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

(2S)-7-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one

中文名称
——
中文别名
——
英文名称
(2S)-7-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one
英文别名
——
(2S)-7-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one化学式
CAS
——
化学式
C27H32O14
mdl
——
分子量
580.543
InChiKey
DFPMSGMNTNDNHN-NPDMSNFISA-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):
    -0.5
  • 重原子数:
    41
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.52
  • 拓扑面积:
    225
  • 氢给体数:
    8
  • 氢受体数:
    14

文献信息

  • Methods of Using Substituted Tetracycline Compounds to Modulate RNA
    申请人:Levy Stuart B.
    公开号:US20120245130A1
    公开(公告)日:2012-09-27
    A method for modulating RNA with tetracycline compounds is described.
    本文描述了一种使用四环素化合物调节RNA的方法。
  • SubstitutedTetracycline Compounds for the Treatment of Malaria
    申请人:DRAPER Michael
    公开号:US20120101071A1
    公开(公告)日:2012-04-26
    This invention provides a method for treating or preventing malaria in a subject. The method includes administering to the subject an effective amount of a substituted tetracycline compound, such that malaria is treated or prevented. In one aspect, the invention relates to pharmaceutical compositions which include an effective amount of a tetracycline compound to treat malaria in a subject and a pharmaceutically acceptable carrier. The substituted tetracycline compounds of the invention can be used to in combination with one or more anti-malarial compounds or can be used to treat or prevent malaria which is resistant to one or more other anti-malarial compounds.
    本发明提供了一种治疗或预防疟疾的方法。该方法包括向受试者施用足够量的取代四环素化合物,以治疗或预防疟疾。在一方面,本发明涉及制药组合物,其包括足够量的四环素化合物以治疗受试者的疟疾和药学上可接受的载体。本发明的取代四环素化合物可以与一种或多种抗疟疾化合物结合使用,或者可以用于治疗或预防对一种或多种其他抗疟疾化合物产生耐药性的疟疾。
  • ELECTROCATALYTIC SYNTHESIS OF DIHYDROCHALCONES
    申请人:BOARD OF TRUSTEES OF MICHIGAN STATE UNIVERSITY
    公开号:US20220089630A1
    公开(公告)日:2022-03-24
    The disclosure relates to methods of forming a dihydrochalcone using electrocatalytic dehydrogenation. In particular, the disclosure relates to methods of forming a dihydrochalcone electrocatalytically hydrogenating (ECH) a reactant compound over a catalytic cathode in a reaction medium having a non-alkaline pH value, thereby forming a dihydrochalcone product; wherein the reactant compound has a structure according to Formula (I). The method can be used to prepare dihydrochalcone sweeteners, such as, for example, naringin dihydrochalcone and neohesperidin dihydrochalcone.
  • US8088820B2
    申请人:——
    公开号:US8088820B2
    公开(公告)日:2012-01-03
  • US9562003B2
    申请人:——
    公开号:US9562003B2
    公开(公告)日:2017-02-07
查看更多