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9-(2H-1,3-Benzodioxol-5-yl)-6,7-dimethoxy-1-oxo-1,3-dihydronaphtho[2,3-c]furan-4-yl hexopyranoside

中文名称
——
中文别名
——
英文名称
9-(2H-1,3-Benzodioxol-5-yl)-6,7-dimethoxy-1-oxo-1,3-dihydronaphtho[2,3-c]furan-4-yl hexopyranoside
英文别名
9-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3H-benzo[f][2]benzofuran-1-one
9-(2H-1,3-Benzodioxol-5-yl)-6,7-dimethoxy-1-oxo-1,3-dihydronaphtho[2,3-c]furan-4-yl hexopyranoside化学式
CAS
——
化学式
C27H26O12
mdl
——
分子量
542.5
InChiKey
BJGIWVGXMRUMNA-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

计算性质

  • 辛醇/水分配系数(LogP):
    1.8
  • 重原子数:
    39
  • 可旋转键数:
    6
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.37
  • 拓扑面积:
    163
  • 氢给体数:
    4
  • 氢受体数:
    12

文献信息

  • [EN] ANTITUMOR ARYLNAPHTHALENE LIGAND GLYCOSIDES<br/>[FR] GLYCOSIDES DE LIGANDS ARYLNAPHTALÈNES ANTITUMORAUX
    申请人:OHIO STATE INNOVATION FOUNDATION
    公开号:WO2017147624A1
    公开(公告)日:2017-08-31
    Described are arylnaphthalene lactone derivatives. Also disclosed herein are methods of use of the arylnaphthalene lactone derivatives as anticancer agents.
    描述了芳基萘内酯衍生物。本文还披露了将芳基萘内酯衍生物用作抗癌剂的方法。
  • Antitumor arylnaphthalene ligand glycosides
    申请人:OHIO STATE INNOVATION FOUNDATION
    公开号:US10682367B2
    公开(公告)日:2020-06-16
    Described are arylnaphthalene lactone derivatives. Also disclosed herein are methods of use of the arylnaphthalene lactone derivatives as anticancer agents.
    本文描述的是芳基萘内酯衍生物。 本文还公开了使用芳基萘内酯衍生物作为抗癌剂的方法。
  • ARYLNAPHTHALENE LACTONE DERIVATIVES AND METHODS OF MAKING AND USING THEREOF
    申请人:OHIO STATE INNOVATION FOUNDATION
    公开号:US20170119806A1
    公开(公告)日:2017-05-04
    A series of natural products including phyllanthusum, an arylnaphthalene lignan derivative, with anticancer and antitumor and immunostimulating activity are disclosed. The invention further encompasses methods of adding water solubilizing groups to the arylrings that include phosphonyl groups.
  • ANTITUMOR ARYLNAPHTHALENE LIGAND GLYCOSIDES
    申请人:OHIO STATE INNOVATION FOUNDATION
    公开号:US20190054105A1
    公开(公告)日:2019-02-21
    Described are arylnaphthalene lactone derivatives. Also disclosed herein are methods of use of the arylnaphthalene lactone derivatives as anticancer agents.
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同类化合物

鹅掌楸碱 罗汉松树脂酚-4'-O-β-龙胆二糖苷 络石苷元-4'-O-BETA-龙胆二糖苷 络石苷 牛蒡苷 柑属苷B 松脂醇二葡萄糖苷 松脂醇-4-O-beta-D-吡喃葡萄糖苷 松脂醇 beta-D-吡喃葡萄糖苷 木須皮苷 异落叶松脂素-9'-O-beta-D-吡喃葡萄糖苷 开环异落叶松脂素BETA-D-葡糖苷 地菲林葡萄糖苷 南烛木糖甙 刺五加苷D 刺五加甙E 刺五加甙 E 刺五加提取物 丁香树脂醇双葡萄糖苷 b-D-吡喃葡萄糖苷,4-[(1R,2R)-1,3-二羟基-2-[4-[(1E)-3-羟基-1-丙烯-1-基]-2-甲氧基苯氧基]丙基]-2-甲氧苯基 Ssioriside; (2S,3S)-4-羟基-2,3-双[(4-羟基-3,5-二甲氧基苯基)甲基]丁基 beta-D-吡喃木糖苷 8-羟基松脂醇二葡萄糖苷 8-O-(α-阿拉伯呋喃糖)-β-àpeltatin 4-(1,3-苯并二氧戊环-5-基)-9-[(2S,3R,4S,5R)-3,4-二甲氧基-5-[(2S,3R,4S,5S,6R)-3,4,5-三羟基-6-(羟基甲基)四氢吡喃-2-基]氧基四氢吡喃-2-基]氧基-6,7-二甲氧基-1H-苯并[f][2]苯并呋喃-3-酮 4-(1,3-苯并二氧戊环-5-基)-6,7-二甲氧基-9-[(2S,3R,4S,5S,6R)-3,4,5-三羟基-6-(羟基甲基)四氢吡喃-2-基]氧基-1H-苯并[f][2]苯并呋喃-3-酮 3-[2,3-二氢-6-羟基-2-(1-羟基-1-甲基乙基)苯并呋喃-5-基]-8-(beta-D-吡喃葡萄糖基)-2,3-二氢-5,7-二羟基-4H-1-苯并吡喃-4-酮 2,3-双(3-甲氧基-4-羟基苄基)丁烷-1,4-二醇 1,4-二葡萄糖甙 (3S,4R)-4-(苯并[1,3]二氧杂环戊烯-5-基甲基)-3-[(S)-[(2R,3R,4S,5R,6R)-3,4,5-三羟基-6-(羟基甲基)四氢吡喃-2-基]氧基-(3,4,5-三甲氧基苯基)甲基]四氢呋喃-2-酮 (3R,4S)-3-[[4-(beta-D-吡喃葡萄糖基氧基)-3-甲氧基苯基]甲基]-4,5-二氢-4-[(4-羟基-3-甲氧基苯基)甲基]呋喃-2(3H)-酮 (-)-异落叶松脂素-9'-O-BETA-D-吡喃葡萄糖苷 (+)-南烛木树脂酚9'-O-葡萄糖甙 4-O-[2"-O-[6-[4-hydroxypiperidin-1-yl]hexyl]-3",4"-di-O-methyl-β-D-xylopyranosyl]diphyllin 4-O-[2"-O-[8-[4-hydroxypiperidin-1-yl]octyl]-3",4"-di-O-methyl-β-D-xylopyranosyl]diphyllin phyllanthusmin B (2S,3R,4S,5S)-2-((9-(benzo[d][1,3]dioxol-5-yl)-6,7-dimethoxy-1,3-dihydronaphtho[2,3-c]furan-4-yl)oxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate (2S,3R,4S,5S)-2-((9-(benzo[d][1,3]dioxol-5-yl)-6,7-dimethoxy-3-oxo-1,3-dihydronaphtho[2,3-c]furan-4-yl)oxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate tri-O-acetylpatentiflorin A phyllanthusmin D 2")-β-D-xylopyranosyl-(1""->5")-β-D-apiofuranosyl]diphyllin">4-O-[α-L-arabinopyranosyl-(1"'->2")-β-D-xylopyranosyl-(1""->5")-β-D-apiofuranosyl]diphyllin (+)-syringaresinol 4-O-β-D-glucopyranosyl(1->6)-β-D-glucopyranoside liriodendrin 4-O-[6-O-(5-O-sinapoyl-β-D-apiofuranosyl)-β-D-glucopyranosyl]-(+)-(7S,7'S,8R,8'R)-4'-hydroxy-3,3',5,5'-tetramethoxy-7,9':7',9-diepoxylignane 4-O-[3″,4″-di-O-methyl-β-d-xylopyranosyl]diphyllin (+)-medioresinol di-O-β-D-glucopyranoside (-)-(8S,8'R)-4,4'-dihydroxy-3,3',5'-trimethoxylignan-4'-O-β-D-glucopyranoside (-)-nectandrin B-β-D-glucopyranoside (3S)-4''-O-β-D-Glucopyranosylhinokiresinol 4'-O-β-D-glucopyranosylhinokiresinol (7R,8R)-4,7,9,3′,9′-pentahydroxy-3-methoxy-8,4′-oxyneolignan-3′-O-β-D-glucopyranoside (7S,7'R,8R,8'S)-7'-butoxy-7,9'-epoxy-4,4',9-trihydroxy-3,3'-dimethoxylignane 9-O-β-D-glucopyranoside