Expanding the scope of alkyne-mediated bioconjugations utilizing unnatural amino acids.

about

Synthesis and incorporation of a caged tyrosine amino acid possessing a bioorthogonal handle.Development of optimized conditions for Glaser-Hay bioconjugations.Playing with the molecules of life.Utilization of alkyne bioconjugations to modulate protein function.

P2860

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P2860

Expanding the scope of alkyne-mediated bioconjugations utilizing unnatural amino acids.

Item

http://www.wikidata.org/entity/Q42217668

description

2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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2015年论文

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2015年论文

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name

Expanding the scope of alkyne-mediated bioconjugations utilizing unnatural amino acids.

@en

Expanding the scope of alkyne-mediated bioconjugations utilizing unnatural amino acids.

@nl

type

Item

label

Expanding the scope of alkyne-mediated bioconjugations utilizing unnatural amino acids.

@en

Expanding the scope of alkyne-mediated bioconjugations utilizing unnatural amino acids.

@nl

prefLabel

Expanding the scope of alkyne-mediated bioconjugations utilizing unnatural amino acids.

@en

Expanding the scope of alkyne-mediated bioconjugations utilizing unnatural amino acids.

@nl

P1476

Expanding the scope of alkyne-mediated bioconjugations utilizing unnatural amino acids.

@en

P2093

Douglas D Young

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

Johnathan C Maza

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

Zachary M Nimmo

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

P2860

Cu-free click cycloaddition reactions in chemical biology

Bioorthogonal chemistry: fishing for selectivity in a sea of functionality

Hydrolytic stability of hydrazones and oximes

An Evolved Aminoacyl-tRNA Synthetase with Atypical Polysubstrate Specificity,

A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes

Beyond the canonical 20 amino acids: expanding the genetic lexicon

Adding new chemistries to the genetic code

Advances in Bioconjugation

A strain-promoted [3 + 2] azide-alkyne cycloaddition for covalent modification of biomolecules in living systems

Synthesis of naturally occurring polyynes

P304

88-91

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

P31

scholarly article

P356

10.1039/C5CC08287K

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

P407

English

P433

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

P478

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

P577

2015-10-26T00:00:00Z

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

P698

26499242

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

P921

bioconjugation

P932

5461652

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

Expanding the scope of alkyne-mediated bioconjugations utilizing unnatural amino acids.

about

P2860

P2860

Expanding the scope of alkyne-mediated bioconjugations utilizing unnatural amino acids.

description

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type

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P1433

P1476

P2093

P2860

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P356

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P698

P921

P932

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P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P921

P932