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Treatment of K562 cells with the various oxicam complexes and the oxicam ligands showed different inhibition effects in a concentration dependent manner. The cell inhibition was measured after 48 h by the MTT assay.
(A) (A)tThe docked trans-[Cu(Pir)2(THF)2] complex in the binding pocket of BSA using MVD. The complex is depicted in a stick model, with BSA represented in a wireframe model; (B) two-dimensional interactions generated by LIGPLOT+.
(A) The docked trans-[Co(Mel)2(EtOH)2] complex in the binding pocket of BSA using MVD. The complex is depicted in a stick model, with BSA represented in a wireframe model; (B) two-dimensional interactions generated by LIGPLOT+.
(A) (A)tA molecular docking perspective of trans-[Cu(Pir)2(THF)2] with the major groove of DNA using UCSF Chimera. The complex is depicted in a stick model, and DNA is represented in a wireframe model; (B) two-dimensional interactions generated byLIGPLOT+
Molecular docking of the complex with DNA (A) and BSA (B)
Relative energy level diagram for the electronic transition (absorption) of the [Cu(tptz)(dppz)]2+ complex upon binding with CT-DNA
(a) Molecular docking of the Rh(III) complex with DNA. (b) The bases of DNA with dominant interactions with the complex in the active site
Mouteh Gold Complex 1
Mouteh Gold Complex 2
Mouteh Gold Complex 3
Mouteh Gold Complex 4
Mouteh Gold Complex 5
Mouteh Gold Complex 6
Mouteh Gold Complex 7
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