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

5,7-二羟基-6-(3-甲基-2-丁烯基)-8-(3-甲基丁酰)-4-苯基-2H-1-苯并吡喃-2-酮 | 5224-54-4

中文名称
5,7-二羟基-6-(3-甲基-2-丁烯基)-8-(3-甲基丁酰)-4-苯基-2H-1-苯并吡喃-2-酮
中文别名
——
英文名称
5,7-dihydroxy-8-(3-methylbutanoyl)-6-(3-methylbut-2-enyl)-4-phenyl-2H-chromen-2-one
英文别名
mammea A/BA;5,7-dihydroxy-6-(3-methyl-but-2-enyl)-8-(3-methyl-butyryl)-4-phenyl-chromen-2-one;5,7-dihydroxy-8-(3-methylbutanoyl)-6-(3-methylbut-2-enyl)-4-phenylchromen-2-one
5,7-二羟基-6-(3-甲基-2-丁烯基)-8-(3-甲基丁酰)-4-苯基-2H-1-苯并吡喃-2-酮化学式
CAS
5224-54-4
化学式
C25H26O5
mdl
——
分子量
406.478
InChiKey
SBHOAZQBEGVQLJ-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:
    629.1±54.0 °C(Predicted)
  • 密度:
    1.219±0.06 g/cm3(Predicted)
  • 物理描述:
    Solid
  • 熔点:
    125-126°C

计算性质

  • 辛醇/水分配系数(LogP):
    5.8
  • 重原子数:
    30
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    83.8
  • 氢给体数:
    2
  • 氢受体数:
    5

SDS

SDS:b2b1a56ef025220e62b599d609c3fcd1
查看

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
  • 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:
    描述:
    5,7-二羟基-6-(3-甲基-2-丁烯基)-8-(3-甲基丁酰)-4-苯基-2H-1-苯并吡喃-2-酮氧气 、 tetraphenylporphyrin 、 三苯基膦 作用下, 以 二氯甲烷 为溶剂, 反应 1.5h, 以63%的产率得到5,7-dihydroxy-6-(2-hydroxy-3-methylbut-3-enyl)-8-(3-methyl-1-oxobutyl)-2H-4-phenyl-benzopyran-2-one
    参考文献:
    名称:
    Synthesis of 2-hydroxy-3-methylbut-3-enyl substituted coumarins and xanthones as natural products. Application of the Schenck ene reaction of singlet oxygen with ortho-prenylphenol precursors
    摘要:
    Application of our original photooxidation-reduction methodology to prenylated dihydroxycoumarin and trihydroxyxanthone compounds led to the corresponding ortho-(2-hydroxy-3-methylbut-3-enyl)phenol derivatives with yields ranging from 8 to 65%. In most of the reported experiments, the oxidation products distribution, after the photooxygenation step, was controlled by the competition between the large group effect and the stabilising phenolic assistance effect. We also showed that ortho-(3-hydroxy-3-methylbut-1-enyl)phenol derivatives could be considered as biogenetic precursors of 2,2-dimethylbenzopyranic structures. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2004.01.033
  • 作为产物:
    参考文献:
    名称:
    mammeins和surangin a的合成
    摘要:
    据报道,天然的4-烷基和4-芳基香豆素与六取代的芳环(氧化磷酸化的解偶联剂)的合成。合成的Mammea B / BB是(S)-(-)-化合物。
    DOI:
    10.1016/s0040-4039(00)98874-9
点击查看最新优质反应信息

文献信息

  • Methods and compositions for lowering levels of blood lipids
    申请人:Pharmacia Corporation
    公开号:US20040014806A1
    公开(公告)日:2004-01-22
    Disclosed are methods to lower blood cholesterol levels or inhibit ileal apical sodium co-dependent bile acid transport (ASBT) protein using coumarin and anthracene dione derivatives. Pharmaceutical compositions are also disclosed.
    揭示了使用香豆素和蒽醌二酮衍生物降低血液胆固醇水平或抑制回肠顶端钠依赖性胆汁酸转运蛋白(ASBT)的方法。同时还公开了相关的药物组合物。
  • PLANT EXTRACT OBTAINED FROM KIELMEYERA AUREOVINOSA WHICH HAS ANTIBIOTIC ACTIVITY, ISOLATED CHEMICAL COMPOUND, COMPOSITIONS COMPRISING SAME, USES THEREOF AND METHODS FOR PREVENTING AND TREATING BACTERIAL INFECTIONS
    申请人:Extracta Moléculas Naturais S/A
    公开号:EP2735311A1
    公开(公告)日:2014-05-28
    The present invention refers primarily to a plant extract obtained from Kielmeyera aureovinosa which has accentuated antibiotic activity. In a second modality, the invention describes a new chemical compound isolated from the same, as well as variations thereof. In other terms, the present invention provides compositions comprising a phytotherapic obtained from said plant extract, as well as veterinary pharmaceutical compositions comprising isolated compounds and variations of the same. Additionally, the present invention provides uses of the plant extract, chemical compounds and compositions comprising the same for the preparation of medicines for the prevention or treatment of bacterial infections, as well as methods of prevention or treatment of the same.
    本发明主要涉及一种从 Kielmeyera aureovinosa 中提取的植物提取物,它具有更强的抗生素活性。在第二种模式中,本发明描述了从该提取物中分离出来的一种新化合物及其变体。换言之,本发明提供了包含从上述植物提取物中获得的植物治疗剂的组合物,以及包含分离化合物及其变体的兽药组合物。 此外,本发明还提供了植物提取物、化合物和包含上述物质的组合物在制备预防或治疗细菌感染的药物中的用途,以及预防或治疗细菌感染的方法。
  • Crombie, Leslie; Jones, Raymond C. F.; Palmer, Christopher J., Journal of the Chemical Society. Perkin transactions I, 1987, p. 317 - 332
    作者:Crombie, Leslie、Jones, Raymond C. F.、Palmer, Christopher J.
    DOI:——
    日期:——
  • Synthesis of 2-hydroxy-3-methylbut-3-enyl substituted coumarins and xanthones as natural products. Application of the Schenck ene reaction of singlet oxygen with ortho-prenylphenol precursors
    作者:Jean-Jacques Helesbeux、Olivier Duval、Caroline Dartiguelongue、Denis Séraphin、Jean-Michel Oger、Pascal Richomme
    DOI:10.1016/j.tet.2004.01.033
    日期:2004.3
    Application of our original photooxidation-reduction methodology to prenylated dihydroxycoumarin and trihydroxyxanthone compounds led to the corresponding ortho-(2-hydroxy-3-methylbut-3-enyl)phenol derivatives with yields ranging from 8 to 65%. In most of the reported experiments, the oxidation products distribution, after the photooxygenation step, was controlled by the competition between the large group effect and the stabilising phenolic assistance effect. We also showed that ortho-(3-hydroxy-3-methylbut-1-enyl)phenol derivatives could be considered as biogenetic precursors of 2,2-dimethylbenzopyranic structures. (C) 2004 Elsevier Ltd. All rights reserved.
  • Synthesis of mammeins and surangin a
    作者:Leslie Crombie、Raymond C.F. Jones、Christopher J. Palmer
    DOI:10.1016/s0040-4039(00)98874-9
    日期:1985.1
    Syntheses of natural 4-alkyl and 4-aryl coumarins with hexasubstituted aromatic rings, uncouplers of oxidative phosphorylation, are reported. Mammea B/BB, by synthesis, is the (S)-(−)-compound.
    据报道,天然的4-烷基和4-芳基香豆素与六取代的芳环(氧化磷酸化的解偶联剂)的合成。合成的Mammea B / BB是(S)-(-)-化合物。
查看更多

同类化合物

黄檀色烯 黄檀素 铁力木苦素 贝伐他汀 红厚壳内酯 头孢克肟侧链酸活性酯 外消旋6-甲氧羰基-4-苯基-3,4-二氢香豆素 外消旋-6-甲基-4-苯基-2-色满醇 塞曲司特 四甲基罗丹明-5-马来酰亚胺 乙酮,1-[8-(4-羟基-3,5-二甲氧苯基)-6-甲基-8H-1,3-二噁唑并[4,5-g][1]苯并吡喃-7-基]- N,N-二乙基-4-(5-羟基螺[2H-1-苯并吡喃-2,4'-哌啶]-4-基)苯甲酰胺盐酸盐 L-苯丙氨酸,N-[(7-羟基-2-羰基-4-苯基-2H-1-苯并吡喃-8-基)甲基]- Atto590NHS酯 8-羟基-4-苯基-2-3,4-二氢苯并吡喃酮 8-乙酰基-5,7-二羟基-4-苯基色烯-2-酮 8-(4-甲氧苯基)-6-甲基-7,8-二氢-6H-[1,3]二噁唑并[4,5-g]色烯-6-醇 8-(2-羟基-3-甲氧苯基)-7-甲基-7,8-二氢-6H-[1,3]二噁唑并[4,5-g]色烯-6-醇 8-(2-甲氧苯基)-6,7-二甲基-7,8-二氢-6H-[1,3]二噁唑并[4,5-g]色烯-6-醇 8-(2,4-二甲氧基苯基)-6-甲氧基-6,7-二甲基-7,8-二氢吡喃并[6,5-f][1,3]苯并二氧戊环 7-羟基-8-甲基-4-苯基-2H-色烯-2-酮 7-羟基-6-戊基-4-苯基色烯-2-酮 7-羟基-4-苯基香豆素 7-羟基-4-苯基-3-(4-羟基苯基)香豆素 7-羟基-4-苯基-3-(3-吡啶基)-2H-1-苯并吡喃-2-酮 7-羟基-4-(4-甲氧基苯基)-3,4-二氢-2H-1-苯并吡喃-2-酮 7-羟基-4-(3-三氟甲基苯基)香豆素 7-羟基-3-甲基-4-苯基香豆素 7-羟基-3-(4-甲氧苯基)-4-苯基-2H-色烯-2-酮 7-甲氧基-8-甲基-4-苯基色烯-2-酮 7-甲氧基-4-苯基色烯-2-酮 7-甲氧基-3-甲基-4-苯基-2H-色烯-2-酮 7-甲基-4-苯基-3,4-二氢色烯-2-酮 7-溴-4-(3-甲基苯基)-2H-色烯-2-酮 7-乙酰氧基-4-苯基-色烯-2-酮 7-乙氧基-4-苯基-2H-色烯-2-酮 7-[4-(1-乙基-1-羟基-丙基)-[1,2,3]三唑-1-基甲基]-4-(3-氟-苯基)-色烯-2-酮 7-(溴甲基)-4-(3-氟苯基)-2H-色烯-2-酮 7-(叠氮甲基)-4-(3-甲基苯基)-2H-色烯-2-酮 7-(叠氮甲基)-4-(3-氟苯基)-2H-色烯-2-酮 7,8-二羟基-4-苯基香豆素 7,8-二乙酰氧基-4-苯基香豆素 6-羧基-4-苯基-3,4-二氢香豆素 6-羟基-4-苯基-3,4-二氢色烯-2-酮 6-甲氧基-7-甲基-8-(3,4,5-三甲氧苯基)-7,8-二氢-6H-[1,3]二噁唑并[4,5-g]色烯 6-甲基-6-吡咯烷-1-基-8-(3,4,5-三甲氧基苯基)-7,8-二氢吡喃并[6,5-f][1,3]苯并二氧戊环-7-羧酸乙酯 6-甲基-4-苯基香豆素 6-甲基-4-苯基色满-2-酮 6-甲基-4-(4-甲基苯基)-3-苯基色烯-2-酮 6-溴-3,4-二氢-4-苯基-2H-1-苯并吡喃-2-酮