Phthalazine Derivatives as VEGFR‐2 Inhibitors: Docking, ADMET, Synthesis, Design, Anticancer Evaluations, and Apoptosis Inducers DOI Open Access

Hatem Hussein Bayoumi,

Mohamed‐Kamal Ibrahim,

Mohammed A. Dahab

et al.

Drug Development Research, Journal Year: 2024, Volume and Issue: 86(1)

Published: Dec. 24, 2024

New phthalazine-derived inhibitors for VEGFR-2 were synthesized anticancer evaluations. Also, docking studies performed to explore the suggested binding orientations of novel derivatives inside site VEGFR-2. The achieved biological data extremely interrelated that study. In specific, derivative 3f was greatest effective compound against HepG2 and MCF-7 cancer cell lines with IC

Language: Английский

Recent advances on anticancer activity of benzodiazine heterocycles through kinase inhibition DOI Creative Commons
Mohamed S. Nafie, Sherif Ashraf Fahmy,

Shaima H. Kahwash

et al.

RSC Advances, Journal Year: 2025, Volume and Issue: 15(7), P. 5597 - 5638

Published: Jan. 1, 2025

This is an updated review for the anticancer activity of benzodiazine heterocyclic derivatives through kinase inhibition.

Language: Английский

Citations

0

In silico exploration of Aloe Vera leaf compounds as dual AChE and BChE inhibitors for Alzheimer’s disease therapy DOI Creative Commons

Meriem Khedraoui,

Fatima Zahra Guerguer,

El Mehdi Karim

et al.

Current Pharmaceutical Analysis, Journal Year: 2025, Volume and Issue: unknown

Published: March 1, 2025

Language: Английский

Citations

0

Rationale, in silico docking, ADMET profile, design, synthesis and cytotoxicity evaluations of phthalazine derivatives as VEGFR-2 inhibitors and apoptosis inducers DOI Creative Commons

Hatem Hussein Bayoumi,

Mohamed‐Kamal Ibrahim,

Mohammed A. Dahab

et al.

RSC Advances, Journal Year: 2024, Volume and Issue: 14(37), P. 27110 - 27121

Published: Jan. 1, 2024

New phthalazine derivatives as vascular endothelial growth factor receptor-2 (VEGFR-2) inhibitors were synthesized joined to different spacers including pyrazole, α,β-unsaturated ketonic fragment, pyrimidinone and/or pyrimidinthione.

Language: Английский

Citations

2

Phthalazine Derivatives as VEGFR‐2 Inhibitors: Docking, ADMET, Synthesis, Design, Anticancer Evaluations, and Apoptosis Inducers DOI Open Access

Hatem Hussein Bayoumi,

Mohamed‐Kamal Ibrahim,

Mohammed A. Dahab

et al.

Drug Development Research, Journal Year: 2024, Volume and Issue: 86(1)

Published: Dec. 24, 2024

New phthalazine-derived inhibitors for VEGFR-2 were synthesized anticancer evaluations. Also, docking studies performed to explore the suggested binding orientations of novel derivatives inside site VEGFR-2. The achieved biological data extremely interrelated that study. In specific, derivative 3f was greatest effective compound against HepG2 and MCF-7 cancer cell lines with IC

Language: Английский

Citations

0