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European Journal of Medicinal Chemistry|May 23, 2026
Thioureas, thiosemicarbazones, hydroxamic acids and related compounds as copper-chelating tyrosinase inhibitorsRomain HaudecoeurChemistry (Weinheim an Der Bergstrasse, Germany)|August 8, 2013
Multitasking water-soluble synthetic G-quartets: from preferential RNA-quadruplex interaction to biocatalytic activityRomain Haudecoeur, Loic Stefan, David MonchaudJournal of Medicinal Chemistry|August 14, 2020
Advances in the Design of Genuine Human Tyrosinase Inhibitors for Targeting Melanogenesis and Related PigmentationsBrayan Roulier, Basile Pérès, Romain HaudecoeurJournal of the American Chemical Society|January 10, 2013
A model of smart G-quadruplex ligandRomain Haudecoeur, Loic Stefan, Franck Denat, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|February 19, 2024
Expanding Chemical Frontiers: Approaches for Generating Diverse and Bioactive Natural Product-Like Compounds Libraries from ExtractsAurélien Beato, Romain Haudecoeur, Benjamin Boucherle, et al.Phytochemistry|July 14, 2017
Occurrences, biosynthesis and properties of aurones as high-end evolutionary productsBenjamin Boucherle, Marine Peuchmaur, Ahcène Boumendjel, et al.Chemmedchem|August 6, 2024
Tyrosinase Inhibition and Antimelanogenic Effects of Resorcinol-Containing CompoundsMorane Beaumet, Leticia M Lazinski, Marc Maresca, et al.European Journal of Medicinal Chemistry|July 24, 2023
Catechol-mimicking transition-state analogues as non-oxidizable inhibitors of tyrosinasesMorane Beaumet, Leticia M Lazinski, Marc Maresca, et al.Journal of Medicinal Chemistry|February 2, 2021
β-Carboline as a Privileged Scaffold for Multitarget Strategies in Alzheimer's Disease TherapyAurélien Beato, Anthonin Gori, Benjamin Boucherle, et al.Journal of Medicinal Chemistry|September 20, 2022
Bioactive Aurones, Indanones, and Other Hemiindigoid Scaffolds: Medicinal Chemistry and Photopharmacology PerspectivesLeticia M Lazinski, Guy Royal, Maxime Robin, et al.Pageof 4