Organometallic Nucleosides: Synthesis and Biological Evaluation of Substituted Dicobalt Hexacarbonyl 2'-Deoxy-5-oxopropynyluridines.

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Organometallic Nucleosides: Synthesis and Biological Evaluation of Substituted Dicobalt Hexacarbonyl 2'-Deoxy-5-oxopropynyluridines.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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2018年學術文章

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name

Organometallic Nucleosides: Sy ...... '-Deoxy-5-oxopropynyluridines.

@en

Organometallic Nucleosides: Sy ...... '-Deoxy-5-oxopropynyluridines.

@nl

type

Item

label

Organometallic Nucleosides: Sy ...... '-Deoxy-5-oxopropynyluridines.

@en

Organometallic Nucleosides: Sy ...... '-Deoxy-5-oxopropynyluridines.

@nl

prefLabel

Organometallic Nucleosides: Sy ...... '-Deoxy-5-oxopropynyluridines.

@en

Organometallic Nucleosides: Sy ...... '-Deoxy-5-oxopropynyluridines.

@nl

P1476

Organometallic Nucleosides: Sy ...... '-Deoxy-5-oxopropynyluridines.

@en

P2093

Agnieszka Mikus

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Dariusz Korczyński

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Ferman A Chavez

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Karolina Królewska-Golińska

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Kraig A Wheeler

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Renata Kaczmarek

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Roman Dembinski

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An organometallic structure-activity relationship study reveals the essential role of a Re(CO)3 moiety in the activity against gram-positive pathogens including MRSA.

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Organometallic nucleosides induce non-classical leukemic cell death that is mitochondrial-ROS dependent and facilitated by TCL1-oncogene burden.

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Synthesis and EPR studies of 2'-deoxyuridines with alkynyl, rodlike linkages.

P304

237-247

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P31

scholarly article

P356

10.1002/OPEN.201700168

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2018-01-18T00:00:00Z

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P698

29531887

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P932

5838391

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