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liriodendrin octaacetate | 66007-45-2

中文名称
——
中文别名
——
英文名称
liriodendrin octaacetate
英文别名
[(2R,3R,4S,5R,6S)-6-[4-[(3S,3aR,6S,6aR)-6-[3,5-dimethoxy-4-[(2S,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-3,4,5-triacetyloxyoxan-2-yl]methyl acetate
liriodendrin octaacetate化学式
CAS
66007-45-2
化学式
C50H62O26
mdl
——
分子量
1079.03
InChiKey
BYBBEORPMYUPIS-RFMFFHAESA-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):
    2.1
  • 重原子数:
    76
  • 可旋转键数:
    28
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    303
  • 氢给体数:
    0
  • 氢受体数:
    26

反应信息

  • 作为反应物:
    描述:
    liriodendrin octaacetatesodium methylate 作用下, 以 甲醇 为溶剂, 生成 鹅掌楸碱
    参考文献:
    名称:
    Synthesis of biologically active tetrahydro-furofuranlignan-(syringin, pinoresinol)- mono- and bis-glucosides
    摘要:
    The naturally occurring tetrahydrofurofuran-lignan-(syringaresinol, pinoresinol)-mono- and bis-glucosides were synthesized and their structures thereby confirmed.
    DOI:
    10.1016/s0031-9422(00)98258-x
  • 作为产物:
    描述:
    反式芥子醇氢氧化钾aircopper(II) sulfate 作用下, 以 丙酮 为溶剂, 反应 96.0h, 生成 liriodendrin octaacetate
    参考文献:
    名称:
    Synthesis of biologically active tetrahydro-furofuranlignan-(syringin, pinoresinol)- mono- and bis-glucosides
    摘要:
    The naturally occurring tetrahydrofurofuran-lignan-(syringaresinol, pinoresinol)-mono- and bis-glucosides were synthesized and their structures thereby confirmed.
    DOI:
    10.1016/s0031-9422(00)98258-x
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文献信息

  • New Iridoid Glucosides and a Lignan Diglucoside fromGlobularia alypumL
    作者:Ratan K. Chaudhuri、Otto Sticher
    DOI:10.1002/hlca.19810640103
    日期:1981.2.4
    The four new iridoid glucosides globularicisin (2), globularidin (5), globularimin (9), and globularinin (13), the lignan diglucoside liriodendrin (18), and syringin (20) have been isolated from Globularia alypum L. along with the previously reported glucosides globularin (1) and catalpol (4). Compound 2 is the first report of any cinnamoyl iridoid with a cis-configuration at the acyl double bond.
    从球藻中分离出了四个新的虹彩糖苷球蛋白(2),球蛋白(5),球蛋白(9)和球蛋白(13),木脂素二糖苷鸟苷(18)和丁香素(20)。先前报道的糖苷球蛋白(1)和catalpol (4)。化合物2是在酰基双键上具有顺式构型的任何肉桂酰基烯酮类化合物的首次报道。化合物5是另一种新的虹彩化合物,其在糖苷配基部分中缺乏特征性的C(3),C(4)双键。化合物9和13是非对映异构体,并含有高度氧化的糖苷结构。liriodendrin的隔离,从Globularia alypum是在家庭中的木素的产生的第一个示范Globulariaceae。
  • Studies on the constituents of Cistanchis Herba. V. Isolation and structures of two new phenylpropanoid glycosides, cistanosides E and F.
    作者:HIROMI KOBAYASHI、HIROKO KARASAWA、TOSHIO MIYASE、SEIGO FUKUSHIMA
    DOI:10.1248/cpb.33.1452
    日期:——
    Two new phenylpropanoid glycosides, named cistanosides E (III) and F (IV), were isolated from Cistanchis Herba, the whole plant of Cistanche salsa (C. A. MEY.) G. BECK (Orobanchaceae), together with two known lignan glycosides, liriodendrin (I) and (+)-syringaresinol O-β-D-glucopyranoside (II). The structures of III and IV were determined to be 2-(4-hydroxy-3-methoxyphenyl) ethyl O-α-L-rhamnopyranosyl-(1→3)-O-β-D-glucopyranoside and α-L-rhamnopyranosyl (1→3)-O-(4-O-caffeoyl)-D-glucopyranose, respectively, on the basis of chemical and spectral data.
    从列当科肉苁蓉 (C. A. MEY.) G. BECK (C. A. MEY.) G. BECK (C. A. MEY.) G. BECK (C. A. MEY.) G. BECK (C. A. MEY.) G. BECK (C. A. MEY.) G. BECK (C. A. MEY.) G. BECK (C. A. MEY.) G. BECK (C. A. MEY.) G. BECK (列当科) 的全草中分离得到两种新的苯丙素苷,命名为肉苁蓉苷 E (III) 和 F (IV)。 I) 和 (+)-丁香树脂醇 O-β-D-吡喃葡萄糖苷 (II)。 III和IV的结构确定为2-(4-羟基-3-甲氧基苯基)乙基O-α-L-鼠李糖基-(1→3)-O-β-D-吡喃葡萄糖苷和α-L-鼠李糖基( 1→3)-O-(4-O-咖啡酰基)-D-吡喃葡萄糖,分别基于化学和光谱数据。
  • Liriodendrin, a New Lignan Diglucoside from the Inner Bark of Yellow Poplar (Liriodendron tulipifera L.)
    作者:EDGAR E. DICKEY
    DOI:10.1021/jo01096a007
    日期:1958.2
  • Deyama, Takeshi, Chemical and pharmaceutical bulletin, 1983, vol. 31, # 9, p. 2993 - 2997
    作者:Deyama, Takeshi
    DOI:——
    日期:——
  • Cytotoxic agent from Penstemon deustus (Scrophulariaceae): isolation and stereochemistry of liriodendrin, a symmetrically substituted furofuranoid lignan diglucoside
    作者:Shivanand D. Jolad、Joseph J. Hoffmann、Jack R. Cole、Michael S. Tempesta、Robert B. Bates
    DOI:10.1021/jo01295a038
    日期:1980.3
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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