Synthesis of gem-difluorinated nucleoside analogues of the liposidomycins and evaluation as MraY inhibitors.

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5'-Methylene-triazole-substituted-aminoribosyl uridines as MraY inhibitors: synthesis, biological evaluation and molecular modeling.Total Synthesis of (−)-Caprazamycin A Total Synthesis of (−)-Caprazamycin A

P2860

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P2860

Synthesis of gem-difluorinated nucleoside analogues of the liposidomycins and evaluation as MraY inhibitors.

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2007 nî lūn-bûn

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2007年の論文

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年學術文章

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2007年學術文章

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name

Synthesis of gem-difluorinated ...... evaluation as MraY inhibitors.

@en

Synthesis of gem-difluorinated ...... evaluation as MraY inhibitors.

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type

Item

label

Synthesis of gem-difluorinated ...... evaluation as MraY inhibitors.

@en

Synthesis of gem-difluorinated ...... evaluation as MraY inhibitors.

@nl

prefLabel

Synthesis of gem-difluorinated ...... evaluation as MraY inhibitors.

@en

Synthesis of gem-difluorinated ...... evaluation as MraY inhibitors.

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P1476

Synthesis of gem-difluorinated ...... evaluation as MraY inhibitors.

@en

P2093

Amy E Trunkfield

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Feng-Ling Qing

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

Timothy D H Bugg

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

Xiu-Hua Xu

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

P2860

On the initial stage in peptidoglycan synthesis. Phospho-N-acetylmuramyl-pentapeptide translocase (uridine monophosphate)

Synthesis of analogues of the O-beta-D-ribofuranosyl nucleoside moiety of liposidomycins. Part 1: contribution of the amino group and the uracil moiety upon the inhibition of MraY.

Synthesis of analogues of the O-beta-D-ribofuranosyl nucleoside moiety of liposidomycins. Part 2: role of the hydroxyl groups upon the inhibition of MraY.

Synthesis of the nucleoside moiety of liposidomycins: elucidation of the pharmacophore of this family of MraY inhibitors.

Application of the synthetic aminosugars for glycodiversification: synthesis and antimicrobial studies of pyranmycin.

Multiple drug resistance.

2',2'-Difluoro-deoxycytidine (gemcitabine) incorporation into RNA and DNA of tumour cell lines.

Fluoro carbocyclic nucleosides: synthesis and antiviral activity of 2'- and 6'-fluoro carbocyclic pyrimidine nucleosides including carbocyclic 1-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)-5-methyluracil and carbocyclic 1-(2-deoxy-2-fluoro-beta-D-ara

Synthesis of 2,3-dideoxy-2,2-difluoro-L-glycero-pentofuranosyl nucleosides.

Structure-activity relationships of 2'-deoxy-2',2'-difluoro-L-erythro-pentofuranosyl nucleosides.

P304

157-161

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scholarly article

P356

10.1039/B713068F

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P478

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

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2007-11-16T00:00:00Z

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5772197

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18075661

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Synthesis of gem-difluorinated nucleoside analogues of the liposidomycins and evaluation as MraY inhibitors.

about

P2860

P2860

Synthesis of gem-difluorinated nucleoside analogues of the liposidomycins and evaluation as MraY inhibitors.

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label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698