Advanced Search
QSARStudyonAntiarhythmicActivityofSomeMethanesulfonamidoPhenethylaminoDerivativesJiMin,LiuHong,JinSong,LiuLigang,HuaWeiyi,JiNianningDivisionofMedicinalChemistry,ChinaPharmaceuticalUniversity,Nanjing210009AbstractStructuresof12substitutedmethanesulfonamido[J]. Journal of China Pharmaceutical University, 1998, (4): 7-10.
Citation: QSARStudyonAntiarhythmicActivityofSomeMethanesulfonamidoPhenethylaminoDerivativesJiMin,LiuHong,JinSong,LiuLigang,HuaWeiyi,JiNianningDivisionofMedicinalChemistry,ChinaPharmaceuticalUniversity,Nanjing210009AbstractStructuresof12substitutedmethanesulfonamido[J]. Journal of China Pharmaceutical University, 1998, (4): 7-10.
shu

QSARStudyonAntiarhythmicActivityofSomeMethanesulfonamidoPhenethylaminoDerivativesJiMin,LiuHong,JinSong,LiuLigang,HuaWeiyi,JiNianningDivisionofMedicinalChemistry,ChinaPharmaceuticalUniversity,Nanjing210009AbstractStructuresof12substitutedmethanesulfonamido

    Graphical Abstract
    • Abstract
  • Structures of 12 substituted methanesulfonamido phenethylamino derivatives were mimicked by computer aided molecular modeling. The POLYGEN software and the method of clique coordinate transformation were involved in these modeling processes. 12 parameter
    • FullText(HTML)
  • loading
    • References (0)
    • Related Articles

Catalog

    Turn off MathJax
    Article Contents

    Total visits：

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return