Unusual truncation of N-acylated peptoids under acidic conditions.

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Advances in Development of Antimicrobial Peptidomimetics as Potential Drugs.On-resin N-terminal peptoid degradation: Toward mild sequencing conditions.In situ deprotection and dynamic covalent assembly using a dual role catalyst.

P2860

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P2860

Unusual truncation of N-acylated peptoids under acidic conditions.

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http://www.wikidata.org/entity/Q51075439

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2014 nî lūn-bûn

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2014年の論文

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2014年学术文章

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2014年學術文章

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name

Unusual truncation of N-acylated peptoids under acidic conditions.

@en

Unusual truncation of N-acylated peptoids under acidic conditions.

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type

Item

label

Unusual truncation of N-acylated peptoids under acidic conditions.

@en

Unusual truncation of N-acylated peptoids under acidic conditions.

@nl

prefLabel

Unusual truncation of N-acylated peptoids under acidic conditions.

@en

Unusual truncation of N-acylated peptoids under acidic conditions.

@nl

P1476

Unusual truncation of N-acylated peptoids under acidic conditions.

@en

P2093

Arim Kim

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

Eunsook Park

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

Hyunjung Park

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

Jeongmi Kim

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

Shinae Park

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

Soomin Kim

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

Yong-Uk Kwon

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

P2860

Toward the synthesis of artificial proteins: the discovery of an amphiphilic helical peptoid assembly.

Solid-phase synthesis and characterization of N-methyl-rich peptides.

Efficient solid-phase synthesis of a series of cyclic and linear peptoid-dexamethasone conjugates for the cell permeability studies.

Ring-closing metathesis approaches for the solid-phase synthesis of cyclic peptoids.

Deletion of Ac-NMePhe(1) from [NMePhe(1) ]arodyn under acidic conditions, part 1: effects of cleavage conditions and N-terminal functionality

Peptoid transporters: effects of cationic, amphipathic structure on their cellular uptake

Quantitative evaluation of the relative cell permeability of peptoids and peptides.

The design, synthesis, and evaluation of molecules that enable or enhance cellular uptake: peptoid molecular transporters.

Synthetic receptors with antibody-like binding affinities.

Solid-phase synthesis of N-substituted glycine oligomers (alpha-peptoids) and derivatives.

P304

5222-5226

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P31

scholarly article

P356

10.1039/C3OB42572J

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P433

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

P478

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

P50

Goutam Biswas

P577

2014-07-01T00:00:00Z

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

P698

24918101

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Unusual truncation of N-acylated peptoids under acidic conditions.

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P2860

P2860

Unusual truncation of N-acylated peptoids under acidic conditions.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698