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Bioorganic Chemistry|April 3, 2025
Structure-activity relationship study of navarixin analogues as dual CXCR2 and CCR7 antagonistsAnže Meden, Sandra Claes, Tom Van Loy, et al.
The Journal of Organic Chemistry|November 19, 2024
Protecting Group Control of Hydroxyketone-Hemiketal Tautomeric Equilibrium Enables the Stereoselective Synthesis of a 1<i>'</i>-Azido <i>C</i>-NucleosideSubhankar Panda, Moyosore O Orimoloye, Tej Narayan Poudel, et al.
Bioorganic Chemistry|August 6, 2023
Synthesis and structure-activity relationship study of phenoxybenzylpiperazine analogues as CCR8 agonistsQifei Li, Sandra Claes, Yenthel Verhaegen, et al.
Organic & Biomolecular Chemistry|October 8, 2016
Bifunctional aryloxyphosphoramidate prodrugs of 2'-C-Me-uridine: synthesis and anti-HCV activityMunmun Maiti, Ling-Jie Gao, Chunsheng Huang, et al.
Bioorganic & Medicinal Chemistry|January 26, 2013
Synthesis of a 2,4,6-trisubstituted 5-cyano-pyrimidine library and evaluation of its immunosuppressive activity in a Mixed Lymphocyte Reaction assayAlessandro Stella, Kristien Van Belle, Steven De Jonghe, et al.
Cancer Immunology, Immunotherapy : CII|January 17, 2024
Development of a cellular model to study CCR8 signaling in tumor-infiltrating regulatory T cellsLibao Liu, Laurie Rangan, Nathan Vanalken, et al.
Biochemical Pharmacology|April 19, 2021
Biological characterization of ligands targeting the human CC chemokine receptor 8 (CCR8) reveals the biased signaling properties of small molecule agonistsLibao Liu, Jordi Doijen, Thomas D'huys, et al.
Chemmedchem|July 10, 2013
Discovery of an acyclic nucleoside phosphonate that inhibits Mycobacterium tuberculosis ThyX based on the binding mode of a 5-alkynyl substrate analogueAnastasia Parchina, Matheus Froeyen, Lia Margamuljana, et al.
Journal of Medicinal Chemistry|November 6, 2014
Imidazopyridine- and purine-thioacetamide derivatives: potent inhibitors of nucleotide pyrophosphatase/phosphodiesterase 1 (NPP1)Lei Chang, Sang-Yong Lee, Piotr Leonczak, et al.
Nature Communications|December 9, 2021
Sliding of HIV-1 reverse transcriptase over DNA creates a transient P pocket - targeting P-pocket by fragment screeningAbhimanyu K Singh, Sergio E Martinez, Weijie Gu, et al.
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