Lu Y - Search Results

1

Enantiomerically pure hexahydropyrazinoquinolines as potent and selective dopamine 3 subtype receptor ligands.

Ding K, Chen J, Ji M, Wu X, Varady J, Yang CY, Lu Y, Deschamps JR, Levant B, Wang S. Ding K, et al. Among authors: lu y. J Med Chem. 2005 May 5;48(9):3171-81. doi: 10.1021/jm049031l. J Med Chem. 2005. PMID: 15857123

2

The PDBbind database: methodologies and updates.

Wang R, Fang X, Lu Y, Yang CY, Wang S. Wang R, et al. Among authors: lu y. J Med Chem. 2005 Jun 16;48(12):4111-9. doi: 10.1021/jm048957q. J Med Chem. 2005. PMID: 15943484

3

Structure-based design of spiro-oxindoles as potent, specific small-molecule inhibitors of the MDM2-p53 interaction.

Ding K, Lu Y, Nikolovska-Coleska Z, Wang G, Qiu S, Shangary S, Gao W, Qin D, Stuckey J, Krajewski K, Roller PP, Wang S. Ding K, et al. Among authors: lu y. J Med Chem. 2006 Jun 15;49(12):3432-5. doi: 10.1021/jm051122a. J Med Chem. 2006. PMID: 16759082

4

Comparative evaluation of 11 scoring functions for molecular docking.

Wang R, Lu Y, Wang S. Wang R, et al. Among authors: lu y. J Med Chem. 2003 Jun 5;46(12):2287-303. doi: 10.1021/jm0203783. J Med Chem. 2003. PMID: 12773034

5

The PDBbind database: collection of binding affinities for protein-ligand complexes with known three-dimensional structures.

Wang R, Fang X, Lu Y, Wang S. Wang R, et al. Among authors: lu y. J Med Chem. 2004 Jun 3;47(12):2977-80. doi: 10.1021/jm030580l. J Med Chem. 2004. PMID: 15163179

6

Structure-based design of potent non-peptide MDM2 inhibitors.

Ding K, Lu Y, Nikolovska-Coleska Z, Qiu S, Ding Y, Gao W, Stuckey J, Krajewski K, Roller PP, Tomita Y, Parrish DA, Deschamps JR, Wang S. Ding K, et al. Among authors: lu y. J Am Chem Soc. 2005 Jul 27;127(29):10130-1. doi: 10.1021/ja051147z. J Am Chem Soc. 2005. PMID: 16028899

7

Discovery of a nanomolar inhibitor of the human murine double minute 2 (MDM2)-p53 interaction through an integrated, virtual database screening strategy.

Lu Y, Nikolovska-Coleska Z, Fang X, Gao W, Shangary S, Qiu S, Qin D, Wang S. Lu Y, et al. J Med Chem. 2006 Jun 29;49(13):3759-62. doi: 10.1021/jm060023+. J Med Chem. 2006. PMID: 16789731

8

Binding free energy contributions of interfacial waters in HIV-1 protease/inhibitor complexes.

Lu Y, Yang CY, Wang S. Lu Y, et al. J Am Chem Soc. 2006 Sep 13;128(36):11830-9. doi: 10.1021/ja058042g. J Am Chem Soc. 2006. PMID: 16953623

9

Analysis of ligand-bound water molecules in high-resolution crystal structures of protein-ligand complexes.

Lu Y, Wang R, Yang CY, Wang S. Lu Y, et al. J Chem Inf Model. 2007 Mar-Apr;47(2):668-75. doi: 10.1021/ci6003527. Epub 2007 Feb 1. J Chem Inf Model. 2007. PMID: 17266298

10

Structure-based discovery of nonpeptidic small organic compounds to block the T cell response to myelin basic protein.

Koehler NK, Yang CY, Varady J, Lu Y, Wu XW, Liu M, Yin D, Bartels M, Xu BY, Roller PP, Long YQ, Li P, Kattah M, Cohn ML, Moran K, Tilley E, Richert JR, Wang S. Koehler NK, et al. Among authors: lu y. J Med Chem. 2004 Oct 7;47(21):4989-97. doi: 10.1021/jm030362s. J Med Chem. 2004. PMID: 15456243

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