| Entry ID | Original Release date | Data summary | Entry Title | Citation Title | Authors | 
    
    
        | 20071 | 2009-03-09 | Chemical Shifts: 1 set 
 | Probing the Bioactive Conformation of an Archetypal Natural Product HDAC Inhibitor Using Conformationally Homogeneous Triazole-Modified Cyclic Tetrapeptides | Probing the Bioactive Conformation of an Archetypal Natural Product HDAC Inhibitor with Conformationally Homogeneous Triazole-Modified Cyclic Tetrapeptides   | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri, W Seth Horne | 
    
        | 20073 | 2009-03-09 | Chemical Shifts: 1 set 
 | Probing the Bioactive Conformation of an Archetypal Natural Product HDAC Inhibitor Using Conformationally Homogeneous Triazole-Modified Cyclic Tetrapeptides | Probing the Bioactive Conformation of an Archetypal Natural Product HDAC Inhibitor with Conformationally Homogeneous Triazole-Modified Cyclic Tetrapeptides   | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri, W Seth Horne | 
    
        | 20072 | 2009-03-09 | Chemical Shifts: 1 set 
 | Probing the Bioactive Conformation of an Archetypal Natural Product HDAC Inhibitor Using Conformationally Homogeneous Triazole-Modified Cyclic Tetrapeptides | Probing the Bioactive Conformation of an Archetypal Natural Product HDAC Inhibitor with Conformationally Homogeneous Triazole-Modified Cyclic Tetrapeptides   | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri, W Seth Horne | 
    
        | 20065 | 2009-02-26 | Chemical Shifts: 1 set 
 | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-tetrapeptide architectures | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-Tetrapeptide Architectures   | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri | 
    
        | 20064 | 2009-02-26 | Chemical Shifts: 1 set 
 | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-tetrapeptide architectures | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-Tetrapeptide Architectures   | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri | 
    
        | 20066 | 2009-02-26 | Chemical Shifts: 1 set 
 | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-tetrapeptide architectures | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-Tetrapeptide Architectures   | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri | 
    
        | 20067 | 2009-02-26 | Chemical Shifts: 1 set 
 | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-tetrapeptide architectures | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-Tetrapeptide Architectures   | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri | 
    
        | 20068 | 2009-02-26 | Chemical Shifts: 1 set 
 | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-tetrapeptide architectures | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-Tetrapeptide Architectures   | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri | 
    
        | 20069 | 2009-02-26 | Chemical Shifts: 1 set 
 | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-tetrapeptide architectures | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-Tetrapeptide Architectures   | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri | 
    
        | 20070 | 2009-02-26 | Chemical Shifts: 1 set 
 | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-tetrapeptide architectures | Design, Synthesis, Biological Evaluation, and Structural Characterization of Potent Histone Deacetylase Inhibitors Based on Cyclic alpha/beta-Tetrapeptide Architectures   | Ana Montero, Christian A Olsen, John M Beierle, M Reza Ghadiri | 
    
        | 20038 | 2009-03-06 | Chemical Shifts: 1 set 
 | Cyclic Pseudotetrapeptide L-Phe-D-Trp-L-Lys-L-Thr | Conformationally Homogeneous Heterocyclic Pseudotetrapeptides as Three-Dimensional Scaffolds for Rational Drug Design: Receptor-Selective Somatostatin Analogues   | Beatrice Waser, Jan H van Maarseveen, Jean Claude Reubi, John M Beierle, M Reza Ghadiri, W Seth Horne | 
    
        | 20037 | 2009-03-06 | Chemical Shifts: 1 set 
 | Cyclic Pseudotetrapeptide D-Phe-L-Trp-L-Lys-L-Thr | Conformationally Homogeneous Heterocyclic Pseudotetrapeptides as Three-Dimensional Scaffolds for Rational Drug Design: Receptor-Selective Somatostatin Analogues   | Beatrice Waser, Jan H van Maarseveen, Jean Claude Reubi, John M Beierle, M Reza Ghadiri, W Seth Horne | 
    
        | 20040 | 2009-03-06 | Chemical Shifts: 1 set 
 | Cyclic Pseudotetrapeptide D-Phe-D-Trp-D-Lys-L-Thr | Conformationally Homogeneous Heterocyclic Pseudotetrapeptides as Three-Dimensional Scaffolds for Rational Drug Design: Receptor-Selective Somatostatin Analogues   | Beatrice Waser, Jan H van Maarseveen, Jean Claude Reubi, John M Beierle, M Reza Ghadiri, W Seth Horne | 
    
        | 20041 | 2009-03-06 | Chemical Shifts: 1 set 
 | Cyclic Pseudotetrapeptide L-Phe-D-Trp-D-Lys-L-Thr | Conformationally Homogeneous Heterocyclic Pseudotetrapeptides as Three-Dimensional Scaffolds for Rational Drug Design: Receptor-Selective Somatostatin Analogues   | Beatrice Waser, Jan H van Maarseveen, Jean Claude Reubi, John M Beierle, M Reza Ghadiri, W Seth Horne | 
    
        | 20042 | 2009-03-06 | Chemical Shifts: 1 set 
 | Cyclic Pseudotetrapeptide L-Phe-L-Trp-D-Lys-D-Thr | Conformationally Homogeneous Heterocyclic Pseudotetrapeptides as Three-Dimensional Scaffolds for Rational Drug Design: Receptor-Selective Somatostatin Analogues   | Beatrice Waser, Jan H van Maarseveen, Jean Claude Reubi, John M Beierle, M Reza Ghadiri, W Seth Horne | 
    
        | 20043 | 2009-03-06 | Chemical Shifts: 1 set 
 | Cyclic Pseudotetrapeptide L-Phe-D-Trp-L-Lys-D-Thr | Conformationally Homogeneous Heterocyclic Pseudotetrapeptides as Three-Dimensional Scaffolds for Rational Drug Design: Receptor-Selective Somatostatin Analogues   | Beatrice Waser, Jan H van Maarseveen, Jean Claude Reubi, John M Beierle, M Reza Ghadiri, W Seth Horne | 
    
        | 20039 | 2009-03-06 | Chemical Shifts: 1 set 
 | Cyclic Pseudotetrapeptide L-Phe-L-Trp-D-Lys-L-Thr | Conformationally Homogeneous Heterocyclic Pseudotetrapeptides as Three-Dimensional Scaffolds for Rational Drug Design: Receptor-Selective Somatostatin Analogues   | Beatrice Waser, Jan H van Maarseveen, Jean Claude Reubi, John M Beierle, M Reza Ghadiri, W Seth Horne | 
    
        | 20036 | 2009-03-06 | Chemical Shifts: 1 set 
 | Cyclic Pseudotetrapeptide L-Phe-L-Trp-L-Lys-L-Thr | Conformationally Homogeneous Heterocyclic Pseudotetrapeptides as Three-Dimensional Scaffolds for Rational Drug Design: Receptor-Selective Somatostatin Analogues   | Beatrice Waser, Jan H van Maarseveen, Jean Claude Reubi, John M Beierle, M Reza Ghadiri, W Seth Horne |