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Synthesis and Structure–Activity Relationship of Naphtho[1,2-b]furan-2-carboxamide Derivatives as Melanin Concentrating Hormone Receptor 1 Antagonists

Chemical and Pharmaceutical Bulletin, 2013/12/01, Vol.61(12), pp.1239-1247

2013

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Identification of new target proteins of a Urotensin-II receptor antagonist using transcriptome-based drug repositioning approach

Scientific reports, 2021-08, Vol.11 (1), p.17138-17138, Article 17138

2021

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Accurate prediction of protein–ligand interactions by combining physical energy functions and graph-neural networks

Journal of cheminformatics, 2024-11, Vol.16 (1), p.121-15, Article 121

2024

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KR-39038, a Novel GRK5 Inhibitor, Attenuates Cardiac Hypertrophy and Improves Cardiac Function in Heart Failure

Biomolecules & Therapeutics, 2020, 28(5), , pp.482-489

2020

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KR-39038, a Novel GRK5 Inhibitor, Attenuates Cardiac Hypertrophy and Improves Cardiac Function in Heart Failure

Biomolecules & therapeutics, 2020-09, Vol.28 (5), p.482-489

2020

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Enantioselective Conjugate Radical Addition to α‘-Hydroxy Enones

Organic letters, 2006-09, Vol.8 (19), p.4311-4313

2006

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4-Heteroaryl Phthalazin-1(2H)-one Derivatives as Potent Melanin Concentrating Hormone Receptor 1 (MCH-R1) Antagonists

Bulletin of the Korean Chemical Society, 2012, 33(7), , pp.2389-2392

2012

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4-Arylphthalazin-1(2H)-one derivatives as potent antagonists of the melanin concentrating hormone receptor 1 (MCH-R1)

Bioorganic & medicinal chemistry letters, 2012-01, Vol.22 (1), p.427-430

2012

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Design, synthesis and evaluation of 3-(2-(substituted benzyloxy)benzylidene) pyrrolidine-2,5-dione derivatives for novel ATX inhibitor

Bioorganic & medicinal chemistry letters, 2024-12, Vol.114, p.130006, Article 130006

2024

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Synthesis and SAR investigations of novel 2-arylbenzimidazole derivatives as melanin-concentrating hormone receptor 1 (MCH-R1) antagonists

Bioorganic & medicinal chemistry letters, 2011-04, Vol.21 (8), p.2309-2312

2011

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A urotensin II receptor antagonist, KR36676, decreases vascular remodeling and inflammation in experimental pulmonary hypertension

International immunopharmacology, 2016-11, Vol.40, p.196-202

2016

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β-Elimination of a Phosphonate Group from an Alkoxy Radical: An Intramolecular Acylation Approach Using an Acylphosphonate as a Carbonyl Group Acceptor

Journal of the American Chemical Society, 2003-08, Vol.125 (32), p.9574-9575

2003

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A novel urotensin II receptor antagonist, KR-36996, improved cardiac function and attenuated cardiac hypertrophy in experimental heart failure

European journal of pharmacology, 2017-03, Vol.799, p.94-102

2017

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Benzo[b]thiophene-2-carboxamide derivatives as potent urotensin-II receptor antagonists

Bioorganic & medicinal chemistry letters, 2016-10, Vol.26 (19), p.4684-4686

2016

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Synthesis and SAR of 5-aryl-furan-2-carboxamide derivatives as potent urotensin-II receptor antagonists

Bioorganic & medicinal chemistry letters, 2019-02, Vol.29 (4), p.577-580

2019

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Decarboxylative acylation approach of thiohydroxamate esters

Chemical communications (Cambridge, England), 2001-01 (15), p.1410-1411

2001

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4-Substituted quinazoline derivatives as novel EphA2 receptor tyrosine kinase inhibitors

Bioorganic & medicinal chemistry letters, 2014-09, Vol.24 (17), p.4080-4083

2014

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Novel Radical Alkylation of Carboxylic Imides

Journal of the American Chemical Society, 2002-12, Vol.124 (48), p.14306-14307

2002

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Synthesis and SAR of thieno[3,2-b]pyridinyl urea derivatives as urotensin-II receptor antagonists

Bioorganic & medicinal chemistry letters, 2014-12, Vol.24 (24), p.5832-5835

2014

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Synthesis and SAR study of pyrrolo[3,4-b]pyridin-7(6H)-one derivatives as melanin concentrating hormone receptor 1 (MCH-R1) antagonists

Bioorganic & medicinal chemistry letters, 2013-03, Vol.23 (6), p.1736-1739

2013

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Indole‐2‐carboxamide Derivatives as Potent Urotensin‐II Receptor (UT) Antagonists

Bulletin of the Korean Chemical Society, 2017, 38(9), , pp.1109-1112

2017

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Tin-Free Radical-Mediated C----C-Bond Formations with Alkyl Allyl Sulfones as Radical Precursors

Angewandte Chemie (International ed.), 2002-09, Vol.41 (17), p.3265-3267

2002

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Radical-Mediated γ-Functionalizations of α,β-Unsaturated Carboxylic Amides

Angewandte Chemie International Edition, 2004-10, Vol.43 (40), p.5378-5380

2004

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Predicted Ligands for the Human Urotensin-II GProtein-Coupled Receptor with Some Experimental Validation

ChemMedChem, 2014-08, Vol.9 (8), p.1732

2014

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Predicted Ligands for the Human Urotensin-II G Protein-Coupled Receptor with Some Experimental Validation

ChemMedChem, 2014-08, Vol.9 (8), p.1732-1743

2014

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Synthesis and Structure–Activity Relationship of Naphtho[1,2-b]furan-2-carboxamide Derivatives as Melanin Concentrating Hormone Receptor 1 Antagonists

Identification of new target proteins of a Urotensin-II receptor antagonist using transcriptome-based drug repositioning approach

Accurate prediction of protein–ligand interactions by combining physical energy functions and graph-neural networks

KR-39038, a Novel GRK5 Inhibitor, Attenuates Cardiac Hypertrophy and Improves Cardiac Function in Heart Failure

KR-39038, a Novel GRK5 Inhibitor, Attenuates Cardiac Hypertrophy and Improves Cardiac Function in Heart Failure

Enantioselective Conjugate Radical Addition to α‘-Hydroxy Enones

4-Heteroaryl Phthalazin-1(2H)-one Derivatives as Potent Melanin Concentrating Hormone Receptor 1 (MCH-R1) Antagonists

4-Arylphthalazin-1(2H)-one derivatives as potent antagonists of the melanin concentrating hormone receptor 1 (MCH-R1)

Design, synthesis and evaluation of 3-(2-(substituted benzyloxy)benzylidene) pyrrolidine-2,5-dione derivatives for novel ATX inhibitor

Synthesis and SAR investigations of novel 2-arylbenzimidazole derivatives as melanin-concentrating hormone receptor 1 (MCH-R1) antagonists

A urotensin II receptor antagonist, KR36676, decreases vascular remodeling and inflammation in experimental pulmonary hypertension

β-Elimination of a Phosphonate Group from an Alkoxy Radical: An Intramolecular Acylation Approach Using an Acylphosphonate as a Carbonyl Group Acceptor

A novel urotensin II receptor antagonist, KR-36996, improved cardiac function and attenuated cardiac hypertrophy in experimental heart failure

Benzo[b]thiophene-2-carboxamide derivatives as potent urotensin-II receptor antagonists

Synthesis and SAR of 5-aryl-furan-2-carboxamide derivatives as potent urotensin-II receptor antagonists

Decarboxylative acylation approach of thiohydroxamate esters

4-Substituted quinazoline derivatives as novel EphA2 receptor tyrosine kinase inhibitors

Novel Radical Alkylation of Carboxylic Imides

Synthesis and SAR of thieno[3,2-b]pyridinyl urea derivatives as urotensin-II receptor antagonists

Synthesis and SAR study of pyrrolo[3,4-b]pyridin-7(6H)-one derivatives as melanin concentrating hormone receptor 1 (MCH-R1) antagonists

Indole‐2‐carboxamide Derivatives as Potent Urotensin‐II Receptor (UT) Antagonists

Tin-Free Radical-Mediated C----C-Bond Formations with Alkyl Allyl Sulfones as Radical Precursors

Radical-Mediated γ-Functionalizations of α,β-Unsaturated Carboxylic Amides

Predicted Ligands for the Human Urotensin-II GProtein-Coupled Receptor with Some Experimental Validation

Predicted Ligands for the Human Urotensin-II G Protein-Coupled Receptor with Some Experimental Validation

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