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(+/-)-1,2-dihydro-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]-1-acenaphthylenecarboxamide | 208649-57-4

中文名称
——
中文别名
——
英文名称
(+/-)-1,2-dihydro-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]-1-acenaphthylenecarboxamide
英文别名
(+/-)-1,2-dihydro-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]-1-acenaphthylencarboxamide;N-methyl-N-(2-pyrrolidin-1-ylcyclohexyl)-1,2-dihydroacenaphthylene-1-carboxamide
(+/-)-1,2-dihydro-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]-1-acenaphthylenecarboxamide化学式
CAS
208649-57-4
化学式
C24H30N2O
mdl
——
分子量
362.515
InChiKey
GYUFHXLKZVIHEO-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):
    4.5
  • 重原子数:
    27
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    23.6
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • 1,2-cyclohexylaminoaryl amides useful as analgesic agents
    申请人:WARNER-LAMBERT COMPANY
    公开号:EP0380063A1
    公开(公告)日:1990-08-01
    Novel 1,2-cyclohexylaminoaryl amides of formula I are useful as analgesic agents having very high kappa-opioid affinity and selectivity and potency and are useful as analgesics, diuretics, antiinflammatory and psychotherapeutic agents. Methods for making the compounds and pharmaceutical compositions containing them are also disclosed.
    式 I 的新型 1,2-环己基基芳酰胺可用作镇痛剂,具有极高的卡巴阿片亲和力、选择性和药效。 可用作镇痛剂,具有极高的卡帕-阿片类亲和力、选择性和效力,可用作镇痛剂、利尿剂、消炎剂和精神治疗剂。 此外,还公开了制造这些化合物的方法以及含有这些化合物的药物组合物。
  • REMEDIES FOR SEPSIS
    申请人:TORAY INDUSTRIES, INC.
    公开号:EP1402899A1
    公开(公告)日:2004-03-31
    A therapeutic agent for sepsis and various symptoms accompanying sepsis (such as septic shock, disseminated intravascular coagulation syndrome, adult respiratory distress syndrome and multiple organ dysfunction) is disclosed. The therapeutic agent for sepsis according to the present invention comprises as an effective ingredient an opioid κ receptor agonist compound such as (-)-17-(cyclopropylmethyl)-3,14β-dihydroxy-4,5α-epoxy-6β[N-methyl-trans-3-(3-furyl)acrylamide] oxide derivative. The opioid κ receptor agonist compound may be administered as it is or in the form of a pharmaceutical composition prepared by mixing the compound with a known pharmaceutically acceptable acid, carrier or vehicle orally or parenterally.
    本发明公开了一种治疗败血症和败血症伴随的各种症状(如脓毒性休克、弥散性血管内凝血综合征、成人呼吸窘迫综合征和多器官功能障碍)的药物。根据本发明的败血症治疗剂包括作为有效成分的阿片类κ受体激动剂化合物,如(-)-17-(环丙基甲基)-3,14β-二羟基-4,5α-环氧-6β[N-甲基-反式-3-(3-呋喃基)丙烯酰胺]氧化物衍生物。阿片κ受体激动剂化合物可以原样给药,也可以通过将该化合物与已知的药学上可接受的酸、载体或载体混合制备的药物组合物的形式口服或肠外给药。
  • Remedies for sepsis
    申请人:——
    公开号:US20040147536A1
    公开(公告)日:2004-07-29
    A therapeutic agent for sepsis and various symptoms accompanying sepsis (such as septic shock, disseminated intravascular coagulation syndrome, adult respiratory distress syndrome and multiple organ dysfunction) is disclosed. The therapeutic agent for sepsis according to the present invention comprises as an effective ingredient an opioid &kgr; receptor agonist compound such as (−)-17-(cyclopropylmethyl)-3,14&bgr;-dihydroxy-4,5&agr;-epoxy-6&bgr;[N-methyl-trans-3-(3-furyl)acrylamide] oxide derivative. The opioid &kgr; receptor agonist compound may be administered as it is or in the form of a pharmaceutical composition prepared by mixing the compound with a known pharmaceutically acceptable acid, carrier or vehicle orally or parenterally.
    本发明公开了一种治疗败血症和败血症伴随的各种症状(如脓毒性休克、弥散性血管内凝血综合征、成人呼吸窘迫综合征和多器官功能障碍)的药物。根据本发明的败血症治疗剂包括作为有效成分的阿片受体激动剂化合物,如(-)-17-(环丙基甲基)-3,14&bgr;-二羟基-4,5&agr;-环氧-6&bgr;[N-甲基-反式-3-(3-呋喃基)丙烯酰胺]氧化物衍生物。阿片类&kgr;受体激动剂化合物可以原样给药,也可以通过将该化合物与已知的药学上可接受的酸、载体或载体混合制备的药物组合物的形式口服或肠外给药。
  • KAPPA AGONIST ANTI-PRURITIC PHARMACEUTICAL FORMULATIONS AND METHOD OF TREATING PRURITUS THEREWITH
    申请人:Adolor Corporation
    公开号:EP0996434A1
    公开(公告)日:2000-05-03
  • EP0996434A4
    申请人:——
    公开号:EP0996434A4
    公开(公告)日:2001-10-10
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