Anti-cancer activity of derivatives of 1, 3, 4-oxadiazole

T Glomb, K Szymankiewicz, P Świątek - Molecules, 2018 - mdpi.com
Compounds containing 1, 3, 4-oxadiazole ring in their structure are characterised by
multidirectional biological activity. Their anti-proliferative effects associated with various …

Isatin containing heterocycles for different biological activities: Analysis of structure activity relationship

R Nath, S Pathania, G Grover, MJ Akhtar - Journal of Molecular Structure, 2020 - Elsevier
Isatin has been widely used in drug discovery. The ring is part of many naturally occurring
compounds and is used to design compounds with diverse biological activities. These isatin …

[HTML][HTML] 1, 3, 4-Oxadiazole-containing hybrids as potential anticancer agents: Recent developments, mechanism of action and structure-activity relationships

S Nayak, SL Gaonkar, EA Musad… - Journal of Saudi Chemical …, 2021 - Elsevier
Chemotherapy is an important therapeutic approach for the treatment of cancer. Currently,
many anticancer drugs are available in the market that plays an important role in cancer …

An understanding of mechanism-based approaches for 1, 3, 4-oxadiazole scaffolds as cytotoxic agents and enzyme inhibitors

D Kumar, N Aggarwal, A Deep, H Kumar, H Chopra… - Pharmaceuticals, 2023 - mdpi.com
The world's health system is plagued by cancer and a worldwide effort is underway to find
new drugs to treat cancer. There has been a significant improvement in understanding the …

Design, click synthesis, anticancer screening and docking studies of novel benzothiazole-1, 2, 3-triazoles appended with some bioactive benzofused heterocycles

MR Aouad, MA Almehmadi, N Rezki, FF Al-blewi… - Journal of Molecular …, 2019 - Elsevier
Abstract New series of benzothiazole-1, 2, 3-triazoles; appended with benzothiazole, isatin
and/or benzimidazole moiety; were designed and synthesized through the click chemistry …

1, 3, 4-oxadiazole/chalcone hybrids: Design, synthesis, and inhibition of leukemia cell growth and EGFR, Src, IL-6 and STAT3 activities

MAA Fathi, AA Abd El-Hafeez, D Abdelhamid… - Bioorganic …, 2019 - Elsevier
Abstract A new series of 1, 3, 4-oxadiazole/chalcone hybrids was designed, synthesized,
identified with different spectroscopic techniques and biologically evaluated as inhibitors of …

Isatin-derived azoles as new potential antimicrobial agents: Design, synthesis and biological evaluation

VKR Tangadanchu, YF Sui, CH Zhou - Bioorganic & Medicinal Chemistry …, 2021 - Elsevier
Novel antibiotics are forced to be developed on account of multidrug-resistant bacteria with
serious threats to human health. This work developed isatin-derived azoles as new potential …

Identification of 1, 2, 4-triazoles as new thymidine phosphorylase inhibitors: Future anti-tumor drugs

SA Shahzad, M Yar, ZA Khan, L Shahzadi… - Bioorganic …, 2019 - Elsevier
Thymidine phosphorylase (TP) is over expressed in several solid tumors and its inhibition
can offer unique target suitable for drug discovery in cancer. A series of 1, 2, 4-triazoles 3a …

A quick microwave preparation of isatin hydrazone schiff base conjugated organosilicon compounds: Exploration of their antibacterial, antifungal, and antioxidative …

G Singh, P Kalra, A Singh, G Sharma… - Journal of …, 2021 - Elsevier
In the current study, five isatin hydrazone schiff base linked acetylinic scaffolds have been
synthesized via condensation reaction of isatin hydrazone with aldehydic groups. In order to …

1, 3, 4-Oxadiazole containing compounds as therapeutic targets for cancer therapy

MJ Ahsan - Mini Reviews in Medicinal Chemistry, 2022 - ingentaconnect.com
Background: Cancer is the first or second leading cause of premature death in 134 of 183
countries in the world. 1, 3, 4-Oxadiazoles are five membered heterocyclic rings containing …