[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 …

Naturally derived indole alkaloids targeting regulated cell death (RCD) for cancer therapy: from molecular mechanisms to potential therapeutic targets

R Qin, FM You, Q Zhao, X **e, C Peng, G Zhan… - Journal of hematology & …, 2022 - Springer
Regulated cell death (RCD) is a critical and active process that is controlled by specific
signal transduction pathways and can be regulated by genetic signals or drug interventions …

Recent advances in the development of pyrazole derivatives as anticancer agents

Y Zhang, C Wu, N Zhang, R Fan, Y Ye, J Xu - International Journal of …, 2023 - mdpi.com
Pyrazole derivatives, as a class of heterocyclic compounds, possess unique chemical
structures that confer them with a broad spectrum of pharmacological activities. They have …

A Review of the Recent Developments of Molecular Hybrids Targeting Tubulin Polymerization

O Ebenezer, M Shapi, JA Tuszynski - International Journal of Molecular …, 2022 - mdpi.com
Microtubules are cylindrical protein polymers formed from α β-tubulin heterodimers in the
cytoplasm of eukaryotic cells. Microtubule disturbance may cause cell cycle arrest in the …

Pyrazolo-benzothiazole hybrids: Synthesis, anticancer properties and evaluation of antiangiogenic activity using in vitro VEGFR-2 kinase and in vivo transgenic …

VG Reddy, TS Reddy, C Jadala, MS Reddy… - European journal of …, 2019 - Elsevier
A series of new pyrazolo-benzothiazole hybrids (7–26) were synthesised and screened for
their cytotoxic activity towards several cancer cell lines [colon (HT-29), prostate (PC-3), lung …

A close look into the biological and synthetic aspects of fused pyrazole derivatives

MM Li, H Huang, Y Pu, W Tian, Y Deng, J Lu - European journal of …, 2022 - Elsevier
The fusion of pyrazole scaffold with other skeletons creates a class of attractive molecules,
demonstrating significant biological and chemical potentiality in the development of …

Indole derivatives as tubulin polymerization inhibitors for the development of promising anticancer agents

Y Hong, YY Zhu, Q He, SX Gu - Bioorganic & medicinal chemistry, 2022 - Elsevier
The α-and β-tubulins are the major polypeptide components of microtubules (MTs), which
are attractive targets for anticancer drug development. Indole derivatives display a variety of …

Recent progress in anticancer agents incorporating pyrazole scaffold

S Mor, M Khatri, R Punia… - Mini Reviews in Medicinal …, 2022 - benthamdirect.com
The search for new anticancer agents is considered a dynamic field of medicinal chemistry.
In recent years, the synthesis of compounds with anticancer potential has increased and a …

Cinnamide derived pyrimidine-benzimidazole hybrids as tubulin inhibitors: synthesis, in silico and cell growth inhibition studies

S Sana, VG Reddy, TS Reddy, R Tokala, R Kumar… - Bioorganic …, 2021 - Elsevier
An approach in modern medicinal chemistry to discover novel bioactive compounds is by
mimicking diverse complementary pharmacophores. In extension of this strategy, a new …

Bromide-catalyzed electrochemical trifluoromethylation/cyclization of N-arylacrylamides with low catalyst loading

YY Jiang, GY Dou, K Xu, CC Zeng - Organic Chemistry Frontiers, 2018 - pubs.rsc.org
Bromide-catalyzed electrochemical trifluoromethylation/cyclization of N -arylacrylamides with low
catalyst loading - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C8QO00645H …