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Psyche and Symbol: A Selection from the Writings of C.G. Jung

2021

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The Basic Writings of C.G. Jung: Revised Edition

2021

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Marine recreation with a purpose: an emerging form of marine citizen science in the Ocean Decade

Frontiers in sustainable tourism, 2023-12, Vol.2

2023

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Psyche and Symbol: A Selection from the Writings of C.G. Jung

2021

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Potent, orally absorbed glucagon receptor antagonists

Bioorganic & medicinal chemistry letters, 1999-03, Vol.9 (5), p.641-646

1999

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Substituted Imidazoles as Glucagon Receptor Antagonists

Bioorganic & medicinal chemistry letters, 2001-09, Vol.11 (18), p.2549-2553

2001

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Characterization of a Novel, Non-peptidyl Antagonist of the Human Glucagon Receptor

The Journal of biological chemistry, 1999-03, Vol.274 (13), p.8694-8697

1999

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The discovery of sulfonylated dipeptides as Potent VLA-4 antagonists

Bioorganic & medicinal chemistry letters, 2001-10, Vol.11 (20), p.2709-2713

2001

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Pyrroles and other heterocycles as inhibitors of P38 kinase

Bioorganic & medicinal chemistry letters, 1998-10, Vol.8 (19), p.2689-2694

1998

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Psyche and Symbol: A Selection from the Writings of C. G. Jung

1, 1991

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Deprotection of N- tert-butoxycarbonyl (Boc) groups in the presence of tert-butyl esters

Tetrahedron letters, 2000-09, Vol.41 (36), p.7013-7016

2000

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Carbohydroxamido-oxazolidines: antibacterial agents that target lipid A biosynthesis

Bioorganic & medicinal chemistry letters, 1999-02, Vol.9 (3), p.313-318

1999

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N-(3-Phenylsulfonyl-3-piperidinoyl)-phenylalanine derivatives as potent, selective VLA-4 antagonists

Bioorganic & medicinal chemistry letters, 2003-03, Vol.13 (5), p.885-890

2003

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A potent, orally active, balanced affinity angiotensin II AT1 antagonist and AT2 binding inhibitor

Journal of medicinal chemistry, 1993-10, Vol.36 (21), p.3207-3210

1993

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N-Tetrahydrofuroyl-( l)-phenylalanine derivatives as potent VLA-4 antagonists

Bioorganic & medicinal chemistry letters, 2002-06, Vol.12 (11), p.1497-1500

2002

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Identification of Unique VLA-4 Antagonists from a Combinatorial Library

Bioorganic & medicinal chemistry letters, 2002-02, Vol.12 (4), p.685-688

2002

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N-(Arylacetyl)-biphenylalanines as Potent VLA-4 Antagonists

Bioorganic & medicinal chemistry letters, 2002-08, Vol.12 (16), p.2141-2144

2002

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Amidines as amide bond replacements in VLA-4 antagonists

Bioorganic & medicinal chemistry letters, 2004-05, Vol.14 (9), p.2323-2326

2004

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N-Aryl-prolyl-dipeptides as potent antagonists of VLA-4

Bioorganic & medicinal chemistry letters, 2002-08, Vol.12 (16), p.2205-2208

2002

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Molecular Basis for p38 Protein Kinase Inhibitor Specificity

Biochemistry (Easton), 1998-11, Vol.37 (47), p.16573-16581

1998

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Alpha(4)beta(7)/alpha(4)beta(1) dual integrin antagonists block alpha(4)beta(7)-dependent adhesion under shear flow

The Journal of pharmacology and experimental therapeutics, 2002-07, Vol.302 (1), p.153

2002

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Synthesis and use of 3-amino-4-phenyl-2-piperidones and 4-amino-2-benzazepin-3-ones as conformationally restricted phenylalanine isosteres in renin inhibitors

Journal of medicinal chemistry, 1992-03, Vol.35 (5), p.833-846

1992

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Molecular Basis for p38 Protein Kinase Inhibitor Specificity

Biochemistry (Easton), 1999-03, Vol.38 (11), p.3456-3456

1999

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A nonpeptidic agonist ligand of the human C5a receptor: Synthesis, binding affinity optimization and functional characterization

Bioorganic & medicinal chemistry letters, 1997-01, Vol.7 (2), p.213-218

1997

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TWO CHAPTERS FROM SYNCHRONICITY

Psyche and Symbol, 2021, p.275

2021

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Psyche and Symbol: A Selection from the Writings of C.G. Jung

The Basic Writings of C.G. Jung: Revised Edition

Marine recreation with a purpose: an emerging form of marine citizen science in the Ocean Decade

Psyche and Symbol: A Selection from the Writings of C.G. Jung

Potent, orally absorbed glucagon receptor antagonists

Substituted Imidazoles as Glucagon Receptor Antagonists

Characterization of a Novel, Non-peptidyl Antagonist of the Human Glucagon Receptor

The discovery of sulfonylated dipeptides as Potent VLA-4 antagonists

Pyrroles and other heterocycles as inhibitors of P38 kinase

Psyche and Symbol: A Selection from the Writings of C. G. Jung

Deprotection of N- tert-butoxycarbonyl (Boc) groups in the presence of tert-butyl esters

Carbohydroxamido-oxazolidines: antibacterial agents that target lipid A biosynthesis

N-(3-Phenylsulfonyl-3-piperidinoyl)-phenylalanine derivatives as potent, selective VLA-4 antagonists

A potent, orally active, balanced affinity angiotensin II AT1 antagonist and AT2 binding inhibitor

N-Tetrahydrofuroyl-( l)-phenylalanine derivatives as potent VLA-4 antagonists

Identification of Unique VLA-4 Antagonists from a Combinatorial Library

N-(Arylacetyl)-biphenylalanines as Potent VLA-4 Antagonists

Amidines as amide bond replacements in VLA-4 antagonists

N-Aryl-prolyl-dipeptides as potent antagonists of VLA-4

Molecular Basis for p38 Protein Kinase Inhibitor Specificity

Alpha(4)beta(7)/alpha(4)beta(1) dual integrin antagonists block alpha(4)beta(7)-dependent adhesion under shear flow

Synthesis and use of 3-amino-4-phenyl-2-piperidones and 4-amino-2-benzazepin-3-ones as conformationally restricted phenylalanine isosteres in renin inhibitors

Molecular Basis for p38 Protein Kinase Inhibitor Specificity

A nonpeptidic agonist ligand of the human C5a receptor: Synthesis, binding affinity optimization and functional characterization

TWO CHAPTERS FROM SYNCHRONICITY

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