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Journal of Medicinal Chemistry|January 6, 2016
4-Acyl Pyrrole Derivatives Yield Novel Vectors for Designing Inhibitors of the Acetyl-Lysine Recognition Site of BRD4(1)Martin Hügle, Xavier Lucas, Gerhard Weitzel, et al.Nature Chemical Biology|March 14, 2017
Structural basis of PROTAC cooperative recognition for selective protein degradationMorgan S Gadd, Andrea Testa, Xavier Lucas, et al.Angewandte Chemie (International Ed. in English)|August 3, 2017
Beyond the BET Family: Targeting CBP/p300 with 4-Acyl PyrrolesMartin Hügle, Xavier Lucas, Dmytro Ostrovskyi, et al.Journal of Medicinal Chemistry|December 4, 2020
4-Acyl Pyrroles as Dual BET-BRD7/9 Bromodomain Inhibitors Address BETi Insensitive Human Cancer Cell LinesMartin Hügle, Pierre Regenass, Robin Warstat, et al.Nucleic Acids Research|November 29, 2015
StreptomeDB 2.0--an extended resource of natural products produced by streptomycetesDennis Klementz, Kersten Döring, Xavier Lucas, et al.Data in Brief|May 10, 2016
Preparation data of the bromodomains BRD3(1), BRD3(2), BRD4(1), and BRPF1B and crystallization of BRD4(1)-inhibitor complexesMartin Hügle, Xavier Lucas, Gerhard Weitzel, et al.Journal of the American Chemical Society|June 28, 2018
3-Fluoro-4-hydroxyprolines: Synthesis, Conformational Analysis, and Stereoselective Recognition by the VHL E3 Ubiquitin Ligase for Targeted Protein DegradationAndrea Testa, Xavier Lucas, Guilherme V Castro, et al.Nature Structural & Molecular Biology|October 31, 2023
The molecular basis of drug selectivity for α5 subunit-containing GABAA receptorsVikram Babu Kasaragod, Tomas Malinauskas, Ayla A Wahid, et al.Journal of Chemical Information and Modeling|November 26, 2022
Collaborative Assessment of Molecular Geometries and Energies from the Open Force FieldLorenzo D'Amore, David F Hahn, David L Dotson, et al.Journal of Chemical Theory and Computation|September 22, 2021
Development and Benchmarking of Open Force Field v1.0.0-the Parsley Small-Molecule Force FieldYudong Qiu, Daniel G A Smith, Simon Boothroyd, et al.Pageof 4