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Z-(9RS,10RS)-9,10-dihydroxy-6-phenyl-2-cyclodecen-1-one | 471910-76-6

中文名称
——
中文别名
——
英文名称
Z-(9RS,10RS)-9,10-dihydroxy-6-phenyl-2-cyclodecen-1-one
英文别名
(2Z)-9,10-dihydroxy-6-phenylcyclodec-2-en-1-one
Z-(9RS,10RS)-9,10-dihydroxy-6-phenyl-2-cyclodecen-1-one化学式
CAS
471910-76-6
化学式
C16H20O3
mdl
——
分子量
260.333
InChiKey
CAQQNQUFMGBDKG-UITAMQMPSA-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):
    2.4
  • 重原子数:
    19
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    57.5
  • 氢给体数:
    2
  • 氢受体数:
    3

文献信息

  • Cyclooctanone derivatives and cyclodecanone derivative, and use thereof
    申请人:——
    公开号:US20040082805A1
    公开(公告)日:2004-04-29
    The present invention provides a compound which has cytokine production inhibitory activity and is useful for the treatment of diseases which is associated with cytokine. The compound is represented by the following general formula (I) [wherein A represents a cyclic group which may be substituted; the partial structure -D E- represents a group represented by —CH 2 CH 2 — or —CH═CH—; W represents a group represented by —CH 2 —, —CH 2 CH 2 —, —CH═CH— or —CH═; the partial structure >X Y—represents a group represented by >CH—(CH 2 ) n —, >C═CH—, >CH—CH 2 —CH(OH)—, >CH—CH 2 —C(═O)—, >CH—O— or >CH—O—CO—, provided that when W is —CH═, then X Y— represents C—(CH 2 ) p —; Z represents a divalent aliphatic hydrocarbon group; R 1 and R 2 , which may be the same or different, each represents a hydrogen atom, or a hydroxyl, alkoxy or alkoxyalkoxy group; m is an integer of 0 or 1].
    本发明提供了一种具有细胞因子生产抑制活性的化合物,可用于治疗与细胞因子相关的疾病。该化合物由以下通式(I)表示:[其中,A表示可以被取代的环状基团;部分结构-DE-表示由— —或—CH═CH—表示的基团;W表示由—CH2—、— —、—CH═CH—或—CH═—表示的基团;部分结构>XY-表示由>CH—( )n—、>C═CH—、>CH— —CH(OH)—、>CH— —C(═O)—、>CH—O—或>CH—O—CO—表示的基团,但当W为—CH═时,XY—表示C—( )p—;Z表示二价的脂肪族碳氢基团;R1和R2,可以相同也可以不同,每个表示氢原子或羟基、烷氧基或烷氧基烷基;m是0或1的整数。]
  • PYRROLIDINE DERIVATIVE AND PROCESS FOR PRODUCING THE SAME
    申请人:Eisai Co., Ltd.
    公开号:EP1375479A1
    公开(公告)日:2004-01-02
    The present invention provides a compound which has cytokine production inhibitory activity and is useful for the treatment of diseases which is associated with cytokine. The compound is represented by the following general formula (I) [wherein A represents a cyclic group which may be substituted; the partial structure -D---E- represents a group represented by -CH2CH2- or -CH=CH-; W reprensents a group represented by -CH2-, - CHzCH2-, -CH=CH- or -CH=; the partial structure >X---Y- represents a group represented by >CH-(CH2)n-, >C=CH-, >CH-CH2-CH(OH)-, >CH-CH2-C (=O) -, >CH-O- or >CH-O-CO-, provided that when W is -CH=, then X---Y- represents C-(CH2)p-; Z represents a divalent aliphatic hydrocarbon group; R1 and R2, which may be the same or different, each represents a hydrogen atom, or a hydroxyl, alkoxy or alkoxyalkoxy group; m is an integer of 0 or 1] .
    本发明提供了一种化合物,它具有抑制细胞因子产生的活性,可用于治疗与细胞因子有关的疾病。该化合物由以下通式(I)表示[其中 A 代表可被取代的环状基团;部分结构-D--E-代表由- -或-CH=CH-代表的基团;W 代表由-CH2-、-CHz -、-CH=CH-或-CH=;部分结构 >X---Y- 代表由 >CH-( )n-、>C=CH-、>CH- -CH(OH)-、>CH- -C (=O) -、>CH-O- 或 >CH-O-CO- 所代表的基团,条件是当 W 为 -CH= 时,则 X---Y- 代表 C-( )p-;Z 代表二价脂肪族烃基; R1 和 R2 可以相同或不同,各自代表氢原子或羟基、烷氧基或烷氧烷氧基; m 是 0 或 1 的整数]。
  • CYCLOOCTANONE DERIVATIVE AND CYCLODECANONE DERIVATIVE, AND USE THEREOF
    申请人:Eisai Co., Ltd.
    公开号:EP1375465A9
    公开(公告)日:2004-04-14
    The present invention provides a compound which has cytokine production inhibitory activity and is useful for the treatment of diseases which is associated with cytokine. The compound is represented by the following general formula (I) [wherein A represents a cyclic group which may be substituted; the partial structure -D---E- represents a group represented by -CH2CH2- or -CH=CH-; W reprensents a group represented by -CH2-, - CH2CH2-, -CH=CH- or -CH=; the partial structure >X---Y- represents a group represented by >CH-(CH2)n-, >C=CH-, >CH-CH2-CH(OH)-, >CH-CH2-C (=O) -, >CH-O- or >CH-O-CO-, provided that when W is -CH=, then X---Y- represents C-(CH2)p-; Z represents a divalent aliphatic hydrocarbon group; R1 and R2, which may be the same or different, each represents a hydrogen atom, or a hydroxyl, alkoxy or alkoxyalkoxy group; m is an integer of 0 or 1] .
    本发明提供了一种化合物,它具有抑制细胞因子产生的活性,可用于治疗与细胞因子有关的疾病。该化合物由以下通式(I)表示[其中 A 代表可被取代的环状基团;部分结构-D--E-代表由- -或-CH=CH-代表的基团;W 代表由-CH2-、- -、-CH=CH-或-CH=;部分结构 >X---Y- 代表由 >CH-( )n-、>C=CH-、>CH- -CH(OH)-、>CH- -C (=O) -、>CH-O- 或 >CH-O-CO- 所代表的基团,条件是当 W 为 -CH= 时,则 X---Y- 代表 C-( )p-;Z 代表二价脂肪族烃基; R1 和 R2 可以相同或不同,各自代表氢原子或羟基、烷氧基或烷氧烷氧基; m 是 0 或 1 的整数]。
  • US6949585B2
    申请人:——
    公开号:US6949585B2
    公开(公告)日:2005-09-27
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