Quinazoline based HDAC dual inhibitors as potential anti-cancer agents

J Dhuguru, OA Ghoneim - Molecules, 2022 - mdpi.com
Cancer is the most devastating disease and second leading cause of death around the
world. Despite scientific advancements in the diagnosis and treatment of cancer which can …

New Quinazolin-4(3H)-one Derivatives Incorporating Hydrazone and Pyrazole Scaffolds as Antimicrobial Agents Targeting DNA Gyraze Enzyme

EM Mohi El-Deen, ES Nossier, EA Karam - Scientia Pharmaceutica, 2022 - mdpi.com
The present work includes the synthesis of a new series of quinazolin-4 (3 H)-one
compounds (4a–f, 5a–d) as antimicrobial agents. The starting compound, 2 …

Development of novel ecto-nucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) inhibitors for tumor immunotherapy

X Wang, X Lu, D Yan, Y Zhou, X Tan - International Journal of Molecular …, 2022 - mdpi.com
The cyclic guanosine monophosphate–adenosine monophosphate synthase–stimulator of
interferon genes–TANK-binding kinase 1–interferon regulating factor 3 (cGAS-STING-TBK1 …

An oleanolic acid derivative, K73‐03, inhibits pancreatic cancer cells proliferation in vitro and in vivo via blocking EGFR/Akt pathway

Z Zhou, Y Dong, N Li, M Niu, S Wang… - Cell Biology …, 2022 - Wiley Online Library
Oleanolic acid (OA) and its derivatives show potent anticancer function. Pancreatic cancer
(PC) is the fourth core motive of cancer‐related deaths worldwide. Epidermal growth factor …

Study of the anticancer effect of new quinazolinone hydrazine derivatives as receptor tyrosine kinase inhibitors

M Mortazavi, M Divar, T Damghani, F Moosavi… - Frontiers in …, 2022 - frontiersin.org
The advent of novel receptor tyrosine kinase inhibitors has provided an important
therapeutic tool for cancer patients. In this study, a series of quinazolinone hydrazide triazole …

Synthesis, antitumor activity, 3D-QSAR and molecular docking studies of new iodinated 4-(3 H)-quinazolinones 3 N-substituted

M Pérez-Fehrmann, V Kesternich, A Puelles… - RSC …, 2022 - pubs.rsc.org
A novel series of 6-iodo-2-methylquinazolin-4-(3H)-one derivatives, 3a–n, were synthesized
and evaluated for their in vitro cytotoxic activity. Compounds 3a, 3b, 3d, 3e, and 3h showed …

Synthesis and tyrosinase inhibitory activities of novel isopropylquinazolinones

A Hashemi, M Noori, N Dastyafteh, SE Sadat-Ebrahimi… - BMC chemistry, 2023 - Springer
To find new anti-browning and whitening agents in this study, new series of
isopropylquinazolinone derivatives were designed and synthesized. All derivatives were …

[PDF][PDF] SYNTHESIS, In-vitro CYTOTOXICITY AND IN SILICO INVESTIGATIONS OF QUINAZOLINONE INTEGRATED CHALCONES: AS NOVEL POTENTIAL DUAL …

PK Arora, S Kumar, SK Bansal… - Rasayan Journal of …, 2023 - rasayanjournal.co.in
The present study focuses on the synthesis of some 2-methoxyphenylquinazolin-4-one
incorporated chalcone hybrids to evaluate their cytotoxic potential by MTT assay, and their …

[HTML][HTML] ПОИСК МУЛЬТИТАРГЕТНЫХ ВЕЩЕСТВ С АНТИМИКРОБНЫМ ЭФФЕКТОМ–ПЕРСПЕКТИВНОЕ НАПРАВЛЕНИЕ СОВРЕМЕННОЙ …

АА Старикова, ДВ Мережкина… - … вестник медицины и …, 2024 - cyberleninka.ru
Представлен обзор литературных данных о принципах создания мультитаргетных
препаратов и механизмах их действия. Проведен анализ результатов изучения …