Translational synthetic chemistry. - Wikidata - awgldk - TriplyDB

Translational synthetic chemistry.

Translational synthetic chemistry.

http://www.wikidata.org/entity/Q34626958

about

Convergent diversity-oriented side-chain macrocyclization scan for unprotected polypeptides.Remodeling of fumagillol: discovery of an oxygen-directed oxidative Mannich reaction.Large-scale classification of P-glycoprotein inhibitors using SMILES-based descriptors.

P2860

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P2860

Translational synthetic chemistry.

http://www.wikidata.org/entity/Q34626958

description

2013 nî lūn-bûn

@nan

2013 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

name

Translational synthetic chemistry.

@ast

Translational synthetic chemistry.

@en

Translational synthetic chemistry.

@nl

type

label

Translational synthetic chemistry.

@ast

Translational synthetic chemistry.

@en

Translational synthetic chemistry.

@nl

prefLabel

Translational synthetic chemistry.

@ast

Translational synthetic chemistry.

@en

Translational synthetic chemistry.

@nl

P1433

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P1476

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P2093

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P2860

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P356

P1433

Nature Chemical Biology

P1476

Translational synthetic chemistry.

@en

P2093

Lisa A Marcaurelle

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

Sarathy Kesavan

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

P2860

Inhibition of oncogenic Wnt signaling through direct targeting of -catenin

Fragment-based discovery of bromodomain inhibitors part 2: optimization of phenylisoxazole sulfonamides

Small-molecule ligands bind to a distinct pocket in Ras and inhibit SOS-mediated nucleotide exchange activity

Discovery of Small Molecules that Bind to K-Ras and Inhibit Sos-Mediated Activation

Natural-product-derived fragments for fragment-based ligand discovery

Diversity-oriented synthesis of a cytisine-inspired pyridone library leading to the discovery of novel inhibitors of Bcl-2.

Recent progress in fragment-based lead discovery.

An aldol-based build/couple/pair strategy for the synthesis of medium- and large-sized rings: discovery of macrocyclic histone deacetylase inhibitors.

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

Route to three-dimensional fragments using diversity-oriented synthesis.

P2888

P304

210-213

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

P31

scholarly article

P356

10.1038/NCHEMBIO.1207

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

P433

4

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

P478

9

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

P577

2013-04-01T00:00:00Z

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

P698

23508175

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