P129, a pyrazole ring-containing isolongifolanone-derivate: synthesis and investigation of anti-glioma action mechanism

Y Jiang, Y Wang, L Zhao, W Yang, L Pan, Y Bai… - Discover Oncology, 2024 - Springer
Abstract Background Cyclin-dependent kinase-2 (CDK-2) is an important regulatory factor in
the G1/S phase transition. CDK-2 targeting has been shown to suppress the viability of …

[HTML][HTML] Pyrazole ring-containing isolongifolanone derivatives as potential CDK2 inhibitors: Evaluation of anticancer activity and investigation of action mechanism

Y Wang, W Shi, C Wu, L Wan, Y Zhao, C Zhang… - Biomedicine & …, 2021 - Elsevier
Isolongifolanone is a high value-added sustainable natural product. Recent studies have
demonstrated that isolongifolanone possesses anticancer activities. In this study, a series of …

A Potential Anti-Glioblastoma Compound LH20 Induces Apoptosis and Arrest of Human Glioblastoma Cells via CDK4/6 Inhibition

Y Wang, Y Li, D Liu, D Zheng, X Li, C Li, C Huang… - Molecules, 2023 - mdpi.com
Glioblastoma (GBM) is a deadly brain tumor characterized by signaling dysregulation and
aberrant cell cycle control. The CDK4/6-Rb axis is dysregulated in approximately 80% of all …

A highly potent CDK4/6 inhibitor was rationally designed to overcome blood brain barrier in gliobastoma therapy

L Yin, H Li, W Liu, Z Yao, Z Cheng, H Zhang… - European journal of …, 2018 - Elsevier
Glioblastoma multiforme (GBM) is the most common and deadliest of malignant brain tumors
in adults. Disease development is associated with dysregulation of the cyclin D-CDK4/6 …

Design, synthesis, and activity assays of cyclin-dependent kinase 1 inhibitors with flavone scaffolds

L Fu, J Mou, Y Deng, X Ren, S Qiu - Frontiers in Chemistry, 2022 - frontiersin.org
Cyclin-dependent kinase 1 (CDK1) plays an indispensable role in the whole cell cycle. It has
become a new target for cancer therapy. According to the binding mode of a pan-CDK …

[HTML][HTML] A novel trifluoromethyl quinoline derivative targeting SGK1 inducing autophagy and apoptosis via regulating mTOR/FOXO3a pathway in glioblastoma

Y Xiong, C Li, J Yu, X Chen, S Cheng, X Liu… - Arabian Journal of …, 2024 - Elsevier
Glioblastoma (GBM) is known for its aggressive nature and poor prognosis, with currently no
effective treatment available. Research has shown that introducing fluorinated functional …

Evaluation of anti-glioma effects of benzothiazoles as efficient apoptosis inducers and DNA cleaving agents

B Sever, H Ciftci - Molecular and Cellular Biochemistry, 2023 - Springer
Glioma is the fast-growing, aggressive, and prevalent brain cancer with a great level of
morbidity and mortality. Current therapy is usually found insufficient for glioma treatment. In …

Anti-Glioma Effects of Ligustilide or n-Butylphthalide on Their Own and the Synergistic Effects with Temozolomide via PI3K/Akt Signaling Pathway

ZQ Li, GS Zhang, RQ Liu, SY Shuai, PY Hu… - OncoTargets and …, 2023 - Taylor & Francis
Background Ligustilide (LIG) and n-butylphthalide (NBP) have neuroprotective effects in
cerebral ischemia; however, their roles in gliomas are not well-known. This study aimed to …

EGFR-targeted pentacyclic triterpene analogues for glioma therapy

HI Ciftci, MO Radwan, B Sever, AK Hamdy… - International Journal of …, 2021 - mdpi.com
Glioma, particularly its most malignant form, glioblastoma multiforme (GBM), is the most
common and aggressive malignant central nervous system tumor. The drawbacks of the …

Synthesis and in vitro evaluation of novel 1, 2, 3, 4-tetrahydroisoquinoline derivatives as potent antiglioma agents

R Patil, A Hosni-Ahmed, TS Jones… - Anti-Cancer Agents …, 2014 - ingentaconnect.com
Glioblastoma Multiforme (GBM) continues to demand improved chemotherapeutic solutions.
In order to discover novel chemotherapeutic agents for GBM, we identified novel …