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(2R,3R)-N-[2-(4-hydroxyphenyl)ethyl]-3-methoxy-2-methyl-3-[(2S)-pyrrolidin-2-yl]propanamide;hydrobromide | 1307229-21-5

中文名称
——
中文别名
——
英文名称
(2R,3R)-N-[2-(4-hydroxyphenyl)ethyl]-3-methoxy-2-methyl-3-[(2S)-pyrrolidin-2-yl]propanamide;hydrobromide
英文别名
——
(2R,3R)-N-[2-(4-hydroxyphenyl)ethyl]-3-methoxy-2-methyl-3-[(2S)-pyrrolidin-2-yl]propanamide;hydrobromide化学式
CAS
1307229-21-5
化学式
BrH*C17H26N2O3
mdl
——
分子量
387.317
InChiKey
KYBWFQQWURMFRD-YHOVMROISA-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):
    2.03
  • 重原子数:
    23
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.59
  • 拓扑面积:
    70.6
  • 氢给体数:
    4
  • 氢受体数:
    4

反应信息

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文献信息

  • [EN] AURISTATIN TYRAMINE PHOSPHATE SALTS AND AURISTATIN AMINOQUINOLINE DERIVATIVES AND PRODRUGS THEREOF<br/>[FR] SELS DE TYRAMINE PHOSPHATE D'AURISTATINE ET DÉRIVÉS D'AMINOQUINOLÉINE D'AURISTATINE ET PROMÉDICAMENTS DE CEUX-CI
    申请人:UNIV ARIZONA
    公开号:WO2012135440A1
    公开(公告)日:2012-10-04
    The present invention relates to new auristatin compounds and prodrugs thereof, compositions comprising them and uses thereof.
    本发明涉及新的奥利斯泰汀化合物及其前药,包含它们的组合物和用途。
  • Antineoplastic Agents. 592. Highly Effective Cancer Cell Growth Inhibitory Structural Modifications of Dolastatin 10
    作者:George R. Pettit、Fiona Hogan、Steven Toms
    DOI:10.1021/np1007334
    日期:2011.5.27
    The dolastatin series of unique peptides, originally discovered as constituents of the sea hare Dolabella auricularia, is of increasing importance in providing biological leads, especially to new and useful anticancer drugs. Dolastatin 10 and three analogues, minor structural modifications designated auristatins, are currently in human cancer clinical trials. The present study was undertaken to explore delivery to the cancer sites by way of phosphate or quinoline modifications. The initial objectives, auristatin TP as sodium phosphate 3b (GI(50) 10(-2)-10(-4) mu g/mL), auristatin 2-AQ (4, GI(50) 10(-2)-10(-3) mu g/mL), and auristatin 6-AQ(5, GI(50) 10(-4) mu g/mL), exhibited superior cancer cell growth inhibitory properties.
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