N-hydroxysuccinimide ester of undecylinic acid | 110661-49-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯烷类
• 英文名称: N-hydroxysuccinimide ester of undecylinic acid
• 英文别名: N-hydroxysuccinimide ester of undecylenic acid；10-undecylenic acid N-hydroxysuccinimide ester；N-ω-undecenoylsuccinimide；succinimidyl undec-10-enoate；10-undecenoic acid N-hydroxysuccinic ester；10-undecenoic acid NHS-ester；N-succinimidyl undecylenate；2,5-Pyrrolidinedione, 1-[(1-oxo-10-undecenyl)oxy]-；(2,5-dioxopyrrolidin-1-yl) undec-10-enoate
• CAS: 110661-49-9
• 化学式: C₁₅H₂₃NO₄
• 分子量: 281.352
• InChiKey: OGMHSLIKBSLUAR-UHFFFAOYSA-N

物化性质

• 沸点：
  387.1±35.0 °C(Predicted)
• 密度：
  1.09±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  20
• 可旋转键数：
  11
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  63.7
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  N-hydroxysuccinimide ester of undecylinic acid 在 偶氮二异丁腈 、 氨 作用下， 以 四氢呋喃 、 N,N-二甲基甲酰胺 为溶剂， 反应 14.0h， 生成
  参考文献：
  名称：

  Arrays for the Combinatorial Exploration of Cell Adhesion

  摘要：

  A new method for the fabrication of arrays of self-assembled monolayers (SAMs) of alkane thiols (ATs) on gold to combinatorially assay surfaces for cell adhesion is reported. A fluorous SAM, which is both cytophobic and solvophobic, was used as the background between the array features. The resulting solvophobic background permits the application of an assembly after conjugation strategy for fabrication. SAMs containing mixtures of ATs and peptide-terminated ATs were generated. Multiple cell types demonstrated differential and specific binding to these surfaces. Additionally, pluripotent human embryonic stem cells proliferated on surfaces generated by this method.

  DOI：

  10.1021/ja0474291
• 作为产物：
  描述：

  2-十一烯酸 在 氯化亚砜 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 37.0h， 生成 N-hydroxysuccinimide ester of undecylinic acid
  参考文献：
  名称：

  Losset, D.; Dupas, G.; Duflos, J., Bulletin de la Societe Chimique de France, 1991, # 5, p. 721 - 729

  摘要：

  DOI：

文献信息

• Development of small-molecule inhibitors of fatty acyl-AMP and fatty acyl-CoA ligases in Mycobacterium tuberculosis
  作者：Marzena Baran、Kimberly D. Grimes、Paul A. Sibbald、Peng Fu、Helena I.M. Boshoff、Daniel J. Wilson、Courtney C. Aldrich

  DOI：10.1016/j.ejmech.2020.112408

  日期：2020.9

  biochemical roles of many FACLs remain poorly characterized while the functionally non-redundant FAALs are much better understood. Here we describe the systematic investigation of 5′-O-[N-(alkanoyl)sulfamoyl]adenosine (alkanoyl adenosine monosulfamate, alkanoyl-AMS) analogs as potential multitarget FadD inhibitors for their antitubercular activity and biochemical selectivity towards representative FAAL and

  结核分枝杆菌( Mtb ) 的脂质代谢依赖 34 种脂肪酸腺苷酸化酶 (FadDs)，可分为两类：参与脂质和胆固醇分解代谢的脂肪酰基辅酶 A 连接酶 (FACL) 和长链脂肪酰基-AMP 连接酶 (FAAL) ) 参与Mtb 中发现的许多必需和赋予毒力的脂质的生物合成。许多 FACL 的精确生化作用仍不清楚，而功能非冗余的 FAAL 则更好理解。这里，我们描述的5'-系统调查ö - [ ñ - （链烷酰基）氨磺酰基]腺苷（烷酰基一denosine米ONO小号ulfamate, alkanoyl-AMS) 类似物作为潜在的多靶点 FadD 抑制剂，因为它们具有抗结核活性和对代表性 FAAL 和 FACL 酶的生化选择性。我们鉴定了几种有效的化合物，包括 12-叠氮十二烷酰基-AMS 28、11-苯氧基十一烷酰基-AMS 32和壬氧基乙酰基-AMS 36，其对结核分枝杆菌的最小抑制浓度 (MIC)范围为
• Examination of Structural Changes of Polymeric Amino Acid-Based Surfactants on Enantioselectivity:  Effect of Amino Acid Order, Steric Factors, and Number and Position of Chiral Centers
  作者：Eugene Billiot、Isiah M. Warner

  DOI：10.1021/ac9908804

  日期：2000.4.1

  In this study, a large number of polymeric chiral surfactants were examined and their performances in terms of enantiomeric resolution compared for a variety of chiral analytes. The surfactants investigated in this study include all possible dipeptide combinations of the l-form of alanine, valine, leucine, and the achiral amino acid glycine (except glycine-glycine). Also included in this study were the single amino acid surfactants of alanine, valine, and leucine as well as the single chiral center dipeptide surfactant poly(sodium undecyl-l-leucine-β-alanine) (poly l-SULβA). Several different aspects of polymeric dipeptide surfactants, as they pertain to chiral separations, are examined. Some of the factors investigated in this report include the effect of position and number of chiral centers, amino acid order, and steric effects.

  在本研究中，考察了大量聚合物手性表面活性剂，并比较了它们在多种手性分析物中对映体分辨性能的表现。本研究所调查的表面活性剂包括了所有可能的l-型丙氨酸、缬氨酸、亮氨酸以及非手性氨基酸甘氨酸（甘氨酸-甘氨酸除外）的二肽组合。研究中还包括了单一氨基酸表面活性剂的丙氨酸、缬氨酸和亮氨酸，以及具有单一手性中心的二肽表面活性剂聚（十一烷基-l-亮氨酸-β-丙氨酸钠）（聚l-SULβA）。本研究审查了与手性分离相关的聚二肽表面活性剂的几个不同方面。报告中调查的一些因素包括手性中心位置和数量的效应、氨基酸顺序及立体效应。
• Multifunctional multivalency: a focused library of polymeric cholera toxin antagonists
  作者：Huu-Anh Tran、Pavel I. Kitov、Eugenia Paszkiewicz、Joanna M. Sadowska、David R. Bundle

  DOI：10.1039/c0ob01089h

  日期：——

  the multivalent ligands is important for successful interaction with multimeric proteins. Polymer-based heterobifunctional ligands that contain pendant groups prearranged into heterodimers can be used to probe the active site and surrounding area of the receptor. Here we describe the synthesis and activities of a series of galactose conjugates on polyacrylamide and dextran. Conjugation of a second fragment

  多价配体的结构预组织对于与多聚体蛋白成功相互作用很重要。包含预先排列成异二聚体的侧基的基于聚合物的异双功能配体可用于探测受体的活性位点和周围区域。在这里，我们描述了一系列半乳糖结合物对聚丙烯酰胺和葡聚糖的合成和活性。第二个片段的缀合导致霍乱毒素的纳摩尔抑制剂，而仅半乳糖的祖细胞显示没有可检测的活性。
• Chiral Separations Using Dipeptide Polymerized Surfactants:  Effect of Amino Acid Order
  作者：Eugene Billiot、Javier Macossay、Stefan Thibodeaux、Shahab A. Shamsi、Isiah M. Warner

  DOI：10.1021/ac9709561

  日期：1998.4.1

  Chiral separations using various polymerized dipeptide surfactants in electrokinetic capillary chromatography (EKC) are investigated. The two main dipeptide surfactants used in this study were sodium N-undecylenyl-l-valine-l-leucine (l-SUVL), and sodium N-undecylenyl-l-leucine-l-valine (l-SULV). These studies were performed in order to determine if the order of amino acids in dipeptide surfactants is important in terms of chiral recognition and separations. Both the monomer and the polymer of these two surfactants were compared for the separation of two model atropisomers, (±)-1,1‘-bi-2-naphthol (BOH) and (±)-1,1‘-bi-2-naphthyl-2,2‘-diyl hydrogen phosphate (BNP). Some advantages and disadvantages of the polymer relative to the monomer are discussed. Four other surfactants, the polymers of sodium N-undecylenyl-l-leucine-l-leucine (l-SULL), sodium N-undecylenyl-l-valine-l-valine (l-SUVV), sodium N-undecylenyl-l-valine (l-SUV), and sodium N-undecylenyl-l-leucine (l-SUL), were also used in this study, and their performance was compared to that of poly(l-SULV). These data show conclusively that the order of amino acids in dipeptide surfactants has a dramatic effect on chiral recognition. Our investigations indicate that poly(l-SULV) provides the best enantioselectivity among the four dipeptide and two single amino acid surfactants for the separation of BNP and BOH. The advantages of poly(l-SULV) are demonstrated via the ultrafast separation of the enantiomers of BNP and BOH in less than 1 min.

  使用电动力学毛细管色谱法(EKC)研究了各种聚二肽表面活性剂的手性分离。本研究中使用的两种主要二肽表面活性剂是钠N-十一烯基-L-缬氨酸-L-亮氨酸(L-SUVL)和钠N-十一烯基-L-亮氨酸-L-缬氨酸(L-SULV)。这些研究的目的是确定二肽表面活性剂中氨基酸的顺序是否在手性识别和分离方面起着重要作用。比较了这两种表面活性剂的单体和聚合物，用于分离两个模型旋转异构体，即(±)-1,1'-双-2-萘酚(BOH)和(±)-1,1'-双-2-萘基-2,2'-二基磷酸氢(BNP)。讨论了聚合物相对于单体的一些优点和缺点。本研究还使用了其他四种表面活性剂，即钠N-十一烯基-L-亮氨酸-L-亮氨酸(L-SULL)、钠N-十一烯基-L-缬氨酸-L-缬氨酸(L-SUVV)、钠N-十一烯基-L-缬氨酸(L-SUV)和钠N-十一烯基-L-亮氨酸(L-SUL)的聚合物，并将其性能与聚(L-SULV)进行了比较。这些数据显示，二肽表面活性剂中氨基酸的顺序对手性识别有显著影响。我们的研究表明，在四种二肽和两种单氨基酸表面活性剂中，聚(L-SULV)在分离BNP和BOH方面提供了最佳的对映选择性。通过在不到1分钟的时间内超快分离BNP和BOH的对映体，展示了聚(L-SULV)的优势。
• Selective esterifications of alcohols and phenols through carbodiimide couplingsElectronic supplementary information (ESI) available: the characterization of new compounds and literature references for known compounds. See http://www.rsc.org/suppdata/ob/b3/b312559a/
  作者：Rimma Shelkov、Moshe Nahmany、Artem Melman

  DOI：10.1039/b312559a

  日期：——

  Esterification of carboxylic acids capable of forming ketene intermediates upon treatment with carbodiimides permits the selective acylation of alcohols in the presence of phenols lacking strong electron-withdrawing groups. The selectivity of acylations involving highly acidic phenols could be reversed through the addition of catalytic amount of acid. Esterification of other carboxylic acids was found

  在用碳二亚胺处理后能够形成烯酮中间体的羧酸的酯化反应可在缺乏强吸电子基团的酚存在下对醇进行选择性酰化。可以通过添加催化量的酸来逆转涉及高酸性酚的酰化反应的选择性。发现其他羧酸的酯化反应通过对称酸酐的形成进行，并提供相反的化学选择性。在这两种情况下，取代酚的相对酰化速率均与反应机理一致，该机理涉及酚盐阴离子攻击亲电子中间体（例如乙烯酮和对称酸酐），而碳二亚胺既用作活化剂，又用作碱性催化剂。