Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Dean A. Kirby"'
Autor:
Renzo Cescato, Beatrice Waser, Jean E. F. Rivier, Dean A Kirby, Véronique Eltschinger, Judit Erchegyi, Jean Claude Reubi
Publikováno v:
Journal of Medicinal Chemistry. 48:515-522
The binding affinity of short chain somatostatin (SRIF) analogues at the five human SRIF receptors (sst) was determined to identify sterically constrained somatostatin receptor subtype 1 (sst(1)) selective scaffolds. Des-AA(1,2,4,13)-[d-Trp(8)]SRIF (
Autor:
Wylie Vale, Jean Claude Reubi, J. Gulyas, Lei Wang, Dean A. Kirby, V Martinez, Marilyn H. Perrin, Steven C. Koerber, Jean Rivier, William Low, Koichi S. Kunitake, Beatrice Waser, Michael R. DiGruccio, Yvette Taché, Joan Vaughan
Publikováno v:
Journal of Medicinal Chemistry. 45:4737-4747
We present evidence that members of the corticotropin releasing factor (CRF) family assume distinct structures when interacting with the CRF(1) and CRF(2) receptors. Predictive methods, physicochemical measurements, and structure-activity relationshi
Publikováno v:
European Journal of Mass Spectrometry. 7:259-266
We report the electrospray mass spectra and tandem mass (MS/MS) spectra of a series of chemically-stable somatostatin (SRIF) and gonadotropin-releasing hormone (GnRH) analogs which incorporate acylated or alkylated/acylated aminoglycine residues (bet
Autor:
Struthers Rs, Catherine Rivier, A. G. Craig, Jean Rivier, Guangcheng Jiang, Dean A. Kirby, Laura A. Cervini, S. C. Koerber, John B. Porter
Publikováno v:
Journal of Medicinal Chemistry. 43:807-818
In three earlier papers, the structures and biological potencies of numerous mono- and dicyclic antagonists of GnRH were reported. Among these, two families, each containing two to four members were identified that had very high antagonist potencies
Publikováno v:
Journal of Medicinal Chemistry. 42:3175-3182
In an earlier report we identified specific modifications and substitutions of corticotropin releasing factor (CRF) that led to the discovery of antagonists with extended duration of action as compared to that of astressin {cyclo(30-33)[DPhe(12),Nle(
Publikováno v:
Psychopharmacology. 132:6-13
This investigation examined receptor subtype specificity and possible modulation by GABAa receptor ligands of NPY-induced behavioral responses to stressful stimuli. First, a series of NPY receptor agonists were examined for their potential effects on
Publikováno v:
Journal of Chromatography A. 648:257-265
Separation of analogues of neuropeptide Y (NPY) in which a single d -amino acid replaced the corresponding naturally occurring residue was performed by chromatographic techniques to ensure the quality of the synthetic peptides to be used for structur
Autor:
Dean A. Kirby, S. C. Koerber, Jean Rivier, A. G. Craig, R. D. Feinstein, L. Delmas, Marvin R. Brown
Publikováno v:
Journal of Medicinal Chemistry. 36:385-393
To further elucidate the minimum bioactive conformation of neuropeptide Y (NPY), a series of truncated and conformationally constrained analogues has been prepared. The synthesis and purification of these peptides was achieved using routine laborator
Autor:
Steven C. Koerber, Catherine Rivier, A. Grey Craig, Laura A. Cervini, John S. Porter, R. Scott Struthers, Dean A. Kirby, Jean Rivier, Guangcheng Jiang
Publikováno v:
ChemInform. 31
Autor:
R. Scott Struthers, S L Lahrichi, Laura A. Cervini, Steven C. Koerber, Catherine Rivier, Jean Rivier, Dean A. Kirby, Guangcheng Jiang, Michel Ibea, John S. Porter
Publikováno v:
ChemInform. 31