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地菲林葡萄糖苷 | 25047-48-7

中文名称
地菲林葡萄糖苷
中文别名
——
英文名称
9-(benzo[d][1,3]dioxol-5-yl)-6,7-dimethoxy-4-(tetrahydro-3-hydroxy-4,5-dimethoxy-2H-pyran-2-yloxy)naphtho[2,3-c]furan-1(3H)-one
英文别名
Cleistanthin;9-(1,3-benzodioxol-5-yl)-4-(3-hydroxy-4,5-dimethoxyoxan-2-yl)oxy-6,7-dimethoxy-3H-benzo[f][2]benzofuran-1-one
地菲林葡萄糖苷化学式
CAS
25047-48-7
化学式
C28H28O11
mdl
——
分子量
540.524
InChiKey
FCOQWUOWHWHTJP-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:
    135.5°C
  • 沸点:
    535.98°C (rough estimate)
  • 密度:
    1.2852 (rough estimate)

计算性质

  • 辛醇/水分配系数(LogP):
    3
  • 重原子数:
    39
  • 可旋转键数:
    7
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    120
  • 氢给体数:
    1
  • 氢受体数:
    11

文献信息

  • Agents for Eliminating Tumour-Initiating Cells
    申请人:GODAVARI BIOREFINERIES LIMITED
    公开号:US20150328245A1
    公开(公告)日:2015-11-19
    The present invention provides agents useful for eliminating tumour initiating cells, compositions thereof, uses thereof and methods of using the same.
  • 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.
  • [EN] AGENTS FOR ELIMINATING TUMOUR-INITIATING CELLS<br/>[FR] AGENTS POUR ÉLIMINER DES CELLULES D'INITIATION TUMORALE
    申请人:GODAVARI BIOREFINERIES LTD
    公开号:WO2014097318A2
    公开(公告)日:2014-06-26
    The present invention provides agents useful for eliminating tumour initiating cells, compositions thereof, uses thereof and methods of using the same.
  • [EN] USE OF COMPOUNDS FOR TREATING VIRAL INFECTIONS<br/>[FR] UTILISATION DE COMPOSÉS POUR LE TRAITEMENT D'INFECTIONS VIRALES
    申请人:GODAVARI BIOREFINERIES LTD
    公开号:WO2021229602A1
    公开(公告)日:2021-11-18
    The invention relates to use of a compound of Formula I for inhibition of V-ATPase activity in a cell and a method of treating viral infections using the compounds of Formula I.
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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 牛蒡子苷元-4'-O-Β-龙胆二糖苷 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'-BETA-D-吡喃木糖苷 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 去甲络石苷 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-[(5S,5aR,8aS)-10-羟基-6-羰基-5,5a,6,8,8a,9-六氢呋喃并[3',4':6,7]萘并[2,3-d][1,3]二噁唑-5-基]-2,6-二甲氧苯基α-L-呋喃阿拉伯糖苷 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 (3-苯甲酰氧基-2-羟基-4,5-二苯基-四氢-[2]呋喃基)-苯基酮 (2S)-5,7-二羟基-2-[4-[2,4,6-三羟基-3-[(E)-3-(4-羟基苯基)丙-2-烯酰基]-5-[(2S,3R,4R,5S,6R)-3,4,5-三羟基-6-(羟基甲基)四氢吡喃-2-基]苯氧基]苯基]色满-4-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-[6-O-(5-O-syringoyl-β-D-apiofuranosyl)-β-D-glucopyranosyl]-(+)-(7S,7'R,8R,8'R)-4'-hydroxy-3,3',5,5'-tetramethoxy-7,9':7',9-diepoxylignane (+)-1-hydroxypinoresinol 4'-O-β-glucopyranoside hexaacetate (+)-1-hydroxypinoresinol 4''-O-β-glucopyranoside 2''',3''',4''',4',6'''-O-pentaacetate (+)-1-hydroxypinoresinol 4''-O-β-glucopyranoside hexaacetate Acetic acid (3R,4S,5R)-2-(9-benzo[1,3]dioxol-5-yl-8-oxo-6,8-dihydro-furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-5-yloxy)-4,5-dimethoxy-tetrahydro-pyran-3-yl ester (+)-1-hydroxypinoresinol 4'-O-β-glucopyranoside 2''',3''',4''',4'',6'''-O-pentaacetate 4'-acetoxy-6-C-(2,3,4-tri-O-acetyl-α-D-arabinopyranosyl)-8-C-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-5,7-dihydroxyflavan (2S,3R,4S,5S,6R)-2-[4-[(2R,3R)-4-hydroxy-3-[(4-hydroxy-3-methoxyphenyl)methyl]-2-(hydroxymethyl)butyl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol Acetic acid (2S,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-[(5S,5aR,8aR)-9-(4-hydroxy-3,5-dimethoxy-phenyl)-8-oxo-5,5a,6,8,8a,9-hexahydro-furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-5-ylsulfanyl]-tetrahydro-pyran-3-yl ester 2,2-difluoro-N-((5S,5aS,8aR,9R)-8-oxo-9-(3,4,5-trimethoxyphenyl)-5,5a,6,8,8a,9-hexahydrofuro[3',4':6,7]naphtho[2,3-d][1,3]dioxol-5-yl)-2-((2R,3R,4S,5S,6R)-2,3,4,5-tetrahydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)acetamide 2,2-difluoro-N-((5S,5aS,8aR,9R)-9-(4-hydroxy-3,5-dimethoxyphenyl)-8-oxo-5,5a,6,8,8a,9-hexahydrofuro[3',4':6,7]naphtho[2,3-d][1,3]dioxol-5-yl)-2-((2R,3R,4S,5R,6R)-2,3,4,5-tetrahydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)acetamide 2,2-difluoro-N-((5S,5aS,8aR,9R)-8-oxo-9-(3,4,5-trimethoxyphenyl)-5,5a,6,8,8a,9-hexahydrofuro[3',4':6,7]naphtho[2,3-d][1,3]dioxol-5-yl)-2-((2R,3R,4S,5R,6R)-2,3,4,5-tetrahydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)acetamide