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Identification of highly selective and potent orexin receptor 1 antagonists derived from a dual orexin receptor 1/2 antagonist based on the structural framework of pyrazoylethylbenzamide

Bioorganic & medicinal chemistry, 2017-10, Vol.25 (20), p.5203-5215

2017

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A Novel Potent and Selective Histamine H 3 Receptor Antagonist Enerisant: In Vitro Profiles, In Vivo Receptor Occupancy, and Wake-Promoting and Procognitive Effects in Rodents

The Journal of pharmacology and experimental therapeutics, 2020-11, Vol.375 (2), p.276-285

2020

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Identification of Arginine Analogues as Antagonists and Agonists for the Melanocortin-4 Receptor

Chemical and Pharmaceutical Bulletin, 2007/08/01, Vol.55(8), pp.1232-1239

2007

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Discovery of ORN0829, a potent dual orexin 1/2 receptor antagonist for the treatment of insomnia

Bioorganic & medicinal chemistry, 2020-07, Vol.28 (13), p.115489, Article 115489

2020

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Synthesis of Diphenylmethyl Analogues and Their Affinity for the Melanocortin-4 Receptor and the Serotonin Transporter

Chemical and Pharmaceutical Bulletin, 2007, Vol.55(7), pp.1044-1050

2007

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Discovery of novel indole derivatives as potent and selective inhibitors of proMMP-9 activation

Bioorganic & medicinal chemistry letters, 2024-01, Vol.97, p.129541-129541, Article 129541

2024

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Identification of Arginine Analogues as Antagonists and Agonists for the Melanocortin-4 Receptor

Chemical & Pharmaceutical Bulletin, 2007, Vol.55 (8), p.1232-1239

2007

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Synthesis of Diphenylmethyl Analogues and Their Affinity for the Melanocortin-4 Receptor and the Serotonin Transporter

Chemical & Pharmaceutical Bulletin, 2007, Vol.55 (7), p.1044-1050

2007

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Synthesis of sulfobacin A and B, new sulfonolipids isolated from Chryseobacterium sp

Tetrahedron letters, 1998-09, Vol.39 (38), p.6931-6934

1998

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Novel piperazines: Potent melanocortin-4 receptor antagonists with anxiolytic-like activity

Bioorganic & medicinal chemistry, 2007-03, Vol.15 (6), p.2375-2385

2007

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Triterpenoid total synthesis. Part 5. Synthetic disproof of the triterpene structure proposed for naurol A, a cytotoxic metabolite of a Pacific sponge

Perkin 1 : an international journal of organic and bio-organic chemistry, 2000 (13), p.2043-2046

2000

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Synthesis of sphingosine relatives. Part 22. Synthesis of sulfobacin A, B and flavocristamide A, new sulfonolipids isolated from Chryseobacterium sp

Journal of the Chemical Society, Perkin Transactions 1, 1999 (17), p.2467-2477

1999

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Synthesis and absolute configuration of Stellettadine A: A marine alkaloid that induces larval metamorphosis in Ascidians

Bioorganic & medicinal chemistry letters, 2001-06, Vol.11 (12), p.1481-1483

2001

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Synthesis and absolute configuration of Stellettadine A

Bioorganic & medicinal chemistry letters, 2001-06, Vol.11 (12), p.1481-1483

2001

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Gene Expression Signature in Surgical Tissues and Endoscopic Biopsies Identifies High-Risk T1 Colorectal Cancers

Gastroenterology (New York, N.Y. 1943), 2019-06, Vol.156 (8), p.2338-2341.e3

2019

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Synthesis and absolute configuration of stellettadine A, a bisguanidinium alkaloid isolated from a marine sponge Stelletta sp

Perkin 1 : an international journal of organic and bio-organic chemistry, 2001 (7), p.657-661

2001

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Synthesis of Diphenylmethyl Analogues and Their Affinity for the Melanocortin-4 Receptor and the Serotonin Transporter

ChemInform, 2007-11, Vol.38 (48), p.no-no

2007

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ChemInform Abstract: Synthesis and Absolute Configuration of Stellettadine A, a Bisguanidinium Alkaloid Isolated from a Marine Sponge Stelletta sp

ChemInform, 2001-09, Vol.32 (38), p.no-no

2001

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ChemInform Abstract: Synthesis and Absolute Configuration of Stellettadine A: A Marine Alkaloid that Induces Larval Metamorphosis in Ascidians

ChemInform, 2001-09, Vol.32 (38), p.no-no

2001

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ChemInform Abstract: Triterpenoid Total Synthesis. Part 5. Synthetic Disproof of the Triterpene Structure Proposed for Naurol A, a Cytotoxic Metabolite of a Pacific Sponge

ChemInform, 2000-11, Vol.31 (45), p.no-no

2000

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ChemInform Abstract: Synthesis of Sphingosine Relatives. Part 22. Synthesis of Sulfobacin A, B and Flavocristamide A, New Sulfonolipids Isolated from Chryseobacterium sp

ChemInform, 2000-01, Vol.31 (2), p.no-no

2000

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Improved Climate Simulation by MIROC5: Mean States, Variability, and Climate Sensitivity

Journal of climate, 2010-12, Vol.23 (23), p.6312-6335

2010

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Radiation-induced amorphization of M23C6 in F82H steel: An atomic-scale observation

Journal of nuclear materials, 2022-01, Vol.558, p.153345, Article 153345

2022

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Chemical and topological disordering in M23C6 due to irradiation: An atomic-scale observation

Journal of nuclear materials, 2023-12, Vol.587, p.154733, Article 154733

2023

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Transmission electron microscopy study of the radiation-induced amorphization in the Cr-W-C ternary M23C6

Journal of nuclear materials, 2024-06, Vol.594, p.155012, Article 155012

2024

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Identification of highly selective and potent orexin receptor 1 antagonists derived from a dual orexin receptor 1/2 antagonist based on the structural framework of pyrazoylethylbenzamide

A Novel Potent and Selective Histamine H 3 Receptor Antagonist Enerisant: In Vitro Profiles, In Vivo Receptor Occupancy, and Wake-Promoting and Procognitive Effects in Rodents

Identification of Arginine Analogues as Antagonists and Agonists for the Melanocortin-4 Receptor

Discovery of ORN0829, a potent dual orexin 1/2 receptor antagonist for the treatment of insomnia

Synthesis of Diphenylmethyl Analogues and Their Affinity for the Melanocortin-4 Receptor and the Serotonin Transporter

Discovery of novel indole derivatives as potent and selective inhibitors of proMMP-9 activation

Identification of Arginine Analogues as Antagonists and Agonists for the Melanocortin-4 Receptor

Synthesis of Diphenylmethyl Analogues and Their Affinity for the Melanocortin-4 Receptor and the Serotonin Transporter

Synthesis of sulfobacin A and B, new sulfonolipids isolated from Chryseobacterium sp

Novel piperazines: Potent melanocortin-4 receptor antagonists with anxiolytic-like activity

Triterpenoid total synthesis. Part 5. Synthetic disproof of the triterpene structure proposed for naurol A, a cytotoxic metabolite of a Pacific sponge

Synthesis of sphingosine relatives. Part 22. Synthesis of sulfobacin A, B and flavocristamide A, new sulfonolipids isolated from Chryseobacterium sp

Synthesis and absolute configuration of Stellettadine A: A marine alkaloid that induces larval metamorphosis in Ascidians

Synthesis and absolute configuration of Stellettadine A

Gene Expression Signature in Surgical Tissues and Endoscopic Biopsies Identifies High-Risk T1 Colorectal Cancers

Synthesis and absolute configuration of stellettadine A, a bisguanidinium alkaloid isolated from a marine sponge Stelletta sp

Synthesis of Diphenylmethyl Analogues and Their Affinity for the Melanocortin-4 Receptor and the Serotonin Transporter

ChemInform Abstract: Synthesis and Absolute Configuration of Stellettadine A, a Bisguanidinium Alkaloid Isolated from a Marine Sponge Stelletta sp

ChemInform Abstract: Synthesis and Absolute Configuration of Stellettadine A: A Marine Alkaloid that Induces Larval Metamorphosis in Ascidians

ChemInform Abstract: Triterpenoid Total Synthesis. Part 5. Synthetic Disproof of the Triterpene Structure Proposed for Naurol A, a Cytotoxic Metabolite of a Pacific Sponge

ChemInform Abstract: Synthesis of Sphingosine Relatives. Part 22. Synthesis of Sulfobacin A, B and Flavocristamide A, New Sulfonolipids Isolated from Chryseobacterium sp

Improved Climate Simulation by MIROC5: Mean States, Variability, and Climate Sensitivity

Radiation-induced amorphization of M23C6 in F82H steel: An atomic-scale observation

Chemical and topological disordering in M23C6 due to irradiation: An atomic-scale observation

Transmission electron microscopy study of the radiation-induced amorphization in the Cr-W-C ternary M23C6

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