Facile synthesis of borofragments and their evaluation in activity-based protein profiling.

about

Boron's journey: advances in the study and application of pharmacokinetics.Synthesis of α-aminoboronic acids.Multicomponent mapping of boron chemotypes furnishes selective enzyme inhibitors.The versatility of boron in biological target engagement.

P2860

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P2860

Facile synthesis of borofragments and their evaluation in activity-based protein profiling.

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http://www.wikidata.org/entity/Q43148837

description

2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

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2015年學術文章

@yue

2015年學術文章

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name

Facile synthesis of borofragme ...... ivity-based protein profiling.

@en

Facile synthesis of borofragme ...... ivity-based protein profiling.

@nl

type

Item

label

Facile synthesis of borofragme ...... ivity-based protein profiling.

@en

Facile synthesis of borofragme ...... ivity-based protein profiling.

@nl

prefLabel

Facile synthesis of borofragme ...... ivity-based protein profiling.

@en

Facile synthesis of borofragme ...... ivity-based protein profiling.

@nl

P1476

Facile synthesis of borofragme ...... ivity-based protein profiling.

@en

P2093

Adam Zajdlik

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Andrei K Yudin

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

Armand B Cognetta

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

Conor C G Scully

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

Jeffrey D St Denis

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

Micah J Niphakis

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

Shinya Adachi

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

Zhi He

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P2860

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Omuralide and vibralactone: differences in the proteasome- β-lactone-γ-lactam binding scaffold alter target preferences

Click Chemistry: Diverse Chemical Function from a Few Good Reactions

Selectivity of kinase inhibitor fragments.

Discovering potent and selective reversible inhibitors of enzymes in complex proteomes.

Academic cross-fertilization by public screening yields a remarkable class of protein phosphatase methylesterase-1 inhibitors.

Synthesis of amidomethyltrifluoroborates and their use in cross-coupling reactions

Mitsunobu and related reactions: advances and applications.

Click-generated triazole ureas as ultrapotent in vivo-active serine hydrolase inhibitors.

P304

3608-3611

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P31

scholarly article

P356

10.1039/C4CC09107H

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P407

English

P433

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P478

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

P50

Benjamin Cravatt III

P577

2015-02-01T00:00:00Z

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25633248

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P932

4330092

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Facile synthesis of borofragments and their evaluation in activity-based protein profiling.

about

P2860

P2860

Facile synthesis of borofragments and their evaluation in activity-based protein profiling.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932