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References from Discovery and biological characterization of 1-[4-(2-difluoromethoxyphenyl)-5-methylthiazol-2-yl]-3-(naphthalen-1-yl)urea (DFMNTU): A novel thiazolyl-urea chemotype targeting yellow fever virus and host casein kinase 2 (CK2). Local targets link to admitted publications; unresolved targets remain external evidence.
Computational pharmacology and pharmacokinetics of betanin: an integrated ADMET, SwissADME, DFT, and target prediction study
2025 · External reference
Molecular recognition of diaryl ureas in their targeted proteins—A data mining and quantum chemical study
10.3390/molecules30051007 · 2025 · External reference
Thiazoles inhibit reactive oxygen and nitrogen species mediated diabetes mellitus: integrated in vitro and in silico insights
10.1039/d6ra01667g · 2026 · External reference
2-aminothiazole derivatives as selective allosteric modulators of the protein kinase CK2. 1. Identification of an allosteric binding site
10.1021/acs.jmedchem.8b01766 · 2019 · External reference
Cytopathic effect inhibition assay for determining the in-vitro susceptibility of herpes simplex virus to antiviral agents
10.1093/jac/44.5.705 · 1999 · External reference
Synthesis and structure-activity relationship of 4, 6-bis (pyrrolidin-1-yl)-1, 3, 5-triazines, their antiviral activity against yellow fever and Tacaribe viruses
10.1016/j.rechem.2026.103613 · 2026 · External reference
Synthesis and reactivity of α-Bromo-4-(difluoromethylthio)acetophenone
10.1023/a:1026114908997 · 2003 · External reference
Preparation and use ofα-bromomono- and-bromobis-difluoromethoxyacetophenones in the synthesis of polymethyleneimidazoles with an angular nitrogen atom
10.1007/bf02290868 · 1997 · External reference
Preparation and use ofα-bromomono- and-bromobis-difluoromethoxyacetophenones in the synthesis of polymethyleneimidazoles with an angular nitrogen atom
10.1007/bf02290868 · 1997 · External reference
Bromine-1,4-Dioxane
2001 · External reference
SuperPred 3.0: drug classification and target prediction—a machine learning approach
10.1093/nar/gkac297 · 2022 · External reference
A note of caution on the role of halogen bonds for protein kinase/inhibitor recognition suggested by high- and low-salt CK2α complex structures
10.1021/acschembio.5b00235 · 2015 · External reference
2-Hydroxyacetophenone via fries rearrangement and related reactions: a comparative applied study
10.1002/jctb.503300182 · 1980 · External reference
MzDOCK : a free ready-to-use GUI -based pipeline for molecular docking simulations
10.1002/jcc.27390 · 2024 · External reference
Urea-functionalized heterocycles: structure, hydrogen bonding and applications
10.3390/molecules28237757 · 2023 · External reference
Discovery of new aurone derivatives as submicromolar CK2 inhibitors
10.1080/14756366.2025.2566780 · 2025 · External reference
O -Acylation of substituted phenols with various alkanoyl chlorides under phase-transfer catalyst conditions
10.1080/00397911.2011.584007 · 2012 · External reference
Evaluation of cell viability dyes in antiviral assays with RNA viruses that exhibit different cytopathogenic properties
10.1016/j.jviromet.2017.03.012 · 2017 · External reference
Insight into the therapeutic potential of pyrazole-thiazole hybrids: a comprehensive review
10.1002/ardp.202400576 · 2024 · External reference
Production of recombinant human apoptosis signal-regulating kinase 1 (ASK1) in Escherichia coli
10.1016/j.pep.2016.05.016 · 2016 · External reference
The allosteric inhibitor ABL001 enables dual targeting of BCR–ABL1
10.1038/nature21702 · 2017 · External reference
In silico ADME profiling of salubrinal and its analogues
10.3390/futurepharmacol2020013 · 2022 · External reference
