A review of progress in o-aminobenzamide-based HDAC inhibitors with dual targeting capabilities for cancer therapy
WX Zhang, J Huang, XY Tian, YH Liu, MQ Jia… - European journal of …, 2023 - Elsevier
Histone deacetylases, as a new class of anticancer targets, could maintain homeostasis by
catalyzing histone deacetylation and play important roles in regulating the expression of …
catalyzing histone deacetylation and play important roles in regulating the expression of …
Quinazoline-based VEGFR-2 inhibitors as potential anti-angiogenic agents: A contemporary perspective of SAR and molecular docking studies
M Moradi, A Mousavi, Z Emamgholipour… - European Journal of …, 2023 - Elsevier
Angiogenesis, the formation of new blood vessels from the existing vasculature, is pivotal in
the migration, growth, and differentiation of endothelial cells in normal physiological …
the migration, growth, and differentiation of endothelial cells in normal physiological …
Vascular endothelial growth factor-D (VEGF-D): An angiogenesis bypass in malignant tumors
SMZ Bokhari, P Hamar - International Journal of Molecular Sciences, 2023 - mdpi.com
Vascular endothelial growth factors (VEGFs) are the key regulators of vasculogenesis in
normal and oncological development. VEGF-A is the most studied angiogenic factor …
normal and oncological development. VEGF-A is the most studied angiogenic factor …
New theobromine derivatives inhibiting VEGFR-2: design, synthesis, antiproliferative, docking and molecular dynamics simulations
HA Mahdy, H Elkady, MS Taghour… - Future Medicinal …, 2023 - Taylor & Francis
Background: VEGFR-2 is one of the most effective targets in cancer treatment. Aim: The
design and semi-synthesis of new theobromine derivatives as potential VEGFR-2 inhibitors …
design and semi-synthesis of new theobromine derivatives as potential VEGFR-2 inhibitors …
Synthesis, characterization, and anticancer activity of new N, N′-Diarylthiourea derivative against breast cancer cells
The goal of the current study was to prepare two new homologous series of N, N′-
diarylurea and N, N′-diarylthiourea derivatives to investigate the therapeutic effects of …
diarylurea and N, N′-diarylthiourea derivatives to investigate the therapeutic effects of …
Imidazopyridine-based kinase inhibitors as potential anticancer agents: A review
F Peytam, Z Emamgholipour, A Mousavi, M Moradi… - Bioorganic …, 2023 - Elsevier
Considering the fundamental role of protein kinases in the mechanism of protein
phosphorylation in critical cellular processes, their dysregulation, especially in cancers, has …
phosphorylation in critical cellular processes, their dysregulation, especially in cancers, has …
Novel 3-phenylquinazolin-2,4(1H,3H)-diones as dual VEGFR-2/c-Met-TK inhibitors: design, synthesis, and biological evaluation
Multitarget anticancer drugs are more superior than single target drugs regarding patient
compliance, drug adverse effects, drug-drug interactions, drug resistance as well as …
compliance, drug adverse effects, drug-drug interactions, drug resistance as well as …
Recent Advances and Future Directions on Small Molecule VEGFR Inhibitors in Oncological Conditions
A Thakur, M Rana, A Mishra, C Kaur, CH Pan… - European Journal of …, 2024 - Elsevier
ABSTRACT “A journey of mixed emotions” is a quote that best describes the progress chart
of vascular endothelial growth factor receptor (VEGFR) inhibitors as cancer therapeutics in …
of vascular endothelial growth factor receptor (VEGFR) inhibitors as cancer therapeutics in …
Structural basis and selectivity of sulfatinib binding to FGFR and CSF-1R
Q Lin, S Dai, L Qu, H Lin, M Guo, H Wei… - Communications …, 2024 - nature.com
Acquired drug resistance poses a challenge for single-target FGFR inhibitors, leading to the
development of dual-or multi-target FGFR inhibitors. Sulfatinib is a multi-target kinase …
development of dual-or multi-target FGFR inhibitors. Sulfatinib is a multi-target kinase …
Recent development of VEGFR small molecule inhibitors as anticancer agents: A patent review (2021–2023)
J Zeng, Q Deng, Z Chen, S Yan, Q Dong, Y Zhang… - Bioorganic …, 2024 - Elsevier
VEGFR, a receptor tyrosine kinase inhibitor (TKI), is an important regulatory factor that
promotes angiogenesis and vascular permeability. It plays a significant role in processes …
promotes angiogenesis and vascular permeability. It plays a significant role in processes …