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1-(10-ethyl-5,6,7,8-tetrahydro-[2]phenanthryl)-2-bromo-ethanone | 6321-61-5

中文名称
——
中文别名
——
英文名称
1-(10-ethyl-5,6,7,8-tetrahydro-[2]phenanthryl)-2-bromo-ethanone
英文别名
1-(10-Aethyl-5,6,7,8-tetrahydro-[2]phenanthryl)-2-brom-aethanon;NSC30820;2-Bromo-1-(10-ethyl-5,6,7,8-tetrahydrophenanthren-2-yl)ethanone
1-(10-ethyl-5,6,7,8-tetrahydro-[2]phenanthryl)-2-bromo-ethanone化学式
CAS
6321-61-5
化学式
C18H19BrO
mdl
——
分子量
331.252
InChiKey
RPZCQYBKVFZDLR-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):
    5.8
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

点击查看最新优质反应信息

文献信息

  • COMPOSITIONS AND METHODS FOR INHIBITING G PROTEIN SIGNALING
    申请人:Smrcka Alan V.
    公开号:US20090221691A1
    公开(公告)日:2009-09-03
    The present invention relates to methods for identifying agents which bind to specific amino acid residues of the protein interaction site of G protein β protein subunit. Compounds identified in accordance with the assay of the invention and methods for using the compound for modulating at least one activity of a G protein are also provide.
  • Compositions and Methods for Inhibiting G Protein Signaling
    申请人:University of Rochester
    公开号:US20130116313A1
    公开(公告)日:2013-05-09
    The present invention relates to methods for identifying agents which bind to specific amino acid residues of the protein interaction site of G protein β protein subunit. Compounds identified in accordance with the assay of the invention and methods for using the compound for modulating at least one activity of a G protein are also provided.
  • US8748480B2
    申请人:——
    公开号:US8748480B2
    公开(公告)日:2014-06-10
  • US8975259B2
    申请人:——
    公开号:US8975259B2
    公开(公告)日:2015-03-10
  • REACTIONS OF 1,2,3,4-TETRAHYDROPHENANTHRENE AND DERIVATIVES. III. ALKYL DERIVATIVES AND ANTIMALARIALS
    作者:W. E. BACHMANN、M. W. CRONYN、W. S. STRUVE
    DOI:10.1021/jo01168a017
    日期:1947.7
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