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(4-(4-amino-1H-pyrazol-1-yl)piperidin-1-yl)(1-methylcyclopropyl)methanone

中文名称
——
中文别名
——
英文名称
(4-(4-amino-1H-pyrazol-1-yl)piperidin-1-yl)(1-methylcyclopropyl)methanone
英文别名
[4-(4-Aminopyrazol-1-yl)piperidin-1-yl]-(1-methylcyclopropyl)methanone;[4-(4-aminopyrazol-1-yl)piperidin-1-yl]-(1-methylcyclopropyl)methanone
(4-(4-amino-1H-pyrazol-1-yl)piperidin-1-yl)(1-methylcyclopropyl)methanone化学式
CAS
——
化学式
C13H20N4O
mdl
——
分子量
248.328
InChiKey
TXMRGRLLUIJYBI-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    0.3
  • 重原子数:
    18
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.69
  • 拓扑面积:
    64.2
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] NOVEL KINASE INHIBITORS<br/>[FR] NOUVEAUX INHIBITEURS DE KINASES
    申请人:ORIGENIS GMBH
    公开号:WO2014060113A1
    公开(公告)日:2014-04-24
    The present invention relates to novel compounds of formula (I) that are capable of inhibiting one or more kinases, especially SYK (Spleen Tyrosine Kinase), LRRK2 (Leucine-rich repeat kinase 2) and/or MYLK (Myosin light chain kinase) or mutants thereof. The compounds find applications in the treatment of a variety of diseases. These diseases include autoimmune diseases, inflammatory diseases, bone diseases, metabolic diseases, neurological and neurodegenerative diseases, cancer, cardiovascular diseases, allergies, asthma, alzheimer's disease, parkinson's disease, skin disorders, eye diseases, infectious diseases and hormone-related diseases.
    本发明涉及一种具有公式(I)的新化合物,能够抑制一个或多个激酶,特别是SYK(脾酪氨酸激酶)、LRRK2(富含亮重复的激酶2)和/或MYLK(肌球蛋白轻链激酶)或其突变体。这些化合物在治疗多种疾病中发挥作用。这些疾病包括自身免疫疾病、炎症性疾病、骨疾病、代谢性疾病、神经和神经退行性疾病、癌症、心血管疾病、过敏、哮喘、阿尔茨海默病、帕森病、皮肤疾病、眼部疾病、传染病和激素相关疾病。
  • [EN] PYRAZOLO[4,3-D]PYRIMIDINES AS KINASE INHIBITORS<br/>[FR] PYRAZOLO[4,3-D]PYRIMIDINES UTILES EN TANT QU'INHIBITEURS DE KINASES
    申请人:ORIGENIS GMBH
    公开号:WO2014060112A1
    公开(公告)日:2014-04-24
    The present invention relates to novel compounds of formula (I) that are capable of inhibiting one or more kinases, especially SYK (Spleen Tyrosine Kinase), LRRK2 (Leucine-rich repeat kinase 2) and/or MYLK (Myosin light chain kinase) or mutants thereof. The compounds find applications in the treatment of a variety of diseases. These diseases include autoimmune diseases, inflammatory diseases, bone diseases, metabolic diseases, neurological and neurodegenerative diseases, cancer, cardiovascular diseases, allergies, asthma, alzheimer's disease, parkinson's disease, skin disorders, eye diseases, infectious diseases and hormone-related diseases.
    本发明涉及具有式(I)的新化合物,其能够抑制一个或多个激酶,特别是SYK(脾酪氨酸激酶)、LRRK2(富含亮重复的激酶2)和/或MYLK(肌球蛋白轻链激酶)或其突变体。这些化合物可用于治疗多种疾病。这些疾病包括自身免疫疾病、炎症性疾病、骨疾病、代谢性疾病、神经和神经退行性疾病、癌症、心血管疾病、过敏、哮喘、阿尔茨海默病、帕森病、皮肤疾病、眼部疾病、传染病和激素相关疾病。
  • NOVEL KINASE INHIBITORS
    申请人:ORIGENIS GMBH
    公开号:US20150259340A1
    公开(公告)日:2015-09-17
    The present invention relates to novel compounds of formula (I) that are capable of inhibiting one or more kinases, especially SYK (Spleen Tyrosine Kinase), LRRK2 (Leucine-rich repeat kinase 2) and/or MYLK (Myosin light chain kinase) or mutants thereof. The compounds find applications in the treatment of a variety of diseases. These diseases include autoimmune diseases, inflammatory diseases, bone diseases, metabolic diseases, neurological and neurodegenerative diseases, cancer, cardiovascular diseases, allergies, asthma, alzheimer's disease, parkinson's disease, skin disorders, eye diseases, infectious diseases and hormone-related diseases.
    本发明涉及式(I)的新型化合物,能够抑制一个或多个激酶,特别是SYK(脾酪氨酸激酶)、LRRK2(富含亮重复的激酶2)和/或MYLK(肌球蛋白轻链激酶)或其突变体。这些化合物可用于治疗各种疾病。这些疾病包括自身免疫性疾病、炎症性疾病、骨病、代谢性疾病、神经和神经退行性疾病、癌症、心血管疾病、过敏、哮喘、阿尔茨海默病、帕森病、皮肤疾病、眼部疾病、传染病和与激素相关的疾病。
  • PYRAZOLO[4,3-D]PYRIMIDINES AS KINASE INHIBITORS
    申请人:ORIGENIS GMBH
    公开号:US20150266882A1
    公开(公告)日:2015-09-24
    The present invention relates to novel compounds of formula (I) that are capable of inhibiting one or more kinases, especially SYK (Spleen Tyrosine Kinase), LRRK2 (Leucine-rich repeat kinase 2) and/or MYLK (Myosin light chain kinase) or mutants thereof. The compounds find applications in the treatment of a variety of diseases. These diseases include autoimmune diseases, inflammatory diseases, bone diseases, metabolic diseases, neurological and neurodegenerative diseases, cancer, cardiovascular diseases, allergies, asthma, alzheimer's disease, parkinson's disease, skin disorders, eye diseases, infectious diseases and hormone-related diseases.
    本发明涉及化合物(I)的新型化合物,能够抑制一个或多个激酶,特别是SYK(脾酪氨酸激酶)、LRRK2(富含亮重复的激酶2)和/或MYLK(肌球蛋白轻链激酶)或其突变体。这些化合物在治疗多种疾病方面有应用。这些疾病包括自身免疫疾病、炎症性疾病、骨病、代谢性疾病、神经和神经退行性疾病、癌症、心血管疾病、过敏、哮喘、阿尔茨海默病、帕森病、皮肤疾病、眼病、传染病和激素相关疾病。
  • Kinase inhibitors
    申请人:Origenis GmbH
    公开号:US10000482B2
    公开(公告)日:2018-06-19
    The present invention relates to novel compounds of formula (I) that are capable of inhibiting one or more kinases, especially SYK (Spleen Tyrosine Kinase), LRRK2 (Leucine-rich repeat kinase 2) and/or MYLK (Myosin light chain kinase) or mutants thereof. The compounds find applications in the treatment of a variety of diseases. These diseases include autoimmune diseases, inflammatory diseases, bone diseases, metabolic diseases, neurological and neurodegenerative diseases, cancer, cardiovascular diseases, allergies, asthma, alzheimer's disease, parkinson's disease, skin disorders, eye diseases, infectious diseases and hormone-related diseases.
    本发明涉及能够抑制一种或多种激酶,特别是 SYK(脾酪氨酸激酶)、LRRK2(富亮重复激酶 2)和/或 MYLK(肌球蛋白轻链激酶)或其突变体的新型式(I)化合物。这些化合物可用于治疗多种疾病。这些疾病包括自身免疫性疾病、炎症性疾病、骨病、代谢性疾病、神经和神经退行性疾病、癌症、心血管疾病、过敏、哮喘、老年痴呆症、帕森病、皮肤病、眼病、传染病和激素相关疾病。
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