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Structure of the human M2 muscarinic acetylcholine receptor bound to an antagonist

Nature (London), 2012-02, Vol.482 (7386), p.547-551

2012

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Metal–Organic Framework with Dual Active Sites in Engineered Mesopores for Bioinspired Synergistic Catalysis

Journal of the American Chemical Society, 2020-05, Vol.142 (19), p.8602-8607

2020

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Novel thymol bearing oxypropanolamine derivatives as potent some metabolic enzyme inhibitors – Their antidiabetic, anticholinergic and antibacterial potentials

Bioorganic chemistry, 2018-12, Vol.81, p.119-126

2018

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The Thermosalient Phenomenon. “Jumping Crystals” and Crystal Chemistry of the Anticholinergic Agent Oxitropium Bromide

Journal of the American Chemical Society, 2010-10, Vol.132 (40), p.14191-14202

2010

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Isorhamnetin and Quercetin Derivatives as Anti-Acetylcholinesterase Principles of Marigold (Calendula officinalis) Flowers and Preparations

International journal of molecular sciences, 2017-08, Vol.18 (8), p.1685

2017

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Hydroxypropyl β-cyclodextrin nanohybrid monoliths for use in capillary electrochromatography with UV detection: application to the enantiomeric separation of adrenergic drugs, anticholinergic drugs, antidepressants, azoles, and antihistamine

Mikrochimica acta (1966), 2020-07, Vol.187 (7), p.381-381, Article 381

2020

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Protein Surface Structural Recognition in Inactive Areas: A New Immobilization Strategy for Acetylcholinesterase

Bioconjugate chemistry, 2018-05, Vol.29 (5), p.1703-1713

2018

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Assessment of Anticholinergic and Antidiabetic Properties of Some Natural and Synthetic Molecules: An In vitro and In silico Approach

Current computer-aided drug design, 2024-01, Vol.20 (5), p.441

2024

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Evidence of a M 1 -muscarinic GPCR homolog in unicellular eukaryotes: featuring Acanthamoeba spp bioinformatics 3D-modelling and experimentations

Journal of receptors and signal transduction, 2017-06, Vol.37 (3), p.267-275

2017

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Risk Prediction Method for Anticholinergic Action Using Auto-quantitative Structure–Activity Relationship and Docking Study with Molecular Operating Environment

Chemical and Pharmaceutical Bulletin, 2020/08/01, Vol.68(8), pp.773-778

2020

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Molecular Basis of Ligand Dissociation from G Protein-Coupled Receptors and Predicting Residence Time

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1705, p.197

2018

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Preparation and evaluation of orally disintegrating tablets of taste masked phencynonate HCl using ion-exchange resin

Drug development and industrial pharmacy, 2015-06, Vol.41 (6), p.934-941

2015

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Chemical aspects of pharmacological prophylaxis against nerve agent poisoning

Current medicinal chemistry, 2009-08, Vol.16 (23), p.2977

2009

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Three new lanostanoid triterpenes from the fruiting bodies of Ganoderma tropicum

Journal of asian natural products research, 2013-04, Vol.15 (4), p.357-362

2013

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Use of inhaled anticholinergic agents in obstructive airway disease

Respiratory care, 2007-07, Vol.52 (7), p.833-851

RESTREPO, Ruben D

2007

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3D-QSAR study of 8-azabicyclo[3.2.1] octane analogs antagonists of cholinergic receptor

Bioorganic & medicinal chemistry letters, 2009-06, Vol.19 (11), p.3108-3112

2009

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Adsorptive stripping voltammetric behavior and determination of anticholinergic agent oxybutynin chloride on a mercury electrode

Journal of colloid and interface science, 2007-10, Vol.314 (2), p.572-577

2007

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Alkyne–quinuclidine derivatives as potent and selective muscarinic antagonists for the treatment of COPD

Bioorganic & medicinal chemistry, 2008-04, Vol.18 (8), p.2675-2678

2008

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Crystal Structure at 1.1 Å Resolution of α-Conotoxin PnIB: Comparison with α-Conotoxins PnIA and GI

Biochemistry (Easton), 1997-09, Vol.36 (38), p.11323-11330

1997

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Simultaneous determination of enantiomers of structurally related anticholinergic analogs in human serum by liquid chromatography–electrospray ionization mass spectrometry with on-line sample cleanup

Journal of chromatography. B, Biomedical sciences and applications, 2001-10, Vol.762 (2), p.181-192

2001

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Trospium chloride: an anticholinergic quaternary ammonium compound for the treatment of overactive bladder

Expert opinion on pharmacotherapy, 2005-07, Vol.6 (8), p.1409-1420

Zinner, Norman R

2005

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Synthesis of Enantiopure 1-Azabicyclo[3.2.2]nonanes via Stereoselective Capture of Chiral Carbocations

Organic letters, 2000-06, Vol.2 (12), p.1661-1664

2000

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New Drugs: Acamprosate Calcium and Solifenacin Succinate

Journal of the American Pharmacists Association, 2005-01, Vol.45 (1), p.109-111

Hussar, Daniel A.

2005

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Jimsonweed poisoning and the anticholinergic syndrome

Ugeskrift for læger, 2005-05, Vol.167 (19), p.2041

Ruhwald, Morten

2005

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Preformulation Studies on the S-Isomer of Oxybutynin Hydrochloride, an Improved Chemical Entity (ICE™)

Drug development and industrial pharmacy, 2001-01, Vol.27 (4), p.321-329

2001

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Structure of the human M2 muscarinic acetylcholine receptor bound to an antagonist

Metal–Organic Framework with Dual Active Sites in Engineered Mesopores for Bioinspired Synergistic Catalysis

Novel thymol bearing oxypropanolamine derivatives as potent some metabolic enzyme inhibitors – Their antidiabetic, anticholinergic and antibacterial potentials

The Thermosalient Phenomenon. “Jumping Crystals” and Crystal Chemistry of the Anticholinergic Agent Oxitropium Bromide

Isorhamnetin and Quercetin Derivatives as Anti-Acetylcholinesterase Principles of Marigold (Calendula officinalis) Flowers and Preparations

Hydroxypropyl β-cyclodextrin nanohybrid monoliths for use in capillary electrochromatography with UV detection: application to the enantiomeric separation of adrenergic drugs, anticholinergic drugs, antidepressants, azoles, and antihistamine

Protein Surface Structural Recognition in Inactive Areas: A New Immobilization Strategy for Acetylcholinesterase

Assessment of Anticholinergic and Antidiabetic Properties of Some Natural and Synthetic Molecules: An In vitro and In silico Approach

Evidence of a M 1 -muscarinic GPCR homolog in unicellular eukaryotes: featuring Acanthamoeba spp bioinformatics 3D-modelling and experimentations

Risk Prediction Method for Anticholinergic Action Using Auto-quantitative Structure–Activity Relationship and Docking Study with Molecular Operating Environment

Molecular Basis of Ligand Dissociation from G Protein-Coupled Receptors and Predicting Residence Time

Preparation and evaluation of orally disintegrating tablets of taste masked phencynonate HCl using ion-exchange resin

Chemical aspects of pharmacological prophylaxis against nerve agent poisoning

Three new lanostanoid triterpenes from the fruiting bodies of Ganoderma tropicum

Use of inhaled anticholinergic agents in obstructive airway disease

3D-QSAR study of 8-azabicyclo[3.2.1] octane analogs antagonists of cholinergic receptor

Adsorptive stripping voltammetric behavior and determination of anticholinergic agent oxybutynin chloride on a mercury electrode

Alkyne–quinuclidine derivatives as potent and selective muscarinic antagonists for the treatment of COPD

Crystal Structure at 1.1 Å Resolution of α-Conotoxin PnIB: Comparison with α-Conotoxins PnIA and GI

Simultaneous determination of enantiomers of structurally related anticholinergic analogs in human serum by liquid chromatography–electrospray ionization mass spectrometry with on-line sample cleanup

Trospium chloride: an anticholinergic quaternary ammonium compound for the treatment of overactive bladder

Synthesis of Enantiopure 1-Azabicyclo[3.2.2]nonanes via Stereoselective Capture of Chiral Carbocations

New Drugs: Acamprosate Calcium and Solifenacin Succinate

Jimsonweed poisoning and the anticholinergic syndrome

Preformulation Studies on the S-Isomer of Oxybutynin Hydrochloride, an Improved Chemical Entity (ICE™)

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