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

2-氨基-1-[4-(甲基磺酰基)苯基]-1-乙酮盐酸盐 | 102871-96-5

中文名称
2-氨基-1-[4-(甲基磺酰基)苯基]-1-乙酮盐酸盐
中文别名
——
英文名称
2-amino-1-[4-(methylsulfonyl)phenyl]-ethanone hydrochloride
英文别名
2-amino-1-(4-(methylsulfonyl)phenyl)ethanone hydrochloride;4-(methylsulfonyl)phenacylamine hydrochloride;2-amino-1-(4-methanesulfonyl-phenyl)-ethanone; hydrochloride;2-Amino-1-(4-methansulfonyl-phenyl)-aethanon; Hydrochlorid;2-Amino-1-[4-(methylsulfonyl)phenyl]-1-ethanone hydrochloride;2-amino-1-(4-methylsulfonylphenyl)ethanone;hydrochloride
2-氨基-1-[4-(甲基磺酰基)苯基]-1-乙酮盐酸盐化学式
CAS
102871-96-5
化学式
C9H11NO3S*ClH
mdl
——
分子量
249.718
InChiKey
JQZLJYCNKBOYGK-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

  • 熔点:
    300°
  • 沸点:
    300°C

计算性质

  • 辛醇/水分配系数(LogP):
    0.65
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    85.6
  • 氢给体数:
    2
  • 氢受体数:
    4

安全信息

  • 危险等级:
    IRRITANT
  • 海关编码:
    2922399090

SDS

SDS:4f8eaed38b446a292bc85f130bac6e6f
查看

反应信息

  • 作为反应物:
    描述:
    2-氨基-1-[4-(甲基磺酰基)苯基]-1-乙酮盐酸盐氢氧化钾三乙胺 作用下, 以 乙醇 为溶剂, 反应 3.0h, 生成 1-(4-Bromophenyl)-5-(4-methylsulfonylphenyl)-2-methylthioimidazole
    参考文献:
    名称:
    Design, synthesis, and biological evaluation of substituted 2-alkylthio-1,5-diarylimidazoles as selective COX-2 inhibitors
    摘要:
    A new type of 1-aryl-5-(4-methylsulfonylphenyl)imidazoles, possessing C-2 alkylthio (We or SEt) substituents, were designed and synthesized for evaluation as selective cyclooxygenase-2 (COX-2) inhibitors with in vivo anti-inflammatory activity. The compound, 1-(4-bromophenyl)-5-(4-methylsulfonylphenyl)-2-methylthioimidazole (11g), was the most potent and selective COX-2 inhibitor (COX-2 IC(50) = 0.43 mu M with no inhibition of COX-1 up to 25 mu M) relative to the reference drug celecoxib (COX-2 IC(50) = 0.21 mu M with no inhibition of COX-1 up to 25 mu M) and also showed very good anti-inflammatory activity compared to celecoxib in carrageenan-induced rat paw edema assay. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2006.12.041
  • 作为产物:
    描述:
    2-amino-1-(4-(methylsulfonyl)phenyl)ethanone盐酸 作用下, 以 乙醇 为溶剂, 反应 2.0h, 以53%的产率得到2-氨基-1-[4-(甲基磺酰基)苯基]-1-乙酮盐酸盐
    参考文献:
    名称:
    [EN] MTH1 INHIBITORS FOR TREATMENT OF CANCER
    [FR] INHIBITEURS MTH1 POUR LE TRAITEMENT DU CANCER
    摘要:
    公式I的化合物(I)或其药用可接受的盐。该化合物在治疗癌症中很有用。
    公开号:
    WO2015187088A1
点击查看最新优质反应信息

文献信息

  • [EN] N-CYCLOPROPYL-N-PIPERIDINYL-AMIDES, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AND USES THEREOF<br/>[FR] N-CYCLOPROPYL-N-PIPÉRIDINYL-AMIDES, COMPOSITIONS PHARMACEUTIQUES LES CONTENANT ET LEURS UTILISATIONS
    申请人:BOEHRINGER INGELHEIM INT
    公开号:WO2014019967A1
    公开(公告)日:2014-02-06
    The present invention relates to compounds of general formula (I), wherein R1, LP, HetAr1, (Het)Ar2 and n are as defined in the application, which have valuable pharmacological properties, and in particular bind to the GPR119 receptor and modulate its activity.
    本发明涉及一般式(I)的化合物,其中R1、LP、HetAr1、(Het)Ar2和n如申请中所定义,具有有价值的药理特性,特别是结合GPR119受体并调节其活性。
  • N-CYCLOPROPYL-N-PIPERIDINYL-AMIDES, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AND USES THEREOF
    申请人:NOSSE Bernd
    公开号:US20140045823A1
    公开(公告)日:2014-02-13
    The present invention relates to compounds of general formula I, wherein R 1 , L P , HetAr 1 , (Het)Ar 2 and n are as defined in the application, which have valuable pharmacological properties, and in particular bind to the GPR119 receptor and modulate its activity.
    本发明涉及一般式I的化合物, 其中R 1 ,LP,HetAr 1 ,(Het)Ar 2 和n如申请中所定义,具有有价值的药理特性,特别是结合GPR119受体并调节其活性。
  • [EN] MTH1 INHIBITORS FOR TREATMENT OF INFLAMMATORY AND AUTOIMMUNE CONDITIONS<br/>[FR] INHIBITEURS DE MTH1 DESTINÉS AU TRAITEMENT DES ÉTATS INFLAMMATOIRES ET AUTO-IMMUNS
    申请人:THOMAS HELLEDAYS STIFTELSE FÖR MEDICINSK FORSKNING
    公开号:WO2015187089A1
    公开(公告)日:2015-12-10
    A compound of formula (I), or a pharmaceutically acceptable salt thereof, for use in the treatment of autoimmune diseases and inflammatory conditions.
    化合物的化学式(I),或其药学上可接受的盐,用于治疗自身免疫性疾病和炎症性疾病。
  • MTH1 inhibitors for treatment of inflammatory and autoimmune conditions
    申请人:THOMAS HELLEDAYS STIFTELSE FOR MEDICINSK FORSKNING
    公开号:US10064869B2
    公开(公告)日:2018-09-04
    A compound of formula (I), or a pharmaceutically acceptable salt thereof, for use in the treatment of autoimmune diseases and inflammatory conditions.
    用于治疗自身免疫性疾病和炎症的式 (I) 化合物或其药学上可接受的盐。
  • MTH1 inhibitors for treatment of cancer
    申请人:THOMAS HELLEDAYS STIFTELSE FOR MEDICINSK FORSKNING
    公开号:US10179790B2
    公开(公告)日:2019-01-15
    A compound of formula I, (I) or a pharmaceutically-acceptable salt thereof. The compound is useful in the treatment of cancer.
    式 I、(I) 的化合物或其药学上可接受的盐。该化合物可用于治疗癌症。
查看更多