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PI3K inhibitors are finally coming of age

Nature reviews. Drug discovery, 2021-10, Vol.20 (10), p.741-769

2021

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Design, Synthesis, and Biological Evaluation of MEK PROTACs

Journal of medicinal chemistry, 2020-01, Vol.63 (1), p.157-162

2020

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Author Correction: PI3K inhibitors are finally coming of age

Nature reviews. Drug discovery, 2021-10, Vol.20 (10), p.798-798

2021

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Impact of Stereospecific Intramolecular Hydrogen Bonding on Cell Permeability and Physicochemical Properties

Journal of medicinal chemistry, 2014-03, Vol.57 (6), p.2746-2754

2014

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Evolution of PI3Kγ and δ Inhibitors for Inflammatory and Autoimmune Diseases

Journal of medicinal chemistry, 2019-05, Vol.62 (10), p.4783-4814

2019

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Structural and conformational determinants of macrocycle cell permeability

Nature chemical biology, 2016-12, Vol.12 (12), p.1065

2016

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Stabilization of protein-protein interactions in drug discovery

Expert opinion on drug discovery, 2017-09, Vol.12 (9), p.925-940

2017

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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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A class of highly selective inhibitors bind to an active state of PI3Kγ

Nature chemical biology, 2019-04, Vol.15 (4), p.348

2019

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Scaffold-hopping with zwitterionic CCR3 antagonists: Identification and optimisation of a series with good potency and pharmacokinetics leading to the discovery of AZ12436092

Bioorganic & medicinal chemistry letters, 2012-11, Vol.22 (21), p.6694-6699

2012

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Identification of Phosphate-Containing Compounds as New Inhibitors of 14-3-3/c-Abl Protein–Protein Interaction

ACS chemical biology, 2020-04, Vol.15 (4), p.1026-1035

2020

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Design and Synthesis of Soluble and Cell-Permeable PI3Kδ Inhibitors for Long-Acting Inhaled Administration

Journal of medicinal chemistry, 2017-06, Vol.60 (12), p.5057-5071

2017

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Spiro-fused Pyrrolidine, Piperidine, and Oxindole Scaffolds from Lactams

Organic letters, 2012-09, Vol.14 (18), p.4846-4849

2012

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14-3-3 modulation of the inflammatory response

Pharmacological research, 2021-01, Vol.163, p.105236-105236, Article 105236

2021

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Designing novel building blocks is an overlooked strategy to improve compound quality

Drug discovery today, 2015-01, Vol.20 (1), p.11-17

2015

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Surprising lipophilicity observations identify unexpected conformational effects

Bioorganic & medicinal chemistry letters, 2022-08, Vol.69, p.128786, Article 128786

2022

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Glucocorticoid receptor Thr524 phosphorylation by MINK1 induces interactions with 14-3-3 protein regulators

The Journal of biological chemistry, 2021-01, Vol.296, p.100551-100551, Article 100551

2021

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Designing Selective Drug-like Molecular Glues for the Glucocorticoid Receptor/14-3‑3 Protein–Protein Interaction

Journal of medicinal chemistry, 2022-12, Vol.65 (24), p.16818-16828

2022

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Correction to “Designing Selective Drug-like Molecular Glues for the Glucocorticoid Receptor/14-3‑3 Protein–Protein Interaction”

Journal of medicinal chemistry, 2023-02, Vol.66 (3), p.2205-2207

2023

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The discovery of CCR3/H1 dual antagonists with reduced hERG risk

Bioorganic & medicinal chemistry letters, 2012-11, Vol.22 (21), p.6688-6693

2012

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A Practical Method for Targeted Library Design Balancing Lead-like Properties with Diversity

ChemMedChem, 2009-05, Vol.4 (5), p.800-808

2009

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On the absolute configuration of 1-cyclopropylethan-1-amine

Tetrahedron: asymmetry, 2017-09, Vol.28 (9), p.1135-1138

2017

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[3 + 2] Cycloaddition Reactions of 4-Alkyl-3-hydroxy-2H-pyrazolo[4,3-c]iso- quinolinium Inner Salts

Journal of organic chemistry, 2003-10, Vol.68 (22), p.8700-8703

2003

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ChemInform Abstract: Scaffold-Hopping with Zwitterionic CCR3 Antagonists: Identification and Optimization of a Series with Good Potency and Pharmacokinetics Leading to the Discovery of AZ12436092 (I)

ChemInform, 2013-03, Vol.44 (12), p.no-no

2013

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PI3K inhibitors are finally coming of age

Design, Synthesis, and Biological Evaluation of MEK PROTACs

Author Correction: PI3K inhibitors are finally coming of age

Impact of Stereospecific Intramolecular Hydrogen Bonding on Cell Permeability and Physicochemical Properties

Evolution of PI3Kγ and δ Inhibitors for Inflammatory and Autoimmune Diseases

Structural and conformational determinants of macrocycle cell permeability

Stabilization of protein-protein interactions in drug discovery

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

A class of highly selective inhibitors bind to an active state of PI3Kγ

Scaffold-hopping with zwitterionic CCR3 antagonists: Identification and optimisation of a series with good potency and pharmacokinetics leading to the discovery of AZ12436092

Discovery of AZD8154, a Dual PI3Kγδ Inhibitor for the Treatment of Asthma

Identification of Phosphate-Containing Compounds as New Inhibitors of 14-3-3/c-Abl Protein–Protein Interaction

Design and Synthesis of Soluble and Cell-Permeable PI3Kδ Inhibitors for Long-Acting Inhaled Administration

Spiro-fused Pyrrolidine, Piperidine, and Oxindole Scaffolds from Lactams

14-3-3 modulation of the inflammatory response

Designing novel building blocks is an overlooked strategy to improve compound quality

Surprising lipophilicity observations identify unexpected conformational effects

Glucocorticoid receptor Thr524 phosphorylation by MINK1 induces interactions with 14-3-3 protein regulators

Designing Selective Drug-like Molecular Glues for the Glucocorticoid Receptor/14-3‑3 Protein–Protein Interaction

Correction to “Designing Selective Drug-like Molecular Glues for the Glucocorticoid Receptor/14-3‑3 Protein–Protein Interaction”

The discovery of CCR3/H1 dual antagonists with reduced hERG risk

A Practical Method for Targeted Library Design Balancing Lead-like Properties with Diversity

On the absolute configuration of 1-cyclopropylethan-1-amine

[3 + 2] Cycloaddition Reactions of 4-Alkyl-3-hydroxy-2H-pyrazolo[4,3-c]iso- quinolinium Inner Salts

ChemInform Abstract: Scaffold-Hopping with Zwitterionic CCR3 Antagonists: Identification and Optimization of a Series with Good Potency and Pharmacokinetics Leading to the Discovery of AZ12436092 (I)

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