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octa-p-amino-octa-O-propoxycalix[8]arene | 628304-56-3

中文名称
——
中文别名
——
英文名称
octa-p-amino-octa-O-propoxycalix[8]arene
英文别名
49,50,51,52,53,54,55,56-Octapropoxynonacyclo[43.3.1.13,7.19,13.115,19.121,25.127,31.133,37.139,43]hexapentaconta-1(48),3,5,7(56),9,11,13(55),15,17,19(54),21,23,25(53),27(52),28,30,33(51),34,36,39(50),40,42,45(49),46-tetracosaene-5,11,17,23,29,35,41,47-octamine
octa-p-amino-octa-O-propoxycalix[8]arene化学式
CAS
628304-56-3
化学式
C80H104N8O8
mdl
——
分子量
1305.75
InChiKey
GUXHRLRQLYKBSS-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

  • 密度:
    1.146±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    16.8
  • 重原子数:
    96
  • 可旋转键数:
    24
  • 环数:
    9.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    282
  • 氢给体数:
    8
  • 氢受体数:
    16

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Novel pH responsive calix[8]arene hydrogelators: self-organization processes at a nanometric scale
    摘要:
    研究发现,水溶性两亲钙[8]烯可在亚毫摩尔浓度下形成 pH 值响应型可逆超分子水凝胶。根据其上缘官能化的不同,pH 值的变化会在碱性或酸性条件下引发水凝胶。报告通过原子力显微镜(AFM)测量不同带电表面的自组织过程进行了研究。
    DOI:
    10.1039/c3cc40374b
  • 作为产物:
    描述:
    5,11,17,23,29,35,41,47-Octanitro-49,50,51,52,53,54,55,56-octapropoxynonacyclo[43.3.1.13,7.19,13.115,19.121,25.127,31.133,37.139,43]hexapentaconta-1(48),3,5,7(56),9,11,13(55),15,17,19(54),21,23,25(53),27(52),28,30,33(51),34,36,39(50),40,42,45(49),46-tetracosaene 在 palladium on activated charcoal 氢气 作用下, 以 甲醇乙酸乙酯 为溶剂, 20.0 ℃ 、200.0 kPa 条件下, 反应 24.0h, 以95%的产率得到octa-p-amino-octa-O-propoxycalix[8]arene
    参考文献:
    名称:
    [EN] ABIOTIC HEPARIN ANTAGONISTS
    [FR] ANTAGONISTES ABIOTIQUES DE L'HEPARINE
    摘要:
    本发明涉及一般式(I)中的肝素结合卡立酮化合物,其中R、R1、L和n的含义如描述中所示,以及它们在生物医学领域中的应用。
    公开号:
    WO2005028422A1
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文献信息

  • [EN] ABIOTIC HEPARIN ANTAGONISTS<br/>[FR] ANTAGONISTES ABIOTIQUES DE L'HEPARINE
    申请人:CONSIGLIO NAZIONALE RICERCHE
    公开号:WO2005028422A1
    公开(公告)日:2005-03-31
    The present invention relates to heparin-binding calixarene compounds of general Formula (I) in which R, R1, L and n have the meanings indicated in the description and their use in the biomedical field.
    本发明涉及一般式(I)中的肝素结合卡立酮化合物,其中R、R1、L和n的含义如描述中所示,以及它们在生物医学领域中的应用。
  • Calix[8]arene-based glycoconjugates as multivalent carbohydrate-presenting systems
    作者:Grazia M.L Consoli、Francesca Cunsolo、Corrada Geraci、Tommaso Mecca、Placido Neri
    DOI:10.1016/j.tetlet.2003.08.039
    日期:2003.9
    An efficient approach for the introduction of eight mono- or disaccharide sugar moieties (D-glucose, N-acetyl-D-glucosamine, D-galactose, L-fucose, D-maltose and D-cellobiose) at the upper rim of calix[8]arene 1, using thioureido linkers, is reported. The obtained water-soluble, nanosized glycocalix[8]arenes 5b-10b may act as biomimetic carbohydrate systems and as hosts for highly polar organic molecules. Preliminary H-1 NMR complexation experiments of octaglycosyl derivative 7b and 10b with ionic guests are also reported. (C) 2003 Elsevier Ltd. All rights reserved.
  • Abiotic heparin antagonists
    申请人:Cunsolo Francesca
    公开号:US20070082951A1
    公开(公告)日:2007-04-12
    The present invention relates to heparin-binding calixarene compounds of general Formula (I) in which R, R 1 , L and n have the meanings indicated in the description and their use in the biomedical field.
  • US7465820B2
    申请人:——
    公开号:US7465820B2
    公开(公告)日:2008-12-16
  • Designed calix[8]arene-based ligands for selective tryptase surface recognition
    作者:Tommaso Mecca、Grazia M.L. Consoli、Corrada Geraci、Francesca Cunsolo
    DOI:10.1016/j.bmc.2004.07.037
    日期:2004.10
    Basic amino acid calix[8]arene receptors for tryptase surface recognition have been synthesized. The tetrameric arrangement and the negative charge distribution close to the active sites of the enzyme, have suggested the design of complementary multifunctional receptors that might bind to the active region of the protein blocking the approach of the substrate. Kinetic inhibition analysis on recombinant lung tryptase have showed a time-dependent competitive inhibition with both initial and steady-state rate constants in the nanomolar range. (C) 2004 Elsevier Ltd. All rights reserved.
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