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1-(5,5-dimethyl-3-propyl-4,5,6,7-tetrahydrobenzo[c]thiophen-1-yl)ethanone

中文名称
——
中文别名
——
英文名称
1-(5,5-dimethyl-3-propyl-4,5,6,7-tetrahydrobenzo[c]thiophen-1-yl)ethanone
英文别名
1-(5,5-Dimethyl-3-propyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-ethanone;1-(5,5-dimethyl-3-propyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)ethanone;1-(5,5-dimethyl-3-propyl-6,7-dihydro-4H-2-benzothiophen-1-yl)ethanone
1-(5,5-dimethyl-3-propyl-4,5,6,7-tetrahydrobenzo[c]thiophen-1-yl)ethanone化学式
CAS
——
化学式
C15H22OS
mdl
——
分子量
250.405
InChiKey
NOXLMKPZSDCZJH-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):
    4.8
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    45.3
  • 氢给体数:
    0
  • 氢受体数:
    2

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1-(5,5-dimethyl-3-propyl-4,5,6,7-tetrahydrobenzo[c]thiophen-1-yl)ethanone盐酸 、 palladium 10% on activated carbon 、 氢气 作用下, 以 四氢呋喃乙醇异丙醇 为溶剂, 20.0 ℃ 、150.0 kPa 条件下, 反应 6.67h, 生成
    参考文献:
    名称:
    Novel S1P1 Receptor Agonists - Part 2: From Bicyclo[3.1.0]hexane-Fused Thiophenes to Isobutyl Substituted Thiophenes
    摘要:
    Previously, we reported on the discovery of a novel series of bicyclo[3.1.0]hexane fused thiophene derivatives that serve as potent and selective S1P(1), receptor agonists. Here, we discuss our efforts to simplify the bicyclohexane fused thiophene head. In a first step the bicyclohexane moiety could be replaced by a simpler, less rigid cyclohexane ring without compromising the SIP receptor affinity profile of these novel compounds. In a second step, the thiophene head was simplified even further by replacing the cyclohexane ring with an isobutyl group attached either to position 4 or position S of the thiophene. These structurally much simpler headgroups again furnished potent and selective S1P(1) agonists (e.g., 87), which efficiently and dose dependently reduced the number of circulating lymphocytes upon oral administration to male Wistar rats. For several compounds discussed in this report lymphatic transport is an important route of absorption that may offer opportunities for a tissue targeted approach with minimal plasma exposure.
    DOI:
    10.1021/jm401456d
  • 作为产物:
    描述:
    参考文献:
    名称:
    Novel S1P1 Receptor Agonists - Part 2: From Bicyclo[3.1.0]hexane-Fused Thiophenes to Isobutyl Substituted Thiophenes
    摘要:
    Previously, we reported on the discovery of a novel series of bicyclo[3.1.0]hexane fused thiophene derivatives that serve as potent and selective S1P(1), receptor agonists. Here, we discuss our efforts to simplify the bicyclohexane fused thiophene head. In a first step the bicyclohexane moiety could be replaced by a simpler, less rigid cyclohexane ring without compromising the SIP receptor affinity profile of these novel compounds. In a second step, the thiophene head was simplified even further by replacing the cyclohexane ring with an isobutyl group attached either to position 4 or position S of the thiophene. These structurally much simpler headgroups again furnished potent and selective S1P(1) agonists (e.g., 87), which efficiently and dose dependently reduced the number of circulating lymphocytes upon oral administration to male Wistar rats. For several compounds discussed in this report lymphatic transport is an important route of absorption that may offer opportunities for a tissue targeted approach with minimal plasma exposure.
    DOI:
    10.1021/jm401456d
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文献信息

  • Hydrogenated Benzo (C) Thiophene Derivatives as Immunomodulators
    申请人:Bolli Martin
    公开号:US20080176926A1
    公开(公告)日:2008-07-24
    The invention relates to novel thiophene derivatives, their preparation and their use as pharmaceutically active compounds. Said compounds particularly act as immunosuppressive agents.
    该发明涉及新型噻吩衍生物,其制备以及其作为药用活性化合物的用途。这些化合物特别作为免疫抑制剂。
  • HYDROGENATED BENZO (C) THIOPHENE DERIVATIVES AS IMMUNOMODULATORS
    申请人:Bolli Martin
    公开号:US20100204198A1
    公开(公告)日:2010-08-12
    The invention relates to novel thiophene derivatives, their preparation and their use as pharmaceutically active compounds. Said compounds particularly act as immunosuppressive agents.
    该发明涉及新型噻吩衍生物,其制备及其作为药物活性化合物的用途。所述化合物特别作为免疫抑制剂。
  • HYDOGRENATED BENZO[C]THIOPHENE DERIVATIVES AS IMMUNOMODULATORS
    申请人:Actelion Pharmaceuticals Ltd.
    公开号:EP1863787B1
    公开(公告)日:2011-05-25
  • US7723378B2
    申请人:——
    公开号:US7723378B2
    公开(公告)日:2010-05-25
  • US8039644B2
    申请人:——
    公开号:US8039644B2
    公开(公告)日:2011-10-18
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