C. Esslinger

发表

Ngamma-aryl glutamine analogues as probes of the ASCT2 neutral amino acid transporter binding site.

C. Esslinger, Kimberly A Cybulski, Joseph F. Rhoderick, 2005, Bioorganic & medicinal chemistry.

Structural determinants of substrates and inhibitors: probing glutamate transporters with 2,4-methanopyrrolidine-2,4-dicarboxylate.

M. Kavanaugh, R. Bridges, C. Thompson, 1998, Bioorganic & medicinal chemistry letters.

Differentiation of substrate and nonsubstrate inhibitors of the high-affinity, sodium-dependent glutamate transporters.

M. Kavanaugh, S. Amara, R. Bridges, 1999, Molecular pharmacology.

The substituted aspartate analogue l-β-threo-benzyl-aspartate preferentially inhibits the neuronal excitatory amino acid transporter EAAT3

M. Kavanaugh, P. A. Wilson, D. Poulsen, 2005, Neuropharmacology.

Design, synthesis, and biological activity of novel triazole amino acids used to probe binding interactions between ligand and neutral amino acid transport protein SN1.

C. Esslinger, M. Gajewski, B. Seaver, 2007, Bioorganic & medicinal chemistry letters.

Synthesis of tri-substituted furans: mild Ti(IV)-mediated couplings to acetals. Construction of the epoxy hemi-amido ketal of fusarin C

Robert M. Williams, C. Esslinger, 1991 .

Discovery and synthesis of hydroxy-L-proline based blockers of the neutral amino acid transporters SLC1A4 (ASCT1) and SLC1A5 (ASCT2)

M. Kavanaugh, C. Esslinger, Derek Silvius, 2021, bioRxiv.

Methylation of L-trans-2,4-pyrrolidine dicarboxylate converts the glutamate transport inhibitor from a substrate to a non-substrate inhibitor.

R. Bridges, C. Esslinger, H. Koch, 2002, Bioorganic & medicinal chemistry.

Synthesis of Tri‐Substituted Furans: Mild Ti(IV)‐Mediated Couplings to Acetals. Construction of the Epoxy Hemi‐Amido Acetal of Fusarin C+.

Robert M. Williams, C. Esslinger, 1992 .

The excitatory amino acid transporters: pharmacological insights on substrate and inhibitor specificity of the EAAT subtypes.

R. Bridges, C. Esslinger, Richard J. Bridges, 2005, Pharmacology & therapeutics.

Synthesis and preliminary pharmacological evaluation of novel derivatives of L-beta-threo-benzylaspartate as inhibitors of the neuronal glutamate transporter EAAT3.

R. Bridges, C. Esslinger, Joseph F. Rhoderick, 2008, Bioorganic & medicinal chemistry.

Substituted quinolines as inhibitors of l-glutamate transport into synaptic vesicles

R. Bridges, C. Thompson, C. Esslinger, 1998, Neuropharmacology.