摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

Boc-Lys(Boc)-Lys(1)-Lys(2)-OH.Boc-Lys(Boc)-Lys(3)-(2).Boc-Lys(Boc)-(1).Boc-Lys(Boc)-(3) | 135467-14-0

中文名称
——
中文别名
——
英文名称
Boc-Lys(Boc)-Lys(1)-Lys(2)-OH.Boc-Lys(Boc)-Lys(3)-(2).Boc-Lys(Boc)-(1).Boc-Lys(Boc)-(3)
英文别名
(2S)-2,6-bis[[(2S)-2,6-bis[[(2S)-2,6-bis[(2-methylpropan-2-yl)oxycarbonylamino]hexanoyl]amino]hexanoyl]amino]hexanoic acid
Boc-Lys(Boc)-Lys(1)-Lys(2)-OH.Boc-Lys(Boc)-Lys(3)-(2).Boc-Lys(Boc)-(1).Boc-Lys(Boc)-(3)化学式
CAS
135467-14-0
化学式
C82H150N14O24
mdl
——
分子量
1716.17
InChiKey
GDNJSXYUNOQIHO-MQEJUTFJSA-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):
    9.3
  • 重原子数:
    120
  • 可旋转键数:
    65
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    519
  • 氢给体数:
    15
  • 氢受体数:
    24

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

  • 作为反应物:
    描述:
    Boc-Lys(Boc)-Lys(1)-Lys(2)-OH.Boc-Lys(Boc)-Lys(3)-(2).Boc-Lys(Boc)-(1).Boc-Lys(Boc)-(3)三氟乙酸 作用下, 以 二氯甲烷 为溶剂, 反应 1.0h, 以100%的产率得到(S)-2,6-Bis-[(S)-2,6-bis-((S)-2,6-diamino-hexanoylamino)-hexanoylamino]-hexanoic acid
    参考文献:
    名称:
    Facile synthesis of poly-(l-lysine) dendrimers with a pentaaminecobalt(III) complex at the core
    摘要:
    The synthesis of second and third generation dendrimers based on poly-(L-lysine) with a pentaamine cobalt(III) metal complex at the core is described. The synthesis and purification of these dendrimers were facilitated by using the metal complex as the C-terminal protecting group. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2005.06.078
  • 作为产物:
    参考文献:
    名称:
    Facile synthesis of poly-(l-lysine) dendrimers with a pentaaminecobalt(III) complex at the core
    摘要:
    The synthesis of second and third generation dendrimers based on poly-(L-lysine) with a pentaamine cobalt(III) metal complex at the core is described. The synthesis and purification of these dendrimers were facilitated by using the metal complex as the C-terminal protecting group. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2005.06.078
点击查看最新优质反应信息

文献信息

  • Syntheses of dendritic branches based on l-lysine: is the stereochemistry preserved throughout the synthesis?
    作者:Malcolm Driffield、David M. Goodall、David K. Smith
    DOI:10.1039/b304410f
    日期:——
    stereochemistry in the dendritic peptide was dependent on the method of synthesis, with divergent methodology being preferred. The results are discussed in terms of the known stereochemical outcomes of traditional peptide coupling processes, and are generalised to the synthesis of other dendritic peptides. Such observations about the chirality of dendritic peptides are of relevance to chemists developing
    本文报道了基于L-赖氨酸并用Boc或Bz表面基团官能化的单个树枝状分支的合成。采用会聚和发散的合成方法,并使用旋光法,NMR和HPLC监测合成过程中立体化学的保留情况。另外,出于比较目的,合成了基于D,L-赖氨酸的外消旋树枝状分支。观察到树突状肽中立体化学的保留取决于合成方法,优选发散方法。根据传统肽偶联方法的已知立体化学结果讨论了结果,并将其推广到其他树突状肽的合成。
  • Controllable mixed-charged co-assembly of dendritic lipopeptides into invisible capsid-like nanoparticles as potential drug carriers
    作者:Qinhan Xu、Chang Shu、Yachao Li、Rong Zhuang、Lei Jiang、Xianghui Xu
    DOI:10.1039/d0cc07953g
    日期:——

    A new type of molecular and supramolecular strategy is proposed to controllably construct mixed-charged nanoparticles with resistance to protein adsorption.

    提出了一种新型的分子和超分子策略,以可控的方式构建具有蛋白质吸附抗性的混合电荷纳米颗粒。
  • Supramolecular dendrimer chemistry: using dendritic crown ethers to reversibly generate functional assemblies
    作者:Graham M. Dykes、David K. Smith
    DOI:10.1016/s0040-4020(03)00468-x
    日期:2003.5
    cations possessing long alkyl spacer chains as templates has also been investigated, and in this case, the 2:1 assembly that forms, goes on to achieve higher order levels of organisation, hence gelating the solvent. This particular system is therefore a rare example in which discrete, characterisable dendritic supermolecules possess an inherent potential for further supramolecular assembly, to yield new
    合成了一系列基于l-赖氨酸重复单元的具有树枝状支化功能的冠醚衍生物。已使用NMR和质谱技术研究了这些受体与阳离子客体相互作用的能力。已经评价了结合常数,其中一些使用竞争性结合测定法,并且这些结合常数表明,封装的冠醚和阳离子客体之间的相互作用强度随着树突状官能度的增加而降低。已经研究了这些树枝状分支与对位铵阳离子官能化模板的相互作用,并且作业图分析表明在MeOH溶液中形成了2:1(分支/模板)化学计量的配合物。这些超分子组装已通过添加钾阳离子而分解,因此实现了模板释放到溶液中的控制释放。该过程已通过NMR方法进行了研究,并报道了抗衡阴离子对这些研究的影响。还研究了使用具有长烷基间隔链的对位铵阳离子作为模板,在这种情况下,形成的2:1组装继续达到更高的组织水平,从而使溶剂胶凝。因此,该特定系统是一个罕见的例子,其中离散的,可表征的树枝状超分子具有进一步超分子组装的内在潜力,可以生产新材料。还研
  • Supramolecular Solubilisation of Hydrophilic Dyes by Using Individual Dendritic Branches
    作者:Graham M. Dykes、Lisa J. Brierley、David K. Smith、P. Terry McGrail、Gordon J. Seeley
    DOI:10.1002/1521-3765(20011105)7:21<4730::aid-chem4730>3.0.co;2-a
    日期:2001.11.5
    Individual dendritic branches can solubilise hydrophilic dyes in apolar media. The functional group at the focal point of the dendritic branch plays a key role in the dye uptake process. Supramolecular interactions between carboxylic acid and amine groups have been shown to be effective in enabling efficient solubilisation to occur. The necessary complementarity of this interaction is further illustrated by a series of control experiments. The extent of dendritic branching (i.e. dendritic generation) plays a key role in controlling the extent of dye uptake, with higher-generation dendritic branches exhibiting more efficient uptake at lower concentrations. UV/Visible spectroscopic methods have shown that the dendritic branches, in addition to the tuning of the extent of dye uptake, also tune the optical properties of the solubilised dye and this provides further insight into the interactions occurring between the solubilised dye and the individual dendritic branches. Furthermore, it is shown that suitably functionalised dendritic branches can transport hydrophilic dyes through an apolar phase and deliver them continuously into an aqueous medium.
  • Controlled Release of a Dendritically Encapsulated Template Molecule
    作者:Graham M. Dykes、David K. Smith、Gordon J. Seeley
    DOI:10.1002/1521-3773(20020902)41:17<3254::aid-anie3254>3.0.co;2-4
    日期:2002.9.2
查看更多

同类化合物

(甲基3-(二甲基氨基)-2-苯基-2H-azirene-2-羧酸乙酯) (±)-盐酸氯吡格雷 (±)-丙酰肉碱氯化物 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素 (S)-(+)-α-氨基-4-羧基-2-甲基苯乙酸 (S)-阿拉考特盐酸盐 (S)-赖诺普利-d5钠 (S)-2-氨基-5-氧代己酸,氢溴酸盐 (S)-2-[3-[(1R,2R)-2-(二丙基氨基)环己基]硫脲基]-N-异丙基-3,3-二甲基丁酰胺 (S)-1-(4-氨基氧基乙酰胺基苄基)乙二胺四乙酸 (S)-1-[N-[3-苯基-1-[(苯基甲氧基)羰基]丙基]-L-丙氨酰基]-L-脯氨酸 (R)-乙基N-甲酰基-N-(1-苯乙基)甘氨酸 (R)-丙酰肉碱-d3氯化物 (R)-4-N-Cbz-哌嗪-2-甲酸甲酯 (R)-3-氨基-2-苄基丙酸盐酸盐 (R)-1-(3-溴-2-甲基-1-氧丙基)-L-脯氨酸 (N-[(苄氧基)羰基]丙氨酰-N〜5〜-(diaminomethylidene)鸟氨酸) (6-氯-2-吲哚基甲基)乙酰氨基丙二酸二乙酯 (4R)-N-亚硝基噻唑烷-4-羧酸 (3R)-1-噻-4-氮杂螺[4.4]壬烷-3-羧酸 (3-硝基-1H-1,2,4-三唑-1-基)乙酸乙酯 (2S,3S,5S)-2-氨基-3-羟基-1,6-二苯己烷-5-N-氨基甲酰基-L-缬氨酸 (2S,3S)-3-((S)-1-((1-(4-氟苯基)-1H-1,2,3-三唑-4-基)-甲基氨基)-1-氧-3-(噻唑-4-基)丙-2-基氨基甲酰基)-环氧乙烷-2-羧酸 (2S)-2,6-二氨基-N-[4-(5-氟-1,3-苯并噻唑-2-基)-2-甲基苯基]己酰胺二盐酸盐 (2S)-2-氨基-3-甲基-N-2-吡啶基丁酰胺 (2S)-2-氨基-3,3-二甲基-N-(苯基甲基)丁酰胺, (2S,4R)-1-((S)-2-氨基-3,3-二甲基丁酰基)-4-羟基-N-(4-(4-甲基噻唑-5-基)苄基)吡咯烷-2-甲酰胺盐酸盐 (2R,3'S)苯那普利叔丁基酯d5 (2R)-2-氨基-3,3-二甲基-N-(苯甲基)丁酰胺 (2-氯丙烯基)草酰氯 (1S,3S,5S)-2-Boc-2-氮杂双环[3.1.0]己烷-3-羧酸 (1R,4R,5S,6R)-4-氨基-2-氧杂双环[3.1.0]己烷-4,6-二羧酸 齐特巴坦 齐德巴坦钠盐 齐墩果-12-烯-28-酸,2,3-二羟基-,苯基甲基酯,(2a,3a)- 齐墩果-12-烯-28-酸,2,3-二羟基-,羧基甲基酯,(2a,3b)-(9CI) 黄酮-8-乙酸二甲氨基乙基酯 黄荧菌素 黄体生成激素释放激素 (1-5) 酰肼 黄体瑞林 麦醇溶蛋白 麦角硫因 麦芽聚糖六乙酸酯 麦根酸 麦撒奎 鹅膏氨酸 鹅膏氨酸 鸦胆子酸A甲酯 鸦胆子酸A 鸟氨酸缩合物