The hydrolysis mechanism of the anticancer ruthenium drugs NAMI-A and ICR investigated by DFT-PCM calculations.
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QM/MM molecular dynamics studies of metal binding proteinsAn omics perspective to the molecular mechanisms of anticancer metallo-drugs in the computational microscope era.Fighting Cancer with Transition Metal Complexes: From Naked DNA to Protein and Chromatin Targeting Strategies.Albumin binding and ligand-exchange processes of the Ru(III) anticancer agent NAMI-A and its bis-DMSO analogue determined by ENDOR spectroscopy.Interaction of anticancer Ru(III) complexes with single stranded and duplex DNA model systems.Aquation Is a Crucial Activation Step for Anticancer Action of Ruthenium(II) Polypyridyl Complexes to Trigger Cancer Cell Apoptosis.Platinum Complexes as Anti-Cancer Drugs: Modeling of Structure, Activation and FunctionThe Spectroscopic and Conductive Properties of Ru(II) Complexes with Potential Anticancer Properties
P2860
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P2860
The hydrolysis mechanism of the anticancer ruthenium drugs NAMI-A and ICR investigated by DFT-PCM calculations.
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2008 nî lūn-bûn
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2008年の論文
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2008年学术文章
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2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
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2008年學術文章
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name
The hydrolysis mechanism of th ...... gated by DFT-PCM calculations.
@en
The hydrolysis mechanism of th ...... gated by DFT-PCM calculations.
@nl
type
label
The hydrolysis mechanism of th ...... gated by DFT-PCM calculations.
@en
The hydrolysis mechanism of th ...... gated by DFT-PCM calculations.
@nl
prefLabel
The hydrolysis mechanism of th ...... gated by DFT-PCM calculations.
@en
The hydrolysis mechanism of th ...... gated by DFT-PCM calculations.
@nl
P50
P356
P1476
The hydrolysis mechanism of th ...... gated by DFT-PCM calculations.
@en
P2093
Alessandra Magistrato
Arturo Robertazzi
P304
P356
10.1021/JP710078Y
P407
P577
2008-03-19T00:00:00Z