Progress towards the broad use of non-peptide synthetic macrocycles in drug discovery.

about

Progress towards the broad use of non-peptide synthetic macrocycles in drug discovery.

Item

http://www.wikidata.org/entity/Q47849835

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

@zh-hant

name

Progress towards the broad use of non-peptide synthetic macrocycles in drug discovery.

@en

Progress towards the broad use of non-peptide synthetic macrocycles in drug discovery.

@nl

type

Item

label

Progress towards the broad use of non-peptide synthetic macrocycles in drug discovery.

@en

Progress towards the broad use of non-peptide synthetic macrocycles in drug discovery.

@nl

prefLabel

Progress towards the broad use of non-peptide synthetic macrocycles in drug discovery.

@en

Progress towards the broad use of non-peptide synthetic macrocycles in drug discovery.

@nl

P1476

Progress towards the broad use of non-peptide synthetic macrocycles in drug discovery.

@en

P2093

Adrian Whitty

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

Lauren A Viarengo

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

Mengqi Zhong

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

P2860

DNA-templated organic synthesis and selection of a library of macrocycles

Macrocyclization Reactions: The Importance of Conformational, Configurational, and Template-Induced Preorganization

Anti-diabetic activity of insulin-degrading enzyme inhibitors mediated by multiple hormones

Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings

Multiple multicomponent macrocyclizations (MiBs): a strategic development toward macrocycle diversity.

Probing the Physicochemical Boundaries of Cell Permeability and Oral Bioavailability in Lipophilic Macrocycles Inspired by Natural Products.

Molecular properties that influence the oral bioavailability of drug candidates.

In vitro selection of anti-Akt2 thioether-macrocyclic peptides leading to isoform-selective inhibitors.

The road less traveled: modulating signal transduction enzymes by inhibiting their protein-protein interactions.

mRNA display: from basic principles to macrocycle drug discovery.

P304

7729-7735

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

P31

scholarly article

P356

10.1039/C7OB00056A

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

P433

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

P478

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

P577

2017-09-06T00:00:00Z

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

P698

28876025

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