N-(2-Aminoethyl)-3-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)propanamide | 820247-10-7

• 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-(2-Aminoethyl)-3-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)propanamide
• 英文别名: N-(2-aminoethyl)-3-(2,5-dioxopyrrol-1-yl)propanamide
• CAS: 820247-10-7
• 化学式: C₉H₁₃N₃O₃
• 分子量: 211.22
• InChiKey: LGOKQXDILYRQRS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -1.1
• 重原子数：
  15
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.44
• 拓扑面积：
  92.5
• 氢给体数：
  2
• 氢受体数：
  4

文献信息

• ANTIBODY DRUG CONJUGATES (ADCS) AND ANTIBODY PRODRUG CONJUGATES (APDCS) WITH ENZYMATICALLY CLEAVABLE GROUPS
  申请人：Bayer Pharma Aktiengesellschaft

  公开号：US20180169256A1

  公开（公告）日：2018-06-21

  The present invention relates to novel binder-prodrug conjugates (APDCs) where binders are conjugated with inactive precursor compounds of kinesin spindle protein inhibitors, and to antibody-drug conjugates ADCs and to processes for producing these APDCs and ADCs.

  这项发明涉及新型结合物-前药偶联物（APDCs），其中结合物与动力蛋白纺锤体抑制剂的非活性前体化合物偶联，以及抗体药物偶联物ADCs以及制备这些APDCs和ADCs的方法。
• ANTIBODY DRUG CONJUGATES OF KINESIN SPINDEL PROTEIN (KSP) INHIBITORS WITH ANTIB7H3-ANTIBODIES
  申请人：BAYER PHARMA AKTIENGESELLSCHAFT

  公开号：US20200138970A1

  公开（公告）日：2020-05-07

  The present application relates to novel binder drug conjugates (ADCs), to active metabolites of these ADCs, to processes for preparing these ADCs, to the use of these ADCs for the treatment and/or prophylaxis of diseases and to the use of these ADCs for preparing medicaments for treatment and/or prophylaxis of diseases, in particular hyperproliferative and/or angiogenic disorders such as, for example, cancer diseases. Such treatments can be effected as monotherapy or else in combination with other medicaments or further therapeutic measures.

  本申请涉及新型结合剂药物偶联物（ADCs），这些ADCs的活性代谢物，制备这些ADCs的过程，将这些ADCs用于治疗和/或预防疾病，以及将这些ADCs用于制备治疗和/或预防疾病的药物，特别是高增殖和/或血管生成异常等疾病，例如癌症等。这种治疗可以作为单独治疗，也可以与其他药物或其他治疗措施结合使用。
• NOVEL WATER-SOLUBLE COMPLEXING AGENTS AND CORRESPONDING LANTHANIDE COMPLEXES
  申请人：CISBIO BIOASSAYS

  公开号：US20150361116A1

  公开（公告）日：2015-12-17

  The invention relates to complexing agents of formula (I): in which A, chrom1, chrom2 and chrom3 are as defined in the description. The invention also relates to the lanthanide complexes obtained from these complexing agents.

  该发明涉及公式（I）中的络合剂：其中A、chrom1、chrom2和chrom3如描述中所定义。该发明还涉及从这些络合剂获得的镧系金属络合物。
• [EN] AURISTATIN COMPOUNDS AND CONJUGATES THEREOF<br/>[FR] COMPOSÉS AURISTATINE ET LEURS CONJUGUÉS
  申请人：MERSANA THERAPEUTICS INC

  公开号：WO2014093379A1

  公开（公告）日：2014-06-19

  An auristatin compound conjugate is provided herein. The conjugate comprises a protein based recognition-molecule (PBRM) and a polymeric carrier substituted with one or more -LD- D, the protein based recognition-molecule being connected to the polymeric carrier by Lp. Each occurrence of D is independently an auristatin compound having a molecular weight ≤ 5 kDa. LD and Lp are distinct linkers connecting the auristatin compound and PBRM to the polymeric earner respectively. Also disclosed are polymeric scaffolds useful for conjugating with a PBRM to form a polymer-auristatin compound-PBRM conjugate described herein, compositions comprising the conjugates, methods of their preparation, and methods of treating various disorders with the conjugates or their compositions.

  本文提供了一种auristatin化合物结合物。该结合物包括基于蛋白质的识别分子（PBRM）和聚合物载体，其被取代一个或多个-LD-D，其中，基于蛋白质的识别分子通过Lp与聚合物载体相连。每个D的出现都是独立的，具有分子量≤5 kDa的auristatin化合物。LD和Lp是连接auristatin化合物和PBRM到聚合物载体的不同连接物。还揭示了用于与PBRM结合形成聚合物-auristatin化合物-PBRM结合物的聚合物支架，以及包括结合物的组合物，其制备方法以及使用结合物或其组合物治疗各种疾病的方法。
• AURISTATIN DRUG LINKER CONJUGATES
  申请人：Seattle Genetics, Inc.

  公开号：US20140050746A1

  公开（公告）日：2014-02-20

  Drug Linker compounds and Drug Linker Ligand conjugates are provided that have auristatins linked via the C-terminus. The conjugates show efficacy without the need for a self-immolative group to release the drug.

  提供了药物连接剂化合物和药物连接剂配体共轭物，这些化合物通过C-末端连接auristatins。这些共轭物表现出疗效，无需自解离基团释放药物。