Visible light-induced Z-scheme V2O5/g-C3N4 heterojunction catalyzed cascade reaction of unactivated alkenes

QW Gui, F Teng, P Yu, YF Wu, ZB Nong… - Chinese Journal of …, 2023 - Elsevier
Abstract The Z-scheme V 2 O 5/gC 3 N 4 heterojunction was firstly applied in heterogeneous
visible light-induced cascade reaction for constructing phosphoryled ring-fused …

Seeking heterocyclic scaffolds as antivirals against dengue virus

S De, B Aamna, R Sahu, S Parida, SK Behera… - European Journal of …, 2022 - Elsevier
Dengue is one of the most typical viral infection categorized in the Neglected Tropical
Diseases (NTDs). It is transmitted via the female Aedes aegypti mosquito to humans and …

Visible‐Light Photosynthesis of CHF2/CClF2/CBrF2‐Substituted Ring‐fused Quinazolinones in Dimethyl Carbonate

QW Gui, F Teng, H Yang, C Xun… - Chemistry–An Asian …, 2022 - Wiley Online Library
With eco‐friendly and sustainable CO2‐derived dimethyl carbonate as the sole solvent, the
visible‐light‐induced cascade radical reactions have been established as a green and …

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 …

Recent insight into the biological activities and SAR of quinolone derivatives as multifunctional scaffold

V Sharma, R Das, DK Mehta, S Gupta… - Bioorganic & Medicinal …, 2022 - Elsevier
Quinolones are a type of bicyclic privileged building block with immense therapeutic
potential. They are known for their crucial role in modulating numerous diseases conditions …

Six‐Membered Aromatic Nitrogen Heterocyclic Anti‐Tumor Agents: Synthesis and Applications

J Li, A Gu, XM Nong, S Zhai, ZY Yue… - The Chemical …, 2023 - Wiley Online Library
Cancer stands as a serious malady, posing substantial risks to human well‐being and
survival. This underscores the paramount necessity to explore and investigate novel …

Identification and exploration of quinazoline-1, 2, 3-triazole inhibitors targeting EGFR in lung cancer

S Kumar, S Sengupta, I Ali, MK Gupta… - Journal of …, 2023 - Taylor & Francis
Epidermal growth factor receptor (EGFR) enhances lung cancer development, due to their
inability to permeate the cell membrane, secreted growth factors work through specialized …

Novel 2‐substituted thioquinazoline‐benzenesulfonamide derivatives as carbonic anhydrase inhibitors with potential anticancer activity

HT Abdel‐Mohsen, MA Omar, A Petreni… - Archiv der …, 2022 - Wiley Online Library
A novel series of 2‐thioquinazoline‐benzenesulfonamide hybrids were designed as
carbonic anhydrase (CA) inhibitors. The design approach relies on molecular hybridization …

Novel quinazolinone derivatives as anticancer agents: Design, synthesis, biological evaluation and computational studies

E Ataollahi, M Behrouz, P Mardaneh, M Emami… - Journal of Molecular …, 2024 - Elsevier
A novel series of quinazoline-pyrimidine derivatives (3a-3i) linked to different aryl
substitutions were designed and synthesized as promising anti-cancer candidates. The …

Discovery of novel thioquinazoline-N-aryl-acetamide/N-arylacetohydrazide hybrids as anti-SARS-CoV-2 agents: Synthesis, in vitro biological evaluation, and …

HT Abdel-Mohsen, MA Omar, O Kutkat… - Journal of Molecular …, 2023 - Elsevier
In the current investigation, two novel series of (tetrahydro) thioquinazoline-N-
arylacetamides and (tetrahydro) thioquinazoline-N-arylacetohydrazides were designed …