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acremomannolipin A | 1403981-83-8

中文名称
——
中文别名
——
英文名称
acremomannolipin A
英文别名
Acremomannolipin A;[(2R,3S,4S,5R,6R)-4,5-di(hexanoyloxy)-6-(hexanoyloxymethyl)-2-[(2R,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexoxy]oxan-3-yl] octanoate
acremomannolipin A化学式
CAS
1403981-83-8
化学式
C38H68O15
mdl
——
分子量
764.949
InChiKey
KXOHHVVQXCNKBM-QDOWTLGRSA-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

  • 沸点:
    818.4±65.0 °C(Predicted)
  • 密度:
    1.18±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.3
  • 重原子数:
    53
  • 可旋转键数:
    34
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    225
  • 氢给体数:
    5
  • 氢受体数:
    15

上下游信息

  • 上游原料
    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:
    acremomannolipin Asodium methylate 作用下, 以 甲醇 为溶剂, 反应 6.0h, 生成 辛酸己酸O1-β-D-mannopyranosyl-D-mannitol
    参考文献:
    名称:
    Acremomannolipin A, the potential calcium signal modulator with a characteristic glycolipid structure from the filamentous fungus Acremonium strictum
    摘要:
    By the newly developed assay method, the glycolipid Acremomannolipin A (1) was isolated from a filamentous fungus Acremonium strictum as a potential calcium signal modulator. The structure of 1 elucidated on the basis of intensive spectroscopic analyses as well as its degradation studies is quite unique: the D-mannopyranose is connected to D-mannitol through a beta-glycoside linkage; all the hydroxyls in the mannose are highly masked as peresters with aliphatic acids, and this moiety is made hydrophobic, whereas the mannitol part exhibits a highly hydrophilic property. The compound (1) showed the characteristic bioactivity property, enabling calcineurin deletion cells to grow in the presence of Cl-, which would be caused by calcium signal modulating. The activity was so potent as to exert the effect at a concentration of 200 nM. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.08.085
  • 作为产物:
    描述:
    phenyl 2-O-p-methoxybenzyl-3-O-benzyl-4,6-O-benzylidene-1-deoxy-1-thio-α-D-mannopyranoside 在 吡啶4-二甲氨基吡啶2,6-二叔丁基-4-甲基吡啶三氟甲磺酸酐 、 palladium 10% on activated carbon 、 氢气间氯过氧苯甲酸三氟乙酸2,3-二氯-5,6-二氰基-1,4-苯醌 作用下, 以 二氯甲烷乙酸乙酯 为溶剂, 反应 23.67h, 生成 acremomannolipin A
    参考文献:
    名称:
    立体选择性全合成acremomannolipin A及其异构体,具有新型糖脂结构的强效钙信号调节剂:在端粒异构中心对活性的立体化学作用
    摘要:
    甲充分考虑的新的糖脂的立体选择性全合成的,acremomannolipin A(1),从分离出的有效的钙信号调制器顶孢strictum,通过采用的4,6-立体选择性β甘露糖基ø -亚苄基保护的甘露糖基砜与d -以甘露醇为关键反应进行了描述。的α端基异构体(EPI - 1)的1,还选择合成。钙调节活性在异头中心在所述构型的反转降低,表明甘露糖部分的β构型是优选的活性。
    DOI:
    10.1016/j.tet.2013.09.086
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文献信息

  • Glycosyl-Acceptor-Derived Borinic Ester-Promoted Direct and β-Stereoselective Mannosylation with a 1,2-Anhydromannose Donor
    作者:Masamichi Tanaka、Junki Nashida、Daisuke Takahashi、Kazunobu Toshima
    DOI:10.1021/acs.orglett.6b00926
    日期:2016.5.6
    in the presence of a glycosyl-acceptor-derived borinic ester. Reactions proceeded smoothly under mild conditions to provide the corresponding β-mannosides with high stereoselectivity in moderate to high yields. In addition, the present glycosylation method was applied successfully to the total synthesis of acremomannolipin A.
    在糖基受体衍生的硼酸酯存在下,使用1,2-脱水甘露糖供体和单醇受体进行β-立体选择性甘露糖基化。反应在温和条件下平稳进行,以中等至高产率提供具有高立体选择性的相应β-甘露糖苷。此外,本糖基化方法已成功地应用于阿莫莫尼脂A的全合成。
  • Construction of β-Mannosidic Bonds via Gold(I)-Catalyzed Glycosylations with Mannopyranosyl<i>ortho</i>-Hexynylbenzoates and Its Application in Synthesis of Acremomannolipin A
    作者:Peng Sun、Peng Wang、Yongzhen Zhang、Xiuli Zhang、Cong Wang、Shaojing Liu、Jinjie Lu、Ming Li
    DOI:10.1021/acs.joc.5b00140
    日期:2015.4.17
    A mild and convenient protocol for direct synthesis of beta-mannosides has been developed. Glycosylation of 4,6-O-benzylidene-protected mannosyl ortho-hexynylbenzoates with various alcohol acceptors catalyzed by gold(I) complex proceeded smoothly at 0 degrees C to room temperature and afforded the corresponding beta-mannoside in high yield and satisfactory stereoselectivity. This reaction was applied to the total synthesis of acremomannolipin A and its analogue.
  • ANTI-TUMOR AGENT
    申请人:Kinki University
    公开号:EP2716293B1
    公开(公告)日:2017-09-06
  • The first total synthesis of acremomannolipin A, the potential Ca2+ signal modulator with a characteristic glycolipid structure, isolated from the filamentous fungus Acremonium strictum
    作者:Nozomi Tsutsui、Genzoh Tanabe、Ayako Kita、Reiko Sugiura、Osamu Muraoka
    DOI:10.1016/j.tetlet.2012.10.128
    日期:2013.2
    The first total synthesis of acremomannolipin A, the potential Ca2+ signal modulator isolated from Acremonium strictum, was achieved by employing the characteristic stereoselective beta-mannosylation of 4,6-O-benzylidene-protected mannosyl sulfoxide with a D-mannitol derivative in the presence of trifluoromethanesulfonic anhydride as the key reaction. (C) 2012 Elsevier Ltd. All rights reserved.
  • Acremomannolipin A, the potential calcium signal modulator with a characteristic glycolipid structure from the filamentous fungus Acremonium strictum
    作者:Reiko Sugiura、Ayako Kita、Nozomi Tsutsui、Osamu Muraoka、Kanako Hagihara、Nanae Umeda、Tatsuki Kunoh、Hirofumi Takada、Dai Hirose
    DOI:10.1016/j.bmcl.2012.08.085
    日期:2012.11
    By the newly developed assay method, the glycolipid Acremomannolipin A (1) was isolated from a filamentous fungus Acremonium strictum as a potential calcium signal modulator. The structure of 1 elucidated on the basis of intensive spectroscopic analyses as well as its degradation studies is quite unique: the D-mannopyranose is connected to D-mannitol through a beta-glycoside linkage; all the hydroxyls in the mannose are highly masked as peresters with aliphatic acids, and this moiety is made hydrophobic, whereas the mannitol part exhibits a highly hydrophilic property. The compound (1) showed the characteristic bioactivity property, enabling calcineurin deletion cells to grow in the presence of Cl-, which would be caused by calcium signal modulating. The activity was so potent as to exert the effect at a concentration of 200 nM. (C) 2012 Elsevier Ltd. All rights reserved.
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