Novel quinazoline-based EGFR kinase inhibitors: A review focussing on SAR and molecular docking studies (2015-2019)

P Bhatia, V Sharma, O Alam, A Manaithiya… - European Journal of …, 2020 - Elsevier
The over expression of EGFR has been recognized as the driver mechanism in the
occurrence and progression of carcinomas such as lung cancer, breast cancer, pancreatic …

An appraisal of anticancer activity with structure–activity relationship of quinazoline and quinazolinone analogues through EGFR and VEGFR inhibition: A review

K Haider, S Das, A Joseph… - Drug Development …, 2022 - Wiley Online Library
Cancer is one of the leading causes of death. Globally a huge number of deaths and new
incidences are reported annually. Heterocyclic compounds have been proved to be very …

Design, synthesis, antimicrobial evaluation, and molecular docking study of some 4-thiazolidinone derivatives containing pyridine and quinazoline moiety

NC Desai, KA Jadeja, DJ Jadeja… - Synthetic …, 2021 - Taylor & Francis
Abstract A series of 5-aryl-3-(4-oxo-2-phenylquinazolin-3 (4 H)-yl)-2-(pyridin-4-yl) thiazolidin-
4-ones were synthesized and evaluated for their antibacterial and antifungal activities …

Current scenario of 1, 3-oxazole derivatives for anticancer activity

X Yan, J Wen, L Zhou, L Fan… - Current Topics in …, 2020 - ingentaconnect.com
Cancer, which has been cursed for human beings for long time is considered as one of the
leading causes of morbidity and mortality across the world. In spite of different types of …

Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors for the treatment of non-small cell lung cancer: a patent review (2014-present)

X Sun, S Xu, Z Yang, P Zheng… - Expert Opinion on …, 2021 - Taylor & Francis
Introduction: EGFR is the receptor for epidermal growth factor (EGF) and belongs to the
protein tyrosine kinase (PTK) receptor. It is closely related to the inhibition of tumor cell …

Quinazolinone Synthesis through Base-Promoted SNAr Reaction of ortho-Fluorobenzamides with Amides Followed by Cyclization

MA Iqbal, L Lu, H Mehmood, DM Khan, R Hua - ACS omega, 2019 - ACS Publications
A transition-metal-free synthesis of quinazolin-4-ones by Cs2CO3-promoted SNAr reaction
of ortho-fluorobenzamides with amides followed by cyclization in dimethyl sulfoxide has …

Recent developments in oxazole derivatives as anticancer agents: Review on synthetic strategies, mechanism of action and SAR studies

S Kulkarni, K Kaur, V Jaitak - Anti-Cancer Agents in Medicinal …, 2022 - ingentaconnect.com
Background: Cancer is the world's third deadliest disease. Despite the availability of
numerous treatments, researchers are focusing on the development of new drugs with no …

Design, synthesis and 3D-QSAR analysis of novel thiopyranopyrimidine derivatives as potential antitumor agents inhibiting A549 and Hela cancer cells

B Zhao, C Zhao, X Hu, S Xu, Z Lan, Y Guo… - European Journal of …, 2020 - Elsevier
Four series of thiopyranopyrimidine AZD9291 derivatives containing acrylamide structure
were designed, synthesized and evaluated for their antiproliferative activity against A549 …

[HTML][HTML] Small heterocyclic ligands as anticancer agents: QSAR with a model G-quadruplex

J Kaneti, V Kurteva, M Georgieva, N Krasteva… - Molecules, 2022 - mdpi.com
G-quadruplexes (GQs) have become valid targets for anticancer studies in recent decades
due to their multifaceted biological function. Herewith, we aim to quantify interactions of …

REVIEW ON THE SIGNIFICANCE OF QUINAZOLINE DERIVATIVES AS BROAD SPECTRUM ANTI-CANCER AGENTS.

M El-Zahabi - Al-Azhar Journal of Pharmaceutical Sciences, 2021 - ajps.journals.ekb.eg
Cancer is one of the major causes of human mortality worldwide. A number of approved
antineoplastic medications and treatment regimens are already working in the field, and …