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

3-[[(2S)-1-hydroxybutan-2-yl]amino]propane-1-sulfonic Acid | 303956-82-3

中文名称
——
中文别名
——
英文名称
3-[[(2S)-1-hydroxybutan-2-yl]amino]propane-1-sulfonic Acid
英文别名
——
3-[[(2S)-1-hydroxybutan-2-yl]amino]propane-1-sulfonic Acid化学式
CAS
303956-82-3
化学式
C7H17NO4S
mdl
——
分子量
211.28
InChiKey
KRTOESVSBQOMBK-ZETCQYMHSA-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):
    -3
  • 重原子数:
    13
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    95
  • 氢给体数:
    3
  • 氢受体数:
    5

文献信息

  • Compositions and methods for treating amyloidosis
    申请人:Queen's University at Kingston
    公开号:US20040198832A1
    公开(公告)日:2004-10-07
    Therapeutic compounds and methods for modulating amyloid aggregation in a subject, whatever its clinical setting, are described. Amyloid aggregation is modulated by the administration to a subject of an effective amount of a therapeutic compound of the formula 1 or a pharmaceutically acceptable salt or ester, such that modulation of amyloid aggregation occurs. R 1 and R 2 are each independently a hydrogen atom or a substituted or unsubstituted aliphatic or aryl group. Z and Q are each independently a carbonyl (C═O), thiocarbonyl (C═S), sulfonyl (SO 2 ), or sulfoxide (S═O) group. “k” and “m” are 0 or 1, provided when k is 1, R 1 is not a hydrogen atom, and when m is 1, R 2 is not a hydrogen atom. In an embodiment, at least one of k or m must equal 1. “p” and “s” are each independently positive integers selected such that the biodistribution of the therapeutic compound for an intended target site is not prevented while maintaining activity of the therapeutic compound. T is a linking group and Y is a group of the formula -A X wherein A is an anionic group at physiological pH, and X is a cationic group.
    本文描述了用于调节淀粉样蛋白聚集的治疗化合物和方法,无论其临床设置如何。通过向受试者施用公式1的治疗化合物的有效量或其药学上可接受的盐或酯,从而调节淀粉样蛋白聚集。其中,R1和R2分别独立地为氢原子或取代或未取代的脂肪族或芳香族基团。Z和Q分别独立地为羰基(C═O)、硫代羰基(C═S)、磺酰基(SO2)或亚磺酸基(S═O)基团。“k”和“m”为0或1,当k为1时,R1不是氢原子,当m为1时,R2不是氢原子。在一种实施方式中,k或m中至少有一个必须等于1。“p”和“s”分别是正整数,选取这些正整数使治疗化合物的生物分布不会阻止预期的靶位点,并保持治疗化合物的活性。T是连接基团,Y是公式-A X的基团,其中A是生理pH下的阴离子基团,X是阳离子基团。
  • Methods and compositions for treating amyloid-related diseases
    申请人:Kong Xianqi
    公开号:US20070010573A1
    公开(公告)日:2007-01-11
    Methods, compounds, pharmaceutical compositions and kits are described for treating or preventing amyloid-related disease.
    描述了用于治疗或预防与淀粉样蛋白相关的疾病的方法、化合物、制药组合物和试剂盒。
  • Methods and Compositions for Treating Amyloid-Related Diseases
    申请人:KONG Xianqi
    公开号:US20100190753A1
    公开(公告)日:2010-07-29
    Methods, compounds, pharmaceutical compositions and kits are described for treating or preventing amyloid-+related disease.
    本文描述了用于治疗或预防淀粉样蛋白相关疾病的方法、化合物、药物组合物和试剂盒。
  • METHODS AND COMPOSITIONS FOR TREATING AMYLOID-RELATED DISEASES
    申请人:Kong Xianqi
    公开号:US20100113591A1
    公开(公告)日:2010-05-06
    Methods, compounds, pharmaceutical compositions and kits are described for treating or preventing amyloid-related disease.
    本发明涉及用于治疗或预防淀粉样蛋白相关疾病的方法、化合物、制药组合物和试剂盒。
  • Amyloid targeting imaging agents and uses thereof
    申请人:——
    公开号:US20020115717A1
    公开(公告)日:2002-08-22
    Amyloid-targeting imaging agents such as radiolabeled amyloid targeting molecules and amyloid targeting molecule-chelator conjugates for imaging, e.g., amyloid plaques in vivo, and/or for the treatment of amyloidosis disorders. The invention provides amyloid-targeting imaging agents that are useful for imaging sites of amyloid disease. Imaging agents of the invention are capable of binding specifically to amyloid plaques, as an aid in diagnosis and/or early treatment of amyloidosis disorders.
    淀粉样蛋白靶向成像剂,如放射性标记的淀粉样蛋白靶向分子和淀粉样蛋白靶向分子-螯合剂共轭物,用于例如体内淀粉样蛋白斑块的成像,和/或用于淀粉样变性疾病的治疗。本发明提供的淀粉样蛋白靶向成像剂可用于淀粉样蛋白疾病部位的成像。本发明的成像剂能够与淀粉样蛋白斑块特异性结合,有助于淀粉样变性疾病的诊断和/或早期治疗。
查看更多