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5-(4-[2-(5-Methyl-2-phenyloxazol-4-yl)ethoxy]benzyl)-5-(naphthalene-2-sulfonyl)thiazolidine-2,4-dione | 500718-73-0

中文名称
——
中文别名
——
英文名称
5-(4-[2-(5-Methyl-2-phenyloxazol-4-yl)ethoxy]benzyl)-5-(naphthalene-2-sulfonyl)thiazolidine-2,4-dione
英文别名
5-[[4-[2-(5-Methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]phenyl]methyl]-5-naphthalen-2-ylsulfonyl-1,3-thiazolidine-2,4-dione
5-(4-[2-(5-Methyl-2-phenyloxazol-4-yl)ethoxy]benzyl)-5-(naphthalene-2-sulfonyl)thiazolidine-2,4-dione化学式
CAS
500718-73-0
化学式
C32H26N2O6S2
mdl
——
分子量
598.7
InChiKey
RDZNIMGZAFFSRJ-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

物化性质

  • 密度:
    1.379±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.6
  • 重原子数:
    42
  • 可旋转键数:
    9
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.16
  • 拓扑面积:
    149
  • 氢给体数:
    1
  • 氢受体数:
    8

文献信息

  • 5-(Substituted)-5-(substitutedsulfonyl or sulfanyl) thiazolidine-2,4-diones useful for inhibition of farnesyl-protein transferase
    申请人:American Cyanamid Company
    公开号:US20030096849A1
    公开(公告)日:2003-05-22
    The invention relates to compounds of Formula (I) wherein R 1 , (R 2 ) v , R 3 and n are defined in the specification and pharmaceutical compositions thereof, that inhibit the Ras farnesyl-protein transferase enzyme (FPTase), and may be used as an alternative to, or in conjunction with, traditional cancer therapy for the treatment of ras oncogene-dependent tumors, such as cancers of the pancreas, colon, bladder, and thyroid. 1
    本发明涉及式(I)的化合物,其中R1,(R2)v,R3和n在规范中定义,并且其制药组合物抑制Ras法尼醇蛋白转移酶(FPTase),可用作替代或与传统癌症治疗相结合,用于治疗ras癌基因依赖性肿瘤,如胰腺癌,结肠癌,膀胱癌和甲状腺癌。
  • US6716862B2
    申请人:——
    公开号:US6716862B2
    公开(公告)日:2004-04-06
  • [EN] 5-(SUBSTITUTED)-5-(SUBSTITUTEDSULFONYL OR SULFANYL)THIAZOLIDINE-2,4-DIONES USEFUL FOR INHIBITION OF FARNESYL-PROTEIN TRANSFERASE<br/>[FR] 5-(SUBSTITUE)-5-(SUBSTITUE SULFONYL OU SULFANYL)THIAZOLIDINE-2,4-DIONES UTILES POUR L'INHIBITION DE LA FARNESYL-PROTEINE TRANSFERASE
    申请人:WYETH CORP
    公开号:WO2003018011A1
    公开(公告)日:2003-03-06
    The invention relates to compounds of Formula (I) wherein R1, (R2)v, R3 and n are defined in the specification, to processes for their preparation and pharmaceutical compositions thereof, that inhibit the Ras farnesyl-protein transferase enzyme (FPTase), and may be used as an alternative to, or in conjunction with, traditional cancer therapy for the treatment of ras oncogene-dependent tumors, such as cancers of the pancreas, colon, bladder, and thyroid.
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