[HTML][HTML] Oxindole and its derivatives: A review on recent progress in biological activities

YM Khetmalis, M Shivani, S Murugesan… - Biomedicine & …, 2021 - Elsevier
Oxindole has been shown to be a pharmacologically advantageous scaffold having many
biological properties that are relevant to medicinal chemistry. The simplicity and widespread …

[HTML][HTML] Target-based anticancer indole derivatives and insight into structure‒activity relationship: A mechanistic review update (2018–2021)

A Dhiman, R Sharma, RK Singh - Acta Pharmaceutica Sinica B, 2022 - Elsevier
Cancer, which is the uncontrolled growth of cells, is the second leading cause of death after
heart disease. Targeting drugs, especially to specific genes and proteins involved in growth …

Recent progress in biologically active indole hybrids: A mini review

E Mahmoud, AM Hayallah, S Kovacic… - Pharmacological …, 2022 - Springer
The indole moiety is one of the most widespread heterocycles found in both natural products
and biological systems. Indoles have important biological activities including anticancer …

In Silico Exploration of Potential Natural Inhibitors against SARS-Cov-2 nsp10

IH Eissa, MM Khalifa, EB Elkaeed, EE Hafez… - Molecules, 2021 - mdpi.com
In continuation of our previous effort, different in silico selection methods were applied to
310 naturally isolated metabolites that exhibited antiviral potentialities before. The applied …

Structural insights of oxindole based kinase inhibitors as anticancer agents: Recent advances

P Dhokne, AP Sakla, N Shankaraiah - European journal of medicinal …, 2021 - Elsevier
Small-molecule kinase inhibitors are being continuously explored as new anticancer
therapeutics. Kinases are the phosphorylating enzymes which regulate numerous cellular …

Development of isatin-thiazolo [3, 2-a] benzimidazole hybrids as novel CDK2 inhibitors with potent in vitro apoptotic anti-proliferative activity: Synthesis, biological and …

WM Eldehna, MA El Hassab, MF Abo-Ashour… - Bioorganic …, 2021 - Elsevier
In the current medical era, human health is experiencing numerous challenges, particularly
the human malignancies. Therefore, the therapeutic arsenal for these malignancies is to be …

Novel oxindole/benzofuran hybrids as potential dual CDK2/GSK-3β inhibitors targeting breast cancer: design, synthesis, biological evaluation, and in silico studies

WM Eldehna, ST Al-Rashood, T Al-Warhi… - Journal of Enzyme …, 2021 - Taylor & Francis
The serine/threonine protein kinases CDK2 and GSK-3β are key oncotargets in breast
cancer cell lines, therefore, in the present study three series of oxindole-benzofuran hybrids …

Multi-phase in silico discovery of potential SARS-CoV-2 RNA-dependent RNA polymerase inhibitors among 3009 clinical and FDA-approved related drugs

EB Elkaeed, H Elkady, A Belal, BA Alsfouk, TH Ibrahim… - Processes, 2022 - mdpi.com
Proceeding our prior studies of SARS-CoV-2, the inhibitory potential against SARS-CoV-2
RNA-dependent RNA polymerase (RdRp) has been investigated for a collection of 3009 …

[HTML][HTML] Computer-aided drug design in anti-cancer drug discovery: what have we learnt and what is the way forward??

I Opeyemi, O Paul, F Olawale, B Olorunfemi… - Informatics in Medicine …, 2023 - Elsevier
The escalating prevalence of cancer on a global scale, coupled with the inadequacies of
present-day therapies and the emergence of drug-resistant cancer strains, has necessitated …

CDK4/6 inhibitors: a brief overview and prospective research directions

T Adon, D Shanmugarajan, HY Kumar - RSC advances, 2021 - pubs.rsc.org
The discovery of cyclin-dependent kinases (CDK) and their mechanism in regulating the cell
cycle process was considered a game-changer in cancer therapy. Cell cycle arrest and …