Virtual fragment screening: exploration of MM-PBSA re-scoring. - Wikidata - wikimedia - TriplyDB

Virtual fragment screening: exploration of MM-PBSA re-scoring.

Virtual fragment screening: exploration of MM-PBSA re-scoring.

http://www.wikidata.org/entity/Q34368348

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Improvements, trends, and new ideas in molecular docking: 2012-2013 in review.Tranilast binds to aβ monomers and promotes aβ fibrillation.

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P2860

Virtual fragment screening: exploration of MM-PBSA re-scoring.

http://www.wikidata.org/entity/Q34368348

description

2012 nî lūn-bûn

@nan

2012 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

name

Virtual fragment screening: exploration of MM-PBSA re-scoring.

@ast

Virtual fragment screening: exploration of MM-PBSA re-scoring.

@en

Virtual fragment screening: exploration of MM-PBSA re-scoring.

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type

label

Virtual fragment screening: exploration of MM-PBSA re-scoring.

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Virtual fragment screening: exploration of MM-PBSA re-scoring.

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Virtual fragment screening: exploration of MM-PBSA re-scoring.

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prefLabel

Virtual fragment screening: exploration of MM-PBSA re-scoring.

@ast

Virtual fragment screening: exploration of MM-PBSA re-scoring.

@en

Virtual fragment screening: exploration of MM-PBSA re-scoring.

@nl

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S10822-012-9590-X

P1433

Journal of Computer - Aided Molecular Design

P1476

Virtual fragment screening: exploration of MM-PBSA re-scoring.

@en

P2093

Demetri Moustakas

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

Diane Joseph-McCarthy

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

Matthew Miller

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

Sameer Kawatkar

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

P2860

The maximal affinity of ligands

van der Waals Volumes and Radii

Discovery of a novel warhead against beta-secretase through fragment-based lead generation

Application of fragment-based lead generation to the discovery of novel, cyclic amidine beta-secretase inhibitors with nanomolar potency, cellular activity, and high ligand efficiency

Novel prostaglandin D synthase inhibitors generated by fragment-based drug design

Recent developments in fragment-based drug discovery

Fragment-based discovery of the pyrazol-4-yl urea (AT9283), a multitargeted kinase inhibitor with potent aurora kinase activity

Docking for fragment inhibitors of AmpC -lactamase

The glutamate receptor GluR5 agonist (S)-2-amino-3-(3-hydroxy-7,8-dihydro-6H-cyclohepta[d]isoxazol-4-yl)propionic acid and the 8-methyl analogue: synthesis, molecular pharmacology, and biostructural characterization

SMILES, a chemical language and information system. 1. Introduction to methodology and encoding rules

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s10822-012-9590-x

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921-934

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scholarly article

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10.1007/S10822-012-9590-X

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8

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26

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2012-08-07T00:00:00Z

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22869295

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