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2-Oleoyl-1-stearoyl-sn-glycero-3-phosphoserine | 124262-93-7

中文名称
——
中文别名
——
英文名称
2-Oleoyl-1-stearoyl-sn-glycero-3-phosphoserine
英文别名
(2S)-2-azaniumyl-3-[hydroxy-[(2R)-3-octadecanoyloxy-2-[(Z)-octadec-9-enoyl]oxypropoxy]phosphoryl]oxypropanoate
2-Oleoyl-1-stearoyl-sn-glycero-3-phosphoserine化学式
CAS
124262-93-7
化学式
C42H80NO10P
mdl
——
分子量
790.1
InChiKey
AJFWREUFUPEYII-PAHWMLEVSA-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):
    11.1
  • 重原子数:
    54
  • 可旋转键数:
    43
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    172
  • 氢给体数:
    3
  • 氢受体数:
    11

文献信息

  • Novel neutral (bio)material
    申请人:Centre National de la Recherche Scientifique (CNRS)
    公开号:EP2444464A1
    公开(公告)日:2012-04-25
    The instant invention concerns - a method for preparing a material comprising the following steps of a) treating the support to obtain a layer having SiH function, b) grafting the SiH layer obtained in step a) with an alkene and a catalyst for covalently bonding the alkene to the coating, said alkene being non-terminal and/or having an hydrophilic part, and c) recovering a material comprising a support coated with a chain covalently grafted with Si-C bonds, - a material comprising a support, optionally comprising a polyhydrosiloxane layer, on which surface is covalently bonded a grafted chain, wherein the covalent bonding between the support and/or the polyhydrosiloxane and the chain is an Si-C bond, and the grafted chain is bonded through a non-terminal carbon, through more than one covalent bond and/or the chain is having at least one hydrophilic part, and - devices comprising such material.
    本发明涉及 - 一种制备材料的方法,包括以下步骤 a) 处理支持物以获得具有 SiH 功能的层;b) 将步骤 a) 中获得的 SiH 层与烯烃和催化剂接枝,以将烯烃共价键合到涂层上,所述烯烃为非末端烯烃和/或具有亲水部分;以及 c) 回收一种材料,该材料包括涂有共价键合的 Si-C 键接枝链的支持物、 - 一种材料,包括支撑体,可选择包括聚氢硅氧烷层,在支撑体表面共价键合了一条接枝链,其中支撑体和/或聚氢硅氧烷与链之间的共价键合是 Si-C 键,接枝链通过非末端碳键、通过一个以上的共价键和/或链具有至少一个亲水部分键合,以及 - 包括这种材料的装置。
  • Compositions and methods for enhancing contrast in imaging
    申请人:Marval Biosciences, Inc.
    公开号:EP2578237A1
    公开(公告)日:2013-04-10
    Example compositions of liposomes with hydrophilic polymers on their surface, and containing relatively high concentrations of contrast- enhancing agents for computed tomography are provided. Example pharmaceutical compositions of such liposomes, when administered to a subject, provide for increased contrast of extended duration, as measured by computed tomography, in the bloodstream and other tissues of the subject. Also provided are example methods for making liposomes containing high concentrations of contrast-enhancing agents, and example methods for using the compositions.
    本发明提供了一些脂质体组合物实例,这些脂质体表面具有亲水性聚合物,并含有相对高浓度的计算机断层扫描造影剂。这种脂质体的药物组合物范例在给受试者用药时,可使受试者血液和其他组织中的对比度增加,持续时间延长,如计算机断层扫描所测。此外,还提供了制造含有高浓度造影剂的脂质体的示例方法,以及使用这些组合物的示例方法。
  • FUSOGENIC PROPERTIES OF SAPOSIN C AND RELATED PROTEINS AND POLYPEPTIDES FOR APPLICATION TO TRANSMEMBRANE DRUG DELIVERY SYSTEMS
    申请人:Children's Hospital Medical Center
    公开号:EP3357490A1
    公开(公告)日:2018-08-08
    The present invention includes pharmaceutical and/or imaging agents and methods for delivering the agent(s) within and/or through the dermal, mucosal and other cellular membranes. The agents can include a fusogenic protein. This technology can be used for applications in which the objective is delivery of active agent within and/or beneath biological membranes and/or across the blood-brain barrier and neuronal membranes.
    本发明包括药物和/或成像制剂以及在皮肤、粘膜和其他细胞膜内和/或通过皮肤、粘膜和其他细胞膜输送制剂的方法。这些制剂可包括致熔蛋白。该技术可用于在生物膜内和/或生物膜下和/或穿过血脑屏障和神经元膜输送活性剂的应用。
  • MICROFLUIDIC PRODUCTION OF BIOFUNCTIONALIZED GIANT UNILAMELLAR VESICLES FOR TARGETED INTRACELLULAR CARGO DELIVERY
    申请人:Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V.
    公开号:EP3838266A1
    公开(公告)日:2021-06-23
    The present invention relates to a method for preparation of monodisperse cell-targeting giant unilamellar vesicles based on symmetrically division of a parent polymer shell-stabilized giant unilamellar vesicle into smaller polymer shell-stabilized giant unilamellar vesicles with a diameter smaller than 10 µm using a microfluidic splitting device. The inventive method allows preparation of differently charged giant unilamellar vesicles as well as bioligand- and PEG-conjugated giant unilamellar vesicles, which are useful for targeted cellular delivery at high efficiency and specificity. A further advantage of the present invention is that the giant unilamellar vesicles can deliver huge cargos such as drug releasing porous microparticles, high amounts of in vivo imaging probes, viruses, or up-and-coming DNA origami robots.
    本发明涉及一种制备单分散细胞靶向巨型单拉美米尔囊泡的方法,其基础是利用微流体分割装置将母体聚合物壳稳定巨型单拉美米尔囊泡对称分割成直径小于10微米的较小聚合物壳稳定巨型单拉美米尔囊泡。 本发明的方法可制备不同电荷的巨型单拉米分子囊泡以及生物配体和 PEG 共轭巨型单拉米分子囊泡,这些囊泡可用于高效、特异性的细胞靶向递送。本发明的另一个优点是,巨型单拉美拉尔囊泡可以输送巨大的载体,如释放药物的多孔微颗粒、大量的体内成像探针、病毒或新兴的 DNA 折纸机器人。
  • BOTTOM-UP ASSEMBLY OF SYNTHETIC EXTRACELLULAR VESICLES
    申请人:Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V.
    公开号:EP3858332A1
    公开(公告)日:2021-08-04
    The present invention relates to a method for producing synthetic extracellular vesicles comprising a lipid bilayer including at least two lipids, optionally one or more extracellular vesicle associated proteins, and optionally one or more nucleic acid molecules. The inventive synthetic extracellular vesicles are formed by emulsification using a mechanic emulsifier in the form of polymer shell stabilized synthetic extracellular vesicles. The inventive method allows producing synthetic extracellular vesicles miming the composition and function of natural extracellular vesicles. Therefore, synthetic extracellular vesicles with specific protein and nucleic acids compositions are also disclosed herein, as well as their therapeutic uses.
    本发明涉及一种生产合成细胞外囊泡的方法,该囊泡包括一个脂质双分子层,其中至少包括两种脂质、一种或多种细胞外囊泡相关蛋白,以及一种或多种核酸分子。本发明的合成细胞外囊泡是通过使用机械乳化剂乳化形成的聚合物壳稳定合成细胞外囊泡。本发明的方法可以生产出模拟天然细胞外囊泡成分和功能的合成细胞外囊泡。因此,本文还公开了具有特定蛋白质和核酸成分的合成细胞外囊泡及其治疗用途。
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