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2-异丙基-4-嘧啶羧酸 | 1060817-57-3

中文名称
2-异丙基-4-嘧啶羧酸
中文别名
——
英文名称
2-Isopropylpyrimidine-4-carboxylic acid
英文别名
2-propan-2-ylpyrimidine-4-carboxylic acid
2-异丙基-4-嘧啶羧酸化学式
CAS
1060817-57-3
化学式
C8H10N2O2
mdl
——
分子量
166.18
InChiKey
VSALLHNSJLKESM-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:
    293.2±13.0 °C(Predicted)
  • 密度:
    1.200±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.2
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    63.1
  • 氢给体数:
    1
  • 氢受体数:
    4

安全信息

  • WGK Germany:
    3

文献信息

  • [EN] CYCLOBUTYL SUBSTITUTED PYRROLOPYRIDINE AND PYRROLOPYRIMIDINE DERIVATIVES AS JAK INHIBITORS<br/>[FR] DÉRIVÉS PYRROLOPYRIDINE ET PYRROLOPYRIMIDINE À SUBSTITUTION CYCLOBUTYLE UTILISÉS COMME INHIBITEURS DES JAK
    申请人:INCYTE CORP
    公开号:WO2012068450A1
    公开(公告)日:2012-05-24
    The present invention provides cyclobutyl substituted pyrrolopyrimidines and pyrrolopyridines of Formula I: wherein X, Y, Z, L, A, R5, n and m are defined above, as well as their compositions and methods of use, that modulate the activity of Janus kinases (JAKs) and are useful in the treatment of diseases related to the activity of JAKs including, for example, inflammatory disorders, autoimmune disorders, cancer, and other diseases.
    本发明提供了式I的环丁基取代的吡咯嘧啶吡咯吡啶:其中X、Y、Z、L、A、R5、n和m如上定义,以及它们的组合物和使用方法,用于调节Janus激酶(JAKs)的活性,并且在治疗与JAKs活性相关的疾病中是有用的,例如炎症性疾病、自身免疫疾病、癌症和其他疾病。
  • NEW 2-SUBSTITUTED INDAZOLES, METHODS FOR PRODUCING SAME, PHARMACEUTICAL PREPARATIONS THAT CONTAIN SAME, AND USE OF SAME TO PRODUCE DRUGS
    申请人:Bayer Pharma Aktiengesellschaft
    公开号:US20190071432A1
    公开(公告)日:2019-03-07
    The present application relates to novel substituted indazoles, to processes for preparation thereof, to the use thereof alone or in combinations for treatment and/or prophylaxis of diseases, and to the use thereof for production of medicaments for treatment and/or prophylaxis of diseases, especially for treatment and/or prophylaxis of endometriosis and endometriosis-associated pain and other endometriosis-associated symptoms such as dysmenorrhoea, dyspareunia, dysuria and dyschezia, of lymphoma, rheumatoid arthritis, spondyloarthritis (especially psoriatic spondyloarthritis and Bekhterev's disease), lupus erythematosus, multiple sclerosis, macular degeneration, COPD, gout, fatty liver disorders, insulin resistance, neoplastic disorders and psoriasis.
    本申请涉及新型取代吲唑并[1,2,3]三唑化合物,其制备方法,其单独或组合用于治疗和/或预防疾病的用途,以及其用于制备用于治疗和/或预防疾病的药物的用途,特别是用于治疗和/或预防子宫内膜异位症及其相关疼痛和其他子宫内膜异位症症状,如经痛、性交痛、排尿困难和排便困难,淋巴瘤、类风湿关节炎、脊柱关节炎(特别是屑病性脊柱关节炎和贝赫切夫病)、红斑狼疮、多发性硬化、黄斑变性、慢性阻塞性肺病、痛风、脂肪肝疾病、胰岛素抵抗、肿瘤性疾病和屑病。
  • CYCLOBUTYL SUBSTITUTED PYRROLOPYRIDINE AND PYRROLOPYRIMIDINE DERIVATIVES AS JAK INHIBITORS
    申请人:RODGERS JAMES D.
    公开号:US20120149681A1
    公开(公告)日:2012-06-14
    The present invention provides cyclobutyl substituted pyrrolopyrimidines and pyrrolopyridines of Formula I: wherein X, Y, Z, L, A, R 5 , n and m are defined above, as well as their compositions and methods of use, that modulate the activity of Janus kinases (JAKs) and are useful in the treatment of diseases related to the activity of JAKs including, for example, inflammatory disorders, autoimmune disorders, cancer, and other diseases.
    本发明提供了式I中的环丁基取代的吡咯嘧啶吡咯吡啶:其中X、Y、Z、L、A、R5、n和m如上所定义,以及它们的组合物和使用方法,可以调节Janus激酶(JAKs)的活性,并且对于与JAKs活性相关的疾病是有用的,包括例如炎症性疾病、自身免疫性疾病、癌症和其他疾病。
  • CYCLOBUTYL SUBSTITUTED PYRROLOPYRIDINE AND PYRROLOPYRIMIDINES DERIVATIVES AS JAK INHIBITORS
    申请人:Incyte Corporation
    公开号:US20150087632A1
    公开(公告)日:2015-03-26
    The present invention provides cyclobutyl substituted pyrrolopyrimidines and pyrrolopyridines of Formula I: wherein X, Y, Z, L, A, R 5 , n and m are defined above, as well as their compositions and methods of use, that modulate the activity of Janus kinases (JAKs) and are useful in the treatment of diseases related to the activity of JAKs including, for example, inflammatory disorders, autoimmune disorders, cancer, and other diseases.
    本发明提供了公式I的环丁基取代的吡咯嘧啶吡咯吡啶化合物:其中X,Y,Z,L,A,R5,n和m如上所定义,以及它们的组合物和使用方法,调节Janus激酶(JAKs)的活性,并且对于治疗与JAKs活性相关的疾病,例如炎症性疾病,自身免疫性疾病,癌症和其他疾病非常有用。
  • 2-substituted indazoles, methods for producing same, pharmaceutical preparations that contain same, and use of same to produce drugs
    申请人:Bayer Pharma Aktiengesellschaft
    公开号:US10435396B2
    公开(公告)日:2019-10-08
    The present application relates to novel substituted indazoles, to processes for preparation thereof, to the use thereof alone or in combinations for treatment and/or prophylaxis of diseases, and to the use thereof for production of medicaments for treatment and/or prophylaxis of diseases, especially for treatment and/or prophylaxis of endometriosis and endometriosis-associated pain and other endometriosis-associated symptoms such as dysmenorrhoea, dyspareunia, dysuria and dyschezia, of lymphoma, rheumatoid arthritis, spondyloarthritis (especially psoriatic spondyloarthritis and Bekhterev's disease), lupus erythematosus, multiple sclerosis, macular degeneration, COPD, gout, fatty liver disorders, insulin resistance, neoplastic disorders and psoriasis.
    本申请涉及新型取代吲唑、其制备工艺、其单独使用或组合使用以治疗和/或预防疾病,以及其用于生产治疗和/或预防疾病的药物,特别是用于治疗和/或预防子宫内膜异位症、子宫内膜异位症相关疼痛和其他子宫内膜异位症相关症状,如痛经、淋巴瘤、类风湿性关节炎、脊柱关节炎(尤其是屑病性脊柱关节炎和 Bekhterev 病)、红斑狼疮、多发性硬化症、黄斑变性、慢性阻塞性肺病、痛风、脂肪肝、胰岛素抵抗、肿瘤性疾病和屑病。
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