2-氨基-3-(4-甲氧基-1H-吲哚-3-基)丙酸 | 199540-73-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 中文名称: 2-氨基-3-(4-甲氧基-1H-吲哚-3-基)丙酸
• 英文名称: 4-Methoxy-tryptophan
• 英文别名: 2-amino-3-(4-methoxy-1H-indol-3-yl)propanoic Acid
• CAS: 199540-73-3
• 化学式: C₁₂H₁₄N₂O₃
• 分子量: 234.255
• InChiKey: VYXPKRIKQJEAOO-UHFFFAOYSA-N

物化性质

• 沸点：
  478.3±45.0 °C(Predicted)
• 密度：
  1.347±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  -1.2
• 重原子数：
  17
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  88.3
• 氢给体数：
  3
• 氢受体数：
  4

安全信息

• 海关编码：
  2933990090

反应信息

• 作为产物：
  描述：

  4-甲氧基芦竹碱 在 乙醇 、 sodium ethanolate 、 sodium carbonate 、 硫酸二甲酯 作用下， 生成 2-氨基-3-(4-甲氧基-1H-吲哚-3-基)丙酸
  参考文献：
  名称：

  Doig et al., Journal of the Chemical Society, 1952, p. 3912,3915

  摘要：

  DOI：

文献信息

• Method for Producing Intermediates for the Production of Novel Macrocycles that are Inhibitors of the Proteasomic Degradation of p27, such as Argyrin and Derivatives Thereof, and Uses of Said Macrocycles
  申请人：Kalesse Markus

  公开号：US20110311564A1

  公开（公告）日：2011-12-22

  The present invention relates to the use of particular macrocycles that are inhibitors of the proteasomic degradation of p27, in particular argyrin and derivatives thereof, for a treatment in a variety of conditions, such as the induction of immunotolerance, autoimmune diseases, bacterial infections, and proliferative diseases, such as cancers.

  本发明涉及使用特定的大环化合物，这些大环化合物是p27蛋白质降解的蛋白酶体抑制剂的抑制剂，尤其是精胺及其衍生物，用于治疗多种病症，如诱导免疫耐受、自身免疫疾病、细菌感染以及增殖性疾病，如癌症。
• MITHRAMYCIN DERIVATIVES HAVING INCREASED SELECTIVITY AND ANTI-CANCER ACTIVITY
  申请人：University of Kentucky Research Foundation

  公开号：US20190083519A1

  公开（公告）日：2019-03-21

  Mithramycin side chain carboxylic acid (MTM-SA) derivative are provided, which include a substituted amino acid derivative, a substituted amino acid dipeptide derivative, or an unsubstituted dipeptide derivative. The MTM-SA derivatives are useful for treatment of cancer or neuro-diseases associated with an aberrant erythroblast transformation-specific transcription factor. Unique MTM-SA derivatives have increased selectively toward ETS transcription factor.

  米司麦霉素侧链羧酸（MTM-SA）衍生物包括一种取代氨基酸衍生物、一种取代氨基酸二肽衍生物或一种未取代的二肽衍生物。这些MTM-SA衍生物对于治疗与异常红细胞转化特异性转录因子相关的癌症或神经疾病很有用。独特的MTM-SA衍生物对ETS转录因子具有增强的选择性。
• [EN] IMPROVED METHOD FOR PRODUCING INTERMEDIATES FOR THE PRODUCTION OF MACROCYCLES THAT ARE INHIBITORS OF THE PROTEASOMIC DEGRADATION OF P27, SUCH AS ARGYRIN AND DERIVATIVES THEREOF<br/>[FR] PROCÉDÉ AMÉLIORÉ DE PRODUCTION D'INTERMÉDIAIRES POUR LA PRODUCTION DE MACROCYCLES QUI SONT DES INHIBITEURS DE LA DÉGRADATION PROTÉASOMIQUE DE P27, TELS QUE L'ARGYRINE ET SES DÉRIVÉS
  申请人：HELMHOLTZ INFEKTIONSFORSCHUNG

  公开号：WO2011073173A1

  公开（公告）日：2011-06-23

  The present invention relates to an improved method for the synthesis of particular macrocycles that are inhibitors of the proteasomic degradation of p27, in particular argyrin and derivatives thereof.

  本发明涉及一种改进的方法，用于合成特定的大环化合物，这些大环化合物是p27蛋白质酶解抑制剂，特别是Argyrin及其衍生物。
• Method for producing intermediates for the production of novel macrocycles that are inhibitors of the proteasomic degradation of p27, such as argyrin and derivatives thereof, and uses of said macrocycles
  申请人：Helmholtz-Zentrum für Infektionsforschung GmbH

  公开号：EP2138507A1

  公开（公告）日：2009-12-30

  The present invention relates to the use of particular macrocycles that are inhibitors of the proteasomic degradation of p27, in particular argyrin and derivatives thereof, for a treatment in a variety of conditions, such as the induction of immunotolerance, autoimmune diseases, bacterial infections, and proliferative diseases, such as cancers.

  本发明涉及使用特定的宏环化合物，如阿吉林及其衍生物，作为p27蛋白酶解抑制剂，用于治疗各种疾病，例如诱导免疫耐受性、自身免疫疾病、细菌感染和增殖性疾病，如癌症。
• PESTICIDAL COMPOSITION COMPRISING INDOLE DERIVATES
  申请人：Bednarek Pawel

  公开号：US20090028796A1

  公开（公告）日：2009-01-29

  The present invention is directed to pesticidal compositions comprising indole derivatives. These indole derivatives are especially active against phytopathogenic fungi. Furthermore, the invention relates to the use of indole derivatives for the production of pesticides and the use of the compositions according to the invention as pesticides. The present invention is also directed to a process for producing a pesticidal composition and to pesticidal compositions prepared by this process. In addition, the invention relates to a process for preventing or combating pests and to a process for protecting plants against pests, especially against phytopathogenic fungi. Further, the invention is directed to plants or seeds as well as objects or materials which have been protected against pests by treatment with a composition according to the invention. Further, the invention is directed to a method for identifying a substance having pesticidal activity. Further, the invention is directed to a method of identifying the mode of action of and/or of providing binding proteins for a pesticidal compound of the present invention. Finally, the invention is directed to a method for diagnosing pest infection of a plant and to the use of a pesticidal compound of the present invention as diagnostic markers.

  本发明涉及包含吲哚衍生物的杀虫组合物。这些吲哚衍生物特别对植物病原真菌具有活性。此外，本发明涉及使用吲哚衍生物制备杀虫剂以及使用本发明中的组合物作为杀虫剂。本发明还涉及制备杀虫组合物的过程以及通过该过程制备的杀虫组合物。此外，本发明还涉及预防或对抗害虫的过程以及保护植物免受害虫，特别是植物病原真菌的过程。此外，本发明还涉及经过本发明中的组合物处理后受到保护的植物或种子以及物体或材料。本发明还涉及识别具有杀虫活性的物质的方法。此外，本发明还涉及识别本发明中杀虫化合物的作用方式和/或提供结合蛋白的方法。最后，本发明涉及诊断植物害虫感染的方法以及使用本发明中的杀虫化合物作为诊断标记的方法。