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(R)-2,3-bis(dodecyloxy)propyl trifluoromethane sulfonate | 1239978-03-0

中文名称
——
中文别名
——
英文名称
(R)-2,3-bis(dodecyloxy)propyl trifluoromethane sulfonate
英文别名
(R)-2,3-bis(dodecyloxy)propyl trifluoromethanesulfonate;[(2R)-2,3-didodecoxypropyl] trifluoromethanesulfonate
(R)-2,3-bis(dodecyloxy)propyl trifluoromethane sulfonate化学式
CAS
1239978-03-0
化学式
C28H55F3O5S
mdl
——
分子量
560.803
InChiKey
FOIMMKNACMNYAK-HHHXNRCGSA-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):
    11.8
  • 重原子数:
    37
  • 可旋转键数:
    28
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    70.2
  • 氢给体数:
    0
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    (R)-2,3-bis(dodecyloxy)propyl trifluoromethane sulfonate哌啶potassium carbonate 、 O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate 、 N,N-二异丙基乙胺三氟乙酸 作用下, 以 乙醇二氯甲烷乙腈 为溶剂, 反应 3.0h, 生成 diethyl (14R,18R)-14-amino-18-(dodecyloxy)-13-oxo-3,6,9,20-tetraoxa-16-thia-12-azadotriacontylphosphonate
    参考文献:
    名称:
    [EN] COMPOUNDS (CYSTEIN BASED LIPOPEPTIDES) AND COMPOSITIONS AS TLR2 AGONISTS USED FOR TREATING INFECTIONS, INFLAMMATIONS, RESPIRATORY DISEASES ETC.
    [FR] COMPOSÉS (LIPOPEPTIDES À BASE DE CYSTÉINE) ET COMPOSITIONS EN TANT QU'AGONISTES DES TLR2 UTILISÉS POUR TRAITER DES INFECTIONS, INFLAMMATIONS, MALADIES RESPIRATOIRES ENTRE AUTRES
    摘要:
    这项发明提供了一类新型化合物,即一般类似Pam3CSK4的脂肽类化合物,包括含有这类化合物的免疫原组合物和药物组合物,以及使用这类化合物治疗或预防与Toll样受体2相关的疾病或紊乱的方法。在一个方面,这些化合物可用作增强疫苗效果的佐剂。
    公开号:
    WO2011119759A1
  • 作为产物:
    描述:
    (R)-((2,3-bis(dodecyloxy)propoxy)methyl)benzene 在 palladium(II) hydroxide 吡啶氢气 作用下, 以 乙醇二氯甲烷 为溶剂, 反应 0.33h, 生成 (R)-2,3-bis(dodecyloxy)propyl trifluoromethane sulfonate
    参考文献:
    名称:
    [EN] COMPOUNDS (CYSTEIN BASED LIPOPEPTIDES) AND COMPOSITIONS AS TLR2 AGONISTS USED FOR TREATING INFECTIONS, INFLAMMATIONS, RESPIRATORY DISEASES ETC.
    [FR] COMPOSÉS (LIPOPEPTIDES À BASE DE CYSTÉINE) ET COMPOSITIONS EN TANT QU'AGONISTES DES TLR2 UTILISÉS POUR TRAITER DES INFECTIONS, INFLAMMATIONS, MALADIES RESPIRATOIRES ENTRE AUTRES
    摘要:
    这项发明提供了一类新型化合物,即一般类似Pam3CSK4的脂肽类化合物,包括含有这类化合物的免疫原组合物和药物组合物,以及使用这类化合物治疗或预防与Toll样受体2相关的疾病或紊乱的方法。在一个方面,这些化合物可用作增强疫苗效果的佐剂。
    公开号:
    WO2011119759A1
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文献信息

  • COMPOUNDS (CYSTEIN BASED LIPOPEPTIDES) AND COMPOSITIONS AS TLR2 AGONISTS USED FOR TREATING INFECTIONS, INFLAMMATIONS, RESPIRATORY DISEASES ETC.
    申请人:Wu Tom Yao-Hsiang
    公开号:US20130065861A1
    公开(公告)日:2013-03-14
    The invention provides a novel class of compounds viz. generally lipopeptides like Pam3CSK4, immunogenic compositions and pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with Toll-Like Receptors 2. In one aspect, the compounds are useful as adjuvants for enhancing the effectiveness a vaccine.
    该发明提供了一类新型化合物,即通常为脂肽类似物Pam3CSK4的脂肽类化合物,以及包含这些化合物的免疫原组合物和药物组合物,以及使用这些化合物治疗或预防与Toll样受体2相关的疾病或紊乱的方法。在一个方面,这些化合物可用作增强疫苗有效性的佐剂。
  • Compounds (cystein based lipopeptides) and compositions as TLR2 agonists used for treating infections, inflammations, respiratory diseases etc
    申请人:Wu Tom Yao-Hsiang
    公开号:US08808703B2
    公开(公告)日:2014-08-19
    The invention provides a novel class of compounds viz. generally lipopeptides like Pam3CSK4, immunogenic compositions and pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with Toll-Like Receptors 2. In one aspect, the compounds are useful as adjuvants for enhancing the effectiveness a vaccine.
    本发明提供了一类新型化合物,即通常类似于Pam3CSK4的脂肽类化合物,以及包括这些化合物的免疫原组合物和药物组合物,以及使用这些化合物治疗或预防与Toll-Like受体2相关的疾病或障碍的方法。在一个方面,这些化合物可用作佐剂,以增强疫苗的有效性。
  • COMPOUNDS AND COMPOSITIONS AS TLR2 AGONISTS
    申请人:WU Tom Yao-Hsiang
    公开号:US20140323390A1
    公开(公告)日:2014-10-30
    The invention provides a novel class of compounds, immunogenic compositions and pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with Toll-Like Receptors 2. In one aspect, the compounds are useful as adjuvants for enhancing the effectiveness of a vaccine.
    本发明提供了一种新的化合物类别,免疫原组合物和包含这种化合物的药物组合物,以及使用这种化合物来治疗或预防与Toll样受体2相关的疾病或障碍的方法。在一个方面,这些化合物可用作佐剂,以增强疫苗的有效性。
  • Compounds and compositions as TLR2 agonists
    申请人:Wu Tom Yao-Hsiang
    公开号:US09365506B2
    公开(公告)日:2016-06-14
    The invention provides a novel class of compounds, immunogenic compositions and pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with Toll-Like Receptors 2. In one aspect, the compounds are useful as adjuvants for enhancing the effectiveness of a vaccine.
    该发明提供了一类新型化合物、免疫原组合物和包含这些化合物的药物组合物,以及使用这些化合物治疗或预防与Toll样受体2相关的疾病或疾病的方法。在一个方面,这些化合物可以作为佐剂用于增强疫苗的有效性。
  • Formation of Silica Precipitates on Membrane Surfaces in Two and Three Dimensions
    作者:Anja Bernecker、Joanna Ziomkowska、Svenja Heitmüller、Ralph Wieneke、Armin Geyer、Claudia Steinem
    DOI:10.1021/la1021627
    日期:2010.8.17
    Ether lipids with alkyl chains of uniform length and varying amine headgroups were synthesized and assembled into bilayer structures in aqueous solution, which served as templates for the formation of silica in two and three dimensions produced under ambient conditions. Dynamic light scattering revealed that unilamellar vesicles of the aminolipids are formed by the extrusion method. The alkylation of the polar amine headgroup was systematically increased from a primary, secondary, and tertiary amine to a quaternary ammonium salt, and the amount of silica was quantified by the beta-silicomolybdate method as a function of the headgroup. A lysinol-connected ether lipid harboring two primary amine groups was also investigated. This variation enabled us to compare the influence of the headgroup on the properties of the precipitated silica in detail. By spreading of unilamellar aminolipid vesicles onto planar silicon substrates, two-dimensional planar bilayers can be produced. By means of ellipsometry in conjunction with atomic force microscopy, we were able to demonstrate that very thin silica layers with a thickness of a few nanometers are formed within minutes on the surface of the aminolipid bilayers. All layers are composed of silica nanospheres, and the thickness turned out to be independent of the amine headgroup.
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