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macarangin | 129385-65-5

中文名称
——
中文别名
——
英文名称
macarangin
英文别名
6-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,5,7-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one
macarangin化学式
CAS
129385-65-5
化学式
C25H26O6
mdl
——
分子量
422.478
InChiKey
MBIJQAHZUBUPNM-VIZOYTHASA-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:
    655.4±55.0 °C(Predicted)
  • 密度:
    1.315±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.3
  • 重原子数:
    31
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    107
  • 氢给体数:
    4
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    macarhizinoidin A 在 lithium 1-butanethiolate 作用下, 以 六甲基磷酰三胺 为溶剂, 反应 4.0h, 以65%的产率得到macarangin
    参考文献:
    名称:
    Synthesis of Isoprenyl Flavonoids: (+)-Denticulaflavonol, Macarangin, and Isomacarangin
    摘要:
    本研究描述了两种天然 C-烷基类黄酮的直接合成方法:大黄素、异大黄素和天然 (-)- 丁香黄酮醇的对映体。
    DOI:
    10.1055/s-2008-1072734
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文献信息

  • [EN] PROCESSES FOR THE PREPARATION OF ORTHO-ALLYLATED HYDROXY ARYL COMPOUNDS<br/>[FR] PROCÉDÉS DE PRÉPARATION DE COMPOSÉS HYDROXY-ARYLE ORTHO-ALLYLÉS
    申请人:UNIV MCMASTER
    公开号:WO2021237371A1
    公开(公告)日:2021-12-02
    The present application describes process for preparing an ortho-allylated hydroxy aryl compounds such as compounds of Formula (I) by reacting an allylic alcohol with a hydroxy aryl compound in the presence of aluminum compound selected from alumina and aluminum alkoxides and in a non-protic solvent wherein at least one carbon atom ortho to the hydroxy group in the hydroxy aryl compound is unsubstituted. The present application also includes compounds of Formula (I).
    本申请描述了一种制备邻烯丙基羟基芳基化合物的方法,例如通过在非质子溶剂中,在氧化铝和铝烷氧化物中选择的铝化合物存在下,将烯丙醇与羟基芳基化合物反应,其中羟基芳基化合物中至少有一个碳原子位于羟基的邻位且未被取代。本申请还包括化合物的化学式(I)。
  • LIGAND REGULATED PROTEIN-PROTEIN INTERACTION SYSTEM
    申请人:St. Anna Kinderkrebsforschung
    公开号:EP3502130A1
    公开(公告)日:2019-06-26
    Disclosed is a ligand regulated protein-protein interaction system based on a lipocalin-fold molecule comprising: (a) a lipocalin-fold molecule (b) a lipocalin-fold ligand with a low molecular weight of 1500 Da or below, and (c) a lipocalin-fold binding interaction partner, wherein the lipocalin-fold molecule can bind to the lipocalin-fold ligand; and wherein the lipocalin-fold molecule bound to the lipocalin-fold ligand binds to the lipocalin-fold binding interaction partner with an affinity which is at least 10-fold higher than the affinity of the lipocalin-fold molecule not bound to the lipocalin-fold ligand, and wherein the lipocalin-fold binding interaction partner is not a naturally occurring protein which has an affinity of <10 µM to any naturally occurring lipocalin-fold molecule in the presence of any lipocalin-fold ligand.
    所公开的是一种基于脂蛋白折叠分子的配体调节蛋白质-蛋白质相互作用系统,该系统包括 (a) 脂蛋白折叠分子 (b) 低分子量为 1500 Da 或以下的脂蛋白-折叠配体,以及 (c) 脂蛋白-折叠结合相互作用伙伴、 其中脂素折叠分子可与脂素折叠配体结合;以及 其中与脂蛋白配体结合的脂蛋白-折叠分子与脂蛋白-折叠结合相互作用伙伴结合的亲和力比未与脂蛋白-折叠配体结合的脂蛋白-折叠分子的亲和力至少高 10 倍、 其中脂蛋白-折叠结合相互作用伙伴不是天然存在的蛋白质,它在任何脂蛋白-折叠配体存在下对任何天然存在的脂蛋白-折叠分子的亲和力小于10 µM。
  • A GROUP OF CHIMERIC ANTIGEN RECEPTORS (CARS)
    申请人:St. Anna Kinderkrebsforschung
    公开号:EP3860643A1
    公开(公告)日:2021-08-11
  • PROCESSES FOR THE PREPARATION OF ORTHO-ALLYLATED HYDROXY ARYL COMPOUNDS
    申请人:McMaster University
    公开号:US20210380513A1
    公开(公告)日:2021-12-09
    The present application describes process for preparing an ortho-allylated hydroxy aryl compounds such as compounds of Formula (I) by reacting an allylic alcohol with a hydroxy aryl compound in the presence of aluminum compound selected from alumina and aluminum alkoxides and in a non-protic solvent wherein at least one carbon atom ortho to the hydroxy group in the hydroxy aryl compound is unsubstituted. The present application also includes compounds of Formula (I).
  • [EN] A GROUP OF CHIMERIC ANTIGEN RECEPTORS (CARS)<br/>[FR] GROUPE DE RÉCEPTEURS D'ANTIGÈNES CHIMÉRIQUES (CAR)
    申请人:ST ANNA KINDERKREBSFORSCHUNG
    公开号:WO2020070289A1
    公开(公告)日:2020-04-09
    Disclosed is a group of chimeric antigen receptors (CARs) consisting of two, three or four CAR molecules, wherein each member of the group of CARs is different in its amino acid sequence from one another, and wherein each of the CAR molecules of the group comprise at least a transmembrane domain and an ectodomain, wherein the ectodomain comprises one or two antigen binding moieties and/or one or two binding sites to which other polypeptides each comprising at least an antigen binding moiety are able to bind; wherein the ectodomain of each CAR molecule of the group in its prevalent conformation is free of cysteine amino acid moieties which are able to form intermolecular disulphide bonds with other CAR molecules of the group, respectively, and wherein each CAR molecule of the group comprises at least one heterodimerization domain.
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