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-(2-吡啶基磺酰)硫代乙酰胺 | 175276-91-2

中文名称
2-(2-吡啶基磺酰)硫代乙酰胺
中文别名
2-(2-吡啶基磺酰)硫代乙酰胺,97;2-(吡啶-2-磺酰基)乙烷硫代酰胺
英文名称
2-(2-pyridylsulfonyl)-ethanethioamide
英文别名
2-(2-Pyridylsulfonyl)thioacetamide;2-pyridin-2-ylsulfonylethanethioamide
2-(2-吡啶基磺酰)硫代乙酰胺化学式
CAS
175276-91-2
化学式
C7H8N2O2S2
mdl
MFCD00052951
分子量
216.285
InChiKey
SXZDKXKPNUSOTB-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:
    138°C
  • 稳定性/保质期:
    避氧化物

计算性质

  • 辛醇/水分配系数(LogP):
    0
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.142
  • 拓扑面积:
    114
  • 氢给体数:
    1
  • 氢受体数:
    4

安全信息

  • 海关编码:
    2933399090

SDS

SDS:4257ea4a0bbbcae511887152c9de9d58
查看

反应信息

  • 作为反应物:
    描述:
    2-(2-吡啶基磺酰)硫代乙酰胺氢氧化钾草酰氯N,N-二甲基甲酰胺 作用下, 以 乙醇二氯甲烷 为溶剂, 生成 2-(Pyridine-2-sulfonylmethyl)-thiazole-4-carbonyl chloride
    参考文献:
    名称:
    A catch-and-release strategy for the combinatorial synthesis of 4-acylamino-1,3-thiazoles as potential CDK5 inhibitors
    摘要:
    Two-dimensional libraries of 4-acylamino-1,3-thiazoles 9 were prepared via Curtius rearrangement of 1,3-thiazole-4-carbonyl azides 6, trapping of the intermediate isocyanates with oxime resin, and thermal regeneration of the isocyanates from the washed resin in the presence of nucleophiles. Several compounds proved to be selective inhibitors of CDK5/p25 versus the closely homologous CDK2/cyclin A enzyme, with the best analogue (43) possessing over 100-fold selectivity. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(03)00726-1
点击查看最新优质反应信息

文献信息

  • Pyrid-2-one derivatives and methods of use
    申请人:——
    公开号:US20040147561A1
    公开(公告)日:2004-07-29
    Selected compounds are effective for treatment of diseases, such as cell proliferation or apoptosis mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable derivatives thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving stroke, cancer and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.
    所选化合物对于治疗疾病,如细胞增殖或凋亡介导的疾病,具有有效性。该发明涵盖了新颖的化合物、类似物、前药和其药学上可接受的衍生物,以及用于预防和治疗涉及中风、癌症等疾病和其他疾病或病况的药物组合物和方法。该主题发明还涉及制备此类化合物的方法,以及在这些过程中有用的中间体。
  • Design and synthesis of quinolin-2(1H)-one derivatives as potent CDK5 inhibitors
    作者:Wenge Zhong、Hu Liu、Matthew R. Kaller、Charles Henley、Ella Magal、Thomas Nguyen、Timothy D. Osslund、David Powers、Robert M. Rzasa、Hui-Ling Wang、Weiya Wang、Xiaoling Xiong、Jiandong Zhang、Mark H. Norman
    DOI:10.1016/j.bmcl.2007.07.045
    日期:2007.10
    Using active site homology modeling between CDK5 and CDK2, we explored several different chemical series of potent CDK5 inhibitors. In this report, we describe the design, synthesis, and CDK5 inhibitory activities of quinolin-2(1H)-one derivatives.
    细胞周期蛋白依赖性激酶5(CDK5)是一种丝氨酸/苏氨酸蛋白激酶,其失调与许多神经退行性疾病(例如阿尔茨海默氏病,肌萎缩性侧索硬化症和缺血性中风)有关。使用CDK5和CDK2之间的活性位点同源性建模,我们探索了有效的CDK5抑制剂的几种不同化学系列。在此报告中,我们描述了喹啉2(1H)-one衍生物的设计,合成和CDK5抑制活性。
  • 2-OXOPYRIDIN-3-YL THIA(DI)AZOLE DERIVATIVES FOR USE IN THE TREATMENT OF CELL PROLIFERATION AND APOPTOSIS RELATED DISEASES
    申请人:AMGEN INC.
    公开号:EP1575947A1
    公开(公告)日:2005-09-21
  • COMPOSITIONS FOR REGULATING OR MODULATING QUORUM SENSING IN BACTERIA, METHODS OF USING THE COMPOUNDS, AND METHODS OF REGULATING OR MODULATING QUORUM SENSING IN BACTERIA
    申请人:Wang Binghe
    公开号:US20100137249A1
    公开(公告)日:2010-06-03
    The present disclosure encompasses compounds and compositions that are useful as specific AI-2 antagonists for the control of bacterial quorum sensing. Although the AI-2 antagonists according to the present disclosure may not have bactericidal effect, their ability to attenuate virulence, drug resistance, and/or biofilm formation have therapeutic benefits. In addition, the AI-2 antagonists of the present disclosure can also be used as tools to probe bacterial AI-2 functions. The present disclosure also encompasses methods for inhibiting or attenuating microbial virulence, biofilm formation, and drug resistance. The methods are suitable for preventing bacteria from accruing and forming extensive biofilms that may be a health or hygiene hazard or a physical issue, such as in the blockage of water or fuel lines.
  • US8653258B2
    申请人:——
    公开号:US8653258B2
    公开(公告)日:2014-02-18
查看更多

同类化合物

(S)-氨氯地平-d4 (R,S)-可替宁N-氧化物-甲基-d3 (R)-N'-亚硝基尼古丁 (5E)-5-[(2,5-二甲基-1-吡啶-3-基-吡咯-3-基)亚甲基]-2-亚磺酰基-1,3-噻唑烷-4-酮 (5-溴-3-吡啶基)[4-(1-吡咯烷基)-1-哌啶基]甲酮 (5-氨基-6-氰基-7-甲基[1,2]噻唑并[4,5-b]吡啶-3-甲酰胺) (2S)-2-[[[9-丙-2-基-6-[(4-吡啶-2-基苯基)甲基氨基]嘌呤-2-基]氨基]丁-1-醇 (2R,2''R)-(+)-[N,N''-双(2-吡啶基甲基)]-2,2''-联吡咯烷四盐酸盐 黄色素-37 麦斯明-D4 麦司明 麝香吡啶 鲁非罗尼 鲁卡他胺 高氯酸N-甲基甲基吡啶正离子 高氯酸,吡啶 高奎宁酸 马来酸溴苯那敏 马来酸左氨氯地平 顺式-双(异硫氰基)(2,2'-联吡啶基-4,4'-二羧基)(4,4'-二-壬基-2'-联吡啶基)钌(II) 顺式-二氯二(4-氯吡啶)铂 顺式-二(2,2'-联吡啶)二氯铬氯化物 顺式-1-(4-甲氧基苄基)-3-羟基-5-(3-吡啶)-2-吡咯烷酮 顺-双(2,2-二吡啶)二氯化钌(II) 水合物 顺-双(2,2'-二吡啶基)二氯化钌(II)二水合物 顺-二氯二(吡啶)铂(II) 顺-二(2,2'-联吡啶)二氯化钌(II)二水合物 非那吡啶 非洛地平杂质C 非洛地平 非戈替尼 非尼拉朵 非尼拉敏 阿雷地平 阿瑞洛莫 阿培利司N-6 阿伐曲波帕杂质40 间硝苯地平 间-硝苯地平 锇二(2,2'-联吡啶)氯化物 链黑霉素 链黑菌素 银杏酮盐酸盐 铬二烟酸盐 铝三烟酸盐 铜-缩氨基硫脲络合物 铜(2+)乙酸酯吡啶(1:2:1) 铁5-甲氧基-6-甲基-1-氧代-2-吡啶酮 钾4-氨基-3,6-二氯-2-吡啶羧酸酯 钯,二氯双(3-氯吡啶-κN)-,(SP-4-1)-