[HTML][HTML] Voreloxin is an anticancer quinolone derivative that intercalates DNA and poisons topoisomerase II

RE Hawtin, DE Stockett, JAW Byl, RS McDowell, N Tan… - Plos one, 2010 - journals.plos.org
Background Topoisomerase II is critical for DNA replication, transcription and chromosome
segregation and is a well validated target of anti-neoplastic drugs including the …

[HTML][HTML] Antiproliferative effects of alkaloid evodiamine and its derivatives

X Hu, D Li, C Chu, X Li, X Wang, Y Jia, H Hua… - International journal of …, 2018 - mdpi.com
Alkaloids, a category of natural products with ring structures and nitrogen atoms, include
most US Food and Drug Administration approved plant derived anti-cancer agents …

Combination of DNA damage, autophagy, and ERK inhibition: novel evodiamine-inspired multi-action Pt (IV) prodrugs with high-efficiency and low-toxicity antitumor …

XM Liu, Z Li, XR Xie, JQ Wang, X Qiao… - Journal of Medicinal …, 2023 - ACS Publications
Exploring multi-targeting chemotherapeutants with advantages over single-targeting agents
and drug combinations is of great significance in drug discovery. Herein, we employed …

Design and synthesis of novel C14-urea-tetrandrine derivatives with potent anti-cancer activity

J Lan, L Huang, H Lou, C Chen, T Liu, S Hu… - European journal of …, 2018 - Elsevier
Tetrandrine is a dibenzyltetrahydroisoquinoline alkaloid, isolated from traditional Chinese
medicinal plant Stephania tetrandra, with anti-tumor activity. Our previous study identified …

Synthesis and anticancer activity of epipolythiodiketopiperazine alkaloids

N Boyer, KC Morrison, J Kim, PJ Hergenrother… - Chemical …, 2013 - pubs.rsc.org
The epipolythiodiketopiperazine (ETP) alkaloids are a highly complex class of natural
products with potent anticancer activity. Herein, we report the application of a flexible and …

Collective Synthesis and Biological Evaluation of Tryptophan‐Based Dimeric Diketopiperazine Alkaloids

S Tadano, Y Sugimachi, M Sumimoto… - … A European Journal, 2016 - Wiley Online Library
A concise two one‐pot synthesis of WIN 64821, eurocristatine, 15, 15′‐bis‐epi‐
eurocristatine, ditryptophenaline, ditryptoleucine A, WIN 64745, cristatumin C, asperdimin …

Structure modification and biological evaluation of indole-chalcone derivatives as anti-tumor agents through dual targeting tubulin and TrxR

J Yan, Y Xu, X Jin, Q Zhang, F Ouyang, L Han… - European Journal of …, 2022 - Elsevier
Microtubule target agents (MTAs) are widely-used clinical anti-cancer drugs for decades, but
the acquired drug resistance severely restricted their application. Thioredoxin reductases …

Discovery of plant-derived anti-tumor natural products: Potential leads for anti-tumor drug discovery

Z Hui, H Wen, J Zhu, H Deng, X Jiang, XY Ye… - Bioorganic …, 2023 - Elsevier
Natural products represent a paramount source of novel drugs. Numerous plant-derived
natural products have demonstrated potent anti-tumor properties, thereby garnering …

Designing multi-targeted agents: An emerging anticancer drug discovery paradigm

R Fu, Y Sun, W Sheng, D Liao - European journal of medicinal chemistry, 2017 - Elsevier
The dominant paradigm in drug discovery is to design ligands with maximum selectivity to
act on individual drug targets. With the target-based approach, many new chemical entities …

Concise total syntheses of (–)-jorunnamycin A and (–)-jorumycin enabled by asymmetric catalysis

ER Welin, A Ngamnithiporn, M Klatte, G Lapointe… - Science, 2019 - science.org
The bis-tetrahydroisoquinoline (bis-THIQ) natural products have been studied intensively
over the past four decades for their exceptionally potent anticancer activity, in addition to …