Dany Pechalrieu

发表

Compounds for use in the treatment of mycobacterial infections: a patent evaluation (WO2014049107A1)

Marie Lopez, Dany Pechalrieu, 2015, Expert opinion on therapeutic patents.

Bisubstrate-type chemical probes identify GRP94 as a potential target of cytosine-containing adenosine analogs.

G. Chiosis, O. Burlet-Schiltz, Fanny Assemat, 2020, ACS chemical biology.

Identification of novel quinazoline derivatives as potent antiplasmodial agents.

A. Mai, P. Arimondo, G. Fabrizi, 2019, European journal of medicinal chemistry.

Hemisynthetic derivatives of the natural alkaloid trilobine are fast-acting antimalarial compounds with sustained activity in multi-drug resistant P. falciparum isolates

S. Thiberge, C. Jallet, G. Médard, 2022, bioRxiv.

Chemoproteomics‐Enabled De Novo Discovery of Photoswitchable Carboxylesterase Inhibitors for Optically Controlled Drug Metabolism

A. Adibekian, Nan Qiu, D. Abegg, 2020, Angewandte Chemie.

Chemoproteomics-Enabled De Novo Discovery of Photoswitchable Carboxylesterase Inhibitors for Optically Controlled Drug Metabolism.

A. Adibekian, Nan Qiu, D. Abegg, 2020, Angewandte Chemie.

Hijacking DNA methyltransferase transition state analogues to produce chemical scaffolds for PRMT inhibitors

A. Jeltsch, E. Decroly, P. Arimondo, 2018, Philosophical Transactions of the Royal Society B: Biological Sciences.

Chemoproteomic Profiling by Cysteine Fluoroalkylation Reveals Myrocin G as an Inhibitor of the Nonhomologous End Joining DNA Repair Pathway.

A. Adibekian, Nan Qiu, D. Abegg, 2021, Journal of the American Chemical Society.

Chemoproteomic Profiling by Cysteine Fluoroalkylation Reveals the DNA Repair Protein XRCC5 as a Functional Target of Myrocin G

A. Adibekian, Nan Qiu, D. Abegg, 2021 .

Clinical Antiviral Drug Arbidol Inhibits Infection by SARS-CoV-2 and Variants through Direct Binding to the Spike Protein

H. Choe, A. Adibekian, D. Abegg, 2021, ACS chemical biology.

Synthesis of novel 3-halo-3-nitroflavanones and their activities as DNA methyltransferase inhibitors in cancer cells.

D. Dauzonne, P. Arimondo, Marie Lopez, 2019, European journal of medicinal chemistry.

Hemisynthetic alkaloids derived from trilobine are antimalarials with sustained activity in multidrug-resistant Plasmodium falciparum

S. Thiberge, C. Jallet, G. Médard, 2023, iScience.

DNA methyltransferase inhibitors in cancer: From pharmacology to translational studies.

C. Etiévant, P. Arimondo, Dany Pechalrieu, 2017, Biochemical pharmacology.

Rational Design of Bisubstrate-Type Analogues as Inhibitors of DNA Methyltransferases in Cancer Cells.

M. Bouhlel, P. Arimondo, L. Halby, 2017, Journal of medicinal chemistry.

Novel Quinoline Compounds Active in Cancer Cells through Coupled DNA Methyltransferase Inhibition and Degradation

D. Trisciuoglio, L. Altucci, A. Mai, 2020, Cancers.

Combined Omics Approach Identifies Gambogic Acid and Related Xanthones as Covalent Inhibitors of the Serine Palmitoyltransferase Complex.

H. Riezman, Q. You, J. Hannich, 2020, Cell chemical biology.

Rational Design of Bisubstrate-Type Analogues as Inhibitors of DNA Methyltransferases in Cancer Cells.

M. Bouhlel, P. Arimondo, L. Halby, 2017, Journal of medicinal chemistry.

Chemoproteomic Profiling Maps Zinc-Dependent Cysteine Reactivity.

A. Adibekian, Nan Qiu, D. Abegg, 2024, Chemical research in toxicology.