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4-oxo-4-((2-(prop-2-yn-1-yl)pent-4-yn-1-yl)oxy)butanoic acid

中文名称
——
中文别名
——
英文名称
4-oxo-4-((2-(prop-2-yn-1-yl)pent-4-yn-1-yl)oxy)butanoic acid
英文别名
4-Oxo-4-((2-(prop-2-yn-1-yl)pent-4-yn-1-yl)oxy)butanoic acid;4-oxo-4-(2-prop-2-ynylpent-4-ynoxy)butanoic acid
4-oxo-4-((2-(prop-2-yn-1-yl)pent-4-yn-1-yl)oxy)butanoic acid化学式
CAS
——
化学式
C12H14O4
mdl
——
分子量
222.241
InChiKey
JHWALLYOWBHJRK-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):
    1
  • 重原子数:
    16
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    63.6
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    参考文献:
    名称:
    复分解环聚合引发含偶氮苯纳米结构的自组装
    摘要:
    将偶氮苯(AB)单元成功引入聚(1,6-庚二炔)中,以确保双链和单链聚(1,6-庚二炔)(P1和P2)的顺利合成,同时实现自- 通过 Grubbs-III 催化剂介导的复分解环聚合 (CP) 组装 AB 官能化的双 (1,6-庚二炔) 和 1,6-庚二炔单体 (M1 和 M2)。单体和聚合物通过 1H NMR、质谱和 GPC 技术进行表征。双链聚(1,6-庚二炔)表现出大规模的有序梯形纳米结构。该结果归因于沿聚合物纵轴的端基之间的 π-π 吸引力以及相邻聚合物骨架之间的范德华相互作用。而连接在 P2 侧链上的偶氮发色团在 CP 过程中诱导胶束纳米结构的构象,无需任何后处理。此外,Azo 单元的光异构化对聚合物主链的共轭度有明显不同的调节作用,尤其是对单链 P2,这归因于聚合物中 AB 发色团之间的结构差异和相互作用。
    DOI:
    10.3390/molecules25173767
  • 作为产物:
    描述:
    2-(丙-2-炔-1-基)戊-4-炔-1-醇丁二酸酐4-二甲氨基吡啶 作用下, 以 二氯甲烷 为溶剂, 反应 24.0h, 以89%的产率得到4-oxo-4-((2-(prop-2-yn-1-yl)pent-4-yn-1-yl)oxy)butanoic acid
    参考文献:
    名称:
    复分解环聚合引发含偶氮苯纳米结构的自组装
    摘要:
    将偶氮苯(AB)单元成功引入聚(1,6-庚二炔)中,以确保双链和单链聚(1,6-庚二炔)(P1和P2)的顺利合成,同时实现自- 通过 Grubbs-III 催化剂介导的复分解环聚合 (CP) 组装 AB 官能化的双 (1,6-庚二炔) 和 1,6-庚二炔单体 (M1 和 M2)。单体和聚合物通过 1H NMR、质谱和 GPC 技术进行表征。双链聚(1,6-庚二炔)表现出大规模的有序梯形纳米结构。该结果归因于沿聚合物纵轴的端基之间的 π-π 吸引力以及相邻聚合物骨架之间的范德华相互作用。而连接在 P2 侧链上的偶氮发色团在 CP 过程中诱导胶束纳米结构的构象,无需任何后处理。此外,Azo 单元的光异构化对聚合物主链的共轭度有明显不同的调节作用,尤其是对单链 P2,这归因于聚合物中 AB 发色团之间的结构差异和相互作用。
    DOI:
    10.3390/molecules25173767
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文献信息

  • [EN] POLYMER CONJUGATE FOR DELIVERY OF A BIOACTIVE AGENT<br/>[FR] CONJUGUÉ POLYMÈRE POUR LA DÉLIVRANCE D'UN AGENT BIOACTIF
    申请人:POLYACTIVA PTY LTD
    公开号:WO2014134689A1
    公开(公告)日:2014-09-12
    The present invention relates in general to polymer-bioactive agent conjugates for delivering a bioactive agent to a subject. The polymer-bioactive agent conjugates contain triazole moieties in the polymer backbone and a bioactive moiety selected from prostaglandin analogues, β-blockers and mixtures thereof. The present invention also relates to methods for preparing the polymer conjugates using click chemical reactions, to monomer-bioactive agent conjugates suitable for preparing the polymer conjugates, and to pharmaceutical products comprising the polymer conjugates for the treatment of glaucoma.
    本发明一般涉及用于向受试者传递生物活性剂的聚合物-生物活性剂共轭物。聚合物-生物活性剂共轭物在聚合物骨架中含有三唑基团和从前列腺素类似物、β-受体阻滞剂和二者的混合物中选择的生物活性基团。本发明还涉及使用点击化学反应制备聚合物共轭物的方法,适用于制备聚合物共轭物的单体-生物活性剂共轭物,以及包含用于治疗青光眼的聚合物共轭物的药物产品。
  • Metathesis cyclopolymerization of substituted 1,6-heptadiyne and dual conductivity of doped polyacetylene bearing branched triazole pendants
    作者:Jianhua Wu、Hongfei Li、Dandan Zhou、Xiaojuan Liao、Meiran Xie、Ruyi Sun
    DOI:10.1002/pola.28430
    日期:2017.2.1
    pendant‐contained polyacetylene with trans‐double bonds and five‐membered ring repeating units along the conjugated backbone. The LiTFSI doped polyacetylenes display ionic conductivities of 2.5–1.8 × 10−6 S cm−1; by further doping with iodine, polyacetylenes show the improved ionic and electronic conductivities of 1.3 × 10−5 and 2.1 × 10−7 S cm−1 at 30 °C, respectively. Therefore, these doped polyacetylenes may
    支链三唑基团是通过点击化学反应,通过将AB 2化合物缓慢添加至B 2核的受控方法合成的,并用作1,6-庚二炔单体的取代基。在没有弱配位添加剂的情况下,单体的易位环聚合反应在二氯甲烷中进行得很好,表明支链三唑本身可以稳定活泼的传播链,从而沿着支链产生具有反式双键和五元环重复单元的支链三唑侧基含聚乙炔。共轭骨架。LiTFSI掺杂的聚乙炔的离子电导率为2.5–1.8×10 -6 S cm -1; 通过进一步掺杂,聚乙炔在30°C时分别具有1.3×10 -5和2.1×10 -7 S cm -1的改善的离子电导率。因此,这些掺杂的聚乙炔可以充当新的电解质材料。©2016 Wiley Periodicals,Inc. J. Polym。科学,A部分:Polym。化学 2017年,55,485-494
  • POLYMER CONJUGATE FOR DELIVERY OF A BIOACTIVE AGENT
    申请人:POLYACTIVA PTY LTD
    公开号:US20160000929A1
    公开(公告)日:2016-01-07
    The presentinvention relates in general to polymer-bioactive agent conjugates for delivering a bioactive agent to a subject. The polymer-bioactive agent conjugates contain triazole moieties in the polymer backbone and a bioactive moiety selected from prostaglandin analogues, β-blockers and mixtures thereof. The present invention also relates to methods for preparing the polymer conjugates using click chemical reactions, to monomer-bioactive agent conjugates suitable for preparing the polymer conjugates, and to pharmaceutical products comprising the polymer conjugates for the treatment of glaucoma.
    本发明通常涉及聚合物-生物活性剂共轭物,用于将生物活性剂传递给对象。聚合物-生物活性剂共轭物在聚合物骨架中含有三唑基团和从前列腺素类似物、β受体阻滞剂和其混合物中选择的生物活性基团。本发明还涉及使用点击化学反应制备聚合物共轭物的方法,适用于制备聚合物共轭物的单体-生物活性剂共轭物,以及包含聚合物共轭物的制药产品,用于治疗青光眼。
  • Polymer conjugate for delivery of a bioactive agent
    申请人:POLYACTIVA PTY LTD
    公开号:US10113033B2
    公开(公告)日:2018-10-30
    The present invention relates in general to polymer-bioactive agent conjugates for delivering a bioactive agent to a subject. The polymer-bioactive agent conjugates contain triazole moieties in the polymer backbone and a bioactive moiety comprising prostaglandin analogues. The present invention also relates to methods for preparing the polymer conjugates using click chemical reactions, to monomer-bioactive agent conjugates suitable for preparing the polymer conjugates, and to pharmaceutical products comprising the polymer conjugates for the treatment of glaucoma.
    本发明总体上涉及用于向受试者输送生物活性剂的聚合物-生物活性剂共轭物。聚合物-生物活性剂共轭物的聚合物骨架中含有三唑分子,生物活性分子包括前列腺素类似物。本发明还涉及利用点击化学反应制备聚合物共轭物的方法、适用于制备聚合物共轭物的单体-生物活性剂共轭物,以及包含用于治疗青光眼的聚合物共轭物的药物产品。
  • BIODEGRADABLE DRUG-POLYMER CONJUGATE
    申请人:POLYACTIVA PTY LTD
    公开号:US20200123322A1
    公开(公告)日:2020-04-23
    A drug-polymer conjugate, which is a copolymer of at least one monomer of formula (I): (I) where: X may be the same or different at each occurrence and represents a terminal functional group comprising an alkyne or an azide; Q is independently selected at each occurrence and may be present or absent and when present, represents a linking group; R is selected from the group consisting of linear or branched hydrocarbon, optionally substituted aryl and optionally substituted heteroaryl; D is a releasable drug selected from prostaglandins, β-blockers and mixtures thereof; L is a linker group group; and at least one co-monomer of Formula III III J represents a linking functional group, n is 2 to 8, preferably 3 to 8; Y comprises a polyether of formula (ORa)m wherein Ra is independently ethylene, propylene and butylene and m is from 1 to 300 (preferably 2 to 300) and the polyether is in chain with one or more groups which are preferably selected from one or more of optionally substituted straight or branched Ci to do alkylene, amino, ether, ester, amide, carbonate and carbamate; A may be the same or different at each occurrence and represents a group comprising a terminal functional group comprising an alkyne or an azide functionality, wherein said terminal functional group is complementary to the terminal functional group X of formula (I) providing triazole moieties from reaction of X and A.
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