Research progress on the synthesis and pharmacology of 1, 3, 4-oxadiazole and 1, 2, 4-oxadiazole derivatives: a mini review

JJ Wang, W Sun, WD Jia, M Bian… - Journal of Enzyme …, 2022 - Taylor & Francis
Oxadiazole is a five-membered heterocyclic compound containing two nitrogen atoms and
one oxygen atom. The 1, 3, 4-oxadiazole and 1, 2, 4-oxadiazole have favourable physical …

Selective SIRT2 inhibitors as promising anticancer therapeutics: An update from 2016 to 2020

E Roshdy, M Mustafa, AER Shaltout… - European Journal of …, 2021 - Elsevier
Abstract Sirtuin 2 (SIRT2) is a member of the human sirtuins, which regulates various
biological processes and is deemed as a novel biomarker for different cancers. Depending …

Selective inhibition of SIRT2: A disputable therapeutic approach in cancer therapy

SG Kaya, G Eren - Bioorganic Chemistry, 2023 - Elsevier
Abstract Sirtuin 2 (SIRT2) is involved in a wide range of processes, from transcription to
metabolism to genome stability. Dysregulation of SIRT2 has been associated with the …

Virtual Screening Combined with Enzymatic Assays to Guide the Discovery of Novel SIRT2 Inhibitors

N Scarano, E Abbotto, F Musumeci, A Salis… - International Journal of …, 2023 - mdpi.com
Sirtuin isoform 2 (SIRT2) is one of the seven sirtuin isoforms present in humans, being
classified as class III histone deacetylases (HDACs). Based on the high sequence similarity …

Development of an Environment-Friendly and Electrochemical Method for the Synthesis of an Oxadiazole Drug-Scaffold That Targets Poly (ADP-Ribose) Polymerase …

SM Parameshwaraiah, Z Xi, A Ravish, A Mohan… - Catalysts, 2023 - mdpi.com
The development of environment-friendly new Poly-adenosine diphosphate (ADP)-ribose
Polymerase (PARP) inhibitors are highly essential because of their involvement in the …

Oxadiazole Schiff Base as Fe3+ Ion Chemosensor: “Turn-off” Fluorescent, Biological and Computational Studies

R Mehandi, R Sultana, S Ahmedi, M Rana… - Journal of …, 2023 - Springer
Abstract Compound,(E)-5-(4-((thiophen-2-ylmethylene) amino) phenyl)-1, 3, 4-oxadiazole-2-
thiol (3) was synthesized via condensation reaction of 5-(4-aminophenyl)-1, 3, 4-oxadiazole …

The anticancer activity of indazole compounds: a mini review

C Shang, Y Hou, T Meng, M Shi… - Current Topics in …, 2021 - ingentaconnect.com
The incidence and mortality of cancer continue to grow since the current medical treatments
often fail to produce a complete and durable tumor response and ultimately give rise to …

Role of sirtuins in hepatocellular carcinoma progression and multidrug resistance: mechanistical and pharmacological perspectives

MP Ceballos, AD Quiroga, NF Palma - Biochemical Pharmacology, 2023 - Elsevier
Hepatocellular carcinoma (HCC) is the third most common cause of death from cancer
worldwide. Therapeutic strategies are still challenging due to the high relapse rate after …

In silico approach reveals N-(5-phenoxythiophen-2-yl)-2-(arylthio)acetamides as promising selective SIRT2 inhibitors: the case of structural optimization of virtual …

M Gozelle, F Bakar-Ates, A Massarotti… - Journal of …, 2023 - Taylor & Francis
Epigenetic modifications play an essential role in tumor suppression and promotion. Among
the diverse range of epigenetic regulators, SIRT2, a member of NAD+-dependent protein …

Development of Novel Indazolyl‐Acyl Hydrazones as Antioxidant and Anticancer Agents that Target VEGFR‐2 in Human Breast Cancer Cells

SM Parameshwaraiah, R Shivakumar… - Chemistry & …, 2024 - Wiley Online Library
The increased expression of VEGFR‐2 in a variety of cancer cells promotes a cascade of
cellular responses that improve cell survival, growth, and proliferation. Heterocycles are …