18 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
Organization
Strategies of Targeting CK2 in Drug Discovery: Challenges, Opportunities, and Emerging Prospects.

Sichuan University
Bioactive Aurones, Indanones, and Other Hemiindigoid Scaffolds: Medicinal Chemistry and Photopharmacology Perspectives.

Universite Grenoble Alpes
Molecular hybrids: A five-year survey on structures of multiple targeted hybrids of protein kinase inhibitors for cancer therapy.

Al-Azhar University
Fused-azepinones: Emerging scaffolds of medicinal importance.

National Institute of Pharmaceutical Education and Research (NIPER)
Comprehensive review for anticancer hybridized multitargeting HDAC inhibitors.

Menoufia University
Design, synthesis and biological evaluation of chromone derivatives as novel protein kinase CK2 inhibitors.

China Pharmaceutical University
Structure-Activity Relationship in the Leucettine Family of Kinase Inhibitors.

Manros Therapeutics & Perha Pharmaceuticals
Recent advances in development of hetero-bivalent kinase inhibitors.

Cha University
Discovery of Novel Dual-Target Inhibitor of Bromodomain-Containing Protein 4/Casein Kinase 2 Inducing Apoptosis and Autophagy-Associated Cell Death for Triple-Negative Breast Cancer Therapy.

Sichuan University-Oxford University Huaxi Gastrointestinal Cancer Centre
Discovery of 5-(3-Chlorophenylamino)benzo[

Southeast University
New Dual CK2/HDAC1 Inhibitors with Nanomolar Inhibitory Activity against Both Enzymes.

Universidad San Pablo-Ceu
Inhibitory Properties of ATP-Competitive Coumestrol and Boldine Are Correlated to Different Modulations of CK2 Flexibility.

University of Padua and Institute of Biomolecular Chemistry
2-Aminothiazole Derivatives as Selective Allosteric Modulators of the Protein Kinase CK2. 2. Structure-Based Optimization and Investigation of Effects Specific to the Allosteric Mode of Action.

University of Lyon
Discovery of 4

TBA
A review on flavones targeting serine/threonine protein kinases for potential anticancer drugs.

China Pharmaceutical University
Progress toward B-Cell Lymphoma 6 BTB Domain Inhibitors for the Treatment of Diffuse Large B-Cell Lymphoma and Beyond.

University of Maryland
Dual-Specificity Tyrosine Phosphorylation-Regulated Kinase 1A (DYRK1A) Inhibitors as Potential Therapeutics.

Seoul National University
A new family of densely functionalized fused-benzoquinones as potent human protein kinase CK2 inhibitors.

Instituto Universitario De Bio-Org£Nica Antonio Gonz£Lez (Cibican)