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N-[2-(R)-hydroxy-2-(4-hydroxy-phenyl)ethyl]-3-(4-hydroxy-3-methoxy-phenyl)acrylamide

中文名称
——
中文别名
——
英文名称
N-[2-(R)-hydroxy-2-(4-hydroxy-phenyl)ethyl]-3-(4-hydroxy-3-methoxy-phenyl)acrylamide
英文别名
(2S,E)-N-[2-hydroxy-2-(4-hydroxyphenyl)ethyl]ferulamide;R-(+)-N-trans-feruloyloctopamine;N-trans-feruloyloctopamine;N-[2-(R)-hydroxy-2-(4-hydroxy-phenyl)-ethyl]-3-(4-hydroxy-3-methoxy-phenyl)-acrylamide;(R)-N-trans-Feruloyloctopamine;(E)-N-[(2R)-2-hydroxy-2-(4-hydroxyphenyl)ethyl]-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide
N-[2-(R)-hydroxy-2-(4-hydroxy-phenyl)ethyl]-3-(4-hydroxy-3-methoxy-phenyl)acrylamide化学式
CAS
——
化学式
C18H19NO5
mdl
——
分子量
329.353
InChiKey
VJSCHQMOTSXAKB-CFZDNBDDSA-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):
    1.8
  • 重原子数:
    24
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    99
  • 氢给体数:
    4
  • 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

  • 作为产物:
    描述:
    [(R)-2-hydroxy-2-(4-acetoxy-phenyl)-ethyl]-carbamic acid benzyl ester 在 palladium on activated charcoal 氢氧化钾氢气N,N'-二环己基碳二亚胺 作用下, 以 四氢呋喃乙醇N,N-二甲基甲酰胺 为溶剂, 20.0~25.0 ℃ 、101.33 kPa 条件下, 反应 19.0h, 生成 N-[2-(R)-hydroxy-2-(4-hydroxy-phenyl)ethyl]-3-(4-hydroxy-3-methoxy-phenyl)acrylamide
    参考文献:
    名称:
    Identification from a Combinatorial Library of a Small Molecule that Selectively Induces Apoptosis in Cancer Cells
    摘要:
    The selective induction of death in cancer cells is a major challenge in modern medicine. In this communication we describe the synthesis of an 88-membered combinatorial library, and the subsequent evaluation of these compounds for their ability to selectively induce apoptosis in cancerous cells. A compound was identified from the library that induces apoptosis in U-937 and HL-60 cell lines. This compound is a remarkably selective pro-apoptotic agent for these cancer cell lines, as it does not induce significant death in noncancerous white blood cells, even at concentrations as high as 1000 muM.
    DOI:
    10.1021/ja038043d
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文献信息

  • Compounds and methods for treatment of cancer and modulation of programmed cell death for melanoma and other cancer cells
    申请人:Hergenrother J. Paul
    公开号:US20050197511A1
    公开(公告)日:2005-09-08
    Compounds and related methods for synthesis, and the use of compounds and combination therapies for the treatment of cancer and modulation of apoptosis in cells are disclosed. The generation of synthetic combinatorial libraries and the evaluation of library member compounds regarding induction of apoptosis selectively in cancer cells are disclosed. Compounds, methods of making the compounds, and therapeutic methods with application against breast cancer cells, melanoma cancer cells, colon cancer cells, and other cancer cells are described.
    本文披露了合成化合物及相关方法,并使用化合物和联合疗法治疗癌症和调节细胞凋亡。本文还披露了合成组合库的生成以及评估库成员化合物在选择性诱导癌细胞凋亡方面的应用。描述了化合物、制备化合物的方法以及应用于乳腺癌细胞、黑色素瘤癌细胞、结肠癌细胞和其他癌症细胞的治疗方法。
  • [EN] COMPOUNDS AND METHODS FOR TREATMENT OF CANCER AND MODULATION OF PROGRAMMED CELL DEATH FOR MELANOMA AND OTHER CANCER CELLS<br/>[FR] COMPOSES ET PROCEDES DE TRAITEMENT DU CANCER ET MODULATION DE LA MORT CELLULAIRE PROGRAMMEE DE MELANOMES ET D'AUTRES CELLULES CANCEREUSES
    申请人:UNIV ALABAMA
    公开号:WO2005044191A3
    公开(公告)日:2005-10-20
  • US7632972B2
    申请人:——
    公开号:US7632972B2
    公开(公告)日:2009-12-15
  • Identification from a Combinatorial Library of a Small Molecule that Selectively Induces Apoptosis in Cancer Cells
    作者:Vitaliy Nesterenko、Karson S. Putt、Paul J. Hergenrother
    DOI:10.1021/ja038043d
    日期:2003.12.1
    The selective induction of death in cancer cells is a major challenge in modern medicine. In this communication we describe the synthesis of an 88-membered combinatorial library, and the subsequent evaluation of these compounds for their ability to selectively induce apoptosis in cancerous cells. A compound was identified from the library that induces apoptosis in U-937 and HL-60 cell lines. This compound is a remarkably selective pro-apoptotic agent for these cancer cell lines, as it does not induce significant death in noncancerous white blood cells, even at concentrations as high as 1000 muM.
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