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4-Hydroxycordoin | 55524-25-9

中文名称
——
中文别名
——
英文名称
4-Hydroxycordoin
英文别名
p-hydroxycordoin;(2E)-1-{2-hydroxy-4-[(3-methylbut-2-enyl)oxy]phenyl}-3-(4-hydroxyphenyl)prop-2-en-1-one;(E)-1-[2-hydroxy-4-(3-methylbut-2-enoxy)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one
4-Hydroxycordoin化学式
CAS
55524-25-9
化学式
C20H20O4
mdl
——
分子量
324.376
InChiKey
SFXYAAFUXNWNQF-BJMVGYQFSA-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):
    5
  • 重原子数:
    24
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    66.8
  • 氢给体数:
    2
  • 氢受体数:
    4

SDS

SDS:c361e03732e46dfd9f7f2388af1a1876
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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

  • 作为产物:
    描述:
    1-[2-羟基-4-(3-甲基-2-丁烯氧基)-苯基]-乙酮对羟基苯甲醛 在 potassium hydroxide 作用下, 以 乙醇 为溶剂, 反应 1.0h, 以32%的产率得到4-Hydroxycordoin
    参考文献:
    名称:
    Prenyloxyphenylpropanoids as a novel class of anticonvulsive agents
    摘要:
    In this study, we synthesized some natural and semi-synthetic prenyloxyphenylpropanoids (e.g., acetophenones, benzoic and cinnamic acids, chalcones, and coumarins), and we assessed their in vivo neuroprotective activity, using the mouse maximal electroshock-induced seizure model (MES test). 7-Iso-pentenyloxycoumarin and (2E)-3-{4-[(3-methylbut-2-enyl)oxy]phenyl}prop-2-enoic acid, administered ip at a dose of 300 mg/kg, suppressed MES-induced seizures in mice in a time- and dose-dependent manner. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.07.110
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文献信息

  • [EN] SKIN PIGMENTATION MODIFIERS TO DARKEN OR LIGHTEN THE SKIN<br/>[FR] AGENTS DE MODIFICATION DE LA PIGMENTATION DE LA PEAU EN VUE DE L'ASSOMBRIR OU DE L'ÉCLAIRCIR
    申请人:AFFICHEM
    公开号:WO2016193220A1
    公开(公告)日:2016-12-08
    The present invention relates to a method for changing the pigmentation of a skin, a mucous membrane or hair with a compound of general formula (I), a cosmetic use of said compound of general formula (I), to cosmetic compositions comprising said compound of general formula (I), and to new depigmenting agents.
    本发明涉及一种改变皮肤、粘膜或头发色素的方法,使用一般式(I)的化合物,以及所述一般式(I)的化合物的化妆用途,包括所述一般式(I)的化合物的化妆组合物,以及新的脱色剂。
  • DEPIGMENTING AGENTS TO LIGHTEN THE SKIN
    申请人:Affichem
    公开号:EP3097904A1
    公开(公告)日:2016-11-30
    The present invention relates to a method for lightening a skin or a mucous membrane with a depigmenting agent, a cosmetic use of said depigmenting agent, to cosmetic compositions comprising said agent, and to new depigmenting agents.
    本发明涉及一种使用脱色剂淡化皮肤或粘膜的方法、所述脱色剂的化妆品用途、包含所述脱色剂的化妆品组合物以及新型脱色剂。
  • Antibacterial and Anti-inflammatory Activities of 4-Hydroxycordoin: Potential Therapeutic Benefits
    作者:Mark Feldman、Shinichi Tanabe、Francesco Epifano、Salvatore Genovese、Massimo Curini、Daniel Grenier
    DOI:10.1021/np100547b
    日期:2011.1.28
    4-Hydroxycordoin (1), a natural isopentenyloxychalcone, is a plant secondary metabolite that is relatively rare. Since there are very few reports about the biological activities of 1, its potential benefits for periodontal disease were investigated. A marked and dose-dependent antibacterial activity of 1 was observed against the three major periodontal pathogens, Porphyromonas gingivalis, Fusobacterium nucleatum, and Prevotella intermedia. Moreover, compound 1 showed an antiadhesion effect, since it inhibited attachment of P. gingivalis to oral epithelial cells. Finally, using a macrophage model, the ability of 1 to inhibit the secretion of inflammatory mediators induced by Aggregatibacter actinomycetemcomitans lipopolysaccharide was demonstrated. The anti-inflammatory effect observed was associated with reduced activation of the nuclear factor-kappa B (NF-kappa B) p65 and activator protein-1 (AP-1) pathways.
  • CHALCONES AND ESTERS THEREOF WITH ANTIPROLIFERATIVE ACTIVITY IN UTERUS, OVARY AND BREAST TUMOURS
    申请人:INDENA S.p.A.
    公开号:EP0800387A1
    公开(公告)日:1997-10-15
  • MRGPRX2 ANTAGONIST FOR THE TREATMENT OF PSEUDO ALLERGIC REACTIONS
    申请人:The University of Hong Kong
    公开号:US20220401435A1
    公开(公告)日:2022-12-22
    Compounds that have antiallergic and/or anti-inflammatory properties and methods of making thereof are disclosed. These compounds can block MMRGPRX2 and prevent or reduce mast cells activation. Pharmaceutical formulations in a unit dosage form suitable for the delivery of the compounds to a subject in need thereof are disclosed. The pharmaceutical formulations may include one or more active agents in addition to the compounds, such as one or more additional antiallergic and/or anti-inflammatory agents. The pharmaceutical formulation can be administered by oral administration, parenteral administration, inhalation, mucosal administration, or a combination thereof. Methods for preventing or treating pseudo allergic reactions, pseudo allergic diseases, and/or pseudo inflammatory diseases, or treating or ameliorating one or more symptoms associated with a pseudo allergic reaction, a pseudo allergic disease, and/or a pseudo inflammatory disease in a subject are also disclosed.
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