Cyclin dependent kinase (CDK) inhibitors as anticancer drugs: Recent advances (2015–2019)

C Sánchez-Martínez, MJ Lallena… - Bioorganic & medicinal …, 2019 - Elsevier
Sustained proliferative capacity and gene dysregulation are hallmarks of cancer. In
mammalian cells, cyclin-dependent kinases (CDKs) control critical cell cycle checkpoints …

PROTACs to address the challenges facing small molecule inhibitors

P Martín-Acosta, X Xiao - European journal of medicinal chemistry, 2021 - Elsevier
Small molecule inhibitors of proteins represent important medicines and critical chemical
tools to investigate the biology of the target proteins. Advances in various-omics …

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 …

Progress in targeted therapeutic drugs for oral squamous cell carcinoma

L Liu, J Chen, X Cai, Z Yao, J Huang - Surgical oncology, 2019 - Elsevier
With the rapid development of biomedicine, people have a deeper understanding with the
biological characteristics of malignant tumors, and begin to notice that in most tumors, there …

Eco-friendly sequential one-pot synthesis, molecular docking, and anticancer evaluation of arylidene-hydrazinyl-thiazole derivatives as CDK2 inhibitors

AM El-Naggar, MA El-Hashash, EB Elkaeed - Bioorganic Chemistry, 2021 - Elsevier
One current approach in the treatment of cancer is the inhibition of cyclin dependent kinase
(CDK) enzymes with small molecules. CDK are a class of enzymes, which catalyze the …

Identification of 3-(piperazinylmethyl)benzofuran derivatives as novel type II CDK2 inhibitors: design, synthesis, biological evaluation, and in silico insights

WM Eldehna, RM Maklad, H Almahli… - Journal of Enzyme …, 2022 - Taylor & Francis
In the current work, a hybridisation strategy was adopted between the privileged building
blocks, benzofuran and piperazine, with the aim of designing novel CDK2 type II inhibitors …

CDK regulators—Cell cycle progression or apoptosis—Scenarios in normal cells and cancerous cells

M D'costa, A Bothe, S Das, SU Kumar… - Advances in Protein …, 2023 - Elsevier
Serine/threonine kinases called cyclin-dependent kinases (CDKs) interact with cyclins and
CDK inhibitors (CKIs) to control the catalytic activity. CDKs are essential controllers of RNA …

A comprehensive insight on the recent development of cyclic dependent kinase inhibitors as anticancer agents

BN Marak, J Dowarah, L Khiangte, VP Singh - European Journal of …, 2020 - Elsevier
Cancer is one of the major leading causes of death worldwide despite many breakthroughs
in the development of novel anticancer drugs. The heterodimer CDK-Cyclin complex plays …

[HTML][HTML] An insight into the risk factors of brain tumors and their therapeutic interventions

S Rasheed, K Rehman, MSH Akash - Biomedicine & Pharmacotherapy, 2021 - Elsevier
Brain tumors are an abnormal growth of cells in the brain, also known as multifactorial
groups of neoplasm. Incidence rates of brain tumors increase rapidly, and it has become a …

Proteomic signatures of 16 major types of human cancer reveal universal and cancer-type-specific proteins for the identification of potential therapeutic targets

Y Zhou, TM Lih, J Pan, N Höti, M Dong, L Cao… - Journal of Hematology & …, 2020 - Springer
Background Proteomic characterization of cancers is essential for a comprehensive
understanding of key molecular aberrations. However, proteomic profiling of a large cohort …