量
482.626
InChiKey
DGFFFLQTZGBNHX-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):
    4.3
  • 重原子数:
    36
  • 可旋转键数:
    8
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    52.8
  • 氢给体数:
    0
  • 氢受体数:
    5

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

  • Piperazine-containing compounds useful in the treatment of pain
    申请人:AstraZeneca AB
    公开号:US06784181B2
    公开(公告)日:2004-08-31
    The present invention is directed to a compound of general formula (I), wherein R1 is selected from phenyl, pyridinyl, thiophenyl, furanyl, imidazolyl; each phenyl ring and heteroaromatic ring optionally and independently being further substituted by 1, 2 or 3 substituents selected from straight and branched C1-C6 alkyl, NO2, CF3, C1-C6 alkoxy, chloro, fluoro, bromo, and iodo, as well as their pharmaceutically acceptable salts. The invention includes pharmaceutical compositions comprising these compounds and the use of the compounds in therapy, in particular in the management of pain.
    本发明涉及一种通式(I)的化合物,其中R1从苯基、吡啶基、噻吩基、呋喃基、咪唑基中选择;每个苯环和杂环环可以选择地独立地进一步被1、2或3个取代基所取代,所述取代基选择自直链和支链C1-C6烷基、NO2、CF3、C1-C6烷氧基、氯、氟、溴和碘,以及其药学上可接受的盐。本发明还包括包含这些化合物的制药组合物以及这些化合物在治疗中的使用,特别是在疼痛管理中的使用。
  • NOVEL COMPOUNDS
    申请人:AstraZeneca AB
    公开号:EP1242402A2
    公开(公告)日:2002-09-25
  • US6784181B2
    申请人:——
    公开号:US6784181B2
    公开(公告)日:2004-08-31
  • [EN] NOVEL COMPOUNDS<br/>[FR] NOUVEAUX COMPOSES
    申请人:ASTRAZENECA AB
    公开号:WO2001045637A2
    公开(公告)日:2001-06-28
    Compounds of general formula (I), wherein R1 is selected from phenyl, pyridinyl, thiophenyl, furanyl and imidazolyl; each phenyl ring and heteroaromatic ring otpionally and independently being further substituted by 1,2 or 3 substituents selected from straight and branched C¿1?-C6 alkyl, NO2, CF3, C1-C6 alkoxy, chloro, fluoro, bromo, and iodo; are disclosed and claimed in the present application, as well as their pharmaceutically acceptable salts, pharmaceutical compositions comprising the novel compounds and their use in therapy, in particular in the management of pain.
  • Novel compounds
    申请人:——
    公开号:US20030119845A1
    公开(公告)日:2003-06-26
    Compounds of general formula (I), wherein R 1 is selected from phenyl, pyridinyl, thiophenyl, furanyl, imidazolyl; each phenyl ring and heteroaromatic ring optionally and independently being further substituted by 1, 2 or 3 substituents selected from straight and branched C 1 -C 6 alkyl, NO 2 , CF 3 , C 1 -C 6 alkoxy, chloro, fluoro, bromo, and iodo; are disclosed and claimed in the present application, as well as their pharmaceutically acceptable salts, pharmaceutical compositions comprising the novel compounds and their use in therapy, in particular in the management of pain.
    通式(I)的化合物,其中R1选择自苯基、吡啶基、噻吩基、呋喃基、咪唑基;每个苯环和杂环可能且独立地进一步被1、2或3个取代基所取代,所述取代基选择自直链和支链的C1-C6烷基、NO2、CF3、C1-C6烷氧基、氯、氟、溴和碘;在本申请中披露并声明了这些化合物及其药学上可接受的盐、包含这些新化合物的药物组合物以及它们在治疗中的用途,特别是在疼痛管理中的用途。
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