Rationale, in silico docking, ADMET profile, design, synthesis and cytotoxicity evaluations of phthalazine derivatives as VEGFR-2 inhibitors and apoptosis inducers
HH Bayoumi, MK Ibrahim, MA Dahab, F Khedr… - RSC …, 2024 - pubs.rsc.org
New phthalazine derivatives as vascular endothelial growth factor receptor-2 (VEGFR-2)
inhibitors were synthesized joined to different spacers including pyrazole, α, β-unsaturated …
inhibitors were synthesized joined to different spacers including pyrazole, α, β-unsaturated …
Exploration of the VEGFR-2 inhibition activity of phthalazine derivatives: design, synthesis, cytotoxicity, ADMET, molecular docking and dynamic simulation
HH Bayoumi, MK Ibrahim, MA Dahab, F Khedr… - RSC …, 2024 - pubs.rsc.org
Novel phthalazine derivatives were designed, synthesized and evaluated against Hep G2
and MCF-7 as VEGFR-2 inhibitors. In particular, compounds 2g and 4a were found to be the …
and MCF-7 as VEGFR-2 inhibitors. In particular, compounds 2g and 4a were found to be the …
Exploration of cytotoxicity of iodoquinazoline derivatives as inhibitors of both VEGFR‐2 and EGFRT790M: Molecular docking, ADMET, design, and syntheses
Novel inhibitors of epidermal growth factor receptor (EGFR) T790M/vascular endothelial
growth factor receptor‐2 (VEGFR‐2) were synthesized based on the iodoquinazoline …
growth factor receptor‐2 (VEGFR‐2) were synthesized based on the iodoquinazoline …
Anticancer evaluations of iodoquinazoline substituted with allyl and/or benzyl as dual inhibitors of EGFR WT and EGFR T790M: design, synthesis, ADMET and …
Fifteen new iodoquinazoline derivatives, 5a, b to 18, are reported in this study and their
anticancer evaluation as dual inhibitors of EGFRWT and EGFRT790M. The new derivatives …
anticancer evaluation as dual inhibitors of EGFRWT and EGFRT790M. The new derivatives …
Rational design, docking, syntheses, ADMET and cytotoxicity assessments of iodoquinazoline derivatives as inhibitors of EGFRT790M and VEGFR-2
Multi-targeted anticancer agents demonstrated synergistic properties as they met in
inhibition of signaling pathways targeting diverse receptors with less toxicity. Thus, dual …
inhibition of signaling pathways targeting diverse receptors with less toxicity. Thus, dual …
[HTML][HTML] Cerbera odollam fruit extracts enhance anti-cancer activity of sorafenib in HCT116 and HepG2 cells
S Parhira, O Simanurak, K Pansooksan… - Chinese Herbal …, 2025 - Elsevier
Objective While higher therapeutic doses of toxic cardiac glycosides derived from Cerbera
odollam are frequently employed in cases of suicide or homicide, ongoing research is …
odollam are frequently employed in cases of suicide or homicide, ongoing research is …