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Organic Solution Advanced Spray-Dried Microparticulate/Nanoparticulate Dry Powders of Lactomorphin for Respiratory Delivery: Physicochemical Characterization, In Vitro Aerosol Dispersion, and Cellular Studies

Pharmaceutics, 2020-12, Vol.13 (1), p.26

2020

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Synthesis, Physicochemical Characterization, In Vitro 2D/3D Human Cell Culture, and In Vitro Aerosol Dispersion Performance of Advanced Spray Dried and Co-Spray Dried Angiotensin (1-7) Peptide and PNA5 with Trehalose as Microparticles/Nanoparticles for Targeted Respiratory Delivery as Dry Powder Inhalers

Pharmaceutics, 2021-08, Vol.13 (8), p.1278

2021

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Monoclonal 1- and 3-Phosphohistidine Antibodies: New Tools to Study Histidine Phosphorylation

Cell, 2015-07, Vol.162 (1), p.198-210

2015

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Terpenes from Cannabis sativa induce antinociception in a mouse model of chronic neuropathic pain via activation of adenosine A2A receptors

Pain (Amsterdam), 2024-05

2024

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Flow Plex—A tool for unbiased comprehensive flow cytometry data analysis

Immunity, Inflammation and Disease, 2019-09, Vol.7 (3), p.105-111

2019

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Protein tyrosine kinases: Structure, substrate specificity, and drug discovery

BIOPOLYM, 1998, Vol.47 (3), p.197-223

1998

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Microwave-assisted solid-phase synthesis (MASS): parallel and combinatorial chemical library synthesis

Mini reviews in medicinal chemistry, 2003-08, Vol.3 (5), p.449

2003

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Development of inhibitors for protein tyrosine kinases: Tyrosine Kinases

Oncogene, 2000-11, Vol.19 (49), p.5690-5701

2000

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Factor Xa inhibitors by classical and combinatorial chemistry

Drug discovery today, 1998-05, Vol.3 (5), p.223-231

1998

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Potent and prolonged-acting cyclic lactam analogs of .alpha.-melanotropin: design based on molecular dynamics

Journal of medicinal chemistry, 1989-12, Vol.32 (12), p.2555-2561

1989

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Structure-Based Design of Glycosylated Oxytocin Analogues with Improved Selectivity and Antinociceptive Activity

ACS medicinal chemistry letters, 2023-02, Vol.14 (2), p.163-170

2023

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alpha.-Melanotropin: the minimal active sequence in the frog skin bioassay

Journal of medicinal chemistry, 1987-11, Vol.30 (11), p.2126-2130

1987

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Design of a new class of superpotent cyclic .alpha.-melanotropins based on quenched dynamic simulations

Journal of the American Chemical Society, 1989-04, Vol.111 (9), p.3413-3416

1989

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Microwave assisted solid-phase synthesis of trisubstituted 2-(2,6-purin-9-yl)acetamides

Tetrahedron letters, 2005-04, Vol.46 (16), p.2873-2875

2005

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Microwave-assisted solid-phase synthesis (MASS) of 2,6,9-trisubstituted purines

Tetrahedron letters, 2002-08, Vol.43 (35), p.6169-6171

2002

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Synthesis of 2,5-dihalothiazole-4-carboxylates

Tetrahedron letters, 2002-09, Vol.43 (39), p.7051-7053

2002

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Novel factor Xa inhibitors based on a benzoic acid scaffold and incorporating a neutral P1 ligand

Bioorganic & medicinal chemistry letters, 2004-06, Vol.14 (11), p.2801-2805

2004

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An alternative method for the preparation of resin-bound secondary amines

Tetrahedron letters, 2002-05, Vol.43 (19), p.3555-3556

2002

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Synthesis of 2,5-Dihalothiazole-4-carboxylates

ChemInform, 2002-12, Vol.33 (51), p.139-139

2002

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Design, Synthesis, and Conformation of Superpotent and Prolonged Acting Melanotropins

Annals of the New York Academy of Sciences, 1993-05, Vol.680 (1), p.51-63

1993

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Microwave-Assisted Solid-Phase Synthesis (MASS): Parallel and Combinatorial Chemical Library Synthesis

ChemInform, 2004-02, Vol.35 (7), p.no-no

2004

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Using a Noncovalent Protection Strategy to Enhance Solid-Phase Synthesis

ChemInform, 2003-07, Vol.34 (30), p.no-no

2003

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Synthesis and Actions of a Melanotropin Conjugate, Ac-[Nle4, Glu(gamma-4′-hydroxyanilide)5, D-Phe7]α-MSH4–10-NH2, on Melanocytes and Melanoma Cells In Vitro

Journal of pharmaceutical sciences, 1990-06, Vol.79 (6), p.500-504

1990

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Design and Quantitative Structure−Activity Relationship of 3-Amidinobenzyl-1H-indole-2-carboxamides as Potent, Nonchiral, and Selective Inhibitors of Blood Coagulation Factor Xa

Journal of medicinal chemistry, 2002-06, Vol.45 (13), p.2749-2769

2002

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Cyclic lactam .alpha.-melanotropin analogs of Ac-Nle4-cyclo[Asp5,D-Phe7,Lys10]-.alpha.-melanocyte-stimulating hormone-(4-10)-NH2 with bulky aromatic amino acids at position 7 show high antagonist potency and selectivity at specific melanocortin receptors

Journal of medicinal chemistry, 1995-09, Vol.38 (18), p.3454-3461

1995

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Organic Solution Advanced Spray-Dried Microparticulate/Nanoparticulate Dry Powders of Lactomorphin for Respiratory Delivery: Physicochemical Characterization, In Vitro Aerosol Dispersion, and Cellular Studies

Monoclonal 1- and 3-Phosphohistidine Antibodies: New Tools to Study Histidine Phosphorylation

Terpenes from Cannabis sativa induce antinociception in a mouse model of chronic neuropathic pain via activation of adenosine A2A receptors

Flow Plex—A tool for unbiased comprehensive flow cytometry data analysis

Protein tyrosine kinases: Structure, substrate specificity, and drug discovery

Microwave-assisted solid-phase synthesis (MASS): parallel and combinatorial chemical library synthesis

Development of inhibitors for protein tyrosine kinases: Tyrosine Kinases

Factor Xa inhibitors by classical and combinatorial chemistry

Potent and prolonged-acting cyclic lactam analogs of .alpha.-melanotropin: design based on molecular dynamics

Structure-Based Design of Glycosylated Oxytocin Analogues with Improved Selectivity and Antinociceptive Activity

alpha.-Melanotropin: the minimal active sequence in the frog skin bioassay

Design of a new class of superpotent cyclic .alpha.-melanotropins based on quenched dynamic simulations

Microwave assisted solid-phase synthesis of trisubstituted 2-(2,6-purin-9-yl)acetamides

Microwave-assisted solid-phase synthesis (MASS) of 2,6,9-trisubstituted purines

Synthesis of 2,5-dihalothiazole-4-carboxylates

Novel factor Xa inhibitors based on a benzoic acid scaffold and incorporating a neutral P1 ligand

An alternative method for the preparation of resin-bound secondary amines

Synthesis of 2,5-Dihalothiazole-4-carboxylates

Design, Synthesis, and Conformation of Superpotent and Prolonged Acting Melanotropins

Microwave-Assisted Solid-Phase Synthesis (MASS): Parallel and Combinatorial Chemical Library Synthesis

Using a Noncovalent Protection Strategy to Enhance Solid-Phase Synthesis

Synthesis and Actions of a Melanotropin Conjugate, Ac-[Nle4, Glu(gamma-4′-hydroxyanilide)5, D-Phe7]α-MSH4–10-NH2, on Melanocytes and Melanoma Cells In Vitro

Design and Quantitative Structure−Activity Relationship of 3-Amidinobenzyl-1H-indole-2-carboxamides as Potent, Nonchiral, and Selective Inhibitors of Blood Coagulation Factor Xa

Cyclic lactam .alpha.-melanotropin analogs of Ac-Nle4-cyclo[Asp5,D-Phe7,Lys10]-.alpha.-melanocyte-stimulating hormone-(4-10)-NH2 with bulky aromatic amino acids at position 7 show high antagonist potency and selectivity at specific melanocortin receptors

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