Blandine Baratte

CNRS FR2424, Plateforme De Criblage KISSf Station Biologique, Place Georges Teissier, CS90074
Roscoff, 29688, France

Last Updated: 09/26/2026

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Found 43 publications

An Experimentally Validated Structure-Based Virtual Screening Approach to Identify Nucleotide-Binding Protein Inhibitors as a New Source of Kinase Inhibitors.

An Experimentally Validated Structure-Based Virtual Screening Approach to Identify Nucleotide-Binding Protein Inhibitors as a New Source of Kinase Inhibitors.

Journal: Pharmaceuticals (Basel, Switzerland)

Published: June 01, 2026

Sibiriline, a novel dual inhibitor of necroptosis and ferroptosis, prevents RIPK1 kinase activity and (phospho)lipid peroxidation as a potential therapeutic strategy.

Sibiriline, a novel dual inhibitor of necroptosis and ferroptosis, prevents RIPK1 kinase activity and (phospho)lipid peroxidation as a potential therapeutic strategy.

Journal: Cell death discovery

Published: September 18, 2025

Research towards selective inhibition of the CLK3 kinase.

Research towards selective inhibition of the CLK3 kinase.

Journal: Beilstein journal of organic chemistry

Published: July 03, 2025

New Insights into the Anticancer Effects and Toxicogenomic Safety of Two β-Lapachone Derivatives.

New Insights into the Anticancer Effects and Toxicogenomic Safety of Two β-Lapachone Derivatives.

Journal: Pharmaceuticals (Basel, Switzerland)

Published: April 08, 2025

Pharmacophore-guided optimization of the hit compound CTN1122 in the design of promising imidazo[1,2-a]pyrazine derivatives targeting the casein kinase 1 for antileishmanial therapy.

Pharmacophore-guided optimization of the hit compound CTN1122 in the design of promising imidazo[1,2-a]pyrazine derivatives targeting the casein kinase 1 for antileishmanial therapy.

Journal: RSC medicinal chemistry

Published: March 25, 2025

Investigating the C2 Modulation of the Imidazo[1,2-a]pyrazine-Based Hit Compound CTN1122: Synthesis, in vitro Antileishmanial Activity, Cytotoxicity and Casein Kinase 1 Inhibition.

Investigating the C2 Modulation of the Imidazo[1,2-a]pyrazine-Based Hit Compound CTN1122: Synthesis, in vitro Antileishmanial Activity, Cytotoxicity and Casein Kinase 1 Inhibition.

Journal: ChemMedChem

Published: October 29, 2024

Novel Thiazole-Fused [4,5-g] or [5,4-g]Quinazolin-8-ones and Their Quinazoline Analogues: Synthesis and Biological Evaluation.

Novel Thiazole-Fused [4,5-g] or [5,4-g]Quinazolin-8-ones and Their Quinazoline Analogues: Synthesis and Biological Evaluation.

Journal: Pharmaceuticals (Basel, Switzerland)

Published: October 14, 2024

New Fusarochromanone Derivatives from the Marine Fungus Fusarium equiseti UBOCC-A-117302.

New Fusarochromanone Derivatives from the Marine Fungus Fusarium equiseti UBOCC-A-117302.

Journal: Marine drugs

Published: August 27, 2024

Ethaverine and Papaverine Target Cyclin-Dependent Kinase 5 and Inhibit Lung Cancer Cell Proliferation and Migration.

Ethaverine and Papaverine Target Cyclin-Dependent Kinase 5 and Inhibit Lung Cancer Cell Proliferation and Migration.

Journal: ACS pharmacology & translational science

Published: January 18, 2024

Imidazo[1,2-a]quinazolines as novel, potent EGFR-TK inhibitors: Design, synthesis, bioactivity evaluation, and in silico studies.

Imidazo[1,2-a]quinazolines as novel, potent EGFR-TK inhibitors: Design, synthesis, bioactivity evaluation, and in silico studies.

Journal: Bioorganic chemistry

Published: October 17, 2022

Structure Activity Relationship Studies around DB18, a Potent and Selective Inhibitor of CLK Kinases.

Structure Activity Relationship Studies around DB18, a Potent and Selective Inhibitor of CLK Kinases.

Journal: Molecules (Basel, Switzerland)

Published: August 26, 2022

Synthesis and biological evaluation of Haspin inhibitors: Kinase inhibitory potency and cellular activity.

Synthesis and biological evaluation of Haspin inhibitors: Kinase inhibitory potency and cellular activity.

Journal: European journal of medicinal chemistry

Published: March 15, 2022

Showing 1-12 of 43

Last Updated: 09/26/2026