Target-based drug design strategies to overcome resistance to antiviral agents: Opportunities and challenges

S Du, X Hu, L Menéndez-Arias, P Zhan, X Liu - Drug Resistance Updates, 2024 - Elsevier
Viral infections have a major impact in human health. Ongoing viral transmission and
escalating selective pressure have the potential to favor the emergence of vaccine-and …

Immune response in influenza virus infection and modulation of immune injury by viral neuraminidase

H Jiang, Z Zhang - Virology Journal, 2023 - Springer
Influenza A viruses cause severe respiratory illnesses in humans and animals. Overreaction
of the innate immune response to influenza virus infection results in hypercytokinemia …

Novel thiazolidin-4-one benzenesulfonamide hybrids as PPARγ agonists: Design, synthesis and in vivo anti-diabetic evaluation

IH Ali, RM Hassan, AM El Kerdawy… - European Journal of …, 2024 - Elsevier
In the current study, two series of novel thiazolidin-4-one benzenesulfonamide arylidene
hybrids 9a-l and 10a-f were designed, synthesized and tested in vitro for their PPARɣ …

Synthesis and application of dual-channel fluorescent probes for selective recognition of SO2/H2O2

HC Xia, H Li, WL Zhang, YY Kong - Sensors and Actuators B: Chemical, 2023 - Elsevier
The balance between active oxidizing species and active reducing species plays an
important role in cell metabolism. A multitude of excellent probes can be used for the …

Discovery of Novel Boron-Containing N-Substituted Oseltamivir Derivatives as Anti-Influenza A Virus Agents for Overcoming N1-H274Y Oseltamivir-Resistant

R Jia, J Zhang, J Zhang, C Bertagnin, A Bonomini… - Molecules, 2022 - mdpi.com
To address drug resistance to influenza virus neuraminidase inhibitors (NAIs), a series of
novel boron-containing N-substituted oseltamivir derivatives were designed and …

Discovery of 4-benzyloxy and 4-(2-phenylethoxy) chalcone fibrate hybrids as novel PPARα agonists with anti-hyperlipidemic and antioxidant activities: Design …

RM Hassan, ME Aboutabl, M Bozzi, MF El-Behairy… - Bioorganic …, 2021 - Elsevier
In the current work, a series of novel 4-benzyloxy and 4-(2-phenylethoxy) chalcone fibrate
hybrids (10a-o) and (11a-e) were synthesized and evaluated as new PPARα agonists in …

Design, synthesis, and biological evaluation of novel penindolone derivatives as potential inhibitors of hemagglutinin-mediated membrane fusion

B Li, L Huang, J Lin, X Ma, Y Luo, W Gai, Y Xie… - European Journal of …, 2023 - Elsevier
Abstract Development and design of anti-influenza drugs with novel mechanisms is of great
significance to combat the ongoing threat of influenza A virus (IAV). Hemagglutinin (HA) is …

Discovery of N-substituted oseltamivir derivatives as novel neuraminidase inhibitors with improved drug resistance profiles and favorable drug-like properties

R Jia, J Zhang, F Shi, A Bonomini, C Lucca… - European Journal of …, 2023 - Elsevier
To yield potent neuraminidase inhibitors with improved drug resistance and favorable drug-
like properties, two series of novel oseltamivir derivatives targeting the 150-cavity of …

Modular Biomimetic Strategy Enables Discovery and SAR Exploration of Oxime Macrocycles as Influenza A Virus (H1N1) Inhibitors

D Xu, Y Gong, L Zhang, F Xiao, X Wang… - Journal of Medicinal …, 2024 - ACS Publications
Although vaccination remains the prevalent prophylactic means for controlling Influenza A
virus (IAV) infections, novel structural antivirus small-molecule drugs with new mechanisms …

Elaborate Structural Modifications Yielding Novel Boron-Containing N-Substituted Oseltamivir Derivatives as Potent Neuraminidase Inhibitors with Significantly …

J Zhang, R Jia, H Jia, P Li, Y Jiang… - Journal of Medicinal …, 2024 - ACS Publications
Inspired by our previous finding that targeting the 150-cavity with a multisite-binding strategy
emerged as an effective approach to obtain more potent and selective neuraminidase (NA) …