A bicyclic and hsst2 selective somatostatin analogue: design, synthesis, conformational analysis and binding
| Autor: | Murray Goodman, Roberto Olender, Pninit Litman, Eliezer Falb, Tamar Yechezkel, Moshe Bracha, Shaokai Jiang, Rakefet Rosenfeld, Yoseph Salitra, Hanoch Senderowitz |
|---|---|
| Rok vydání: | 2001 |
| Předmět: |
Models
Molecular Magnetic Resonance Spectroscopy Molecular model Stereochemistry Clinical Biochemistry Drug Evaluation Preclinical Pharmaceutical Science CHO Cells Ring (chemistry) Biochemistry chemistry.chemical_compound Radioligand Assay Cricetinae Drug Discovery Side chain Animals Receptors Somatostatin Molecular Biology Cells Cultured chemistry.chemical_classification Bicyclic molecule Molecular Structure Chemistry Somatostatin receptor Organic Chemistry Ligand (biochemistry) Cyclic peptide Drug Design Lactam Molecular Medicine Somatostatin |
| Zdroj: | Bioorganicmedicinal chemistry. 9(12) |
| ISSN: | 0968-0896 |
| Popis: | A backbone bridged and disulfide bridged bicyclic somatostatin analogue, compound 1 (PTR-3205), was designed and synthesized by solid-phase methodology. The binding of compound 1 to the five different somatostatin receptors, expressed in CHO or COS-7 cells, indicate a high degree of selectivity towards hsstr2. The three-dimensional structure of this compound has been determined in DMSO-d6 and in water by 1H NMR and by molecular dynamics simulations. Similar backbone conformations were observed in both solvents. We have established direct evidence that the backbone of this bicyclic somatostatin analogue assumes a ‘folded’ conformation in solution, where the lactam ring extends roughly in the plane of the β-turn. The pharmacophoric region Phe-( d )-Trp-Lys-Thr of compound 1 is in accord with that of both the Veber compound L-363,301 (Merck) and sandostatin. We believe that the enhanced selectivity towards the hsst2 receptor, in comparison with other analogues, is due to its large hydrophobic region, composed of the lactam ring and the Phe side chains at positions 1 and 8. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Full Text from ScienceDirect