摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

6-(Methylsulfonyl)-1H-indazole | 261953-48-4

中文名称
——
中文别名
——
英文名称
6-(Methylsulfonyl)-1H-indazole
英文别名
6-methylsulfonyl-1H-indazole
6-(Methylsulfonyl)-1H-indazole化学式
CAS
261953-48-4
化学式
C8H8N2O2S
mdl
MFCD12401612
分子量
196.23
InChiKey
XKPZHKXZWDTBOR-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):
    1.5
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.125
  • 拓扑面积:
    71.2
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • [EN] PYRROLOPYRAZINE KINASE INHIBITORS<br/>[FR] INHIBITEURS DE PYRROLOPYRAZINE KINASE
    申请人:HOFFMANN LA ROCHE
    公开号:WO2013030138A1
    公开(公告)日:2013-03-07
    The present invention relates to the use of novel pyrrolopyrazine derivatives of Formula I, wherein the variables are defined as described herein, which inhibit JAK and SYK and are useful for the treatment of auto-immune and inflammatory diseases.
    本发明涉及式I的新型吡咯并吡嗪衍生物的使用,其中变量如本文所述定义,其抑制JAK和SYK,并可用于治疗自身免疫和炎症性疾病。
  • [EN] PYRROLIDINE-PYRAZOLES AS PYRUVATE KINASE ACTIVATORS<br/>[FR] PYRROLIDINE-PYRAZOLES EN TANT QU'ACTIVATEURS DE LA PYRUVATE KINASE
    申请人:GLOBAL BLOOD THERAPEUTICS INC
    公开号:WO2021202796A1
    公开(公告)日:2021-10-07
    The subject matter described herein is directed to pyruvate kinase activating compounds of Formula I and pharmaceutical salts thereof, methods of preparing the compounds, pharmaceutical compositions comprising the compounds and methods of administering the compounds for the treatment of diseases associated with PKR and/or PKM2, such as pyruvate kinase deficiency, sickle cell disease, and beta-thalassemia.
    本文描述的主题是针对式I的丙酮酸激酶激活化合物及其药用盐,制备这些化合物的方法,包含这些化合物的药物组合物以及用于治疗与PKR和/或PKM2相关疾病的化合物的给药方法,例如丙酮酸激酶缺乏症、镰状细胞病和β地中海贫血。
  • PYRROLOPYRAZINE KINASE INHIBITORS
    申请人:Chen Shaoqing
    公开号:US20130059834A1
    公开(公告)日:2013-03-07
    The present invention relates to the use of novel pyrrolopyrazine derivatives of Formula I, wherein the variables are defined as described herein, which inhibit JAK and SYK and are useful for the treatment of auto-immune and inflammatory diseases.
    本发明涉及使用新型吡咯吡嗪衍生物(式I)的使用,其中变量如此处所述,其抑制JAK和SYK并且适用于治疗自身免疫和炎症性疾病。
  • US8658646B2
    申请人:——
    公开号:US8658646B2
    公开(公告)日:2014-02-25
  • [EN] CHEMICAL COMPOUNDS VIII<br/>[FR] COMPOSES CHIMIQUES VIII
    申请人:CEREBRUS PHARM LTD
    公开号:WO2000017170A2
    公开(公告)日:2000-03-30
    A chemical compound of formula (I): wherein R1 to R3 are independently selected from hydrogen and alkyl; R5 is selected from alkylthio, arylthio, alkylsulfoxyl, arylsulfoxyl, alkylsulfonyl and arylsulfonyl; R4, R6, and R7 are independently selected from hydrogen, halogen, hydroxy, alkyl, aryl, alkoxy, aryloxy, alkylthio, arylthio, arylsulfoxyl, alkylsulfoxyl, alkylsulfonyl, arylsulfonyl, amino, monoalkylamino, dialkylamino, nitro, cyano, carboxaldehyde, alkylcarbonyl, arylcarbonyl, aminocarbonyl, monoalkylaminocarbonyl, dialkylaminocarbonyl, alkoxycarbonylamino, aminocarbonyloxy, monoalkylaminocarbonyloxy, dialkylaminocarbonyloxy, monoalkylaminocarbonylamino and dialkylaminocarbonylamino, and pharmaceutically acceptable salts and prodrugs thereof, and the use thereof in therapy, particularly for the treatment of disorders of the central nervous system; damage to the central nervous system; cardiovascular disorders; gastrointestinal disorders; diabetes insipidus; and sleep apnea, and particularly for the treatment of obesity.
查看更多