3-amino-N-(3-(4-amino-4-methylpiperidin-1-yl)pyridin-2-yl)-6-(3-(trifluoromethoxy)pyridin-2-yl)pyrazine-2-carboxamide | 1874276-79-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 3-amino-N-(3-(4-amino-4-methylpiperidin-1-yl)pyridin-2-yl)-6-(3-(trifluoromethoxy)pyridin-2-yl)pyrazine-2-carboxamide
• 英文别名: 3-Amino-N-[3-(4-amino-4-methyl-1-piperidinyl)-2-pyridinyl]-6-[3-(trifluoromethoxy)-2-pyridinyl]-2-pyrazinecarboxamide；3-amino-N-[3-(4-amino-4-methylpiperidin-1-yl)pyridin-2-yl]-6-[3-(trifluoromethoxy)pyridin-2-yl]pyrazine-2-carboxamide
• CAS: 1874276-79-5
• 化学式: C₂₂H₂₃F₃N₈O₂
• 分子量: 488.472
• InChiKey: XNMSYXSCPKOHED-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  35
• 可旋转键数：
  5
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.32
• 拓扑面积：
  145
• 氢给体数：
  3
• 氢受体数：
  12

文献信息

• [EN] PROTEIN KINASE C INHIBITORS AND METHODS OF THEIR USE<br/>[FR] INHIBITEURS DE PROTÉINE KINASE C ET LEURS PROCÉDÉS D'UTILISATION
  申请人：NOVARTIS AG

  公开号：WO2016020864A1

  公开（公告）日：2016-02-11

  PKC inhibitors are disclosed. The PKC inhibitors are useful for treating PKC associated diseases, including certain cancers. The PKC inhibitors have improved efficacy at lower dosage amounts to achieve tumor regression, improved potency, PK profile, absorption, gastrointestinal tolerance and kinase selectivity.

  PKC抑制剂已被披露。这些PKC抑制剂对治疗与PKC相关的疾病，包括某些癌症，非常有用。这些PKC抑制剂在更低剂量下具有改善的疗效，可实现肿瘤的退化，提高了效力、PK特性、吸收、胃肠耐受性和激酶选择性。
• PROTEIN KINASE C INHIBITORS AND METHODS OF THEIR USE
  申请人：VISSER Michael Scott

  公开号：US20160046605A1

  公开（公告）日：2016-02-18

  PKC inhibitors are disclosed. The PKC inhibitors are useful for treating PKC associated diseases, including certain cancers. The PKC inhibitors have improved efficacy at lower dosage amounts to achieve tumor regression, improved potency, PK profile, absorption, gastrointestinal tolerance and kinase selectivity.

  本文披露了PKC抑制剂。这些PKC抑制剂可用于治疗PKC相关疾病，包括某些癌症。这些PKC抑制剂在更低剂量下具有改进的疗效，可实现肿瘤回归，改善了药效、PK剖面、吸收、胃肠耐受性和激酶选择性。
• PROTEIN KINASE C INHIBITORS AND METHODS OF THEIR USE
  申请人：Novartis AG

  公开号：EP3514151A1

  公开（公告）日：2019-07-24

  PKC inhibitors are disclosed. The PKC inhibitors are useful for treating PKC associated diseases, including certain cancers. The PKC inhibitors have improved efficacy at lower dosage amounts to achieve tumor regression, improved potency, PK profile, absorption, gastrointestinal tolerance and kinase selectivity.

  本研究公开了 PKC 抑制剂。这些 PKC 抑制剂可用于治疗 PKC 相关疾病，包括某些癌症。这些 PKC 抑制剂具有更低剂量下的更佳疗效，可实现肿瘤消退，并具有更好的效力、PK 特性、吸收、胃肠道耐受性和激酶选择性。
• Dose and regimen for HDM2-p53 interaction inhibitors
  申请人：Novartis AG

  公开号：US10966978B2

  公开（公告）日：2021-04-06

  The present invention relates to HDM2-p53 interaction inhibitors for use in the treatment of cancer, wherein the drug is administered by a high dose intermittent dosing regimen. The present invention relates in particular to the HDM2-p53 interaction inhibitor HDM20I and the dosing regimen di, d8 of a 4 week cycle.

  本发明涉及用于治疗癌症的HDM2-p53相互作用抑制剂，其中通过大剂量间歇给药方案给药。本发明尤其涉及HDM2-p53相互作用抑制剂HDM20I和4周周期的di、d8给药方案。
• Protein kinase C inhibitors and methods of their use
  申请人：Novartis AG

  公开号：US11059804B2

  公开（公告）日：2021-07-13

  PKC inhibitors are disclosed. The PKC inhibitors are useful for treating PKC associated diseases, including certain cancers. The PKC inhibitors have improved efficacy at lower dosage amounts to achieve tumor regression, improved potency, PK profile, absorption, gastrointestinal tolerance and kinase selectivity.

  本研究公开了 PKC 抑制剂。这些 PKC 抑制剂可用于治疗 PKC 相关疾病，包括某些癌症。这些 PKC 抑制剂具有更低剂量下的更佳疗效，可实现肿瘤消退，并具有更好的效力、PK 特性、吸收、胃肠道耐受性和激酶选择性。