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1-tert-butyl-3-cyclobutyl-1H-pyrazol-5-amine | 817641-86-4

中文名称
——
中文别名
——
英文名称
1-tert-butyl-3-cyclobutyl-1H-pyrazol-5-amine
英文别名
2-tert-butyl-5-cyclobutylpyrazol-3-amine
1-tert-butyl-3-cyclobutyl-1H-pyrazol-5-amine化学式
CAS
817641-86-4
化学式
C11H19N3
mdl
——
分子量
193.292
InChiKey
VZZTXMPAZZZOFX-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

物化性质

  • 沸点:
    331.7±30.0 °C(Predicted)
  • 密度:
    1.15±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    43.8
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2933199090
  • 危险性防范说明:
    P261,P280,P301+P312,P302+P352,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335

SDS

SDS:5f59c5ed2aca05d3955c6d190db7007d
查看

反应信息

  • 作为反应物:
    描述:
    1-tert-butyl-3-cyclobutyl-1H-pyrazol-5-amine乙醇 为溶剂, 反应 44.0h, 生成 ethyl 1-tert-butyl-3-cyclobutyl-4-hydroxy-1H-pyrazolo[3,4-b]pyridine-6-carboxylate
    参考文献:
    名称:
    SUBSTITUTED PYRAZOLO[3,4-b]PYRIDIN-6-CARBOXYLIC ACIDS AND METHOD OF USE
    摘要:
    本发明提供了式(I)的化合物 其中R 1 ,R 2 ,R 3 和R 4 具有规范中定义的任何值,以及其药学上可接受的盐,这些化合物在治疗由CFTR介导和调节的疾病和症状中是有用的,包括囊性纤维化、Sjögren综合征、胰腺功能不全、慢性阻塞性肺病和慢性阻塞性气道疾病。还提供了由一个或多个式(I)的化合物组成的药物组合物。
    公开号:
    US20170101406A1
  • 作为产物:
    描述:
    参考文献:
    名称:
    [EN] N-SULFONYLATED PYRAZOLO[3,4-B]PYRIDIN-6-CARBOXAMIDES AND METHOD OF USE
    [FR] PYRAZOLO[3,4-B]PYRIDIN-6-CARBOXAMIDES N-SULFONYLÉS ET LEUR PROCÉDÉ D'UTILISATION
    摘要:
    本发明提供了一种具有以下结构的化合物(I),其中R1、R2、R3、R4、R5和R6具有规范中定义的任何值,以及其药学上可接受的盐,这些化合物在治疗由CFTR介导和调节的疾病和症状中是有用的,包括囊性纤维化、Sjögren综合征、胰腺功能不全、慢性阻塞性肺病和慢性阻塞性气道疾病。还提供了由一个或多个具有结构(I)的化合物组成的药物组合物。
    公开号:
    WO2017060874A1
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文献信息

  • [EN] PYRAZOLO`3,4-B!PYRIDIN-6-ONES AS GSK-3 INHIBITORS<br/>[FR] PYRAZOLO`3,4-B!PYRIDIN-6-ONES A TITRE D'INHIBITEURS DE GSK-3
    申请人:PFIZER PROD INC
    公开号:WO2005000303A1
    公开(公告)日:2005-01-06
    The invention provides compounds of formula (I), the stereoisomers and prodrugs thereof, and the pharmaceutically acceptable salts of the compounds, stereoisomers, and prodrugs, wherein R1, R2, and R3 are as defined herein; pharmaceutical compositions thereof; and use thereof in the treatment of, inter alia, conditions, diseases, and symptoms such as diabetes, dementia, Alzheimer's Disease, stroke, schizophrenia, depression, hair loss, and cancer.
    该发明提供了公式(I)的化合物,其立体异构体和前药,以及该化合物,立体异构体和前药的药用盐,其中R1、R2和R3如本文所定义; 其药物组成; 以及在治疗糖尿病、痴呆症、阿尔茨海默氏病、中风、精神分裂症、抑郁症、脱发和癌症等疾病、疾病和症状中的使用。
  • Pyrazolo[3,4-b]pyridin-6-ones as GSK-3 inhibitors
    申请人:Pfizer Inc
    公开号:US20040266815A1
    公开(公告)日:2004-12-30
    The present invention provides compounds of formula (I) 1 the stereoisomers and prodrugs thereof, and the pharmaceutically acceptable salts of the compounds, stereoisomers, and prodrugs, wherein R 1 , R 2 and R 3 are as defined herein; pharmaceutical formulations thereof; and use thereof in the treatment of, inter alia, conditions, diseases, and symptoms such as bipolar disorder, diabetes, dementia, Alzheimer's Disease, stroke, schizophrenia, depression, hair loss, and cancer.
    本发明提供了式(I)1的化合物及其立体异构体和前药,以及所述化合物、立体异构体和前药的药用可接受盐,其中R1、R2和R3如本文所定义;其药用制剂;以及在治疗躁郁症、糖尿病、痴呆症、阿尔茨海默病、中风、精神分裂症、抑郁症、脱发和癌症等病症、疾病和症状中的使用。
  • GSK-3 inhibitors
    申请人:Wager T. Travis
    公开号:US20050026946A1
    公开(公告)日:2005-02-03
    The invention provides compounds of formula (I) the stereoisomers and prodrugs thereof, and the pharmaceutically acceptable salts of the compounds, stereoisomers, and prodrugs, wherein R 1 , R 2 , and R 3 are as defined herein; pharmaceutical compositions thereof; and use thereof in the treatment of, inter alia, conditions, diseases, and symptoms such as diabetes, dementia, Alzheimer's Disease, stroke, schizophrenia, depression, hair loss, and cancer.
    本发明提供式(I)的化合物及其立体异构体和前药,以及该化合物、立体异构体和前药的药学上可接受的盐;其中R1、R2和R3如本文所定义;药物组合物;以及在治疗糖尿病、痴呆症、阿尔茨海默病、中风、精神分裂症、抑郁症、脱发和癌症等疾病、症状中的应用。
  • Pyrazole derivatives
    申请人:Sanner A. Mark
    公开号:US20050209297A1
    公开(公告)日:2005-09-22
    The invention provides compounds of formula 1 wherein R 1 , R 2 , R 3 , and R 4 are as defined, and their pharmaceutically acceptable salts. Compounds of formula 1 are indicated to have activity inhibiting cdk5, cdk2, and GSK-3. Pharmaceutical compositions and methods comprising compounds of formula 1 for treating and preventing diseases and conditions comprising abnormal cell growth, such as cancer, and neurodegenerative diseases and conditions and those affected by dopamine neurotransmission. Also described are pharmaceutical compositions and methods comprising compounds of formula 1 for treating male fertility and sperm motility; diabetes mellitus; impaired glucose tolerance; metabolic syndrome or syndrome X; polycystic ovary syndrome; adipogenesis and obesity; myogenesis and frailty, for example age-related decline in physical performance; acute sarcopenia, for example muscle atrophy and/or cachexia associated with burns, bed rest, limb immobilization, or major thoracic, abdominal, and/or orthopedic surgery; sepsis; hair loss, hair thinning, and balding; and immunodeficiency.
    本发明提供了式1的化合物,其中R1、R2、R3和R4如定义所示,并且它们的药学上可接受的盐。式1的化合物被指示具有抑制cdk5、cdk2和GSK-3的活性。本发明还描述了包括式1的化合物的药物组合物和方法,用于治疗和预防包括异常细胞生长的疾病和病况,如癌症和神经退行性疾病和病况以及受到多巴胺神经递质影响的疾病和病况。还描述了包括式1的化合物的药物组合物和方法,用于治疗男性生育能力和精子运动能力;糖尿病;糖耐量受损;代谢综合征或综合征X;多囊卵巢综合征;脂肪生成和肥胖症;肌肉生成和衰弱,例如与年龄相关的身体表现下降;急性肌肉萎缩,例如与烧伤、卧床休息、肢体固定或重大胸腔、腹部和/或骨科手术相关的肌肉萎缩和/或消瘦;败血症;脱发、头发变薄和秃发;以及免疫缺陷症。
  • N-sulfonylated pyrazolo[3,4-b]pyridin-6-carboxamides and method of use
    申请人:AbbVie S.à.r.l.
    公开号:US10259810B2
    公开(公告)日:2019-04-16
    The present invention provides for compounds of formula (I) wherein R1, R2, R3, R4, R5, and R6 have any of the values defined in the specification, and pharmaceutically acceptable salts thereof, that are useful as agents in the treatment of diseases and conditions mediated and modulated by CFTR, including cystic fibrosis, Sjögren's syndrome, pancreatic insufficiency, chronic obstructive lung disease, and chronic obstructive airway disease. Also provided are pharmaceutical compositions comprised of one or more compounds of formula (I).
    本发明提供了式 (I) 的化合物 其中 R1、R2、R3、R4、R5 和 R6 具有说明书中定义的任一值,及其药学上可接受的盐,可作为治疗由 CFTR 介导和调节的疾病和病症的药物,包括囊性纤维化、Sjögren 综合征、胰腺功能不全、慢性阻塞性肺病和慢性阻塞性气道疾病。还提供了由一种或多种式(I)化合物组成的药物组合物。
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