(S)-2-amino-2-(4-difluoromethoxy-phenyl)ethanol | 1213073-80-3

• 英文名称: (S)-2-amino-2-(4-difluoromethoxy-phenyl)ethanol
• 英文别名: (2S)-2-Amino-2-[4-(difluoromethoxy)phenyl]ethan-1-OL；(2S)-2-amino-2-[4-(difluoromethoxy)phenyl]ethanol
• CAS: 1213073-80-3
• 化学式: C₉H₁₁F₂NO₂
• 分子量: 203.189
• InChiKey: YTHACPLZDAHPTP-MRVPVSSYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.1
• 重原子数：
  14
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  55.5
• 氢给体数：
  2
• 氢受体数：
  5

文献信息

• SERINE/THREONINE KINASE INHIBITORS
  申请人：Blake Jim

  公开号：US20140066453A1

  公开（公告）日：2014-03-06

  Compounds having the formula I wherein R 2 , X and Z as defined herein are inhibitors of ERK kinase. Also disclosed are compositions and methods for treating hyperproliferative disorders.

  具有公式I的化合物，其中R2、X和Z如本文所定义，是ERK激酶的抑制剂。还披露了用于治疗过度增殖性疾病的组合物和方法。
• [EN] SERINE/THREONINE KINASE INHIBITORS<br/>[FR] INHIBITEURS DE SÉRINE/THRÉONINE KINASE
  申请人：ARRAY BIOPHARMA INC

  公开号：WO2012118850A1

  公开（公告）日：2012-09-07

  Compounds having the formula I wherein Z, Z1 Z2 Z3, R3a, R3b and Rb and as defined herein are inhibitors of ERK kinase. Also disclosed are compositions and methods for treating hyperproliferative disorders.

  具有公式I的化合物，其中Z，Z1，Z2，Z3，R3a，R3b和Rb如本文所定义，是ERK激酶抑制剂。还公开了用于治疗过度增殖性疾病的组合物和方法。
• SERINE/THREONINE KINASE INHIBITORS FOR THE TREATMENT OF HYPERPROLIFERATIVE!DISEASES
  申请人：Array Biopharma, Inc.

  公开号：EP2888247A1

  公开（公告）日：2015-07-01
• SERINE/THREONINE KINASE INHIBITORS FOR THE TREATMENT OF HYPERPROLIFERATIVE DISEASES
  申请人：Array Biopharma, Inc.

  公开号：EP2888247B1

  公开（公告）日：2020-03-25
• INTRACELLULAR CALCIUM MODULATION FOR CANCER TREATMENT
  申请人：Zeilig Charles E.

  公开号：US20140065246A1

  公开（公告）日：2014-03-06

  Tumor cells exhibit consistent abnormalities in calcium regulation. The present disclosure teaches methods by which such differences are exploited to induce Apoptosis selectively in tumor/cancer cells while sparing normal cells. These methods are based upon employing drugs that, acting in synergistic combinations, trigger selective killing of malignant cells. Since the invention is based upon fundamental cell cycle requirements, to the extent that calcium handling abnormalities are a general characteristic of the malignant state, the methods presented here are widely applicable regardless of tissue of origin and degree of cellular de-differentiation.