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Atulkumar Kamble,Ravindra Kamble,Suneel Dodamani,Sunil Jalalpure,Vijaykumar Rasal,Mahadev Kumbar,Shrinivas Joshi,Sheshagiri Dixit 대한약학회 2017 Archives of Pharmacal Research Vol.40 No.4
In the present paper 5-[40-({4-[(4-aryloxy)methyl]-1H-1,2,3-triazol-1-yl}methyl)[1,10-biphenyl]-2-yl]-1H-tetrazoles(5a–g) and [20 -(1H-tetrazol-5-yl)[1,10-biphenyl]-4-yl]methyl-substituted-1-carbodithioates (11h–q) havebeen designed and synthesized. These compounds weresubjected to docking (against AT1 receptor proteinenzyme in complex with Lisinopril), in vitro angiotensinconverting enzyme inhibition, anti-proliferative, anti-inflammatoryscreening (through egg albumin denaturationinhibition and red blood cell membrane stabilizationassay) and finally anti-fungal activity analyses. Some ofthe compounds have shown significant pharmacologicalproperties.