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A novel non-opioid binding site for endomorphin-1

Journal of physiology and pharmacology : an official journal of the Polish Physiological Society, 2016-08, Vol.67 (4), p.605

2016

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Pharmacological characterization of endomorphin-2-based cyclic pentapeptides with methylated phenylalanine residues

Peptides (New York, N.Y. : 1980), 2014-05, Vol.55, p.145-150

2014

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Specific activation of the μ opioid receptor (MOR) by endomorphin 1 and endomorphin 2

The European journal of neuroscience, 2000-02, Vol.12 (2), p.577-584

2000

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In vitro quantitative study of the degradation of endomorphins

Peptides (New York, N.Y. : 1980), 2002-09, Vol.23 (9), p.1573-1580

2002

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Problems Caused by Thermal Bridges around Windows of Historic Buildings and Renovation Methods

Acta technica Jaurinensis, 2017-03, Vol.10 (1), p.59

Tömböly, C

2017

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Pain Inhibition by Endomorphins

Annals of the New York Academy of Sciences, 1999-12, Vol.897 (1), p.154-164

1999

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Selective and high affinity labeling of neuronal and recombinant nociceptin receptors with the hexapeptide radioprobe [ 3H]Ac-RYYRIK-ol

Neurochemistry international, 2009-12, Vol.55 (7), p.458-466

2009

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Liquid chromatographic study of the enzymatic degradation of endomorphins, with identification by electrospray ionization mass spectrometry

Journal of Chromatography A, 1999-06, Vol.846 (1), p.39-48

1999

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Antinociceptive effects of intrathecal endomorphin-1 and -2 in rats

Life sciences (1973), 1999, Vol.65 (24), p.2635-2641

1999

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Side Chain Modifications Change the Binding and Agonist Properties of Endomorphin 2

Biochemical and biophysical research communications, 2002-01, Vol.290 (1), p.153-161

2002

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Behavioral and neuroendocrine actions of endomorphin-2

Peptides (New York, N.Y. : 1980), 2001-09, Vol.22 (9), p.1459-1463

2001

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Structure−Activity Study on the Phe Side Chain Arrangement of Endomorphins Using Conformationally Constrained Analogues

Journal of medicinal chemistry, 2004-01, Vol.47 (3), p.735-743

2004

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In vitro binding and signaling profile of the novel mu opioid receptor agonist endomorphin 2 in rat brain membranes

Biochemical and biophysical research communications, 1998-09, Vol.250 (3), p.720-725

1998

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Unprecedented Sigmatropic Rearrangements Leading to 2,3-Dihydro-1H-2-benzazepine-3-carboxylic Acid

Journal of organic chemistry, 2001-04, Vol.66 (8), p.2884-2886

2001

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Endomorphin-1 and endomorphin-2 differentially interact with specific binding sites for substance P (SP) aminoterminal SP1-7 in the rat spinal cord

Peptides (New York, N.Y. : 1980), 2006-04, Vol.27 (4), p.753-759

2006

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Influence of Degradation on Binding Properties and Biological Activity of Endomorphin 1

Biochemical and biophysical research communications, 2001-06, Vol.284 (3), p.771-776

2001

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Effects of endomorphin-1 on open-field behavior and on the hypothalamic-pituitary-adrenal system

Endocrine, 2001-03, Vol.14 (2), p.221-224

2001

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Autoradiography in opioid triple knockout mice reveals opioid and opioid receptor like binding of naloxone benzoylhydrazone

Neuropharmacology, 2005-02, Vol.48 (2), p.228-235

2005

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New endomorphin analogs with mu-agonist and delta-antagonist properties

Pure and applied chemistry, 2004-01, Vol.76 (5), p.951-957

2004

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Endomorphin-1 and endomorphin-2 differentially interact with specific binding sites for substance P (SP) aminoterminal SP(1-7) in the rat spinal cord

Peptides (New York, N.Y. : 1980), 2005

2005

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Preparation of specifically tritiated endomorphins

Journal of labelled compounds & radiopharmaceuticals, 2001-04, Vol.44 (5), p.355-363

2001

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Synthesis of tritium labelled endomorphin II and its stability in the radioreceptor assay

Czechoslovak journal of physics, 1999-01, Vol.49 (S1), p.893-896

1999

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β-Methyl Substitution of Cyclohexylalanine in Dmt-Tic-Cha-Phe Peptides Results in Highly Potent δ Opioid Antagonists

Journal of medicinal chemistry, 2007-01, Vol.50 (2), p.328-333

2007

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Unprecedented Sigmatropic Rearrangements Leading to 2,3-Dihydro-1 H -2-benzazepine-3-carboxylic Acid

Journal of organic chemistry, 2001-04, Vol.66 (8), p.2884-2886

2001

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A novel non-opioid binding site for endomorphin-1

Pharmacological characterization of endomorphin-2-based cyclic pentapeptides with methylated phenylalanine residues

Specific activation of the μ opioid receptor (MOR) by endomorphin 1 and endomorphin 2

In vitro quantitative study of the degradation of endomorphins

Problems Caused by Thermal Bridges around Windows of Historic Buildings and Renovation Methods

Pain Inhibition by Endomorphins

Selective and high affinity labeling of neuronal and recombinant nociceptin receptors with the hexapeptide radioprobe [ 3H]Ac-RYYRIK-ol

Liquid chromatographic study of the enzymatic degradation of endomorphins, with identification by electrospray ionization mass spectrometry

Antinociceptive effects of intrathecal endomorphin-1 and -2 in rats

Side Chain Modifications Change the Binding and Agonist Properties of Endomorphin 2

Behavioral and neuroendocrine actions of endomorphin-2

Structure−Activity Study on the Phe Side Chain Arrangement of Endomorphins Using Conformationally Constrained Analogues

In vitro binding and signaling profile of the novel mu opioid receptor agonist endomorphin 2 in rat brain membranes

Unprecedented Sigmatropic Rearrangements Leading to 2,3-Dihydro-1H-2-benzazepine-3-carboxylic Acid

Endomorphin-1 and endomorphin-2 differentially interact with specific binding sites for substance P (SP) aminoterminal SP1-7 in the rat spinal cord

Influence of Degradation on Binding Properties and Biological Activity of Endomorphin 1

Effects of endomorphin-1 on open-field behavior and on the hypothalamic-pituitary-adrenal system

Autoradiography in opioid triple knockout mice reveals opioid and opioid receptor like binding of naloxone benzoylhydrazone

New endomorphin analogs with mu-agonist and delta-antagonist properties

Endomorphin-1 and endomorphin-2 differentially interact with specific binding sites for substance P (SP) aminoterminal SP(1-7) in the rat spinal cord

Preparation of specifically tritiated endomorphins

Synthesis of tritium labelled endomorphin II and its stability in the radioreceptor assay

β-Methyl Substitution of Cyclohexylalanine in Dmt-Tic-Cha-Phe Peptides Results in Highly Potent δ Opioid Antagonists

Unprecedented Sigmatropic Rearrangements Leading to 2,3-Dihydro-1 H -2-benzazepine-3-carboxylic Acid

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