摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2-((1s,4s)-4-azidocyclohexyl)ethanol | 1508307-50-3

中文名称
——
中文别名
——
英文名称
2-((1s,4s)-4-azidocyclohexyl)ethanol
英文别名
——
2-((1s,4s)-4-azidocyclohexyl)ethanol化学式
CAS
1508307-50-3
化学式
C8H15N3O
mdl
——
分子量
169.227
InChiKey
MQVPQTOILBSJMZ-OCAPTIKFSA-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):
    2.24
  • 重原子数:
    12.0
  • 可旋转键数:
    3.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    68.99
  • 氢给体数:
    1.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Optimization of Antitumor Modulators of Pre-mRNA Splicing
    摘要:
    The spliceosome regulates pre-mRNA splicing, which is a critical process in normal mammalian cells. Recently, recurrent mutations in numerous spliceosomal proteins have been associated with a number of cancers. Previously, natural product antitumor agents have been shown to interact with one of the proteins that is subject to recurrent mutations (SF3B1). We report the optimization of a class of tumor-selective spliceosome modulators that demonstrate significant in vivo antitumor activity. This optimization culminated in the discovery of sudemycin D6, which shows potent cytotoxic activity in the melanoma line SK-MEL-2 (IC50 = 39 nM) and other tumor cell lines, including JeKo-1 (IC50 = 22 nM), He La (IC50 = SO nM), and SK-N-AS (IC50 = 81 nM). We also report improved processes for the synthesis of these compounds. Our work supports the idea that sudemycin D6 is worthy of further investigation as a novel preclinical anticancer agent with application in the treatment of numerous human cancers.
    DOI:
    10.1021/jm401370h
  • 作为产物:
    描述:
    2-((1s,4s)-4-aminocyclohexyl)ethan-1-ol1H-咪唑-1-磺酰叠氮盐酸盐copper(ll) sulfate pentahydratepotassium carbonate 作用下, 以 甲醇 为溶剂, 以5 g的产率得到2-((1s,4s)-4-azidocyclohexyl)ethanol
    参考文献:
    名称:
    Optimization of Antitumor Modulators of Pre-mRNA Splicing
    摘要:
    The spliceosome regulates pre-mRNA splicing, which is a critical process in normal mammalian cells. Recently, recurrent mutations in numerous spliceosomal proteins have been associated with a number of cancers. Previously, natural product antitumor agents have been shown to interact with one of the proteins that is subject to recurrent mutations (SF3B1). We report the optimization of a class of tumor-selective spliceosome modulators that demonstrate significant in vivo antitumor activity. This optimization culminated in the discovery of sudemycin D6, which shows potent cytotoxic activity in the melanoma line SK-MEL-2 (IC50 = 39 nM) and other tumor cell lines, including JeKo-1 (IC50 = 22 nM), He La (IC50 = SO nM), and SK-N-AS (IC50 = 81 nM). We also report improved processes for the synthesis of these compounds. Our work supports the idea that sudemycin D6 is worthy of further investigation as a novel preclinical anticancer agent with application in the treatment of numerous human cancers.
    DOI:
    10.1021/jm401370h
点击查看最新优质反应信息

文献信息

  • ANTICANCER COMPOUNDS
    申请人:ST. JUDE CHILDREN'S RESEARCH HOSPITAL
    公开号:US20160009728A1
    公开(公告)日:2016-01-14
    In one aspect, the invention relates to compounds having anticancer activity; synthetic methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating disorders associated with uncontrolled cellular proliferation using the compounds and compositions. This abstract is intended to be used as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
    本发明涉及具有抗癌活性的化合物;制备这些化合物的合成方法;包含这些化合物的制药组合物;以及使用这些化合物和组合物治疗与细胞不受控制增殖相关的疾病的方法。本摘要旨在作为在特定领域搜索的扫描工具使用,不旨在限制本发明。
  • US9682993B2
    申请人:——
    公开号:US9682993B2
    公开(公告)日:2017-06-20
  • [EN] ANTICANCER COMPOUNDS<br/>[FR] COMPOSÉS ANTI-CANCER
    申请人:ST JUDE CHILDRENS RES HOSPITAL
    公开号:WO2014089571A1
    公开(公告)日:2014-06-12
    In one aspect, the invention relates to compounds having anticancer activity; synthetic methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating disorders associated with uncontrolled cellular proliferation using the compounds and compositions. This abstract is intended to be used as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
查看更多