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

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  • 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
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