o-t-butyltyrosine t-butyl ester | 61342-80-1

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: o-t-butyltyrosine t-butyl ester
• 英文别名: 2-Amino-3-(4-tert-butoxy-phenyl)-propionic acid tert-butyl ester；tert-butyl 2-amino-3-[4-[(2-methylpropan-2-yl)oxy]phenyl]propanoate
• CAS: 61342-80-1
• 化学式: C₁₇H₂₇NO₃
• 分子量: 293.406
• InChiKey: SHJFQCHBHKANBY-UHFFFAOYSA-N

物化性质

• 沸点：
  379.1±27.0 °C(Predicted)
• 密度：
  1.026±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  21
• 可旋转键数：
  7
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.59
• 拓扑面积：
  61.6
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  o-t-butyltyrosine t-butyl ester 以 四氢呋喃 为溶剂， 以2.65 g (74%)的产率得到(2S)-N-[(2R,4R)-[3-(S-Acetyl-3-mercaptopropanoyl)-2-(2-hydroxyphenyl)-4-thiazolidinyl]carbonyl]-o-t-butyltyrosine t-butyl ester
  参考文献：
  名称：

  Sulfur-containing acylamino acids

  摘要：

  该发明涉及以下一般公式所代表的新噻唑烷和吡咯烷化合物：其中p1，Q.sup.1和Q.sup.2为亚甲基或硫原子；Z为含有1至3个碳原子的烷基；R.sup.1为氢、烷基、芳基或杂环；R.sup.2为氢、烷基、酰基、芳基、杂环或巯基基团；R.sup.3为氢或烷基；R.sup.4为氢、烷基、芳基、与R.sup.3形成的吡咯环，或与R.sup.3形成的噻唑环；R.sup.5为羟基或氨基，可能被烷基或芳基取代。该发明的化合物是通过含硫酰基噻唑烷羧酸或含硫酰基吡咯烷羧酸与氨基酸的缩合反应合成的。该发明的化合物可用作降压药。

  公开号：

  US04425333A1

文献信息

• Vasculostatic agents and methods of use thereof
  申请人：Wrasidlo Wolfgang

  公开号：US20050282814A1

  公开（公告）日：2005-12-22

  Compositions and methods and are provided for treating disorders associated with compromised vasculostasis. Invention methods and compositions are useful for treating a variety of disorders including for example, stroke, myocardial infarction, cancer, ischemia/reperfusion injury, autoimmune diseases such as rheumatoid arthritis, eye diseases such as retinopathies or macular degeneration or other vitreoretinal diseases, inflammatory diseases, vascular leakage syndrome, edema, transplant rejection, adult/acute respiratory distress syndrome (ARDS), and the like.

  提供了用于治疗与血管稳态受损相关的疾病的组合物和方法。发明的方法和组合物可用于治疗各种疾病，包括中风、心肌梗死、癌症、缺血/再灌注损伤、类风湿性关节炎等自身免疫疾病、眼部疾病如视网膜病变或黄斑变性或其他玻璃体视网膜疾病、炎症性疾病、血管渗漏综合征、水肿、移植排斥反应、成人/急性呼吸窘迫综合征（ARDS）等。
• TETRACYCLIC CDK9 KINASE INHIBITORS
  申请人：AbbVie Inc.

  公开号：US20150218165A1

  公开（公告）日：2015-08-06

  Disclosed are compounds of Formula (Ia), and pharmaceutically acceptable salts thereof, wherein X, Y, R 1 , R 2 , R 3A , R 3B , and R 4 are as described herein. The compounds may be used as agents in the treatment of diseases, including cancer. Also disclosed are pharmaceutical compositions comprising one or more compounds of Formula (Ia).

  公开了公式(Ia)的化合物，以及其中X、Y、R1、R2、R3A、R3B和R4如本文所述的药用可接受盐。这些化合物可用作治疗疾病(包括癌症)的药物。还公开了包含一个或多个公式(Ia)化合物的药物组合物。
• Pyrazolopyrimidines as protein kinase inhibitors
  申请人：Paruch Kamil

  公开号：US20060094706A1

  公开（公告）日：2006-05-04

  In its many embodiments, the present invention provides a novel class of pyrazolo[1,5-a]pyrimidine compounds as inhibitors of protein and/or checkpoint kinases, methods of preparing such compounds, pharmaceutical compositions including one or more such compounds, methods of preparing pharmaceutical formulations including one or more such compounds, and methods of treatment, prevention, inhibition, or amelioration of one or more diseases associated with the protein or checkpoint kinases using such compounds or pharmaceutical compositions. The invention also relates to the inhibition of hepatitis C virus (HCV) replication. In particular, embodiments of the invention provide compounds and methods for inhibiting HCV RNA-dependent RNA polymerase enzymatic activity. The invention also provides compositions and methods for the prophylaxis and treatment of HCV infection.

  在其多种实施方式中，本发明提供了一种新型的吡唑并[1,5-a]嘧啶化合物类别，作为蛋白质和/或检查点激酶的抑制剂，制备这种化合物的方法，包括一种或多种这样的化合物的制药组合物，制备一种或多种这样的化合物的制药配方的方法，以及使用这样的化合物或制药组合物治疗、预防、抑制或改善与蛋白质或检查点激酶相关的一种或多种疾病的方法。本发明还涉及抑制丙型肝炎病毒（HCV）复制。具体而言，本发明的实施方式提供了化合物和方法，用于抑制HCV RNA依赖性RNA聚合酶酶活性。本发明还提供了用于预防和治疗HCV感染的组合物和方法。
• Pyrazolo[1,5a]pyrimidine compounds as antiviral agents
  申请人：Neogenesis Pharmaceuticals, Inc.

  公开号：US20040038993A1

  公开（公告）日：2004-02-26

  The invention relates to the inhibition of hepatitis C virus (HCV) replication. In particular, embodiments of the invention provide compounds and methods for inhibiting HCV RNA-dependent RNA polymerase enzymatic activity. The invention also provides compositions and methods for the prophylaxis and treatment of HCV infection.

  本发明涉及抑制丙型肝炎病毒（HCV）复制的方法。具体而言，本发明的实施例提供了抑制HCV RNA依赖性RNA聚合酶酶活性的化合物和方法。本发明还提供了用于预防和治疗HCV感染的组合物和方法。
• VASCULOSTATIC AGENTS AND METHODS OF USE THEREOF
  申请人：Wrasidlo Wolfgang

  公开号：US20100278811A1

  公开（公告）日：2010-11-04

  Compositions and methods and are provided for treating disorders associated with compromised vasculostasis. Invention methods and compositions are useful for treating a variety of disorders including for example, stroke, myocardial infarction, cancer, ischemia/reperfusion injury, autoimmune diseases such as rheumatoid arthritis, eye diseases such as retinopathies or macular degeneration or other vitreoretinal diseases, inflammatory diseases, vascular leakage syndrome, edema, transplant rejection, adult/acute respiratory distress syndrome (ARDS), and the like.

  本发明提供了用于治疗与血管稳态受损相关的疾病的组合物和方法。本发明的方法和组合物可用于治疗各种疾病，例如中风、心肌梗塞、癌症、缺血/再灌注损伤、自身免疫疾病，如类风湿性关节炎、眼部疾病，如视网膜病变或黄斑变性或其他玻璃体视网膜疾病、炎症性疾病、血管渗漏综合症、水肿、移植排斥、成人/急性呼吸窘迫综合症（ARDS）等。