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

1,3,4-三甲基-2,5-哌嗪二酮 | 182067-63-6

中文名称
1,3,4-三甲基-2,5-哌嗪二酮
中文别名
L-丙氨酸,3,3-二氟-2-甲基-(9CI)
英文名称
1,3,4-trimethylpiperazine-2,5-dione
英文别名
——
1,3,4-三甲基-2,5-哌嗪二酮化学式
CAS
182067-63-6
化学式
C7H12N2O2
mdl
——
分子量
156.184
InChiKey
AMADWOODIDMYTQ-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):
    -0.5
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    40.6
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:511b3ba31a0fa9a37dd58d4fcddcd4d1
查看

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Selectivity in Radical Reactions of Alanylglycine Anhydride Derivatives
    摘要:
    描述了在自由基条件下对N,N′-二取代丙氨酰甘氨酸酐进行官能化的过程。自由基(7)是通过N,N'-二取代丙氨酰甘氨酸酐与N-溴代琥珀酰亚胺反应生成,以及通过与三丁基锡氘反应而产生的,根据N-取代基的不同,会以中等到高的对映选择性进行碳-溴和碳-氘键的形成。
    DOI:
    10.1071/ch9960605
  • 作为产物:
    描述:
    参考文献:
    名称:
    Multi-purpose functionality for the structural elaboration of the piperazine-2,5-dione motif
    摘要:
    Mild methods for controlled C- and N-alkylation of 3-benzyloxycarbonylpiperazine-2,5-diones are reported. The benzyloxylcarbonyl substituent can also serve as latent functionality for N-acyliminium ion formation and subsequent trapping enables installation of new carbon and/or heteroatom substituents. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(02)02571-6
点击查看最新优质反应信息

文献信息

  • [EN] EPIDITHIODIOXOPIPERAZINE COMPOUND OR ITS DERIVATIVES, AND THE USE THEREOF<br/>[FR] COMPOSÉ ÉPIDITHIODIOXOPIPÉRAZINE OU SES DÉRIVÉS, ET LEUR UTILISATION
    申请人:UNIV EWHA IND COLLABORATION
    公开号:WO2014189343A1
    公开(公告)日:2014-11-27
    The present invention relates to an epidithiodioxopiperazine derivative represented by the Chemical Formula 1 or its reduced derivative; a method for preparing a compound represented by Chemical Formula 1 having improved intracellular permeability and mimicking the activity of 2-Cys-Prx in its reduced form in the cells; a pharmaceutical composition for preventing or treating vascular diseases comprising an epidithiodioxopiperazine compound or its derivatives or pharmaceutically acceptable salts thereof as an active ingredient; a drug delivery device for local administration including the pharmaceutical composition; and a pharmaceutical composition for inhibiting melanoma metastasis comprising the epidithiodioxopiperazine compound or its derivatives or pharmaceutically acceptable salts thereof as an active ingredient.
    本发明涉及一种由化学式1表示的二硫代二氧哌嗪衍生物或其还原衍生物;一种制备化学式1所代表的化合物的方法,该化合物具有改善细胞内渗透性并在细胞中模拟其还原形式中2-Cys-Prx的活性;一种用作预防或治疗血管疾病的药物组合物,其包括二硫代二氧哌嗪化合物或其衍生物或其药用盐作为活性成分;一种用于局部给药的药物递送装置,包括该药物组合物;以及一种用作抑制黑色素瘤转移的药物组合物,其包括二硫代二氧哌嗪化合物或其衍生物或其药用盐作为活性成分。
  • EPIDITHIODIOXOPIPERAZINE COMPOUND OR ITS DERIVATIVES, AND THE USE THEREOF
    申请人:EWHA University-Industry Collaboration Foundation
    公开号:US20160222031A1
    公开(公告)日:2016-08-04
    The present invention relates to an epidithiodioxopiperazine derivative represented by the following Chemical Formula 1 or its reduced derivative; a method for preparing a compound represented by Chemical Formula 1 having improved intracellular permeability and mimicking the activity of 2-Cys-Prx in its reduced form in the cells; a pharmaceutical composition for preventing or treating vascular diseases comprising an epidithiodioxopiperazine compound or its derivatives or pharmaceutically acceptable salts thereof as an active ingredient; a drug delivery device for local administration including the pharmaceutical composition; and a pharmaceutical composition for inhibiting melanoma metastasis comprising the epidithiodioxopiperazine compound or its derivatives or pharmaceutically acceptable salts thereof as an active ingredient.
    本发明涉及以下化学式1所表示的表皮二硫二氧哌嗪衍生物或其还原衍生物;一种制备化学式1所表示的化合物的方法,该方法具有改善细胞内渗透性并在其还原形式下模拟2-Cys-Prx在细胞中的活性;一种预防或治疗血管疾病的制药组合物,包括表皮二硫二氧哌嗪化合物或其衍生物或其药学上可接受的盐作为活性成分;一种用于局部给药的药物递送装置,包括该制药组合物;以及一种抑制黑色素瘤转移的制药组合物,包括表皮二硫二氧哌嗪化合物或其衍生物或其药学上可接受的盐作为活性成分。
  • Epidithiodioxopiperazine compound or its derivatives, and the use thereof
    申请人:VASTHERA Co. Ltd.
    公开号:US10450327B2
    公开(公告)日:2019-10-22
    The present invention relates to an epidithiodioxopiperazine derivative represented by the following Chemical Formula 1 or its reduced derivative; a method for preparing a compound represented by Chemical Formula 1 having improved intracellular permeability and mimicking the activity of 2-Cys-Prx in its reduced form in the cells; a pharmaceutical composition for preventing or treating vascular diseases comprising an epidithiodioxopiperazine compound or its derivatives or pharmaceutically acceptable salts thereof as an active ingredient; a drug delivery device for local administration including the pharmaceutical composition; and a pharmaceutical composition for inhibiting melanoma metastasis comprising the epidithiodioxopiperazine compound or its derivatives or pharmaceutically acceptable salts thereof as an active ingredient.
    本发明涉及一种由以下化学式1代表的表二硫代二酮哌嗪衍生物或其还原衍生物;一种制备由化学式1代表的化合物的方法,该化合物具有更好的细胞内渗透性,并能模拟细胞内还原形式的2-Cys-Prx的活性;一种用于预防或治疗血管疾病的药物组合物,其活性成分包括表二硫基二氧代哌嗪化合物或其衍生物或其药学上可接受的盐类;一种用于局部给药的给药装置,其活性成分包括该药物组合物;以及一种用于抑制黑色素瘤转移的药物组合物,其活性成分包括表二硫基二氧代哌嗪化合物或其衍生物或其药学上可接受的盐类。
  • Age-Related Differences in Supervisory Attentional System Functions
    作者:P. Andres、M. Van der Linden
    DOI:10.1093/geronb/55.6.p373
    日期:2000.11.1
    The authors explored the effect of age on executive functions by using 3 tasks (Tower of London, Hayling, and Brixton tests) designed to assess specific executive processes (planning, inhibition, and abstraction of logical rules) that were also sensitive to frontal dysfunction. The performance of elderly participants (n = 48) was significantly poorer than that of young participants (n = 47) in all 3 tasks. Processing speed, measured by means of a color-naming task, explained some but not all of the age-related differences. These results are discussed in terms of general and specific factors in cognitive aging.
  • US7772190B2
    申请人:——
    公开号:US7772190B2
    公开(公告)日:2010-08-10
查看更多

同类化合物

(甲基3-(二甲基氨基)-2-苯基-2H-azirene-2-羧酸乙酯) (±)-盐酸氯吡格雷 (±)-丙酰肉碱氯化物 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素 (S)-(+)-α-氨基-4-羧基-2-甲基苯乙酸 (S)-阿拉考特盐酸盐 (S)-赖诺普利-d5钠 (S)-2-氨基-5-氧代己酸,氢溴酸盐 (S)-2-[3-[(1R,2R)-2-(二丙基氨基)环己基]硫脲基]-N-异丙基-3,3-二甲基丁酰胺 (S)-1-(4-氨基氧基乙酰胺基苄基)乙二胺四乙酸 (S)-1-[N-[3-苯基-1-[(苯基甲氧基)羰基]丙基]-L-丙氨酰基]-L-脯氨酸 (R)-乙基N-甲酰基-N-(1-苯乙基)甘氨酸 (R)-丙酰肉碱-d3氯化物 (R)-4-N-Cbz-哌嗪-2-甲酸甲酯 (R)-3-氨基-2-苄基丙酸盐酸盐 (R)-1-(3-溴-2-甲基-1-氧丙基)-L-脯氨酸 (N-[(苄氧基)羰基]丙氨酰-N〜5〜-(diaminomethylidene)鸟氨酸) (6-氯-2-吲哚基甲基)乙酰氨基丙二酸二乙酯 (4R)-N-亚硝基噻唑烷-4-羧酸 (3R)-1-噻-4-氮杂螺[4.4]壬烷-3-羧酸 (3-硝基-1H-1,2,4-三唑-1-基)乙酸乙酯 (2S,3S,5S)-2-氨基-3-羟基-1,6-二苯己烷-5-N-氨基甲酰基-L-缬氨酸 (2S,3S)-3-((S)-1-((1-(4-氟苯基)-1H-1,2,3-三唑-4-基)-甲基氨基)-1-氧-3-(噻唑-4-基)丙-2-基氨基甲酰基)-环氧乙烷-2-羧酸 (2S)-2,6-二氨基-N-[4-(5-氟-1,3-苯并噻唑-2-基)-2-甲基苯基]己酰胺二盐酸盐 (2S)-2-氨基-3-甲基-N-2-吡啶基丁酰胺 (2S)-2-氨基-3,3-二甲基-N-(苯基甲基)丁酰胺, (2S,4R)-1-((S)-2-氨基-3,3-二甲基丁酰基)-4-羟基-N-(4-(4-甲基噻唑-5-基)苄基)吡咯烷-2-甲酰胺盐酸盐 (2R,3'S)苯那普利叔丁基酯d5 (2R)-2-氨基-3,3-二甲基-N-(苯甲基)丁酰胺 (2-氯丙烯基)草酰氯 (1S,3S,5S)-2-Boc-2-氮杂双环[3.1.0]己烷-3-羧酸 (1R,4R,5S,6R)-4-氨基-2-氧杂双环[3.1.0]己烷-4,6-二羧酸 齐特巴坦 齐德巴坦钠盐 齐墩果-12-烯-28-酸,2,3-二羟基-,苯基甲基酯,(2a,3a)- 齐墩果-12-烯-28-酸,2,3-二羟基-,羧基甲基酯,(2a,3b)-(9CI) 黄酮-8-乙酸二甲氨基乙基酯 黄荧菌素 黄体生成激素释放激素 (1-5) 酰肼 黄体瑞林 麦醇溶蛋白 麦角硫因 麦芽聚糖六乙酸酯 麦根酸 麦撒奎 鹅膏氨酸 鹅膏氨酸 鸦胆子酸A甲酯 鸦胆子酸A 鸟氨酸缩合物