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A MALT1 inhibitor suppresses human myeloid DC, effector T-cell and B-cell responses and retains Th1/regulatory T-cell homeostasis

PloS one, 2020-09, Vol.15 (9), p.e0222548-e0222548

2020

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Plasma Protein Binding as an Optimizable Parameter for Acidic Drugs

Drug metabolism and disposition, 2019-08, Vol.47 (8), p.865-873

2019

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N‑Trifluoromethyl Amines and Azoles: An Underexplored Functional Group in the Medicinal Chemist’s Toolbox

Journal of medicinal chemistry, 2020-11, Vol.63 (21), p.13076-13089

2020

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The powerful symbiosis between synthetic and medicinal chemistry

Future medicinal chemistry, 2021-06, Vol.13 (11), p.941-944

2021

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Small Molecule CXCR3 Antagonists

Journal of medicinal chemistry, 2016-04, Vol.59 (7), p.2894-2917

2016

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Asymmetric, Stereocontrolled Total Synthesis of Paraherquamide A

Journal of the American Chemical Society, 2003-10, Vol.125 (40), p.12172-12178

2003

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Paraherquamides, Brevianamides, and Asperparalines: Laboratory Synthesis and Biosynthesis. An Interim Report

Accounts of chemical research, 2003-02, Vol.36 (2), p.127-139

2003

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Discovery and optimization of cyclohexane-1,4-diamines as allosteric MALT1 inhibitors

European journal of medicinal chemistry, 2022-01, Vol.227, p.113925-113925, Article 113925

2022

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Discovery of Highly Isoform Selective Orally Bioavailable Phosphoinositide 3‑Kinase (PI3K)‑γ Inhibitors

Journal of medicinal chemistry, 2018-06, Vol.61 (12), p.5435-5441

2018

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Efficacious Inhaled PDE4 Inhibitors with Low Emetic Potential and Long Duration of Action for the Treatment of COPD

Journal of medicinal chemistry, 2014-06, Vol.57 (11), p.4661-4676

2014

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Advances in the design of new types of inhaled medicines

Progress in medicinal chemistry, 2022, Vol.61, p.93-162

2022

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Discovery and evaluation of a novel monocyclic series of CXCR2 antagonists

Bioorganic & medicinal chemistry letters, 2015-04, Vol.25 (7), p.1616-1620

2015

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The First Synthesis of the ABC-Ring System of ‘Upenamide

Organic letters, 2007-09, Vol.9 (20), p.4041-4044

2007

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Shedding light on the dark genome: drugging long non-coding RNA

Future drug discovery, 2022-06, Vol.4 (2)

2022

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Synthetic studies towards paraherquamide F: synthesis of the 1,7-dihydropyrano[2,3- g]indole ring system

Tetrahedron letters, 2002-03, Vol.43 (12), p.2149-2152

2002

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A Rapid Entry to Natural and Unnatural Disubstituted Maleic Anhydrides

Synlett, 2002, Vol.2002 (5), p.820-822

2002

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Reinvestigation of the dimerisation process forming isoglaucanic acid

Tetrahedron, 1999-06, Vol.55 (23), p.7363-7374

1999

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Towards a Biomimetic Synthesis of the Marine Alkaloids Papuamine and Haliclonadiamine: Model Studies

Tetrahedron, 2000-01, Vol.56 (4), p.623-628

2000

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Deacetalisation–bicyclisation routes to novel polycyclic heterocycles using stannous chloride dihydrate

Tetrahedron letters, 2007-09, Vol.48 (37), p.6556-6560

2007

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Cepaea nemoralis (L.) in Göteborg, S.W. Sweden: variation in a recent urban invader

Folia malacologica, 2014-08, Vol.22 (3)

2014

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A biomimetic approach to cp-225,917 and cp-263,114

Cox, Rhona J

2001

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Paraherquamides, Brevianamides, and Asperparalines: Laboratory Synthesis and Biosynthesis. An Interim Report

ChemInform, 2003-05, Vol.34 (18), p.no-no

2003

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Asymmetric, Stereocontrolled Total Synthesis of Paraherquamide A

ChemInform, 2004-02, Vol.35 (6), p.no-no

2004

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Deacetalization-Bicyclization Routes to Novel Polycyclic Heterocycles Using Stannous Chloride Dihydrate

ChemInform, 2007-12, Vol.38 (52), p.no-no

2007

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Synthetic Studies Towards Paraherquamide F and Stephacidin A

19th International Congress of Heterocyclic Chemistry, 2003, p.138-138

2003

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A MALT1 inhibitor suppresses human myeloid DC, effector T-cell and B-cell responses and retains Th1/regulatory T-cell homeostasis

Plasma Protein Binding as an Optimizable Parameter for Acidic Drugs

N‑Trifluoromethyl Amines and Azoles: An Underexplored Functional Group in the Medicinal Chemist’s Toolbox

The powerful symbiosis between synthetic and medicinal chemistry

Small Molecule CXCR3 Antagonists

Asymmetric, Stereocontrolled Total Synthesis of Paraherquamide A

Paraherquamides, Brevianamides, and Asperparalines: Laboratory Synthesis and Biosynthesis. An Interim Report

Discovery and optimization of cyclohexane-1,4-diamines as allosteric MALT1 inhibitors

Discovery of Highly Isoform Selective Orally Bioavailable Phosphoinositide 3‑Kinase (PI3K)‑γ Inhibitors

Efficacious Inhaled PDE4 Inhibitors with Low Emetic Potential and Long Duration of Action for the Treatment of COPD

Advances in the design of new types of inhaled medicines

Discovery and evaluation of a novel monocyclic series of CXCR2 antagonists

The First Synthesis of the ABC-Ring System of ‘Upenamide

Shedding light on the dark genome: drugging long non-coding RNA

Synthetic studies towards paraherquamide F: synthesis of the 1,7-dihydropyrano[2,3- g]indole ring system

A Rapid Entry to Natural and Unnatural Disubstituted Maleic Anhydrides

Reinvestigation of the dimerisation process forming isoglaucanic acid

Towards a Biomimetic Synthesis of the Marine Alkaloids Papuamine and Haliclonadiamine: Model Studies

Deacetalisation–bicyclisation routes to novel polycyclic heterocycles using stannous chloride dihydrate

Cepaea nemoralis (L.) in Göteborg, S.W. Sweden: variation in a recent urban invader

A biomimetic approach to cp-225,917 and cp-263,114

Paraherquamides, Brevianamides, and Asperparalines: Laboratory Synthesis and Biosynthesis. An Interim Report

Asymmetric, Stereocontrolled Total Synthesis of Paraherquamide A

Deacetalization-Bicyclization Routes to Novel Polycyclic Heterocycles Using Stannous Chloride Dihydrate

Synthetic Studies Towards Paraherquamide F and Stephacidin A

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