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GPR120 suppresses adipose tissue lipolysis and synergizes with GPR40 in antidiabetic efficacy

Journal of lipid research, 2017-08, Vol.58 (8), p.1561-1578

2017

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A Gpr120-selective agonist improves insulin resistance and chronic inflammation in obese mice

Nature medicine, 2014-08, Vol.20 (8), p.942-947

2014

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Total Synthesis of Gambierol: The Generation of the A-C and F-H Subunits by Using a C-Glycoside Centered Strategy

Chemistry : a European journal, 2006-02, Vol.12 (6), p.1736-1746

2006

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Localized Changes in the gp120 Envelope Glycoprotein Confer Resistance to Human Immunodeficiency Virus Entry Inhibitors BMS-806 and #155

Journal of Virology, 2004-04, Vol.78 (7), p.3742-3752

2004

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Discovery of KIN-3248, An Irreversible, Next Generation FGFR Inhibitor for the Treatment of Advanced Tumors Harboring FGFR2 and/or FGFR3 Gene Alterations

Journal of medicinal chemistry, 2024-02, Vol.67 (3), p.1734-1746

2024

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C-Glycosides to Fused Polycyclic Ethers. A Formal Synthesis of (±)-Hemibrevetoxin B

Journal of organic chemistry, 2001-02, Vol.66 (4), p.1380-1386

2001

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The Discovery of Exarafenib (KIN-2787): Overcoming the Challenges of Pan-RAF Kinase Inhibition

Journal of medicinal chemistry, 2024-02, Vol.67 (3), p.1747-1757

2024

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Exploring antiviral and anti-inflammatory effects of thiol drugs in COVID-19

American journal of physiology. Lung cellular and molecular physiology, 2022-09, Vol.323 (3), p.L372-L389

2022

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Aluminum- and Boron-Mediated C-Glycoside Synthesis from 1,2-Anhydroglycosides

Organic letters, 2000-08, Vol.2 (17), p.2707-2709

2000

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Synthesis of an F−H Gambierol Subunit Using a C-Glycoside-Centered Strategy

Organic letters, 2003-03, Vol.5 (6), p.913-916

2003

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Enol ether–olefin ring closing metathesis using the Grubbs ruthenium imidazole catalyst

Tetrahedron letters, 2001-01, Vol.42 (2), p.179-181

2001

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The discovery of novel 5,6,5- and 5,5,6-tricyclic pyrrolidines as potent and selective DPP-4 inhibitors

Bioorganic & medicinal chemistry letters, 2016-06, Vol.26 (11), p.2622-2626

2016

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An integrin antagonist (MK‐0429) decreases proteinuria and renal fibrosis in the ZSF1 rat diabetic nephropathy model

Pharmacology research & perspectives, 2017-10, Vol.5 (5), p.n/a

2017

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Mineralocorticoid receptor antagonists: Identification of heterocyclic amide replacements in the oxazolidinedione series

Bioorganic & medicinal chemistry letters, 2014-04, Vol.24 (7), p.1681-1684

2014

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Discovery of novel oxazolidinedione derivatives as potent and selective mineralocorticoid receptor antagonists

Bioorganic & medicinal chemistry letters, 2013-08, Vol.23 (15), p.4388-4392

2013

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Nanoporous Microbead Supported Bilayers: Stability, Physical Characterization, and Incorporation of Functional Transmembrane Proteins

Langmuir, 2007-03, Vol.23 (7), p.3864-3872

2007

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Total Synthesis of (−)-2-epi-Peloruside A

Organic letters, 2008-12, Vol.10 (24), p.5501-5504

2008

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Discovery of Benzimidazole Oxazolidinediones as Novel and Selective Nonsteroidal Mineralocorticoid Receptor Antagonists

ACS medicinal chemistry letters, 2015-04, Vol.6 (4), p.461-465

2015

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C-Glycosides to Fused Polycyclic Ethers. An Efficient Entry into the A−D Ring System of Gambierol

Organic letters, 2001-09, Vol.3 (18), p.2919-2922

2001

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Aminopiperidine-fused imidazoles as dipeptidyl peptidase-IV inhibitors

Bioorganic & medicinal chemistry letters, 2009-08, Vol.19 (15), p.4097-4101

2009

Volltextzugriff (PDF)

An integrin antagonist ( MK ‐0429) decreases proteinuria and renal fibrosis in the ZSF 1 rat diabetic nephropathy model

Pharmacology research & perspectives, 2017-10, Vol.5 (5)

2017

Volltextzugriff (PDF)

Discovery of 3-aminopiperidines as potent, selective, and orally bioavailable dipeptidyl peptidase IV inhibitors

Bioorganic & medicinal chemistry letters, 2007-08, Vol.17 (16), p.4579-4583

2007

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A Highly Efficient Synthesis of the Hemibrevetoxin B Ring System

Organic letters, 2000-01, Vol.2 (2), p.231-234

2000

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Dynamic two-dimensional fluorescence correlation spectroscopy. Generalized correlation and experimental factors

Analyst (London), 2001-08, Vol.126 (8), p.1229-1239

2001

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GPR120 suppresses adipose tissue lipolysis and synergizes with GPR40 in antidiabetic efficacy

A Gpr120-selective agonist improves insulin resistance and chronic inflammation in obese mice

Total Synthesis of Gambierol: The Generation of the A-C and F-H Subunits by Using a C-Glycoside Centered Strategy

Localized Changes in the gp120 Envelope Glycoprotein Confer Resistance to Human Immunodeficiency Virus Entry Inhibitors BMS-806 and #155

Discovery of KIN-3248, An Irreversible, Next Generation FGFR Inhibitor for the Treatment of Advanced Tumors Harboring FGFR2 and/or FGFR3 Gene Alterations

C-Glycosides to Fused Polycyclic Ethers. A Formal Synthesis of (±)-Hemibrevetoxin B

The Discovery of Exarafenib (KIN-2787): Overcoming the Challenges of Pan-RAF Kinase Inhibition

Exploring antiviral and anti-inflammatory effects of thiol drugs in COVID-19

Aluminum- and Boron-Mediated C-Glycoside Synthesis from 1,2-Anhydroglycosides

Synthesis of an F−H Gambierol Subunit Using a C-Glycoside-Centered Strategy

Enol ether–olefin ring closing metathesis using the Grubbs ruthenium imidazole catalyst

The discovery of novel 5,6,5- and 5,5,6-tricyclic pyrrolidines as potent and selective DPP-4 inhibitors

An integrin antagonist (MK‐0429) decreases proteinuria and renal fibrosis in the ZSF1 rat diabetic nephropathy model

Mineralocorticoid receptor antagonists: Identification of heterocyclic amide replacements in the oxazolidinedione series

Discovery of novel oxazolidinedione derivatives as potent and selective mineralocorticoid receptor antagonists

Design, Synthesis, and Evaluation of Novel and Selective G‑protein Coupled Receptor 120 (GPR120) Spirocyclic Agonists

Nanoporous Microbead Supported Bilayers: Stability, Physical Characterization, and Incorporation of Functional Transmembrane Proteins

Total Synthesis of (−)-2-epi-Peloruside A

Discovery of Benzimidazole Oxazolidinediones as Novel and Selective Nonsteroidal Mineralocorticoid Receptor Antagonists

C-Glycosides to Fused Polycyclic Ethers. An Efficient Entry into the A−D Ring System of Gambierol

Aminopiperidine-fused imidazoles as dipeptidyl peptidase-IV inhibitors

An integrin antagonist ( MK ‐0429) decreases proteinuria and renal fibrosis in the ZSF 1 rat diabetic nephropathy model

Discovery of 3-aminopiperidines as potent, selective, and orally bioavailable dipeptidyl peptidase IV inhibitors

A Highly Efficient Synthesis of the Hemibrevetoxin B Ring System

Dynamic two-dimensional fluorescence correlation spectroscopy. Generalized correlation and experimental factors

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