Bioactive 1, 2, 3‐Triazoles: An Account on their Synthesis, Structural Diversity and Biological Applications

L da SM Forezi, CGS Lima, AAP Amaral… - The Chemical …, 2021 - Wiley Online Library
The triazole heterocycle is a privileged scaffold in medicinal chemistry, since its structure is
present in a large number of biologically active molecules, including several drugs currently …

From lead to clinic: A review of the structural design of P2X7R antagonists

R Zhang, N Li, M Zhao, M Tang, X Jiang, X Cai… - European Journal of …, 2023 - Elsevier
Abstract P2X7R, which is a member of the purinergic P2 receptor family, is widely expressed
in many immune cells, such as macrophages, lymphocytes, monocytes, and neutrophils …

Usnic acid enaminone-coupled 1, 2, 3-triazoles as antibacterial and antitubercular agents

PK Bangalore, SK Vagolu, RK Bollikanda… - Journal of natural …, 2019 - ACS Publications
(+)-Usnic acid, a product of secondary metabolism in lichens, has displayed a broad range
of biological properties such as antitumor, antimicrobial, antiviral, anti-inflammatory, and …

Design, synthesis, and biological evaluation of novel P2X7 receptor antagonists for the treatment of septic acute kidney injury

R Zhang, K Su, L Yang, M Tang, M Zhao… - Journal of Medicinal …, 2023 - ACS Publications
Sepsis-associated acute kidney injury (AKI) is a serious clinical problem, without effective
drugs. Abnormal activation of the purinergic P2X7 receptor (P2X7R) in septic kidneys makes …

Synthetic 1, 4-Naphthoquinones inhibit P2X7 receptors in murine neuroblastoma cells

E Pislyagin, S Kozlovskiy, E Menchinskaya… - Bioorganic & Medicinal …, 2021 - Elsevier
Abstract The P2X7 receptor (P2X7R) is an ATP-gated ion channel and potential therapeutic
target for new drug development. In this study, we synthesized a series of new 1, 4 …

Juglone: a versatile natural platform for obtaining new bioactive compounds

C dos S. Moreira, TB Santos… - Current Topics in …, 2021 - benthamdirect.com
Juglone is a metabolite produced by several species of plants, in particular Juglans nigra.
Additionally, juglone is a 1, 4-naphthoquinone that has several biological actions …

Structure-activity relationships and therapeutic potential of purinergic P2X7 receptor antagonists

I Ghafir El Idrissi, S Podlewska, C Abate… - Current medicinal …, 2024 - ingentaconnect.com
The purinergic P2X7 receptor (P2X7R), an ATP-gated non-selective cation channel, has
emerged as a gatekeeper of inflammation that controls the release of proinflammatory …

[HTML][HTML] Physalin pool from Physalis angulata L. leaves and physalin D inhibit P2X7 receptor function in vitro and acute lung injury in vivo

JCC Arruda, NC Rocha, EG Santos… - Biomedicine & …, 2021 - Elsevier
P2X7 receptor promotes inflammatory response and neuropathic pain. New drugs capable
of impairing inflammation and pain-reducing adverse effects extracted from plant extracts …

Tetracyclic 1, 4-naphthoquinone thioglucoside conjugate U-556 blocks the purinergic P2X7 receptor in macrophages and exhibits anti-inflammatory activity In Vivo

S Kozlovskiy, E Pislyagin, E Menchinskaya… - International Journal of …, 2023 - mdpi.com
P2X7 receptors (P2X7Rs) are ligand-gated ion channels that play a significant role in
inflammation and are considered a potential therapeutic target for some inflammatory …

Free‐radical Initialized Cyclization of 2‐(3‐Arylpropioloyl) benzaldehydes with Toluene Derivatives: Access to Benzylated 1, 4‐Naphthoquinones via Copper …

B Zhu, H Han, WK Su, C Yu… - Advanced Synthesis & …, 2021 - Wiley Online Library
A copper‐catalyzed cyclization reaction of 2‐(3‐arylpropioloyl) benzaldehydes was
developed, leading to benzylated 1, 4‐naphthoquinones via radical‐triggered cascade …