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(E)-3-(3',4'-bis(benzyloxy)phenyl)-1-(2-hydroxyphenyl)prop-2-en-1-one | 1148010-41-6

中文名称
——
中文别名
——
英文名称
(E)-3-(3',4'-bis(benzyloxy)phenyl)-1-(2-hydroxyphenyl)prop-2-en-1-one
英文别名
(E)-3-(3,4-bis-(benzyloxy)phenyl)-1-(2-hydroxyphenyl)prop-2-en-1-one;3,4-dibenzyloxy-2'-hydroxychalcone;3,4-Dibenzyloxy-2''-hydroxychalcone;(E)-3-[3,4-bis(phenylmethoxy)phenyl]-1-(2-hydroxyphenyl)prop-2-en-1-one
(E)-3-(3',4'-bis(benzyloxy)phenyl)-1-(2-hydroxyphenyl)prop-2-en-1-one化学式
CAS
1148010-41-6
化学式
C29H24O4
mdl
——
分子量
436.507
InChiKey
LHMDXKJKKAITQJ-BMRADRMJSA-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):
    6.8
  • 重原子数:
    33
  • 可旋转键数:
    9
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    55.8
  • 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

点击查看最新优质反应信息

文献信息

  • Enantioselctive Syntheses of Sulfur Analogues of Flavan-3-Ols
    作者:Pradeep K. Sharma、Min He、Jurjus Jurayj、Da-Ming Gou、Richard Lombardy、Leo J. Romanczy、Hagen Schroeter
    DOI:10.3390/molecules15085595
    日期:——
    The first enantioselective syntheses of sulfur flavan-3-ol analogues 1–8 have been accomplished, whereby the oxygen atom of the pyran ring has been replaced by a sulfur atom. The key steps were: (a) Pd(0) catalyzed introduction of –S t-butyl group, (b) Sharpless enantioselective dihydroxylation of the alkene, (c) acid catalyzed ring closure to produce the thiopyran ring, and (d) removal of benzyl groups using N,N-dimethylaniline and AlCl3. The compounds were isolated in high chemical and optical purity.
    首次完成了硫代黄烷-3-醇类似物1-8的手性选择性合成,其中吡喃环上的氧原子被硫原子取代。关键步骤包括:(a) 通过Pd(0)催化引入-S t-丁基,(b) 使用Sharpless方法对烯烃进行手性选择性二羟基化,(c) 酸性催化闭环生成噻吡喃环,以及(d) 利用N,N-二甲基苯胺和AlCl3去除苄基。合成的化合物具有高化学纯度和光学纯度。
  • Inhibitory activity of prostaglandin E2 production by the synthetic 2′-hydroxychalcone analogues: Synthesis and SAR study
    作者:Thanh-Dao Tran、Haeil Park、Hyun Pyo Kim、Gerhard F. Ecker、Khac-Minh Thai
    DOI:10.1016/j.bmcl.2009.02.001
    日期:2009.3
    A series of 2'-hydroxychalcones has been synthesized and screened for their in vitro inhibitory activities of cyclooxygenase-2 catalyzed prostaglandin production from lipopolysaccharide-treated RAW 264.7 cells. Structure-activity relationship study suggested that inhibitory activity against prostaglandin E-2 production was governed to a greater extent by the substituent on B ring of the chalcone, and most of the active compounds have at least two methoxy or benzyloxy groups on B ring. The relationship between chalcone structures and their PGE(2) inhibitory activities was also interpreted by docking study on cyclooxygenase-2. (C) 2009 Elsevier Ltd. All rights reserved.
  • US9975869B2
    申请人:——
    公开号:US9975869B2
    公开(公告)日:2018-05-22
  • NOVEL ANALOGUES OF EPICATECHIN AND RELATED POLYPHENOLS
    申请人:SPHAERA PHARMA PVT. LTD.
    公开号:US20160039781A1
    公开(公告)日:2016-02-11
    The present invention provides novel analogues of epicatechin and related polyphenols, their variously functionalized derivatives, process for preparation of the same, composition comprising these compounds and their method of use.
    本发明提供了表儿茶素及相关多酚的新颖类似物,它们的各种官能化衍生物,以及它们的制备方法、包含这些化合物的组合物和它们的使用方法。
  • Anti-tyrosinase flavone derivatives and their anti-melanogenic activities: Importance of the β-phenyl-α,β-unsaturated carbonyl scaffold
    作者:Jieun Lee、Yeongmu Jeong、Hee Jin Jung、Sultan Ullah、Jeongin Ko、Ga Young Kim、Dahye Yoon、Sojeong Hong、Dongwan Kang、Yujin Park、Pusoon Chun、Hae Young Chung、Hyung Ryong Moon
    DOI:10.1016/j.bioorg.2023.106504
    日期:2023.3
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