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戊巴比妥钠 | 57-33-0

中文名称
戊巴比妥钠
中文别名
戊巴比安钠;5-乙基-5-(1-甲基丁基)-2,4,6-三氧代六氢嘧啶钠盐
英文名称
——
英文别名
——
戊巴比妥钠化学式
CAS
57-33-0
化学式
C11H18N2NaO3
mdl
——
分子量
249.26
InChiKey
UAMVYWFSQGYHFV-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):
    0.8
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    75.3
  • 氢给体数:
    2
  • 氢受体数:
    3

文献信息

  • [EN] S-NITROSOMERCAPTO COMPOUNDS AND RELATED DERIVATIVES<br/>[FR] COMPOSÉS DE S-NITROSOMERCAPTO ET DÉRIVÉS APPARENTÉS
    申请人:GALLEON PHARMACEUTICALS INC
    公开号:WO2009151744A1
    公开(公告)日:2009-12-17
    The present invention is directed to mercapto-based and S- nitrosomercapto-based SNO compounds and their derivatives, and their use in treating a lack of normal breathing control, including the treatment of apnea and hypoventilation associated with sleep, obesity, certain medicines and other medical conditions.
    本发明涉及基于巯基和S-亚硝基巯基的SNO化合物及其衍生物,以及它们在治疗正常呼吸控制缺失方面的用途,包括治疗与睡眠、肥胖、某些药物和其他医疗状况相关的呼吸暂停和低通气。
  • COMPOSITIONS AND METHODS FOR INHIBITING CELLULAR ADHESION OR DIRECTING DIAGNOSTIC OR THERAPEUTIC AGENTS TO RGD BINDING SITES
    申请人:Allegro Pharmaceuticals, LLC
    公开号:US20160022763A1
    公开(公告)日:2016-01-28
    Compounds comprising R-G-Cysteic Acid (i.e., R-G-NH—CH(CH 2 —SO 3 H)COOH or Arg-Gly-NH—CH(CH 2 —SO 3 H)COOH) and derivatives thereof, including pharmaceutically acceptable salts, hydrates, stereoisomers, multimers, cyclic forms, linear forms, drug-conjugates, pro-drugs and their derivatives. Also disclosed are methods for making and using such compounds including methods for inhibiting cellular adhesion to RGD binding sites or delivering other diagnostic or therapeutic agents to RGD binding sites in human or animal subjects.
    包括R-G-半胱氨酸(即R-G-NH—CH(CH2—SO3H)COOH或Arg-Gly-NH—CH(CH2—SO3H)COOH)及其衍生物在内的化合物,包括药用可接受的盐、水合物、立体异构体、多聚体、环形形式、线形形式、药物结合物、前药及其衍生物。还公开了制备和使用这类化合物的方法,包括用于抑制细胞对RGD结合位点的粘附或将其他诊断或治疗剂递送到人类或动物主体中的RGD结合位点的方法。
  • 2-Substituted and 4-substituted aryl nitrone compounds
    申请人:Kelly G. Michael
    公开号:US20050182060A1
    公开(公告)日:2005-08-18
    The present invention provides aryl nitrones, compositions comprising the same and methods of their use for the treatment or prevention of oxidative, ischemic, ischemia/reperfusion-related and chemokine mediated conditions.
    本发明提供芳基亚硝基酮,包括其在内的组合物以及它们用于治疗或预防氧化性、缺血性、缺血/再灌注相关和趋化因子介导的疾病的方法。
  • Dibenzyl Amine Compounds and Derivatives
    申请人:Chang George
    公开号:US20070213371A1
    公开(公告)日:2007-09-13
    Dibenzyl amine compounds and derivatives, pharmaceutical compositions containing such compounds and the use of such compounds to elevate certain plasma lipid levels, including high density lipoprotein-cholesterol and to lower certain other plasma lipid levels, such as LDL-cholesterol and triglycerides and accordingly to treat diseases which are exacerbated by low levels of HDL cholesterol and/or high levels of LDL-cholesterol and triglycerides, such as atherosclerosis and cardiovascular diseases in some mammals, including humans.
    二苯基胺化合物及其衍生物,含有这种化合物的药物组合物以及使用这种化合物提高某些血浆脂质水平,包括高密度脂蛋白胆固醇,并降低其他一些血浆脂质水平,如低密度脂蛋白胆固醇和甘油三酯,并据此治疗由高密度脂蛋白胆固醇水平低和/或低密度脂蛋白胆固醇和甘油三酯水平高加重的疾病,如动脉粥样硬化和心血管疾病在某些哺乳动物,包括人类。
  • Macrocyclic Modulators of the Ghrelin Receptor
    申请人:Ocera Therapeutics, Inc.
    公开号:US20180110824A1
    公开(公告)日:2018-04-26
    The present invention provides novel conformationally-defined macrocyclic compounds that have been demonstrated to be selective modulators of the ghrelin receptor (growth hormone secretagogue receptor, GHS-R1a and subtypes, isoforms and variants thereof). Methods of synthesizing the novel compounds are also described herein. These compounds are useful as agonists of the ghrelin receptor and as medicaments for treatment and prevention of a range of medical conditions including, but not limited to, metabolic and/or endocrine disorders, gastrointestinal disorders, cardiovascular disorders, obesity and obesity-associated disorders, central nervous system disorders, genetic disorders, hyperproliferative disorders and inflammatory disorders.
    本发明提供了一种新颖的构象定义明确的大环化合物,已经证明是生长激素分泌素受体(GHS-R1a及其亚型、异构体和变体)的选择性调节剂。本文还描述了合成这些新型化合物的方法。这些化合物可用作生长激素分泌素受体的激动剂,用于治疗和预防一系列医疗状况,包括但不限于代谢和/或内分泌紊乱、胃肠道紊乱、心血管疾病、肥胖和与肥胖相关的疾病、中枢神经系统疾病、遗传疾病、过度增殖性疾病和炎症性疾病。
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