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4-[5-[4-(4-Fluorophenyl)piperazin-1-yl]sulfonyl-2,3-dihydroindol-1-yl]-4-oxo-butanoic acid | 904447-15-0

中文名称
——
中文别名
——
英文名称
4-[5-[4-(4-Fluorophenyl)piperazin-1-yl]sulfonyl-2,3-dihydroindol-1-yl]-4-oxo-butanoic acid
英文别名
4-(5-(4-(4-fluorophenyl)piperazin-1-ylsulfonyl)indolin-1-yl)-4-oxobutanoic acid;4-[5-[4-(4-Fluorophenyl)piperazin-1-yl]sulfonyl-2,3-dihydroindol-1-yl]-4-oxobutanoic acid
4-[5-[4-(4-Fluorophenyl)piperazin-1-yl]sulfonyl-2,3-dihydroindol-1-yl]-4-oxo-butanoic acid化学式
CAS
904447-15-0
化学式
C22H24FN3O5S
mdl
——
分子量
461.514
InChiKey
YQCMDUVJBCKDSW-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):
    1.6
  • 重原子数:
    32
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    107
  • 氢给体数:
    1
  • 氢受体数:
    8

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    4-[5-[4-(4-Fluorophenyl)piperazin-1-yl]sulfonyl-2,3-dihydroindol-1-yl]-4-oxo-butanoic acid1-(4-氟苯基)哌嗪methyl 4-(5-(chlorosulfonyl)indolin-1-yl)-4-oxobutanoate盐酸 、 Brine 、 magnesium sulfate二氯甲烷甲醇 作用下, 以 二氯甲烷 、 ice water 、 吡啶 为溶剂, 反应 3.0h, 以to give methyl 4-(5-(4-(4-fluorophenyl)piperazin-1-ylsulfonyl)indolin-1-yl)-4-oxobutanoate的产率得到methyl 4-(5-(4-(4-fluorophenyl)piperazin-1-ylsulfonyl)indolin-1-yl)-4-oxobutanoate
    参考文献:
    名称:
    INDOLINE SCAFFOLD SHP-2 INHIBITORS AND CANCER TREATMENT METHOD
    摘要:
    本发明涉及用于抑制Shp2的方法和化合物。在一种实施例中,本发明的化合物具有如公式I或II所示的化学结构:其中X,Y和Z分别是N或S;R1是环烷基,杂环烷基,芳基或杂芳基,其中任何一个可以选择性地被一个或多个卤素;烷基;杂烷基;-COOH;-C(R3)3,其中R3可以独立地是-H或卤素;或-OR4,其中R4可以是H,烷基或杂烷基;R2是烷基,烷基羰基,杂烷基羰基,芳基,芳基羰基,杂环烷基羰基,环烷基羰基或-C(O)NR6R7,其中任何一个可以选择性地被一个或多个卤素;烷基;杂烷基;羰基;-OR4,其中R4可以是-H,烷基或杂烷基;-OH;-C(R3)3,其中R3可以独立地是-H或卤素;芳基,可以被一个或多个卤素或-OR4取代;杂环烷基;或-C(O)OR5,其中R5可以是-H或烷基;R6和R7独立地是-H,烷基,杂烷基,芳基或杂芳基;R'是H或烷基;或其药学上可接受的盐或水合物。
    公开号:
    US20110190315A1
  • 作为产物:
    描述:
    methyl 4-(5-(4-(4-fluorophenyl)piperazin-1-ylsulfonyl)indolin-1-yl)-4-oxobutanoate 、 lithium hydroxide 作用下, 以 甲醇 为溶剂, 反应 0.17h, 以69%的产率得到4-[5-[4-(4-Fluorophenyl)piperazin-1-yl]sulfonyl-2,3-dihydroindol-1-yl]-4-oxo-butanoic acid
    参考文献:
    名称:
    [EN] INDOLINE SCAFFOLD SHP-2 INHIBITORS AND CANCER TREATMENT METHOD
    [FR] INHIBITEURS DE SHP-2 À SQUELETTE INDOLINE ET PROCÉDÉ DE TRAITEMENT DU CANCER
    摘要:
    公开号:
    WO2010011666A3
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文献信息

  • Methods for treating leukemia and myelodysplastic syndrome, and methods for identifying agents for treating same
    申请人:Mustelin Tomas
    公开号:US20090105240A1
    公开(公告)日:2009-04-23
    The present disclosure relates to methods for treating leukemia, pre-leukemic conditions, as well as myelodysplastic syndrome and acute myelogenous leukemia. The present disclosure further relates to compounds that can be used for treating leukemia, pre-leukemic conditions, as well as myelodysplastic syndrome and acute myelogenous leukemia. The present disclosure also relates to methods for identifying compounds that can be used for treating leukemia, pre-leukemic conditions, as well as myelodysplastic syndrome.
    本公开涉及治疗白血病、白血病前期病症、以及骨髓增生异常综合征和急性髓系白血病的方法。本公开还涉及可用于治疗白血病、白血病前期病症、以及骨髓增生异常综合征和急性髓系白血病的化合物。本公开还涉及用于识别可用于治疗白血病、白血病前期病症、以及骨髓增生异常综合征的化合物的方法。
  • INDOLINE SCAFFOLD SHP-2 INHIBITORS AND METHOD OF TREATING CANCER
    申请人:Wu Jie
    公开号:US20120034186A1
    公开(公告)日:2012-02-09
    Protein tyrosine phosphatase (PTP) Shp2 is a non-receptor PTP that involved in cell signaling and regulation of cell proliferation, differentiation, and migration. Shp2 mediates activation of kinases that are involved in the pathogenesis of human carcinoma. A high throughput screen identified compounds that inhibit the PTP Shp2. Several compounds were identified that selectively inhibit Shp2 over Shp1 with low to sub-micromolar activity. Also disclosed are methods of inhibiting a protein tyrosine phosphatase in a cell and treating cancer through selective inhibition of Shp2.
  • METHODS FOR TREATING LEUKEMIA AND MYELODYSPLASTIC SYNDROME, AND METHODS FOR IDENTIFYING AGENTS FOR TREATING SAME
    申请人:Mustelin Tomas
    公开号:US20120095032A1
    公开(公告)日:2012-04-19
    The present disclosure relates to methods for treating leukemia, pre-leukemic conditions, as well as myelodysplastic syndrome and acute myelogenous leukemia. The present disclosure further relates to compounds that can be used for treating leukemia, pre-leukemic conditions, as well as myelodysplastic syndrome and acute myelogenous leukemia. The present disclosure also relates to methods for identifying compounds that can be used for treating leukemia, pre-leukemic conditions, as well as myelodysplastic syndrome.
  • US8623906B2
    申请人:——
    公开号:US8623906B2
    公开(公告)日:2014-01-07
  • US9174969B2
    申请人:——
    公开号:US9174969B2
    公开(公告)日:2015-11-03
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