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Structure of the N-terminal domain of a type B1 G protein-coupled receptor in complex with a peptide ligand

Proceedings of the National Academy of Sciences - PNAS, 2007-03, Vol.104 (12), p.4858-4863

2007

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Discovery, Synthesis, and Structure Activity of a Highly Selective α7 Nicotinic Acetylcholine Receptor Antagonist

Biochemistry (Easton), 2007-06, Vol.46 (22), p.6628-6638

2007

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Synthesis and Nuclear Magnetic Resonance Structure Determination of an .alpha.-Helical, Bicyclic, Lactam-Bridged Hexapeptide

Journal of the American Chemical Society, 1994-07, Vol.116 (14), p.6431-6432

1994

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Characterization of Multisubstituted Corticotropin Releasing Factor (CRF) Peptide Antagonists (Astressins)

Journal of medicinal chemistry, 2016-02, Vol.59 (3), p.854-866

2016

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NMR Structure of the First Extracellular Domain of Corticotropin-releasing Factor Receptor 1 (ECD1-CRF-R1) Complexed with a High Affinity Agonist

The Journal of biological chemistry, 2010-12, Vol.285 (49), p.38580-38589

2010

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Mammalian Neuronal Sodium Channel Blocker μ‑Conotoxin BuIIIB Has a Structured N‑Terminus That Influences Potency

ACS chemical biology, 2013-06, Vol.8 (6), p.1344-1351

2013

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Stressin1-A, a Potent Corticotropin Releasing Factor Receptor 1 (CRF1)-Selective Peptide Agonist

Journal of medicinal chemistry, 2007-04, Vol.50 (7), p.1668-1674

2007

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Definition and Characterization of the Short αA-Conotoxins: A Single Residue Determines Dissociation Kinetics from the Fetal Muscle Nicotinic Acetylcholine Receptor

Biochemistry (Easton), 2006-01, Vol.45 (4), p.1304-1312

2006

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Astressin-amide and astressin-acid are structurally different in dimethylsulfoxide

Biopolymers, 2007-10, Vol.87 (2-3), p.196-205

2007

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κM-Conotoxin RIIIK, Structural and Functional Novelty in a K+ Channel Antagonist

Biochemistry (Easton), 2004-07, Vol.43 (27), p.8625-8635

2004

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αA-Conotoxin OIVA defines a new αA-conotoxin subfamily of nicotinic acetylcholine receptor inhibitors

Toxicon (Oxford), 2004-08, Vol.44 (2), p.207-214

2004

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Discovery, synthesis, and structure activity of a highly selective alpha7 nicotinic acetylcholine receptor antagonist

Biochemistry (Easton), 2007-06, Vol.46 (22), p.6628

2007

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Iterative Approach to the Discovery of Novel Degarelix Analogues: Substitutions at Positions 3, 7, and 8. Part II

Journal of medicinal chemistry, 2005-07, Vol.48 (15), p.4851-4860

2005

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Definition and characterization of the short alphaA-conotoxins: a single residue determines dissociation kinetics from the fetal muscle nicotinic acetylcholine receptor

Biochemistry (Easton), 2006-01, Vol.45 (4), p.1304

2006

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Stressin 1 -A, a Potent Corticotropin Releasing Factor Receptor 1 (CRF 1 )-Selective Peptide Agonist

Journal of medicinal chemistry, 2007-04, Vol.50 (7), p.1668-1674

2007

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Synthesis, in vivo and in vitro biological activity of novel azaline B analogs

Bioorganic & medicinal chemistry letters, 2005-06, Vol.15 (11), p.2894-2897

2005

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KappaM-conotoxin RIIIK, structural and functional novelty in a K+ channel antagonist

Biochemistry (Easton), 2004-07, Vol.43 (27), p.8625

2004

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Potent Somatostatin Undecapeptide Agonists Selective for Somatostatin Receptor 1 (sst1)

Journal of medicinal chemistry, 2001-06, Vol.44 (13), p.2238-2246

2001

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AlphaA-Conotoxin OIVA defines a new alphaA-conotoxin subfamily of nicotinic acetylcholine receptor inhibitors

Toxicon (Oxford), 2004-08, Vol.44 (2), p.207

2004

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Astressin Analogues (Corticotropin-Releasing Factor Antagonists) with Extended Duration of Action in the Rat

Journal of medicinal chemistry, 1998-12, Vol.41 (25), p.5012-5019

1998

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Constrained Corticotropin-Releasing Factor Antagonists with i-(i + 3) Glu−Lys Bridges

Journal of medicinal chemistry, 1997-10, Vol.40 (22), p.3651-3658

1997

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Deductive way of reasoning about the internet AS level topology

Chinese physics B, 2015-11, Vol.24 (11), p.633-642

2015

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Constrained Corticotropin-Releasing Factor (CRF) Agonists and Antagonists with i−(i+3) Glu-Xaa-dXbb-Lys Bridges

Journal of medicinal chemistry, 1998-12, Vol.41 (25), p.5002-5011

1998

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Minimal-Size, Constrained Corticotropin-Releasing Factor Agonists with i−(i+3) Glu−Lys and Lys−Glu Bridges

Journal of medicinal chemistry, 1998-07, Vol.41 (14), p.2614-2620

1998

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Conformationally Restricted Competitive Antagonists of Human/Rat Corticotropin-Releasing Factor

Journal of medicinal chemistry, 1994-05, Vol.37 (10), p.1450-1459

1994

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Structure of the N-terminal domain of a type B1 G protein-coupled receptor in complex with a peptide ligand

Discovery, Synthesis, and Structure Activity of a Highly Selective α7 Nicotinic Acetylcholine Receptor Antagonist

Synthesis and Nuclear Magnetic Resonance Structure Determination of an .alpha.-Helical, Bicyclic, Lactam-Bridged Hexapeptide

Characterization of Multisubstituted Corticotropin Releasing Factor (CRF) Peptide Antagonists (Astressins)

NMR Structure of the First Extracellular Domain of Corticotropin-releasing Factor Receptor 1 (ECD1-CRF-R1) Complexed with a High Affinity Agonist

Mammalian Neuronal Sodium Channel Blocker μ‑Conotoxin BuIIIB Has a Structured N‑Terminus That Influences Potency

Stressin1-A, a Potent Corticotropin Releasing Factor Receptor 1 (CRF1)-Selective Peptide Agonist

Definition and Characterization of the Short αA-Conotoxins: A Single Residue Determines Dissociation Kinetics from the Fetal Muscle Nicotinic Acetylcholine Receptor

Astressin-amide and astressin-acid are structurally different in dimethylsulfoxide

κM-Conotoxin RIIIK, Structural and Functional Novelty in a K+ Channel Antagonist

αA-Conotoxin OIVA defines a new αA-conotoxin subfamily of nicotinic acetylcholine receptor inhibitors

Discovery, synthesis, and structure activity of a highly selective alpha7 nicotinic acetylcholine receptor antagonist

Iterative Approach to the Discovery of Novel Degarelix Analogues: Substitutions at Positions 3, 7, and 8. Part II

Definition and characterization of the short alphaA-conotoxins: a single residue determines dissociation kinetics from the fetal muscle nicotinic acetylcholine receptor

Stressin 1 -A, a Potent Corticotropin Releasing Factor Receptor 1 (CRF 1 )-Selective Peptide Agonist

Synthesis, in vivo and in vitro biological activity of novel azaline B analogs

KappaM-conotoxin RIIIK, structural and functional novelty in a K+ channel antagonist

Potent Somatostatin Undecapeptide Agonists Selective for Somatostatin Receptor 1 (sst1)

AlphaA-Conotoxin OIVA defines a new alphaA-conotoxin subfamily of nicotinic acetylcholine receptor inhibitors

Astressin Analogues (Corticotropin-Releasing Factor Antagonists) with Extended Duration of Action in the Rat

Constrained Corticotropin-Releasing Factor Antagonists with i-(i + 3) Glu−Lys Bridges

Deductive way of reasoning about the internet AS level topology

Constrained Corticotropin-Releasing Factor (CRF) Agonists and Antagonists with i−(i+3) Glu-Xaa-dXbb-Lys Bridges

Minimal-Size, Constrained Corticotropin-Releasing Factor Agonists with i−(i+3) Glu−Lys and Lys−Glu Bridges

Conformationally Restricted Competitive Antagonists of Human/Rat Corticotropin-Releasing Factor

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