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1-溴-10,12-二十五碳二炔 | 94598-32-0

中文名称
1-溴-10,12-二十五碳二炔
中文别名
1-溴-10,12-二十五烷二炔;10,12-二十五烷二炔溴化物;10,12-二十五碳二炔基溴化物;1-溴-10,12-二十五二炔;1-溴-1,12-二十五碳二炔
英文名称
1-bromopentacosa-10,12-diyne
英文别名
1-Bromo-10,12-pentacosadiyne
1-溴-10,12-二十五碳二炔化学式
CAS
94598-32-0
化学式
C25H43Br
mdl
MFCD00059029
分子量
423.52
InChiKey
NUDHYRYEPCJLCL-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

  • 沸点:
    497.7±18.0 °C(Predicted)
  • 密度:
    1.005±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    11.7
  • 重原子数:
    26
  • 可旋转键数:
    19
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.84
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

安全信息

  • 海关编码:
    2903399090

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Glycosyltransferase Microarray Displayed on the Glycolipid LB Membrane
    作者:Noriko Nagahori、Kenichi Niikura、Reiko Sadamoto、Masahiro Taniguchi、Akihiko Yamagishi、Kenji Monde、Shin-Ichiro Nishimura
    DOI:10.1002/adsc.200202204
    日期:2003.6
    ase expressed as a fusion protein with maltose binding protein (MBP-GalT) was displayed specifically on a Langmuir–Blodgett (LB) membrane prepared by photopolymerization of maltotriose-carrying glycolipid (1) with 1,2-bis(10,12-tricosadiynoyl)-sn-glycero-3-phosphocholine (2). The catalytic activity of MBP-GalT on the LB film was directly monitored by the surface plasmon resonance (SPR) method using
    β(14)表示为与麦芽糖结合蛋白(MBP-GalT)融合蛋白的半乳糖基转移酶专门显示在Langmuir-Blodgett(LB)膜上,该膜是通过将携带麦芽三糖糖脂(1)与1,2-bis(10)光聚合制备的(12-三二十二碳酰)-sn-甘油-3-磷酸胆碱(2)。使用携带GlcNAc的溶性聚合物(3)作为受体底物,通过表面等离振子共振(SPR)方法直接监测MBP-GalT在LB膜上的催化活性。高度敏感的S形型信号分别在加入在供体基板,UDP-半乳糖UDP-Gal的)的存在下,受主基片而获得,组成,而结合3缺少UDP-Gal时未检测到。信号强度取决于LB膜上固定的MBP-GalT的量,该量是通过原子力显微镜(AFM)获得的图像估算的。
  • Covalently Linked Perylene Diimide–Polydiacetylene Nanofibers Display Enhanced Stability and Photocurrent with Reversible FRET Phenomenon
    作者:Joonsik Seo、Chandra Kantha、Joonyoung F. Joung、Sungnam Park、Raz Jelinek、Jong‐Man Kim
    DOI:10.1002/smll.201901342
    日期:2019.5
    PDI–BisDA is generated, in which two polymerizable diacetylene (DA) units are covalently linked to a PDI core. Importantly, 254 nm UV irradiation of self‐assembled PDI–BisDA nanofibers forms solvent‐resistant and stable PDI–PDA fibers. Owing to the presence of PDA, the generated polymer fibers display an increased photocurrent. In addition, the existence of PDA and PDI moieties in the fiber leads to the
    由于其独特的结构和光学特性,一维per二酰亚胺(PDI)衍生物已在光电器件中获得关注。但是,含PDI的自组装超分子系统通常用途有限,因为它们具有超分子结构,这些结构通过弱的非共价π-π堆积,氢键和疏相互作用而结合在一起。结果,它们在固溶处理条件下本质上不稳定。为克服此限制,开发了一种基于聚二乙炔PDA)的策略来构建耐溶剂和稳定的PDI组件。为此,首先生成单体PDI-BisDA,其中两个可聚合的二乙炔DA)单元与PDI核共价连接。重要的是,自组装的254 nm紫外线辐射PDI-BisDA纳米纤维可形成耐溶剂性和稳定的PDI-PDA纤维。由于存在PDA,所产生的聚合物纤维显示出增加的光电流。此外,光纤中PDA和PDI部分的存在会导致PDI和可逆热致变色PDA发色团之间发生可切换的开-关荧光共振能量转移(FRET)。
  • Polymerized micelles for diagnosis
    申请人:Commissariat à l'Énergie Atomique et aux Énergies Alternatives
    公开号:EP2425817A1
    公开(公告)日:2012-03-07
    The invention relates to polymerized micelles for diagnosis, in particular of cancer. The polymerized micelles of the invention comprise a diagnostic agent and an amphiphilic polymer obtainable by the polymerization of an amphiphilic monomer, said monomer comprising: a lipophilic chain comprising a polymerizable vinylic or diacetylenic group, and a hydrophilic head comprising a polyoxyethylene or polyoxypropylene chain. The invention finds application in the pharmaceutical field, in particular.
    本发明涉及用于诊断,特别是癌症诊断的聚合胶束。 本发明的聚合胶束由诊断剂和两亲性单体聚合而成的两亲性聚合物组成,两亲性单体包括:由可聚合的乙烯基或二乙炔基组成的亲脂链和由聚氧乙烯或聚氧丙烯链组成的亲头。 本发明尤其适用于制药领域。
  • Impact of the surface charge of polydiacetylene micelles on their interaction with human innate immune protein C1q and the complement system
    作者:Nicole M. Thielens、Agathe Belime、Edmond Gravel、Sarah Ancelet、Charlotte Caneiro、Eric Doris、Wai Li Ling
    DOI:10.1016/j.ijpharm.2017.11.072
    日期:2018.1
    Polydiacetylene (pDA) micelles have been demonstrated to be effective drug carriers for cancer therapy in mouse model. However, little is known about their interaction with the human complement system, which constitutes an important part of the innate immune system and can cause severe hypersensitivity reactions. Herein, we investigate the influence of micelle surface charge on the binding of complement protein C1q, the target recognition unit that activates the classical complement pathway and performs a range of other important physiological functions. Besides the classical pathway, we also investigate the surface charge effect on complement activities through the other activation pathways, namely, the MBL-dependent lectin pathway and the alternative pathway. We synthesized three samples of pDA micelles bearing neutral, anionic, and cationic surface charge motifs, respectively. Surface plasmon resonance showed that none of these micelles interacted with C1q. Results from serum complement activation assays indicated that all micelles were inert to complement, except for the anionic pDA micelles, which activated the alternative pathway.
  • Kolotilo, N. V.; Budilova, I. Yu; Bliznyuk, V. N., Russian Journal of Organic Chemistry, 1993, vol. 29, # 1.2, p. 131 - 135
    作者:Kolotilo, N. V.、Budilova, I. Yu、Bliznyuk, V. N.、Shilov, V. V.、Il'chenko, A. Ya
    DOI:——
    日期:——
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