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N-(1-benzyl-4-vinyl-4-piperidinyl)-2,2,2-trichloroacetamide | 785783-57-5

中文名称
——
中文别名
——
英文名称
N-(1-benzyl-4-vinyl-4-piperidinyl)-2,2,2-trichloroacetamide
英文别名
N-(1-benzyl-4-ethenylpiperidin-4-yl)-2,2,2-trichloroacetamide
N-(1-benzyl-4-vinyl-4-piperidinyl)-2,2,2-trichloroacetamide化学式
CAS
785783-57-5
化学式
C16H19Cl3N2O
mdl
——
分子量
361.699
InChiKey
WQFHHLYAGNDQTH-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):
    3.9
  • 重原子数:
    22
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    32.3
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

点击查看最新优质反应信息

文献信息

  • Spiro-piperidine compounds and medicinal use thereof
    申请人:Nishizawa Rena
    公开号:US20060229301A1
    公开(公告)日:2006-10-12
    The present invention relates to a spiro-piperidine compound represented by formula (I): wherein R 1 represents hydrogen, an aliphatic hydrocarbon group which may have a substituent(s) or a cyclic group which may have a substituent(s); and ring A represents a 5- to 8-membered cyclic group which may have a substituent(s), a salt thereof, an N-oxide thereof, a quaternary ammonium salt thereof or a solvate thereof, or a prodrug thereof. The compounds represented by formula (I) have chemokine antagonistic action, so that they are useful for prevention and/or treatment of various inflammatory diseases, immune diseases such as autoimmune diseases or allergic diseases, or HIV infection.
    本发明涉及一种由式(I)表示的螺环哌啶化合物:其中R1表示,可能具有取代基的脂肪烃基或可能具有取代基的环状基团;环A表示可能具有取代基的5-至8-成员环状基团,其盐,N-化物,季盐或溶剂化物,或其前药。式(I)所表示的化合物具有趋化因子拮抗作用,因此它们对于预防和/或治疗各种炎症性疾病,免疫性疾病如自身免疫性疾病或过敏性疾病,或HIV感染是有用的。
  • SPIRO-PIPERIDINE COMPOUNDS AND MEDICINAL USE THEREOF
    申请人:Nishizawa Rena
    公开号:US20100261641A1
    公开(公告)日:2010-10-14
    The present invention relates to a spiro-piperidine compound represented by formula (I): wherein R 1 represents hydrogen, an aliphatic hydrocarbon group which may have a substituent(s) or a cyclic group which may have a substituent(s); and ring A represents a 5- to 8-membered cyclic group which may have a substituent(s), a salt thereof, an N-oxide thereof, a quaternary ammonium salt thereof or a solvate thereof, or a prodrug thereof. The compounds represented by formula (I) have chemokine antagonistic action, so that they are useful for prevention and/or treatment of various inflammatory diseases, immune diseases such as autoimmune diseases or allergic diseases, or HIV infection.
    本发明涉及一种由式(I)表示的螺环哌啶化合物:其中,R1表示、可能具有取代基的脂肪烃基或可能具有取代基的环状基团;环A表示可能具有取代基的5-至8-成员环状基团,其盐、N-化物、季盐或溶剂化物,或其前药。式(I)所表示的化合物具有趋化因子拮抗作用,因此它们在预防和/或治疗各种炎症性疾病、免疫性疾病,如自身免疫性疾病或过敏性疾病,或HIV感染方面非常有用。
  • SPIROPIPERIDINE COMPOUND AND MEDICINAL USE THEREOF
    申请人:ONO PHARMACEUTICAL CO., LTD.
    公开号:EP1619193A1
    公开(公告)日:2006-01-25
    The present invention relates to a spiro-piperidine compound represented by formula (I): wherein R1 represents hydrogen, an aliphatic hydrocarbon group which may have a substituent(s) or a cyclic group which may have a substituent(s); and ring A represents a 5- to 8-membered cyclic group which may have a substituent(s), a salt thereof, an N-oxide thereof, a quaternary ammonium salt thereof or a solvate thereof, or a prodrug thereof The compounds represented by formula (I) have chemokine antagonistic action, so that they are useful for prevention and/or treatment of various inflammatory diseases, immune diseases such as autoimmune diseases or allergic diseases, or HIV infection.
    本发明涉及一种由式(I)表示的螺哌啶化合物: 其中 R1 代表、可具有取代基的脂肪族烃基或可具有取代基的环状基团;式(I)代表的化合物具有趋化因子拮抗作用,因此可用于预防和/或治疗各种炎症性疾病、免疫性疾病(如自身免疫性疾病或过敏性疾病)或 HIV 感染。
  • Spiro-piperidine compounds as chemokine receptor antagonists and medicinal use thereof
    申请人:ONO Pharmaceutical Co., Ltd.
    公开号:EP2364982A1
    公开(公告)日:2011-09-14
    The present invention relates to a spiro-piperidine compound represented by formula (I): wherein R1 represents hydrogen, an aliphatic hydrocarbon group which may have a substituent(s) or a cyclic group which may have a substituent(s); and ring A represents a 5- to 8-membered cyclic group which may have a substituent(s), a salt thereof, an N-oxide thereof, a quaternary ammonium salt thereof or a solvate thereof, or a prodrug thereof. The compounds represented by formula (I) have chemokine antagonistic action, so that they are useful for prevention and/or treatment of various inflammatory diseases, immune diseases such as autoimmune diseases or allergic diseases, or HIV infection.
    本发明涉及一种由式(I)表示的螺哌啶化合物: 其中 R1 代表、可具有取代基的脂族烃基或可具有取代基的环状基团;环 A 代表可具有取代基的 5 至 8 元环状基团、其盐、其 N-化物、其季盐或其溶液或其原药。式 (I) 所代表的化合物具有趋化因子拮抗作用,因此可用于预防和/或治疗各种炎症性疾病、免疫性疾病(如自身免疫性疾病或过敏性疾病)或 HIV 感染。
  • US7498323B2
    申请人:——
    公开号:US7498323B2
    公开(公告)日:2009-03-03
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