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1-[1-(1-Phenylcyclononyl)-4-piperidinyl]-1,3-dihydro-2H-1,3-benzimidazol-2-one | 231960-88-6

中文名称
——
中文别名
——
英文名称
1-[1-(1-Phenylcyclononyl)-4-piperidinyl]-1,3-dihydro-2H-1,3-benzimidazol-2-one
英文别名
3-[1-(1-phenylcyclononyl)piperidin-4-yl]-1H-benzimidazol-2-one
1-[1-(1-Phenylcyclononyl)-4-piperidinyl]-1,3-dihydro-2H-1,3-benzimidazol-2-one化学式
CAS
231960-88-6
化学式
C27H35N3O
mdl
——
分子量
417.594
InChiKey
OIPCWDBMJJBLIK-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):
    6.7
  • 重原子数:
    31
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.52
  • 拓扑面积:
    35.6
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • 4-(2-KETO-1-BENZIMIDAZOLINYL)PIPERIDINE COMPOUNDS AS ORL1-RECEPTOR AGONISTS
    申请人:PFIZER INC.
    公开号:EP1049689A1
    公开(公告)日:2000-11-08
  • High affinity ligands for nociceptin receptor ORL-1
    申请人:Schering-Plough Corporation
    公开号:US20040067950A1
    公开(公告)日:2004-04-08
    The present invention relates to the method of treating cough with ORL-1 agonists, alone or in combination with additional agents for treating symptoms of cough, allergy or asthma, pharmaceutical compositions comprising the combinations, and to compounds of the formula 1 or a pharmaceutically acceptable salt or solvate thereof, wherein: the dotted line represents an optional double bond; X 1 is optionally substituted alkyl, cycloalkyl, aryl, heteroaryl or heterocycloalkyl; X 2 is —CHO, —CN, optionally substituted amino, alkyl, or aryl; or X 1 is optionally substituted benzofused heterocyclyl and X 2 is hydrogen; or X 1 and X 2 together form an optionally benzofused spiro heterocyclyl group R 1 , R 2 , R 3 and R 4 are independently H and alkyl, or (R 1 and R 4 ) or (R 2 and R 3 ) or (R 1 and R 3 ) or (R 2 and R 4 ) together can form an alkylene bridge of 1 to 3 carbon atoms; Z 1 is optionally substituted alkyl, aryl, heteroaryl, cycloalkyl or heterocycloalkyl, or —CO 2 (alkyl or substituted amino) or CN ; Z 2 is H or Z 1 ; Z 3 is H or alkyl; or Z 1 , Z 2 and Z 3 , together with the carbon to which they are attached, form bicyclic saturated or unsaturated rings; pharmaceutical compositions therefore, and the use of said compounds as nociceptin receptor inhibitors useful in the treatment of pain, anxiety, cough, asthma, depression and alcohol abuse.
  • US6423725B1
    申请人:——
    公开号:US6423725B1
    公开(公告)日:2002-07-23
  • [EN] 4-(2-KETO-1-BENZIMIDAZOLINYL)PIPERIDINE COMPOUNDS AS ORL1-RECEPTOR AGONISTS<br/>[FR] COMPOSES DE 4-(2-CETO-1-BENZIMIDAZOLINYL)PIPERIDINE, UTILES COMME AGONISTES DU RECEPTEUR ORL1
    申请人:PFIZER PHARMACEUTICALS INC.
    公开号:WO1999036421A1
    公开(公告)日:1999-07-22
    (EN) A compound of formula (I) or the pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4 and R5 are defined above are useful as ORL1-receptor agonists, and useful as analgesics or the like in mammalian subjects.(FR) Cette invention se rapporte à un composé représenté par la formule (I) ou aux sels de ce composé acceptables sur le plan pharmaceutique, formule dans laquelle R1, R2, R3, R4 et R5 sont présentés dans les pièces descriptives de l'invention. Ce composé ou ses sels sont utiles comme agonistes du récepteur ORL1 et peuvent servir d'analgésiques ou similaires chez des sujets mammifères.
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