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1-pyrenebutyric acid N-hydroxysuccinimide ester | 192432-85-2

中文名称
——
中文别名
——
英文名称
1-pyrenebutyric acid N-hydroxysuccinimide ester
英文别名
succinimido 1-pyrenebutyrate;1-(4-(Pyren-1-yl)butanoyl)pyrrolidine-2,5-dione;1-(4-pyren-1-ylbutanoyl)pyrrolidine-2,5-dione
1-pyrenebutyric acid N-hydroxysuccinimide ester化学式
CAS
192432-85-2
化学式
C24H19NO3
mdl
——
分子量
369.42
InChiKey
XYJNTRZBYNRQEP-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):
    4.3
  • 重原子数:
    28
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    54.4
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

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文献信息

  • Characterization of daptomycin oligomerization with perylene excimer fluorescence: Stoichiometric binding of phosphatidylglycerol triggers oligomer formation
    作者:Jawad K. Muraih、Jesse Harris、Scott D. Taylor、Michael Palmer
    DOI:10.1016/j.bbamem.2011.10.027
    日期:2012.3
    phosphatidylglycerol in the target membrane. Daptomycin has been shown to form oligomers on liposome membranes. We here use perylene excimer fluorescence to further characterize the membrane-associated oligomer. To this end, the N-terminal fatty acyl chain was replaced with perylene-butanoic acid. The perylene derivative retains one third of the antibacterial activity of native daptomycin. On liposomes containing phosphatidylcholine
    达托霉素是一种脂肽抗生素,可与细菌细胞膜结合并使其去极化。它的抗菌活性需要,并且与靶膜中的磷脂甘油含量有关。已经证明达托霉素在脂质体膜上形成寡聚物。我们在这里使用per准分子荧光来进一步表征膜相关的低聚物。为此,将N-末端脂肪酰基链替换为per-丁酸。ylene衍生物保留了天然达托霉素的三分之一的抗菌活性。在含有磷脂胆碱磷脂甘油的脂质体上,以及在枯草芽孢杆菌细胞上,per标记的达托霉素形成受激准分子,这表明相邻低聚物亚基的N末端酰基链彼此直接接触。在脂质比塞勒系统中,可以用化学计量的磷脂甘油滴定低聚物的形成。因此,达托霉素与单分子磷脂甘油的相互作用足以触发达托霉素寡聚。
  • High-Density Noncovalent Functionalization of DNA by Electrostatic Interactions
    作者:Wei Chen、Jennifer Y. Gerasimov、Pei Zhao、Kai Liu、Andreas Herrmann
    DOI:10.1021/jacs.5b05432
    日期:2015.10.14
    Preserving DNA hybridization in organic solvents could someday serve to significantly extend the applicability of DNA-based technologies. Here, we present a method that can be used to solubilize double-stranded DNA at high concentrations in organic media. This method requires first precipitating a DNA molecule from the aqueous environment with an anilinium derivative and subsequently exchanging this moiety with an amine-containing surfactant in organic solvent. We demonstrate that this method yields complete exchange of the surfactant and allows for the modification of DNA with hydrophobic primary, secondary, and tertiary alkylamines and ordered functional lcsystems. Using this approach, we fabricate a multichromophoric light harvesting system that would be unattainable by traditional methods. Additionally, this method makes it possible to use small, hydrophilic molecules to solubilize DNA in organic solvents, which reduces the shielding around the macromolecule more accessible for further chemical modification. We believe that this approach will prove beneficial in expanding the scope of DNA-based nano- and biotechnologies. DNA and makes the tremendously
  • TELSER, JOSHUA;CRUICKSHANK, KENNETH A.;MORRISON, LARRY E.;NETZEL, THOMAS +, J. AMER. CHEM. SOC., 111,(1989) N8, C. 6966-6976
    作者:TELSER, JOSHUA、CRUICKSHANK, KENNETH A.、MORRISON, LARRY E.、NETZEL, THOMAS +
    DOI:——
    日期:——
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