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聚异己基氰基丙烯酰酸酯 | 107811-81-4

中文名称
聚异己基氰基丙烯酰酸酯
中文别名
——
英文名称
isohexyl 2-cyanoacrylate
英文别名
Isohexylcyanoacrylate;4-methylpentyl 2-cyanoprop-2-enoate
聚异己基氰基丙烯酰酸酯化学式
CAS
107811-81-4;107811-80-3
化学式
C10H15NO2
mdl
——
分子量
181.235
InChiKey
HFQQYIUTYJVYFZ-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

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    13
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    50.1
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    聚异己基氰基丙烯酰酸酯 、 dextran, Mw = 71 kDa 生成 poly(isohexyl 2-cyanoacrylate)-dextran block copolymer
    参考文献:
    名称:
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • Chloroquine combination drugs and methods for their synthesis
    申请人:Kosak M. Kenneth
    公开号:US20070060499A1
    公开(公告)日:2007-03-15
    This invention discloses compositions of chloroquine-coupled active agents, including methods for their preparation. The prior art has shown that chloroquines given as free drug in high enough concentration, enhances the release of various agents from cellular endosomes into the cytoplasm. The purpose of these compositions is to provide a controlled amount of chloroquine at the same site where the active agent is delivered, thereby reducing the overall dosage needed. The compositions comprise a chloroquine substance coupled to an active agent directly or through a variety of pharmaceutical carrier substances. The carrier substances include polysaccharides, synthetic polymers, proteins, micelles and other substances for carrying and releasing the chloroquine compositions in the body for therapeutic effect. The compositions can also include a biocleavable linkage for carrying and releasing active agents for therapeutic or other medical uses. The invention also discloses carrier compositions that are coupled to targeting molecules for targeting the delivery of chloroquine substances and active agents to their site of action.
    这项发明揭示了氯喹偶联活性药剂的组合物,包括其制备方法。先前的技术已经表明,以足够高浓度给予氯喹作为游离药物,可以增强细胞内体内各种药剂从细胞内体释放到细胞质中。这些组合物的目的是在传递活性药剂的相同部位提供受控量的氯喹,从而减少所需的总剂量。这些组合物包括将氯喹物质直接或通过各种药用载体物质偶联到活性药剂。载体物质包括多糖、合成聚合物、蛋白质、胶束和其他用于在体内携带和释放氯喹组合物以产生治疗效果的物质。这些组合物还可以包括用于携带和释放活性药剂以用于治疗或其他医疗用途的生物可降解连接。该发明还揭示了与靶向分子偶联的载体组合物,用于将氯喹物质和活性药剂定位传递到它们的作用部位。
  • [EN] NANOPARTICLES FOR DELIVERY OF A PHARMACOLOGICALLY ACTIVE AGENT<br/>[FR] NANOPARTICLES PERMETTANT DE DISTRIBUER UN AGENT PHARMACEUTIQUEMENT ACTIF
    申请人:IST SUPERIORE SANITA
    公开号:WO2005048997A1
    公开(公告)日:2005-06-02
    Core-shell nanoparticles comprising: (a) a core which comprises a water insoluble polymer or copolymer, and (b) a shell which comprises a hydrophilic polymer or copolymer; said nanoparticles being obtainable by emulsion polymerization of a mixture comprising, in an aqueous solution, at least one water-insoluble styrenic, acrylic or methacrylic monomer and specific hydrophylic monomers or copolymers.
    核壳结构纳米颗粒包括:(a)核心,其中包括水不溶性聚合物或共聚物,和(b)壳层,其中包括亲水性聚合物或共聚物;所述纳米颗粒可以通过乳液聚合制备,其中包括至少一种水不溶性苯乙烯,丙烯酸或甲基丙烯酸单体和特定的亲水性单体或共聚物在水溶液中混合。
  • Chloroquine coupled nucleic acids and methods for their synthesis
    申请人:Kosak M. Kenneth
    公开号:US20060040879A1
    公开(公告)日:2006-02-23
    This invention discloses compositions and methods for preparing chloroquine-coupled nucleic acid compositions. The prior art has shown that chloroquines given as free drug in high enough concentration, enhances the release of various agents from cellular endosomes into the cytoplasm. The purpose of these compositions is to provide a controlled amount of chloroquine at the same site where the nucleic acid needs to be released, thereby reducing the overall dosage needed. The compositions comprise a chloroquine substance coupled to a nucleic acid directly or through a variety of pharmaceutical carrier substances. The carrier substances include polysaccharides, synthetic polymers, proteins, micelles and other substances for carrying and releasing the chloroquine compositions in the body for therapeutic effect. The compositions can also include a biocleavable linkage for carrying and releasing nucleic acids for therapeutic or other medical uses. The invention also discloses nucleic acid carrier compositions that are coupled to targeting molecules for targeting the delivery of nucleic acids to their site of action.
    本发明披露了制备氯喹偶联核酸组合物的组成和方法。先前的研究表明,以足够高的浓度给予氯喹作为自由药物,可以增强细胞内体内各种物质从内体泡中释放到细胞质中。这些组合物的目的是在核酸需要释放的同一位置提供受控量的氯喹,从而降低所需的总剂量。该组合物包括直接或通过各种药物载体物质偶联的氯喹物质和核酸。载体物质包括多糖、合成聚合物、蛋白质、胶束和其他用于在体内携带和释放氯喹组合物以达到治疗效果的物质。该组合物还可以包括生物可降解连接来携带和释放用于治疗或其他医疗用途的核酸。本发明还披露了偶联到靶向分子的核酸载体组合物,用于将核酸传递到其作用位置。
  • DEVICE AND METHOD FOR SOLUBILIZING, SEPARATING, REMOVING AND REACTING CARBOXYLIC ACIDS IN OILS, FATS, AQUEOUS OR ORGANIC SOLUTIONS BY MEANS OF MICRO-OR NANOEMULSIFICATION
    申请人:Dietz Ulrich
    公开号:US20130090488A1
    公开(公告)日:2013-04-11
    The present invention is directed to solubilizing compounds, a device and a method for solubilizing and removing carboxylic acids and especially fatty acids from oils, fats, aqueous emulsion, aqueous media and organic solutions. Devices utilizing the inventive method shall be used for separating carboxylic acids from oils, fats, aqueous emulsion, lipophilic media or organic solutions, respectively by preparing an aqueous micro- or nanoemulsion of the carboxylic acids especially the fatty acids and the solubilizing compound which contains at least one amidino and/or gianidino group. Solubilization effects of solubilizing compounds combined with the inventive use of separation methods for carboxylic acids can be used to treat persons in need of removal of fatty acids or analyze carboxylic acids from blood or process other solutions in food, pharmacy, chemistry, bio fuel industry or other industrial processings.
    本发明涉及溶解化合物、用于从油、脂肪、水乳液、水介质和有机溶液中溶解和去除羧酸,特别是脂肪酸的装置和方法。采用本发明方法的装置将用于通过制备羧酸特别是脂肪酸和含有至少一种氨基甲酰基和/或肼基团的溶解化合物的水微观或纳米乳液,分离油、脂肪、水乳液、亲脂性介质或有机溶液中的羧酸。溶解化合物的溶解效果与本发明所述的羧酸分离方法相结合,可用于治疗需要去除脂肪酸或从血液中分析羧酸或处理食品、药品、化学、生物燃料工业或其他工业加工过程中的其他溶液的人员。
  • Medizinisches Kit zur Anwendung bei der Vakuumversiegelungstherapie
    申请人:AESCULAP AG
    公开号:EP2366721A1
    公开(公告)日:2011-09-21
    Die Erfindung betrifft ein medizinisches Kit, insbesondere zur Vakuumversiegelung und -drainage von Wunden, umfassend die folgenden Komponenten: 1.1 einen Saugkörper zum Aufsaugen von Körperflüssigkeiten, insbesondere Blut, Wundflüssigkeiten oder dergleichen, 1.2 eine polymerisierbare Klebstoffzusammensetzung und 1.3 einen Polymerisationsinitiator.
    本发明涉及一种医疗包,特别是用于真空密封和引流伤口的医疗包,由以下部件组成: 1.1 用于吸收体液,特别是血液、伤口液体或类似液体的吸收体、 1.2 一种可聚合的粘合剂组合物和 1.3 一种聚合引发剂。
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