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2-bromophenoxyethyl tetrahydro-2H-pyran-2-yl ether | 445283-15-8

中文名称
——
中文别名
——
英文名称
2-bromophenoxyethyl tetrahydro-2H-pyran-2-yl ether
英文别名
2-[2-(2-bromo-phenoxy)-ethoxy]-tetrahydropyran;2-[2-(2-bromophenoxy)ethoxy]oxane
2-bromophenoxyethyl tetrahydro-2H-pyran-2-yl ether化学式
CAS
445283-15-8
化学式
C13H17BrO3
mdl
——
分子量
301.18
InChiKey
NDHKPERQHLHPHR-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

  • 沸点:
    385.1±42.0 °C(Predicted)
  • 密度:
    1.37±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.3
  • 重原子数:
    17
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    27.7
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 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:
    参考文献:
    名称:
    Design, Synthesis, and Biological Evaluation of Aryloxyethyl Thiocyanate Derivatives against Trypanosoma cruzi
    摘要:
    As a continuation of our project aimed at the search for new and safe chemotherapeutic and chemoprophylactic agents against American trypanosomiasis (Chagas' disease), several drugs structurally related to 4-phenoxyphenoxyethyl thiocyanate (4) were designed, synthesized, and evaluated as antiproliferative agents against the parasite responsible for this disease, the hemoflagellated protozoan Trypanosoma cruzi. This thiocyanate derivative was previously shown to be an effective and potent agent against T. cruzi proliferation. Several drugs possessing thiocyanate groups proved to be effective growth inhibitors of T. cruzi growth. Among the designed compounds, it is important to point out the extremely potent activity shown by 11, 23, 38, 53, 90, 99, and 117 against the epimastigote forms of the parasite. All of them exhibited IC50 values in the low micromolar range, and these values were comparable with those presented by our lead drug 4 and ketokonazole, a well-known antiparasitic agent. The activity displayed by the nitrogen-containing derivative 90 was very promising with IC50 values of 3.3 muM. Several other thiocyanate derivatives also proved to be very potent inhibitors of the multiplication of T. cruzi epimastigotes, such as compounds 28, 33, 43, 48, 56, 61, 66, 71, 76, and 124. Compound 43 resulted in being a promising drug because it was also very effective against amastigotes, the clinically more relevant form of the parasite. This compound was Mold more potent than 4, while 11 showed nearly the same activity as our lead drug against intracellular T. cruzi. It was very surprising that the experimental juvenoid 124, although fairly devoid of activity against epimastigotes, was very effective against intracellular amastigotes growing in myoblasts. The rest of the designed compounds showed a broad degree of inhibitory action, from moderately active drugs to drugs almost devoid of antiparasitic activity. Compound 43 is an interesting example of an effective antichagasic agent that presents excellent prospectives not only as a lead drug but also to be used for further in vivo studies.
    DOI:
    10.1021/jm0201518
  • 作为产物:
    描述:
    2-(2-溴乙氧基)四氢吡喃2-溴苯酚 在 sodium hydride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 1.0h, 以80%的产率得到2-bromophenoxyethyl tetrahydro-2H-pyran-2-yl ether
    参考文献:
    名称:
    WO2008/144223
    摘要:
    公开号:
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文献信息

  • Triazolyl aminopyrimidine compounds
    申请人:Eli Lilly and Company
    公开号:US08063035B2
    公开(公告)日:2011-11-22
    The present invention provides triazolyl aminopyrimidine compounds useful in the treatment of cancer.
    本发明提供了三唑基氨基嘧啶化合物,用于治疗癌症。
  • TRIAZOLYL AMINOPYRIMIDINE COMPOUNDS
    申请人:Brooks Harold Burns
    公开号:US20100087431A1
    公开(公告)日:2010-04-08
    The present invention provides triazolyl aminopyrimidine compounds useful in the treatment of cancer.
    本发明提供了三唑基氨基嘧啶类化合物,可用于治疗癌症。
  • WO2008/144223
    申请人:——
    公开号:——
    公开(公告)日:——
  • US8063035B2
    申请人:——
    公开号:US8063035B2
    公开(公告)日:2011-11-22
  • [EN] TRIAZOLYL AMINOPYRIMIDINE COMPOUNDS<br/>[FR] COMPOSÉS TRIAZOLYL AMINOPYRIMIDINE
    申请人:LILLY CO ELI
    公开号:WO2008144223A2
    公开(公告)日:2008-11-27
    [EN] The present invention provides triazolyl aminopyrimidine compounds useful in the treatment of cancer.
    [FR] Composés triazolyl aminopyrimidine utiles pour le traitement du cancer.
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