A review exploring therapeutic worth of 1, 3, 4-oxadiazole tailored compounds

G Verma, MF Khan, W Akhtar, MM Alam… - Mini Reviews in …, 2019 - ingentaconnect.com
1, 3, 4-Oxadiazole, a five-membered aromatic ring can be seen in a number of synthetic
molecules. The peculiar structural feature of 1, 3, 4-oxadiazole ring with pyridine type of …

Groundbreaking anticancer activity of highly diversified oxadiazole scaffolds

A Benassi, F Doria, V Pirota - International journal of molecular sciences, 2020 - mdpi.com
Nowadays, an increasing number of heterocyclic-based drugs found application in
medicinal chemistry and, in particular, as anticancer agents. In this context, oxadiazoles …

Discovery of novel benzophenone integrated derivatives as anti-Alzheimer's agents targeting presenilin-1 and presenilin-2 inhibition: A computational approach

RM Martiz, SM Patil, R Ramu, J MK, AP… - PLoS …, 2022 - journals.plos.org
The most commonly accepted hypothesis of Alzheimer's disease (AD) is the amyloid
hypothesis caused due to formation of accumulation of Aβ42 isoform, which leads to …

Design, synthesis, biological evaluation and molecular docking of new 1, 3, 4-oxadiazole homonucleosides and their double-headed analogs as antitumor agents

AEL Mansouri, A Oubella, A Mehdi, MY AitItto… - Bioorganic …, 2021 - Elsevier
A novel series of homonucleosides and their double-headed analogs containing
theophylline, 1, 3, 4-oxadiazole, and variant nucleobases was designed and synthesized …

Exploring target site interactions of 1, 3, 4-Oxadiazole/1, 3, 4-thiadiazole derivatives: Synthesis, characterization in vitro anti-urease and in silico molecular docking …

R Hussain, S Khan, W Rehman, Z Ullah, Y Khan… - Journal of Molecular …, 2025 - Elsevier
Urease enzyme is one of the major causes of severe health issues including urinary catheter
encrustation, gastric cancer, duodenal ulcer and peptic ulcer. In search for potent anti …

[HTML][HTML] Synthesis, docking and biological evaluation of thiadiazole and oxadiazole derivatives as antimicrobial and antioxidant agents

MJN Khadri, AB Begum, MK Sunil, SA Khanum - Results in Chemistry, 2020 - Elsevier
A series of potential biological active substituted thiadiazoles 5a-j and oxadiazoles 6a-j were
obtained via a multistep synthesis sequence with a simple and convenient approach by …

BP-1T, an antiangiogenic benzophenone-thiazole pharmacophore, counteracts HIF-1 signalling through p53/MDM2-mediated HIF-1α proteasomal degradation

P Thirusangu, V Vigneshwaran, T Prashanth… - Angiogenesis, 2017 - Springer
Hypoxia is a feature of all solid tumours, contributing to tumour progression. Activation of HIF-
1α plays a critical role in promoting tumour angiogenesis and metastasis. Since its …

Targeting HIF-1α by newly synthesized Indolephenoxyacetamide (IPA) analogs to induce anti-angiogenesis-mediated solid tumor suppression

FH Al-Ostoot, A Sherapura, VV, G Basappa… - Pharmacological …, 2021 - Springer
Background Hypoxic microenvironment is a common feature of solid tumors, which leads to
the promotion of cancer. The transcription factor, HIF-1α, expressed under hypoxic …

Cluster formation between an oxadiazole derivative with metal nanoclusters (Ag/Au/Cu), graphene quantum dot sheets, SERS studies, and solvent effects

J S. Al-Otaibi, YS Mary, YS Mary, R Trivedi… - Structural Chemistry, 2023 - Springer
Interaction of an oxadiazole derivative, 5-(3, 4-dimethoxyphenyl)-3-(3-methoxyphenyl)-1, 2,
4-oxadiazole (DPMO) with Ag/Au/Cu and graphene quantum dots with different solvents, is …

A tumoural angiogenic gateway blocker, Benzophenone-1B represses the HIF-1α nuclear translocation and its target gene activation against neoplastic progression

P Thirusangu, V Vigneshwaran, VL Ranganatha… - Biochemical …, 2017 - Elsevier
Hypoxia is an important module in all solid tumours to promote angiogenesis, invasion and
metastasis. Stabilization and subsequent nuclear localization of HIF-1α subunits result in the …