Recent updates on thienopyrimidine derivatives as anticancer agents

MTM Sayed, RA Hassan, PA Halim… - Medicinal Chemistry …, 2023 - Springer
Thienopyrimidine derivatives hold a unique place between fused pyrimidine compounds.
They are important and widely represented in medicinal chemistry as they are structural …

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 …

Design and synthesis of novel hexahydrobenzo[4,5]thieno[2,3‐d]pyrimidine derivatives as potential anticancer agents with antiangiogenic activity via VEGFR‐2 …

SE Seif, Z Mahmoud, WW Wardakhan… - Drug Development …, 2023 - Wiley Online Library
Abstract New thieno [2, 3‐d] pyrimidine derivatives were designed and synthesized. The
National Cancer Institute (NCI) evaluated the synthesized novel compounds against a panel …

Exploring a novel thiazole derivatives hybrid with fluorinated-indenoquinoxaline as dual inhibitors targeting VEGFR2/AKT and apoptosis inducers against …

MS Abusaif, A Ragab, EA Fayed, YA Ammar… - Bioorganic …, 2025 - Elsevier
Hepatocellular carcinoma (HCC) ranks as the third most prevalent reason for cancer-related
death on a global scale. Tyrosine kinase inhibitors (TKIs) continue to be the primary …

Design and synthesis of novel quinazolinone-based derivatives as EGFR inhibitors with antitumor activity

A Sonousi, RA Hassan, EO Osman… - Journal of Enzyme …, 2022 - Taylor & Francis
Abstract Nineteen new quinazolin-4 (3 H)-one derivatives 3a–g and 6a–l were designed
and synthesised to inhibit EGFR. The antiproliferative activity of the synthesised compounds …

An expeditious FeCl 3-catalyzed cascade 1, 4-conjugate addition/annulation/1, 5-H shift sequence for modular access of all-pyrano-moiety-substituted chromenes

X He, R Li, PY Choy, J Duan, Z Yin, K Xu, Q Tang… - Chemical …, 2022 - pubs.rsc.org
ortho-Alkynyl quinone methides are well-known four-atom synthons for direct [4+ n]
cycloaddition in constructing useful oxa-heterocyclic compounds owing to their high …

An overview of RAF kinases and their inhibitors (2019-2023)

OM Hashem, AI Shahin, MA Al Hindawi… - European Journal of …, 2024 - Elsevier
Protein kinases (PKs) including RAF, performs a principal role in regulating countless
cellular events such as cell growth, differentiation, and angiogenesis. Overexpression and …

Design, synthesis, anticancer, and antibacterial evaluation of some quinazolinone‐based derivatives as DHFR inhibitors

EO Osman, SH Emam, A Sonousi… - Drug Development …, 2023 - Wiley Online Library
Two series of quinazolinone derivatives were designed and synthesized as dihydrofolate
reductase (DHFR) inhibitors. All compounds were evaluated for their antibacterial and …

Design, synthesis, anticancer evaluation, and in silico studies of some thieno[2,3‐d]pyrimidine derivatives as EGFR inhibitors

MTM Sayed, PA Halim, AK El‐Ansary… - Drug Development …, 2023 - Wiley Online Library
Abstract New series of 20 thieno [2, 3‐d] pyrimidine derivatives have been synthesized. The
National Cancer Institute evaluated all the newly synthesized compounds for their …