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leucosceptoside A | 83529-62-8

中文名称
——
中文别名
——
英文名称
leucosceptoside A
英文别名
leucoseptoside A;[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate
leucosceptoside A化学式
CAS
83529-62-8
化学式
C30H38O15
mdl
——
分子量
638.623
InChiKey
ZMYQRHSOVRDQDL-CPPDSBOHSA-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):
    -0.2
  • 重原子数:
    45
  • 可旋转键数:
    12
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    234
  • 氢给体数:
    8
  • 氢受体数:
    15

安全信息

  • 储存条件:
    室温

SDS

SDS:300a8240333e1a8ec9c70eec471092c5
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制备方法与用途

亮肽苷A是一种具有降血糖和降压作用的苯乙醇糖苷,它还能抑制α-葡萄糖苷酶和PKCα(IC50值为19.0 μM)。

上下游信息

  • 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:
    乙酸酐leucosceptoside A吡啶 作用下, 以76 mg的产率得到(E)-3-(4-Acetoxy-3-methoxy-phenyl)-acrylic acid (2R,3R,4S,5R,6R)-5-acetoxy-2-acetoxymethyl-6-[2-(3,4-diacetoxy-phenyl)-ethoxy]-4-((2S,3R,4R,5S,6S)-3,4,5-triacetoxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl ester
    参考文献:
    名称:
    Studies on the acyl glycosides from Leucoseptrum japonicum (Miq.) Kitamura et Murata.
    摘要:
    从日本白头翁(Leucosceptrum japonicum (MIQ.) KITAMURA et MURATA)中分离出两种新的酰基糖苷,分别为白头翁苷A(IV)和白头翁苷B(V),同时还分离出了马尔丁苷(III)、阿克托苷(I)和阿克托苷异构体(II)。根据化学及光谱数据,IV和V的结构分别被确定为2-(3, 4-二羟基苯基乙基) 1-O-α-L-鼠李糖吡喃糖基-(1→3)-β-D-(4-O-咖啡酸)-葡萄糖吡喃糖苷和2-(3-羟基-4-甲氧基苯基乙基) 1-O-α-L-鼠李糖吡喃糖基-(1→3)-O-[β-D-阿糖苷[1→6]]-β-D-葡萄糖吡喃糖苷。
    DOI:
    10.1248/cpb.30.2732
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文献信息

  • Synergic combination of phenylpropanoids, such as verbascoside or teupolioside, and mesalamine
    申请人:I.R.B. Istituto Di Ricerche Biotecnologiche S.r.l.
    公开号:EP2340808A1
    公开(公告)日:2011-07-06
    The present invention relates to the synergic combination of mesalamine with phenylpropanoids (verbascoside or teupolioside), obtained from plant cell cultures, and the pharmacological and nutritional use thereof for the prevention and treatment of inflammatory disorders of the digestive apparatus. In particular, the present invention relates to a pharmaceutical composition containing mesalamine and one or more phenylpropanoids, together with pharmaceutically acceptable excipients.
    本发明涉及美沙拉敏与从植物细胞培养物中获得的苯丙类化合物(马鞭草甙或茶藨子甙)的协同组合,以及将其用于预防和治疗消化器官炎症性疾病的药理学和营养学用途。 特别是,本发明涉及一种药物组合物,其中含有美沙拉明和一种或多种苯丙酸类物质,以及药学上可接受的赋形剂。
  • Topical macqui berry formula
    申请人:Tracie Martyn International, Inc.
    公开号:US10993897B2
    公开(公告)日:2021-05-04
    The present invention provides a topical formulation and method of use where the formulation comprises macqui berry or a macqui berry extract containing anthocyanins having a very high oxygen radical absorbance capacity (ORAC). The formulation provides the macqui berry in a stabilized form which includes a glucuronide or glycuronide, a photostabilizing agent, encapsulation, or light—and/or air-blocking packaging.
    本发明提供了一种外用制剂和使用方法,其中的制剂包含具有极高氧自由基吸收能力(ORAC)的马奎莓或含有花青素的马奎莓提取物。本发明的制剂提供了稳定形式的马奎莓,其中包括葡萄糖醛酸或糖醛酸、光稳定剂、封装或阻光和/或阻气包装。
  • Topical formulations and methods of use
    申请人:Morariu Marius
    公开号:US20060216251A1
    公开(公告)日:2006-09-28
    A topical composition comprising a lipoic acid, a carnitine, and a carnosine in a suitable vehicle for topical application and a method for treating skin is provided. The present compositions are useful in improving the appearance of aged skin characterized by wrinkles and loss of elasticity. Preferred components include R-lipoic acid or R-dihydrolipoic acid, acetyl-1-carnitine, and 1-carnosine.
    本发明提供了一种外用组合物,该组合物包含硫辛酸、肉毒碱和肉毒碱,并以适合外用的载体形式存在,还提供了一种治疗皮肤的方法。本组合物有助于改善以皱纹和失去弹性为特征的老化皮肤的外观。优选成分包括 R-硫辛酸或 R-二氢硫辛酸、乙酰基-1-肉碱和 1-肉碱。
  • Identification and occurrence of phenylethanoid and iridoid glycosides in six Polish broomrapes (Orobanche spp. and Phelipanche spp., Orobanchaceae)
    作者:Dariusz Jedrejek、Sylwia Pawelec、Renata Piwowarczyk、Łukasz Pecio、Anna Stochmal
    DOI:10.1016/j.phytochem.2019.112189
    日期:2020.2
    There are about 200 holoparasitic broomrapes (Orobanchaceae) known worldwide, however, only several species have been so far investigated phytochemically. Among Orobanche s.l. are both rare and endangered species, as well as onerous crop pests. This study aims to give a phytochemical description, both qualitative and quantitative, of six broomrape species (Orobanche and Phelipanche taxa) growing in Poland, including species that have not been tested in detail (O. caryophyllacea, O. linen, O. picridis, and P. arenaria). Sixteen metabolites, including 14 phenylethanoid glycosides (PhGs) and 2 iridoid glycosides (IrGs), were isolated and identified using NMR spectroscopy and hydrolysis, revealing the presence of two previously undescribed PhGs in P. ramosa, named ramoside A and 2'-acetylramoside A. In addition, in the example of O. caryophyllacea, we have reported as the first occurrence of IrGs in broomrapes. Concentrations of phenylethanoids, the main constituents of broomrapes, in the studied plant material (flowering shoots with haustoria) were determined using the UHPLC-PDA method. It was found that P. ramosa has been the richest source of PhGs. In addition, the differences between broomrapes have been visualized using principal component and cluster analysis. The results of the antiradical DPPH test of 13 PhGs confirmed previous findings on the relation of the antioxidant potential with the structure of phenolic moieties - phenolic acid and phenylethanoid unit.
  • Topical compositions comprising benfotiamine and pyridoxamine
    申请人:Morariu Marius
    公开号:US20060045896A1
    公开(公告)日:2006-03-02
    The present invention provides a composition comprising an effective amount of benfotiamine and an effective amount of pyridoxamine in a suitable vehicle for topical application. The present compositions are useful in improving the appearance of aged skin characterized by wrinkles, loss of elasticity, and hyperpigmentation caused by chronoaging and/or photoaging of skin, by inhibiting particularly skin damage resulting from reactive carbonyl species (RCS), glycation of skin proteins, formation of advanced glycation endproducts (AGEs) and formation of advanced lipoxidation endproducts (ALEs).
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