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N-[4-oxo-4-[(2,3,4,6-tetra-O-acety1-β-D-glucopyranosyl)amino]butyl]carbamic phenylmethyl ester | 1356995-89-5

中文名称
——
中文别名
——
英文名称
N-[4-oxo-4-[(2,3,4,6-tetra-O-acety1-β-D-glucopyranosyl)amino]butyl]carbamic phenylmethyl ester
英文别名
N-[2-oxo-2-[(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)amino]butyl]-carbamic acid phenylmethyl ester;N-[4-oxo-4-[(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)amino]butyl]-carbamic phenylmethyl ester;[(2R,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-[4-(phenylmethoxycarbonylamino)butanoylamino]oxan-2-yl]methyl acetate
N-[4-oxo-4-[(2,3,4,6-tetra-O-acety1-β-D-glucopyranosyl)amino]butyl]carbamic phenylmethyl ester化学式
CAS
1356995-89-5
化学式
C26H34N2O12
mdl
——
分子量
566.562
InChiKey
JVVCKUGHTCLQTE-PRDVQWLOSA-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):
    0.7
  • 重原子数:
    40
  • 可旋转键数:
    17
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    182
  • 氢给体数:
    2
  • 氢受体数:
    12

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:
    N-[4-oxo-4-[(2,3,4,6-tetra-O-acety1-β-D-glucopyranosyl)amino]butyl]carbamic phenylmethyl ester 氢气 作用下, 以 tetrahydrofuran methanol 为溶剂, 反应 5.0h, 以to give the product (760 mg; 98%)的产率得到4-amino-N-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)butyramide
    参考文献:
    名称:
    Compounds targeting the cell invasion protein complex, their pharmaceutical compositions and methods of use thereof
    摘要:
    本申请涉及公式I(I)化合物,以及它们用于抑制AKT-1,FAK和PKCα中至少一种的作用,以及在治疗和/或预防转移性疾病中的应用。
    公开号:
    US09085598B2
  • 作为产物:
    描述:
    2,3,4,6-tetra-O-acetyl-D-glucosyl-1-amineN-苄氧羰基-4-氨基丁酸N,N'-二环己基碳二亚胺 作用下, 以 二氯甲烷 为溶剂, 反应 5.0h, 以90%的产率得到N-[4-oxo-4-[(2,3,4,6-tetra-O-acety1-β-D-glucopyranosyl)amino]butyl]carbamic phenylmethyl ester
    参考文献:
    名称:
    [EN] COMPOUNDS TARGETING THE CELL INVASION PROTEIN COMPLEX, THEIR PHARMACEUTICAL COMPOSITIONS AND METHODS OF USE THEREOF
    [FR] COMPOSÉS CIBLANT LE COMPLEXE PROTÉIQUE D'INVASION CELLULAIRE, LEURS COMPOSITIONS PHARMACEUTIQUES ET LEURS PROCÉDÉS D'UTILISATION
    摘要:
    本申请涉及到I式化合物(I)以及它们在抑制AKT-1、FAK和PKCα中至少一种方面的使用,以及在治疗和/或预防转移性疾病方面的使用。
    公开号:
    WO2013059927A1
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文献信息

  • [EN] COMPOUNDS TARGETING THE CELL INVASION PROTEIN COMPLEX, THEIR PHARMACEUTICAL COMPOSITIONS AND METHODS OF USE THEREOF<br/>[FR] COMPOSÉS CIBLANT LE COMPLEXE PROTÉIQUE D'INVASION CELLULAIRE, LEURS COMPOSITIONS PHARMACEUTIQUES ET LEURS PROCÉDÉS D'UTILISATION
    申请人:ROYAL INST FOR THE ADVANCEMENT OF LEARNING MCGILL UNIVERSITY
    公开号:WO2013059927A1
    公开(公告)日:2013-05-02
    The present application relates to the compounds of formula I (I) as well as their use for inhibiting at least one of AKT-1, FAK and PKCα and in the treatment and/or prevention of metastatic diseases.
    本申请涉及到I式化合物(I)以及它们在抑制AKT-1、FAK和PKCα中至少一种方面的使用,以及在治疗和/或预防转移性疾病方面的使用。
  • Compounds targeting the cell invasion protein complex, their pharmaceutical compositions and methods of use thereof
    申请人:THE ROYAL INSTITUTE FOR THE ADVANCEMENT OF LEARNING/MCGILL UNIVERSITY
    公开号:US09085598B2
    公开(公告)日:2015-07-21
    The present application relates to the compounds of formula I (I) as well as their use for inhibiting at least one of AKT-1, FAK and PKCα and in the treatment and/or prevention of metastatic diseases.
    本申请涉及公式I(I)化合物,以及它们用于抑制AKT-1,FAK和PKCα中至少一种的作用,以及在治疗和/或预防转移性疾病中的应用。
  • US20140256659A1
    申请人:——
    公开号:——
    公开(公告)日:——
  • US9085598B2
    申请人:——
    公开号:US9085598B2
    公开(公告)日:2015-07-21
  • Synthesis and biological activity of novel organoselenium derivatives targeting multiple kinases and capable of inhibiting cancer progression to metastases
    作者:Krikor Bijian、Zhongwei Zhang、Bin Xu、Su Jie、Bo Chen、Shengbiao Wan、JianHui Wu、Tao Jiang、Moulay A. Alaoui-Jamali
    DOI:10.1016/j.ejmech.2011.12.006
    日期:2012.2
    The present study reports synthesis and biological activity of novel benzoisoselenazolone compounds derived from ebselen and conjugated to a sugar molecule. Cell proliferation assay using cancer cells combined with in vitro biochemical assays revealed that benzoisoselenazolone 2d, 5a, and 6a exerted anti-proliferative activity, which correlated with selective in vitro inhibition of focal adhesion kinase, AKT-1, and protein kinase C-alpha. Active molecules were able to significantly inhibit cell migration and invasion in vitro compared to cells treated with the vehicle alone or ebselen. Moreover, in vivo anticancer activity focusing on lead compound 2d and using an invasive human breast cancer orthotopic mouse model revealed a potent anti-metastatic activity at well-tolerated doses. In summary, these novel benzoisoselenazolones we report herein target multiple kinases with established roles in cancer progression and possess anti-invasive and anti-metastatic activity in preclinical models supporting a potential for therapeutic application for human disease. Crown Copyright (C) 2011 Published by Elsevier Masson SAS. All rights reserved.
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