A comprehensive review of topoisomerase inhibitors as anticancer agents in the past decade

X Liang, Q Wu, S Luan, Z Yin, C He, L Yin, Y Zou… - European journal of …, 2019 - Elsevier
The topoisomerase enzymes play an important role in DNA metabolism, and searching for
enzyme inhibitors is an important target in the search for new anticancer drugs. Discovery of …

Discovery of novel topoisomerase II inhibitors by medicinal chemistry approaches

W Hu, XS Huang, JF Wu, L Yang… - Journal of Medicinal …, 2018 - ACS Publications
DNA topoisomerase II (topo II) is an important enzyme involved in DNA replication,
recombination, and repair. Despite the popular applications of topo II inhibitors in cancer …

Design, synthesis and biological evaluation of N-alkyl or aryl substituted isoindigo derivatives as potential dual cyclin-dependent kinase 2 (CDK2)/glycogen synthase …

P Zhao, Y Li, G Gao, S Wang, Y Yan, X Zhan… - European Journal of …, 2014 - Elsevier
A series of N-alkyl or aryl substituted isoindigo derivatives have been synthesized and their
anti-proliferative activity was evaluated by Sulforhodamine B (SRB) assay. Some of the …

Escitalopram oxalate induces apoptosis in U‐87 MG cells and autophagy in GBM 8401 cells

VCH Chen, YH Hsieh, LJ Chen… - Journal of cellular …, 2018 - Wiley Online Library
Glioblastoma multiforme (GBM) is recognized as a most aggressive brain cancer with the
worst prognosis and survival time. Owing to the anatomic location of gliomas, surgically …

Dual inhibition of topoisomerase II and microtubule of podophyllotoxin derivative 5p overcomes cancer multidrug resistance

X Lv, W Cheng, X Li, H Shang, J Zhang, H Hong… - European Journal of …, 2024 - Elsevier
Compound 5p is a 4β-N-substituted podophyllotoxin derivative, which exhibited potent
activity toward drug-resistant K562/A02 cells and decreased MDR-1 mRNA expression …

Structural and biological diversity of natural p-terphenyls

W Li, XB Li, HX Lou - Journal of Asian natural products research, 2018 - Taylor & Francis
Abstract p-Terphenyls consisting of a C-18 tricyclic or polycyclic C-18 aromatic skeleton,
have diverse structures because of the variation of the middle ring and the connections …

Design, semisynthesis, α-glucosidase inhibitory, cytotoxic, and antibacterial activities of p-terphenyl derivatives

XQ Zhang, XF Mou, N Mao, JJ Hao, M Liu… - European Journal of …, 2018 - Elsevier
Abstract Terphenyllin (1), a naturally abundant p-terphenyl metabolite, was isolated from the
coral derived fungus Aspergillus candidus together with four natural analogues 2–5. To …

Anti-inflammatory and anticancer p-terphenyl derivatives from fungi of the genus Thelephora

C Bailly - Bioorganic & Medicinal Chemistry, 2022 - Elsevier
Fungi from the genus Thelephora have been exploited to identify bioactive compounds. The
main natural products characterized are para-terphenyl derivatives, chiefly represented by …

Discovery of a highly active anticancer analogue of cardamonin that acts as an inducer of caspase-dependent apoptosis and modulator of the mTOR pathway

MKB Break, MS Hossan, Y Khoo, ME Qazzaz… - Fitoterapia, 2018 - Elsevier
Cardamonin is a natural chalcone that has been shown to exhibit high anticancer activity. In
an attempt to discover analogues of cardamonin with enhanced anticancer activity, 19 …

p-Terphenyl O-β-glucuronides, DNA topoisomerase inhibitors from Streptomyces sp. LZ35ΔgdmAI

J Deng, C Lu, S Li, H Hao, Z Li, J Zhu, Y Li… - Bioorganic & Medicinal …, 2014 - Elsevier
The analysis of genome sequence indicated that Streptomyces sp. LZ35 has the potential of
producing many types of secondary metabolites, including p-terphenyls and geldanamycins …