Spontaneous head-to-tail cyclization of unprotected linear peptides with the KAHA ligation.

about

A rapid and clean synthetic approach to cyclic peptides via micro-flow peptide chain elongation and photochemical cyclization: synthesis of a cyclic RGD peptide.Synthetic fermentation of β-peptide macrocycles by thiadiazole-forming ring-closing reactions.

P2860

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P2860

Spontaneous head-to-tail cyclization of unprotected linear peptides with the KAHA ligation.

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http://www.wikidata.org/entity/Q44494125

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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

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name

Spontaneous head-to-tail cycli ...... ptides with the KAHA ligation.

@en

Spontaneous head-to-tail cycli ...... ptides with the KAHA ligation.

@nl

type

Item

label

Spontaneous head-to-tail cycli ...... ptides with the KAHA ligation.

@en

Spontaneous head-to-tail cycli ...... ptides with the KAHA ligation.

@nl

prefLabel

Spontaneous head-to-tail cycli ...... ptides with the KAHA ligation.

@en

Spontaneous head-to-tail cycli ...... ptides with the KAHA ligation.

@nl

P1476

Spontaneous head-to-tail cycli ...... ptides with the KAHA ligation.

@en

P2093

Anatol Luther

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

Florian Rohrbacher

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

Gildas Deniau

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

Jeffrey W Bode

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

P2860

Characteristics of Amyloid-Related Oligomers Revealed by Crystal Structures of Macrocyclic β-Sheet Mimics

Conformational selection of inhibitors and substrates by proteolytic enzymes: implications for drug design and polypeptide processing

Macrocyclic beta-sheet peptides that mimic protein quaternary structure through intermolecular beta-sheet interactions.

Protein ligand design: from phage display to synthetic protein epitope mimetics in human antibody Fc-binding peptidomimetics.

Recent progress in the discovery of macrocyclic compounds as potential anti-infective therapeutics.

How proteins bind macrocycles.

The exploration of macrocycles for drug discovery--an underexploited structural class.

Native chemical ligation applied to the synthesis and bioengineering of circular peptides and proteins.

Macrocycles are great cycles: applications, opportunities, and challenges of synthetic macrocycles in drug discovery.

Contemporary strategies for peptide macrocyclization.

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4889-4896

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P31

scholarly article

P356

10.1039/C5SC01774B

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

P433

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

P478

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

P577

2015-06-10T00:00:00Z

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278160375

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29142720

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P932

5664356

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

Spontaneous head-to-tail cyclization of unprotected linear peptides with the KAHA ligation.

about

P2860

P2860

Spontaneous head-to-tail cyclization of unprotected linear peptides with the KAHA ligation.

description

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type

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P932