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4-bromo-3-[2-(tert-butyl-dimethyl-silanyloxy)-3-chloro-phenylmethanesulfonyl]-5-methyl-benzoic acid methyl ester | 887003-18-1

中文名称
——
中文别名
——
英文名称
4-bromo-3-[2-(tert-butyl-dimethyl-silanyloxy)-3-chloro-phenylmethanesulfonyl]-5-methyl-benzoic acid methyl ester
英文别名
4-Bromo-3-[2-(tert-butyl-dimethyl-silanyloxy)-3-chloro-phenyl methane sulfonyl]-5-methyl-benzoic acid methyl ester;methyl 4-bromo-3-[[2-[tert-butyl(dimethyl)silyl]oxy-3-chlorophenyl]methylsulfonyl]-5-methylbenzoate
4-bromo-3-[2-(tert-butyl-dimethyl-silanyloxy)-3-chloro-phenylmethanesulfonyl]-5-methyl-benzoic acid methyl ester化学式
CAS
887003-18-1
化学式
C22H28BrClO5SSi
mdl
——
分子量
547.97
InChiKey
CGPQTNYFMVYQAW-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):
    6.56
  • 重原子数:
    31
  • 可旋转键数:
    8
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    78
  • 氢给体数:
    0
  • 氢受体数:
    5

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

反应信息

点击查看最新优质反应信息

文献信息

  • Fused Tricyclic Compounds as Inhibitors of Tumor Necrosis Factor-Alpha
    申请人:Lal Bansi
    公开号:US20070299050A1
    公开(公告)日:2007-12-27
    Compounds of formula 1: are disclosed, wherein V is CH 2 ; W is S(O) m ; m is the integer 0, 1 or 2; U is O, C(O), CR 13 R 14 or NR 15 ; where R 13 is H, alkyl; R 14 is H, OH, OR 13 or OCOR 13 ; R 15 is H, alkyl, cycloalkyl, alkenyl, C(O)R 13 , C(O)OR 13 or alkylaminocarbonyl; R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are as defined herein. These compounds are inhibitors of tumor necrosis factor-alpha (TNF-α) and are useful as medicaments for the treatment and prevention of disorders caused by increased TNF-α activity, in particular inflammations.
    本文披露了式子1的化合物,其中V为CH2;W为S(O)m;m为0、1或2的整数;U为O、C(O)、CR13R14或NR15;其中R13为H、烷基;R14为H、OH、OR13或OCOR13;R15为H、烷基、环烷基、烯基、C(O)R13、C(O)OR13或烷基氨基甲酰基;R1、R2、R3、R4、R5、R6、R7和R8的定义如本文所述。这些化合物是肿瘤坏死因子-alpha(TNF-α)的抑制剂,并可用作药物治疗和预防由增加的TNF-α活性引起的疾病,特别是炎症。
  • Fused tricyclic compounds as inhibitors of tumor necrosis factor-α
    申请人:Piramal Life Sciences Limited
    公开号:US07964631B2
    公开(公告)日:2011-06-21
    Compounds of formula 1: are disclosed, wherein V is CH2; W is S(O)m; m is the integer 0, 1 or 2; U is O, C(O), CR13R14 or NR15; where R13 is H, alkyl; R14 is H, OH, OR13 or OCOR13; R15 is H, alkyl, cycloalkyl, alkenyl, C(O)R13, C(O)OR13 or alkylaminocarbonyl; R1, R2, R3, R4, R5, R6, R7 and R8 are as defined herein. These compounds are inhibitors of tumor necrosis factor-alpha (TNF-α) and are useful as medicaments for the treatment and prevention of disorders caused by increased TNF-α activity, in particular inflammations.
    公式1的化合物被披露,其中V是CH2; W是S(O)m; m是整数0、1或2; U是O、C(O)、CR13R14或NR15;其中R13是H、烷基; R14是H、OH、OR13或OCOR13; R15是H、烷基、环烷基、烯基、C(O)R13、C(O)OR13或烷基氨基甲酰基; R1、R2、R3、R4、R5、R6、R7和R8如本文所定义。这些化合物是肿瘤坏死因子-alpha(TNF-α)的抑制剂,并且可用作治疗和预防由增加的TNF-α活性引起的疾病的药物,特别是炎症。
  • Fused tricyclic compounds as inhibitors of tumor necrosis factor-alpha
    申请人:Piramal Life Sciences Limited
    公开号:US08163730B2
    公开(公告)日:2012-04-24
    Compounds of formula 1: are disclosed, wherein V is CH2; W is S(O)m; m is the integer 0, 1 or 2; U is O, C(O), CR13R14 or NR15; where R13 is H, alkyl; R14 is H, OH, OR13 or OCOR13; R15 is H, alkyl, cycloalkyl, alkenyl, C(O)R13, C(O)OR13 or alkylaminocarbonyl; R1, R2, R3, R4, R5, R6, R7 and R8 are as defined herein. These compounds are inhibitors of tumor necrosis factor-alpha (TNF-α) and are useful as medicaments for the treatment and prevention of disorders caused by increased TNF-α activity, in particular inflammations.
    公式1的化合物被披露,其中V为CH2;W为S(O)m;m为整数0、1或2;U为O、C(O)、CR13R14或NR15;其中R13为H、烷基;R14为H、OH、OR13或OCOR13;R15为H、烷基、环烷基、烯基、C(O)R13、C(O)OR13或烷基氨基甲酰基;R1、R2、R3、R4、R5、R6、R7和R8的定义如本文所述。这些化合物是肿瘤坏死因子α(TNF-α)的抑制剂,并且可用作药物治疗和预防由增加的TNF-α活性引起的疾病,特别是炎症。
  • FUSED TRICYCLIC COMPOUNDS AS INHIBITORS OF TUMOR NECROSIS FACTOR-ALPHA
    申请人:Lal Bansi
    公开号:US20100305094A1
    公开(公告)日:2010-12-02
    Compounds of formula 1: are disclosed, wherein V is CH 2 ; W is S(O) m ; m is the integer 0, 1 or 2; U is O, C(O), CR 13 R 14 or NR 15 ; where R 13 is H, alkyl; R 14 is H, OH, OR 13 or OCOR 13 ; R 15 is H, alkyl, cycloalkyl, alkenyl, C(O)R 13 , C(O)OR 13 or alkylaminocarbonyl; R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are as defined herein. These compounds are inhibitors of tumor necrosis factor-alpha (TNF-α) and are useful as medicaments for the treatment and prevention of disorders caused by increased TNF-α activity, in particular inflammations.
    本文揭示了式1的化合物,其中V为CH2;W为S(O)m;m为整数0、1或2;U为O、C(O)、CR13R14或NR15;其中R13为H、烷基;R14为H、OH、OR13或OCOR13;R15为H、烷基、环烷基、烯丙基、C(O)R13、C(O)OR13或烷基氨基甲酰基;R1、R2、R3、R4、R5、R6、R7和R8的定义如本文所述。这些化合物是肿瘤坏死因子-α(TNF-α)的抑制剂,并且可用作治疗和预防由于TNF-α活性增加而引起的疾病,特别是炎症的药物。
  • WO2006/51477
    申请人:——
    公开号:——
    公开(公告)日:——
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