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6,7-Dihydro-benzothiophen | 36914-06-4

中文名称
——
中文别名
——
英文名称
6,7-Dihydro-benzothiophen
英文别名
6,7-Dihydrobenzothiophen;6,7-dihydrobenzo[b]thiophene;6,7-dihydrobenzo[b]thiophen;6,7-dihydro-1-benzothiophene
6,7-Dihydro-benzothiophen化学式
CAS
36914-06-4
化学式
C8H8S
mdl
——
分子量
136.218
InChiKey
GCJDEPUAVWAMAG-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):
    2.7
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    28.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Compositions containing 4,5,6,7-tetrahydrobenz[b]thien-4-yl-ureas or
    摘要:
    这份披露描述了一种新颖的方法,通过向兽医同温动物投予一定量的环戊烷基硫代脲或硫脲,以提高饲料效率并加快生长速度。
    公开号:
    US04036979A1
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文献信息

  • HETEROCYCLIC COMPOUNDS, PROCESS FOR PREPARATION OF THE SAME AND USE THEREOF
    申请人:SHANGHAI INSTITUTE OF MATERIA MEDICA, CHINESE ACADEMY OF SCIENCES
    公开号:US20170158680A1
    公开(公告)日:2017-06-08
    The present invention provides a heterocyclic compound represented by the formula (I), its stereoisomers, or a pharmaceutically acceptable salt thereof, pharmaceutical compositions thereof, and their use in preparing a medicament for the prevention and/or treatment of central nervous system disease.
    本发明提供了一种由公式(I)表示的杂环化合物,其立体异构体,或其药用可接受的盐,其药物组合物,以及它们用于制备预防或治疗中枢神经系统疾病的药物。
  • [EN] PYRIMIDINEDIONE CARBOXAMIDE INHIBITORS OF ENDOTHELIAL LIPASE<br/>[FR] INHIBITEURS À BASE DE PYRIMIDINEDIONECARBOXAMIDE DE LIPASE ENDOTHÉLIALE
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2013151877A1
    公开(公告)日:2013-10-10
    The present invention provides compounds of Formula (I), as defined in the specification and compositions comprising any of such novel compounds. These compounds are endothelial lipase inhibitors which may be used as medicaments.
    本发明提供了如规范中定义的Formula (I)的化合物,以及包含任何此类新化合物的组合物。这些化合物是内皮脂酶抑制剂,可用作药物。
  • Substituted tetrahydrobenzothiophenes and method of preparation thereof
    申请人:American Cyanamid Company
    公开号:US04156670A1
    公开(公告)日:1979-05-29
    This disclosure describes novel 4,5,6,7-tetrahydrobenzo[b]thien-4-ylureas useful as herbicidal agents and animal growth regulants and processes for the preparation thereof.
    本公开说明了作为除草剂和动物生长调节剂有用的新型4,5,6,7-四氢苯并[b]噻唑-4-基以及其制备方法。
  • Substituted tetrahydrobenzothiophenes
    申请人:American Cyanamid Company
    公开号:US04191830A1
    公开(公告)日:1980-03-04
    This disclosure describes novel 4,5,6,7-tetrahydrobenzo[b]thien-4-ylureas useful as herbicidal agents and animal growth regulants and processes for the preparation thereof.
    本公开说明了一种新型的4,5,6,7-四氢苯并[b]噻唑-4-基,可用作除草剂和动物生长调节剂,并提供了其制备方法。
  • PYRIMIDINE COMPOUNDS INHIBITING THE FORMATION OF NITRIC OXIDE AND PROSTAGLANDIN E2, METHOD OF PRODUCTION THEREOF AND USE THEREOF
    申请人:Ustav Organicke Chemie A Biochemie Akademie Ved Cr, v.v.i.
    公开号:EP3195867A1
    公开(公告)日:2017-07-26
    The invention provides pyrimidine compounds of general formula (I), which reduce simultaneously the production of nitric oxide (NO) and prostaglandin E2 (PGE2). They have no negative effect on the viability of cells in concentrations decreasing the production of these factors by up to 50%; they are not cytotoxic. Furthermore, a method of preparation of the pyrimidine compounds of general formula (I), carrying 2-formamido group, a pharmaceutical composition comprising the substituted pyrimidine compounds according to the invention, and the use of these compounds for the treatment of inflammatory and cancer diseases are provided.
    本发明提供了通式(I)的嘧啶化合物,它们能同时减少一氧化氮(NO)和前列腺素 E2(PGE2)的产生。它们对细胞的存活能力没有负面影响,在减少这些因子产生达 50%的浓度下,它们没有细胞毒性。此外,本发明还提供了通式(I)嘧啶化合物的制备方法、含有 2-甲酰基的嘧啶化合物的药物组合物,以及这些化合物用于治疗炎症和癌症疾病的方法。
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