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Structural and functional diversification in the teleost S100 family of calcium-binding proteins

BMC evolutionary biology, 2008-02, Vol.8 (1), p.48, Article 48

2008

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Exploiting vulnerabilities of SWI/SNF chromatin remodelling complexes for cancer therapy

Oncogene, 2021-05, Vol.40 (21), p.3637-3654

2021

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Causal analysis approaches in Ingenuity Pathway Analysis

Bioinformatics, 2014-02, Vol.30 (4), p.523-530

2014

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Skipping the Replica Exchange Ladder with Normalizing Flows

The journal of physical chemistry letters, 2022-12, Vol.13 (50), p.11643-11649

2022

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Tracking the PROTAC degradation pathway in living cells highlights the importance of ternary complex measurement for PROTAC optimization

Cell chemical biology, 2023-07, Vol.30 (7), p.753-765.e8

2023

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Cascade Synthesis of Kinase-Privileged 3‑Aminoindazoles via Intramolecular N–N Bond Formation

Journal of organic chemistry, 2022-03, Vol.87 (5), p.3856-3862

2022

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Elimination of mutant SWI/SNF complexes by protein quality control: new opportunities targeting aggressive rhabdoid tumours

Signal transduction and targeted therapy, 2024-09, Vol.9 (1), p.224-3, Article 224

2024

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Pan-SMARCA/PB1 Bromodomain Inhibitors and Their Role in Regulating Adipogenesis

Journal of medicinal chemistry, 2020-12, Vol.63 (23), p.14680-14699

2020

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Development of a potent and selective chemical probe for the pleiotropic kinase CK2

Cell chemical biology, 2021-04, Vol.28 (4), p.546-558.e10

2021

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Synthesis and biological evaluation of 1H-pyrrolo[3,2–g]isoquinolines

Bioorganic & medicinal chemistry, 2024-02, Vol.100, p.117619-117619, Article 117619

2024

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A chemical toolbox for the study of bromodomains and epigenetic signaling

Nature communications, 2019-04, Vol.10 (1), p.1915-14, Article 1915

2019

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Targeting Cavity-Creating p53 Cancer Mutations with Small-Molecule Stabilizers: the Y220X Paradigm

ACS chemical biology, 2020-03, Vol.15 (3), p.657-668

2020

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From data to discovery: AI-guided analysis of disease-relevant molecules in spinal muscular atrophy (SMA)

Human molecular genetics, 2024-07, Vol.33 (15), p.1367-1377

2024

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Synthesis of Pyrazole-Based Macrocycles Leads to a Highly Selective Inhibitor for MST3

Journal of medicinal chemistry, 2024-01, Vol.67 (1), p.674-690

2024

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Structural basis of p53 inactivation by cavity-creating cancer mutations and its implications for the development of mutant p53 reactivators

Cell death & disease, 2024-06, Vol.15 (6), p.408-10

2024

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Synthesis and evaluation of chemical linchpins for highly selective CK2α targeting

European journal of medicinal chemistry, 2024-10, Vol.276, p.116672, Article 116672

2024

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Identification of 4-(6-((2-methoxyphenyl)amino)pyrazin-2-yl)benzoic acids as CSNK2A inhibitors with antiviral activity and improved selectivity over PIM3

Bioorganic & medicinal chemistry letters, 2024-02, Vol.99, p.129617-129617, Article 129617

2024

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MSC-1186, a Highly Selective Pan-SRPK Inhibitor Based on an Exceptionally Decorated Benzimidazole-Pyrimidine Core

Journal of medicinal chemistry, 2023-01, Vol.66 (1), p.837-854

2023

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Macrocyclization of Quinazoline-Based EGFR Inhibitors Leads to Exclusive Mutant Selectivity for EGFR L858R and Del19

Journal of medicinal chemistry, 2022-12, Vol.65 (23), p.15679-15697

2022

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More than an Amide Bioisostere: Discovery of 1,2,4-Triazole-containing Pyrazolo[1,5‑a]pyrimidine Host CSNK2 Inhibitors for Combatting β‑Coronavirus Replication

Journal of medicinal chemistry, 2024-07, Vol.67 (14), p.12261-12313

2024

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Synthesis and Biological Evaluation of 2-Substituted Quinazolin-4(3 H )-Ones with Antiproliferative Activities

Molecules (Basel, Switzerland), 2023-12, Vol.28 (23), p.7912

2023

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Chemical, Biochemical, Cellular, and Physiological Characterization of Leucettinib-21, a Down Syndrome and Alzheimer’s Disease Drug Candidate

Journal of medicinal chemistry, 2023-12, Vol.66 (23), p.15648-15670

2023

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A C‑Degron Structure-Based Approach for the Development of Ligands Targeting the E3 Ligase TRIM7

ACS chemical biology, 2024-07, Vol.19 (7), p.1638-1647

2024

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The nuclear pore proteins Nup88/214 and T-cell acute lymphatic leukemia–associated NUP214 fusion proteins regulate Notch signaling

The Journal of biological chemistry, 2019-08, Vol.294 (31), p.11741-11750

2019

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Multi-phase Boltzmann weighting: accounting for local inhomogeneity in molecular simulations of water–octanol partition coefficients in the SAMPL6 challenge

Journal of computer-aided molecular design, 2020-05, Vol.34 (5), p.471-483

2020

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Structural and functional diversification in the teleost S100 family of calcium-binding proteins

Exploiting vulnerabilities of SWI/SNF chromatin remodelling complexes for cancer therapy

Causal analysis approaches in Ingenuity Pathway Analysis

Skipping the Replica Exchange Ladder with Normalizing Flows

Tracking the PROTAC degradation pathway in living cells highlights the importance of ternary complex measurement for PROTAC optimization

Cascade Synthesis of Kinase-Privileged 3‑Aminoindazoles via Intramolecular N–N Bond Formation

Elimination of mutant SWI/SNF complexes by protein quality control: new opportunities targeting aggressive rhabdoid tumours

Pan-SMARCA/PB1 Bromodomain Inhibitors and Their Role in Regulating Adipogenesis

Development of a potent and selective chemical probe for the pleiotropic kinase CK2

Synthesis and biological evaluation of 1H-pyrrolo[3,2–g]isoquinolines

A chemical toolbox for the study of bromodomains and epigenetic signaling

Targeting Cavity-Creating p53 Cancer Mutations with Small-Molecule Stabilizers: the Y220X Paradigm

From data to discovery: AI-guided analysis of disease-relevant molecules in spinal muscular atrophy (SMA)

Synthesis of Pyrazole-Based Macrocycles Leads to a Highly Selective Inhibitor for MST3

Structural basis of p53 inactivation by cavity-creating cancer mutations and its implications for the development of mutant p53 reactivators

Synthesis and evaluation of chemical linchpins for highly selective CK2α targeting

Identification of 4-(6-((2-methoxyphenyl)amino)pyrazin-2-yl)benzoic acids as CSNK2A inhibitors with antiviral activity and improved selectivity over PIM3

MSC-1186, a Highly Selective Pan-SRPK Inhibitor Based on an Exceptionally Decorated Benzimidazole-Pyrimidine Core

Macrocyclization of Quinazoline-Based EGFR Inhibitors Leads to Exclusive Mutant Selectivity for EGFR L858R and Del19

More than an Amide Bioisostere: Discovery of 1,2,4-Triazole-containing Pyrazolo[1,5‑a]pyrimidine Host CSNK2 Inhibitors for Combatting β‑Coronavirus Replication

Synthesis and Biological Evaluation of 2-Substituted Quinazolin-4(3 H )-Ones with Antiproliferative Activities

Chemical, Biochemical, Cellular, and Physiological Characterization of Leucettinib-21, a Down Syndrome and Alzheimer’s Disease Drug Candidate

A C‑Degron Structure-Based Approach for the Development of Ligands Targeting the E3 Ligase TRIM7

The nuclear pore proteins Nup88/214 and T-cell acute lymphatic leukemia–associated NUP214 fusion proteins regulate Notch signaling

Multi-phase Boltzmann weighting: accounting for local inhomogeneity in molecular simulations of water–octanol partition coefficients in the SAMPL6 challenge

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