γ-Acetylpropionsaeuremethylamid | 98548-88-0

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: γ-Acetylpropionsaeuremethylamid
• 英文别名: Laevulinsaeure-methylamid；N-methyl-4-oxopentanamide
• CAS: 98548-88-0
• 化学式: C₆H₁₁NO₂
• 分子量: 129.159
• InChiKey: KPFALMORZZPMAW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.9
• 重原子数：
  9
• 可旋转键数：
  3
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  46.2
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  当归内酯 、 甲胺 生成 γ-Acetylpropionsaeuremethylamid
  参考文献：
  名称：

  Chiron,R.; Graff,Y., Bulletin de la Societe Chimique de France, 1970, p. 575 - 583

  摘要：

  DOI：

文献信息

• Lipid Compounds Targeting VLA-4
  申请人：BOYLAN John Frederick

  公开号：US20130079383A1

  公开（公告）日：2013-03-28

  The invention relates to the compounds of formula I: and pharmaceutically acceptable salts and esters thereof, wherein n, G, W, X, Y, and R1 are defined in the detailed description and claims. The compounds of formula I bind to or associate with VLA-4 and can be used in delivery formulations to deliver drugs, nucleic acids, or other therapeutic compounds to tissues or cells expressing VLA-4.

  这项发明涉及公式I的化合物： 以及其药用可接受的盐和酯，其中n、G、W、X、Y和R1在详细说明和索赔中有定义。公式I的化合物与VLA-4结合或与之相关，并可用于传递制剂，将药物、核酸或其他治疗化合物传递到表达VLA-4的组织或细胞中。
• FLUORESCENT MOLECULAR ROTORS
  申请人：AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH

  公开号：US20160195519A1

  公开（公告）日：2016-07-07

  The present invention relates to methods and compositions for detecting an interaction between a protein and a ligand, comprising: (i) binding at least one fluorescent molecular rotor to said ligand or protein; and (ii) detecting a change in fluorescence emitted by said fluorescent molecular rotor after contact of the bound fluorescent molecular rotor with the other of said ligand or protein, thereby detecting an interaction between the ligand and the protein, wherein the fluorescent molecular rotor comprises: a rotating ?-bond; an electron-donating moiety; an electron-accepting moiety; and a ?-conjugated linker.

  本发明涉及一种检测蛋白质与配体之间相互作用的方法和组合物，包括：(i)将至少一个荧光分子转子结合到所述配体或蛋白质上；和(ii)在所述结合的荧光分子转子与所述配体或蛋白质中的另一个接触后检测所述荧光分子转子发射的荧光变化，从而检测配体和蛋白质之间的相互作用，其中所述荧光分子转子包括：一个旋转的π键；一个给电子的基团；一个受电子的基团；和一个π共轭连接物。
• Solubilization and Targeted Delivery of Drugs With Self-Assembling Amphiphilic Polymers
  申请人：Diwan Anil

  公开号：US20100260743A1

  公开（公告）日：2010-10-14

  There are provided amphiphilic biodegradable copolymers comprising a hydrophilic backbone with pendant aliphatic groups as the hydrophobic component. The polymers form nanoscale molecular aggregates in aqueous environments, which have hydrophobic interiors that are capable of solubilizing insoluble organic compounds such as drugs, vitamins, dyes, and imaging agents. The polymers optionally feature reactive functional groups that provide attachment points for antibodies, ligands, and other targeting moieties useful for the targeted delivery of drugs and imaging agents.

  提供的两性可降解共聚物包括具有羟基亲水骨架和作为疏水组分的脂肪族侧链的共聚物。这些聚合物在水性环境中形成纳米级分子聚集体，具有疏水内部，能够溶解不溶于水的有机化合物，如药物、维生素、染料和成像剂。这些聚合物可选择性地具有反应性功能基团，提供与抗体、配体和其他靶向基团的结合点，有助于药物和成像剂的靶向传递。
• [EN] FIBROBLAST ACTIVATION PROTEIN (FAP)-TARGETED IMAGING AND THERAPY<br/>[FR] IMAGERIE ET THÉRAPIE CIBLÉES PAR UNE PROTÉINE D'ACTIVATION DES FIBROBLASTES (FAP)
  申请人：PURDUE RESEARCH FOUNDATION

  公开号：WO2018111989A1

  公开（公告）日：2018-06-21

  The present teachings relate generally to conjugates and methods for imaging a tumor microenvironment in a patient, and to conjugates and methods for imaging cancer-associated fibroblasts (CAFs) in the tumor microenvironment of a patient. The present teachings relate generally to method of making conjugates comprising a fibroblast activation protein (FAP) inhibitor.

  本文涉及患者肿瘤微环境成像的共轭物和方法，以及在患者肿瘤微环境中成像癌相关成纤维细胞（CAFs）的共轭物和方法。本文涉及制备含有成纤维细胞激活蛋白（FAP）抑制剂的共轭物的方法。
• SELF ASSEMBLING AMPHIPHILIC POLYMERS AS ANTIVIRAL AGENTS
  申请人：Diwan Anil

  公开号：US20100008938A1

  公开（公告）日：2010-01-14

  There are provided amphiphilic biodegradable copolymers comprising a hydrophilic backbone with pendant aliphatic groups as the hydrophobic component. The polymers form nanoscale molecular aggregates in aqueous environments, which have hydrophobic interiors that are capable of solubilizing insoluble organic compounds and disrupting viral coat proteins. The polymers optionally feature reactive functional groups that provide attachment points for antibodies, ligands, and other targeting moieties which mediate adherence of the aggregate to a viral target.

  提供的两性亲水可生物降解共聚物包括具有侧链脂肪族基作为疏水成分的亲水性骨架。这些聚合物在水性环境中形成纳米级分子聚集体，具有疏水内部，能够溶解不溶性有机化合物并破坏病毒外壳蛋白。这些聚合物可选择性地具有反应性功能基团，提供抗体、配基和其他靶向基团的附着点，介导聚集体与病毒靶标的粘附。