(3R,6R)-1,6-dimethylpiperidin-3-amine

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: (3R,6R)-1,6-dimethylpiperidin-3-amine
• 化学式: C₇H₁₆N₂
• 分子量: 128.22
• InChiKey: LTXJSFOJLSNNLC-RNFRBKRXSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.3
• 重原子数：
  9
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  29.3
• 氢给体数：
  1
• 氢受体数：
  2

文献信息

• Inhibitors of cyclin-dependent kinase 7 (CDK7)
  申请人：Syros Pharmaceuticals, Inc.

  公开号：US10738067B2

  公开（公告）日：2020-08-11

  The present invention provides various compositions, including compounds of Formula (I) or (Ia), or a species thereof, and pharmaceutically acceptable salts, solvates (e.g., hydrates), stereoisomer, tautomers, isotopic and other specified forms thereof. Also provided are methods (or uses) and kits involving the compounds or pharmaceutically acceptable compositions containing them for treating or preventing a disease (e.g., a proliferative disease such as cancer) in a subject. Administration of a compound or pharmaceutical composition described herein is expected to inhibit cyclin-dependent kinase 7 (CDK7), and thereby, induce apoptosis in tumor cells in the subject.

  本发明提供了各种组合物，包括式(I)或(Ia)化合物或其种类，以及其药学上可接受的盐、溶解物（如水合物）、立体异构体、同分异构体、同位素和其它特定形式。还提供了涉及这些化合物或含有它们的药学上可接受的组合物的方法（或用途）和试剂盒，用于治疗或预防受试者的疾病（如癌症等增殖性疾病）。服用本文所述的化合物或药物组合物有望抑制细胞周期蛋白依赖性激酶7（CDK7），从而诱导受试者体内肿瘤细胞的凋亡。
• Inhibitors of cyclin dependent kinase 7 (CDK7)
  申请人：Syros Pharmaceuticals, Inc.

  公开号：US11311542B2

  公开（公告）日：2022-04-26

  The present invention provides, inter alia, compounds having the structures of formulas described herein; pharmaceutically acceptable salts, solvates, hydrates, tautomers, and isotopic forms thereof; and compositions (e.g., pharmaceutical compositions and kits) containing one or more of the foregoing. Also provided are methods of administering and uses involving the compounds and/or pharmaceutical compositions for treating or preventing disease. The disease can be a proliferative disease, such as a cancer (e.g., a blood cancer (e.g., a leukemia or lymphoma), a brain cancer, a breast cancer, melanoma, multiple myeloma, or an ovarian cancer) a benign neoplasm, pathologic angiogenesis, or a fibrotic disease. While no aspect of the invention is limited by the biological events that may transpire, administering a compound or other composition described herein may selectively inhibit the aberrant expression or activity of cyclin-dependent kinase 7 (CDK7) and, thereby, induce cellular apoptosis and/or inhibit the transcription of disease-related genes in the patient (or in a biological sample).

  本发明特别提供了具有本文所述公式结构的化合物；其药学上可接受的盐、溶液剂、水合物、同系物和同位素形式；以及含有一种或多种上述物质的组合物（如药物组合物和试剂盒）。此外，还提供了治疗或预防疾病的化合物和/或药物组合物的施用方法和用途。疾病可以是增殖性疾病，如癌症（如血癌（如白血病或淋巴瘤）、脑癌、乳腺癌、黑色素瘤、多发性骨髓瘤或卵巢癌）良性肿瘤、病理性血管生成或纤维化疾病。虽然本发明的任何方面都不受可能发生的生物事件的限制，但施用本文所述的化合物或其他组合物可选择性地抑制细胞周期蛋白依赖性激酶7（CDK7）的异常表达或活性，从而诱导细胞凋亡和/或抑制患者（或生物样本）中疾病相关基因的转录。
• Inhibitors of Cyclin-Dependent Kinase 7 (CDK7)
  申请人：Syros Pharmaceuticals, Inc.

  公开号：US20200190126A1

  公开（公告）日：2020-06-18

  The present invention provides various compositions, including compounds of Formula (I) or (Ia), or a species thereof, and pharmaceutically acceptable salts, solvates (e.g., hydrates), stereoisomer, tautomers, isotopic and other specified forms thereof. Also provided are methods (or uses) and kits involving the compounds or pharmaceutically acceptable compositions containing them for treating or preventing a disease (e.g., a proliferative disease such as cancer) in a subject. Administration of a compound or pharmaceutical composition described herein is expected to inhibit cyclin-dependent kinase 7 (CDK7), and thereby, induce apoptosis in tumor cells in the subject.
• METHODS OF TREATING CANCER IN BIOMARKER-IDENTIFIED PATIENTS WITH NON-COVALENT INHIBITORS OF CYCLIN-DEPENDENT KINASE 7 (CDK7)
  申请人：Syros Pharmaceuticals, Inc.

  公开号：US20210401859A1

  公开（公告）日：2021-12-30

  The present invention relates to methods of identifying patients suffering from various types of cancer who are more likely to respond to treatment with a CDK7 inhibitor conforming to structural Formula (I), (Ia), a species thereof, or a specified form thereof (as described herein), either when administered or used alone or in combination with a second therapeutic agent (e.g., another anti-cancer therapy). Patients are identified based on one or more features (e.g., gene copy number or expression level) of certain biomarkers (e.g., RB1 or another member of the E2F pathway). In addition, the present invention relates to methods of treating an identified patient with a compound conforming to structural Formula (I), (Ia), a species thereof, or a specified form thereof, either alone or in combination with a second therapeutic agent. In another aspect, the present invention features kits including instructions for treating a patient identified as described herein.
• INHIBITORS OF CYCLIN DEPENDENT KINASE 7 (CDK7)
  申请人：Syros Pharmaceuticals, Inc.

  公开号：US20210379065A1

  公开（公告）日：2021-12-09

  The present invention provides, inter alia, compounds having the structures of formulas described herein; pharmaceutically acceptable salts, solvates, hydrates, tautomers, and isotopic forms thereof; and compositions (e.g., pharmaceutical compositions and kits) containing one or more of the foregoing. Also provided are methods of administering and uses involving the compounds and/or pharmaceutical compositions for treating or preventing disease. The disease can be a proliferative disease, such as a cancer (e.g., a blood cancer (e.g., a leukemia or lymphoma), a brain cancer, a breast cancer, melanoma, multiple myeloma, or an ovarian cancer) a benign neoplasm, pathologic angiogenesis, or a fibrotic disease. While no aspect of the invention is limited by the biological events that may transpire, administering a compound or other composition described herein may selectively inhibit the aberrant expression or activity of cyclin-dependent kinase 7 (CDK7) and, thereby, induce cellular apoptosis and/or inhibit the transcription of disease-related genes in the patient (or in a biological sample).