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(E)-1-(2-hydroxy-5-fluorophenyl)-3-(3-methoxyphenyl)prop-2-en-1-one | 1381931-08-3

中文名称
——
中文别名
——
英文名称
(E)-1-(2-hydroxy-5-fluorophenyl)-3-(3-methoxyphenyl)prop-2-en-1-one
英文别名
(E)-1-(5-fluoro-2-hydroxyphenyl)-3-(3-methoxyphenyl)prop-2-en-1-one
(E)-1-(2-hydroxy-5-fluorophenyl)-3-(3-methoxyphenyl)prop-2-en-1-one化学式
CAS
1381931-08-3
化学式
C16H13FO3
mdl
——
分子量
272.276
InChiKey
BDYRMSHVHBLRSX-FNORWQNLSA-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):
    4
  • 重原子数:
    20
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    4

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

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文献信息

  • [EN] COMPOSITION FOR TREATING DIABETES AND METABOLIC DISEASES AND A PREPARATION METHOD THEREOF<br/>[FR] COMPOSITION POUR LE TRAITEMENT DU DIABÈTE ET DE MALADIES MÉTABOLIQUES, ET SON PROCÉDÉ DE PRÉPARATION
    申请人:UNIV KAOHSIUNG MEDICAL
    公开号:WO2013022951A1
    公开(公告)日:2013-02-14
    Disclosed is a chalcone composition for treating diabetes and metabolic syndromes. In particular, the chalcone compound bound with 2-halogen in ring A significantly decreases the blood glucose level in the in vitro anti-diabetic effect experiment. In the in vivo animal model, the leading chalcone compound can prevent the progression of diabetes and control the blood glucose level, and there is no significant difference in the gains in body weight. Throughout the seven-week administration, there are no hepatic or renal toxicity observed.
    揭示了一种用于治疗糖尿病和代谢综合征的茚素组合物。具体来说,在环A中与2-卤素结合的茚素化合物在体外抗糖尿病效应实验中显着降低了血糖水平。在体内动物模型中,主要的茚素化合物可以预防糖尿病的进展并控制血糖水平,体重增加方面没有显著差异。在为期七周的给药过程中,没有观察到肝脏或肾脏毒性。
  • COMPOSITION FOR TREATING DIABETES AND METABOLIC DISEASES AND A PREPARATION METHOD THEREOF
    申请人:Wu Yang-Chang
    公开号:US20140350304A1
    公开(公告)日:2014-11-27
    Disclosed is a chalcone composition for treating diabetes and metabolic syndromes. In particular, the chalcone compound bound with 2-halogen in ring A significantly decreases the blood glucose level in the in vitro anti-diabetic effect experiment. In the in vivo animal model, the leading chalcone compound can prevent the progression of diabetes and control the blood glucose level, and there is no significant difference in the gains in body weight. Throughout the seven-week administration, there are no hepatic or renal toxicity observed.
    本发明公开了一种治疗糖尿病和代谢综合症的查尔酮组合物。特别是,环A中结合有2-卤素的查尔酮化合物在体外抗糖尿病实验中显著降低血糖水平。在体内动物模型中,主要的查尔酮化合物可以预防糖尿病的进展并控制血糖水平,体重增加也没有显著差异。在七周的给药过程中,没有观察到肝脏或肾脏毒性。
  • Synthesis of chalcone derivatives as potential anti-diabetic agents
    作者:Chi-Ting Hsieh、Tusty-Jiuan Hsieh、Mohamed El-Shazly、Da-Wei Chuang、Yi-Hong Tsai、Chiao-Ting Yen、Shou-Fang Wu、Yang-Chang Wu、Fang-Rong Chang
    DOI:10.1016/j.bmcl.2012.04.108
    日期:2012.6
    Chalcones bearing electron donating or electron withdrawing substitutions were prepared and their glucose uptake activity was evaluated. Chalcone derivatives were synthesized in one step protocol with high purity and yield. Chalcones with chloro, bromo, iodo and hydroxy substitutions at position 2 on A-ring exhibited the highest activity with glucose medium concentration (210 to 236 mg/dl) compared to pioglitazone and rosiglitazone (230 and 263 mg/dl, respectively). Also chalcones with iodo substitution at position 3 on A-ring were comparably active (<= 238 mg/dl). The structure-activity relationship of the tested chalcones was studied and the findings were supported statistically (C) 2012 Elsevier Ltd. All rights reserved.
  • US9085520B2
    申请人:——
    公开号:US9085520B2
    公开(公告)日:2015-07-21
  • Impact of mono- and disubstitution on the colorimetric dynamic covalent switching chalcone/flavanone scaffold
    作者:Brian M. Muller、Jesse Mai、Reid A. Yocum、Marc J. Adler
    DOI:10.1039/c4ob00398e
    日期:——

    The impact of substitution on a novel colorimetric dynamic covalent switching scaffold was investigated using UV/Vis and NMR spectroscopy.

    通过紫外/可见光谱和核磁共振谱,研究了替代对一种新型比色动态共价开关支架的影响。
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