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kaempferol-3-O-rutinoside | 17297-56-2

中文名称
——
中文别名
——
英文名称
kaempferol-3-O-rutinoside
英文别名
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one
kaempferol-3-O-rutinoside化学式
CAS
17297-56-2
化学式
C27H30O15
mdl
——
分子量
594.526
InChiKey
RTATXGUCZHCSNG-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

  • 熔点:
    221-223℃
  • 沸点:
    941.7±65.0 °C(Predicted)
  • 密度:
    1.76
  • 溶解度:
    溶于氯仿、二氯甲烷、乙酸乙酯、DMSO、丙酮等。
  • 物理描述:
    Solid

计算性质

  • 辛醇/水分配系数(LogP):
    -0.9
  • 重原子数:
    42
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    245
  • 氢给体数:
    9
  • 氢受体数:
    15

安全信息

  • 储存条件:
    | 室温 |

SDS

SDS:31b86d85430bf1d04785496c952cfbdd
查看

制备方法与用途

Biorbin(山奈酚3-O-罗宾糖苷)是一种黄酮类化合物,在体外实验中能显著抑制人淋巴细胞的增殖。

文献信息

  • Method For Preparing Kaempferol-3-0-Rutinoside and Composition of Skin External Application Comprising Thereof
    申请人:Park Jun Seong
    公开号:US20100113372A1
    公开(公告)日:2010-05-06
    Disclosed is a method for the preparation of kaempferol-3-O-rutinoside and a composition of a skin external application comprising kaempferol-3-O-rutinoside as an active ingredient. The method for isolating kaempferol-3-O-rutinoside through hydrolysis uses an enzyme or microbe that removes the sugar selectively from kaempferol-3-O-rutinoside glycosides in a plant extract. Disclosed also is a composition of a skin external application comprising kaempferol-3-O-rutinoside that prevents skin wrinkle.
    本文披露了一种制备山奈酚-3-O-鲁丁苷和一种皮肤外用组合物的方法,该组合物包含山奈酚-3-O-鲁丁苷作为活性成分。通过解分离山奈酚-3-O-鲁丁苷的方法使用了一种酶或微生物,可以选择性地从植物提取物中去除山奈酚-3-O-鲁丁苷苷苷。本文还披露了一种包含山奈酚-3-O-鲁丁苷的皮肤外用组合物,可以预防皱纹。
  • Inhibiting corrosion in a downhole environment
    申请人:HALLIBURTON ENERGY SERVICES, INC.
    公开号:US10544356B2
    公开(公告)日:2020-01-28
    A method and system for inhibiting corrosion of a surface in a well including introducing a composition into the well, the composition comprising an acidic medium and Dihydrogen (ethyl) [4-[4-[ethyl(3-sulphonatobenzyl)amino] (4-hydroxy-2-sulphonatobenzhydrylidene]cyclohexa-2,5-dien-1-ylidene](3-sulphonatobenzyl)ammonium), contacting the metal surface with the composition, and inhibiting corrosion of the metal surface with the Dihydrogen (ethyl)[4-[4-[ethyl(3-sulphonatobenzyl)amino](4-hydroxy-2-sulphonatobenzhydrylidene]cyclohexa-2,5-dien-1-ylidene] (3-sulphonatobenzyl)ammonium).
    一种抑制井中表面腐蚀的方法和系统,包括将一种组合物引入井中,该组合物包括酸性介质和二氢(乙基)[4-[4-[乙基(3-磺酸基苄基)基](4-羟基-2-磺酸基苯甲亚基]环己-2、二氢(乙基)[4-[4-[乙基(3-磺酸基苄基)基](4-羟基-2-磺酸基苯甲亚基]环己-2,5-二烯-1-亚基](3-磺酸基苄基)],将组合物与属表面接触,并用二氢(乙基)[4-[4-[乙基(3-磺酸基苄基)基](4-羟基-2-磺酸基苯甲亚基]环己-2,5-二烯-1-亚基](3-磺酸基苄基)]抑制属表面的腐蚀。
  • Compositions for skin diseases or disorders
    申请人:Segond Caroline
    公开号:US20120009290A1
    公开(公告)日:2012-01-12
    Medicaments or cosmetic compositions for the treatment or alleviation of skin or mucous membrane diseases or disorders related to an enhanced level of anti-microbial peptides or proteins comprising Tambourissa plant extracts, which may comprise polyphenols.
  • COMPOSITIONS FOR SKIN DISEASE OR DISORDERS
    申请人:Bayer Consumer Care AG
    公开号:US20130071502A1
    公开(公告)日:2013-03-21
    Medicaments or cosmetic compositions for the treatment or alleviation of skin or mucous membrane diseases or disorders related to an enhanced level of anti-microbial peptides or proteins comprising Tambourissa plant extracts, which may comprise polyphenols.
  • INHIBITING CORROSION IN A DOWNHOLE ENVIRONMENT
    申请人:HALLIBURTON ENERGY SERVICES, INC.
    公开号:US20190218452A1
    公开(公告)日:2019-07-18
    A method and system for inhibiting corrosion of a surface in a well including introducing a composition into the well, the composition comprising an acidic medium and Dihydrogen (ethyl) [4-[4-[ethyl(3-sulphonatobenzyl)amino] (4-hydroxy-2-sulphonatobenzhydrylidene]cyclohexa-2,5-dien-1-ylidene](3-sulphonatobenzyl)ammonium), contacting the metal surface with the composition, and inhibiting corrosion of the metal surface with the Dihydrogen (ethyl)[4-[4-[ethyl(3-sulphonatobenzyl)amino](4-hyodroxy-2-sulphonatobenzhydrylidene]cyclohexa-2,5-dien-1-ylidene] (3-sulphonatobenzyl)ammonium).
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