Recent advances in the chemistry and biology of podophyllotoxins

X Yu, Z Che, H Xu - Chemistry–A European Journal, 2017 - Wiley Online Library
Podophyllotoxin and its related aryltetralin cyclolignans belong to a family of important
products that exhibit various biological properties (eg, cytotoxic, insecticidal, antifungal …

Insight into the molecular mechanism of podophyllotoxin derivatives as anticancer drugs

H Fan, Z Zhu, H Xian, H Wang, B Chen… - Frontiers in Cell and …, 2021 - frontiersin.org
Podophyllotoxin (PTOX) is a biologically active compound derived from the podophyllum
plant, and both it and its derivatives possess excellent antitumor activity. The PTOX …

Podophyllotoxin, a medicinal agent of plant origin: past, present and future

M Guerram, ZZ JIANG, LY Zhang - Chinese Journal of Natural Medicines, 2012 - Elsevier
The aryltetralin-type lignan podophyllotoxin, the main agent present in the resin extracted
from the rhizomes of different podophyllum species, possesses important antineoplastic and …

Synthesis and biological activity, and molecular modelling studies of potent cytotoxic podophyllotoxin-naphthoquinone compounds

HT Nguyen, QGN Thi, THN Thi, PH Thi… - RSC …, 2022 - pubs.rsc.org
A new approach for the synthesis of podophyllotoxin-naphthoquinone compounds using
microwave-assisted three-component reactions is reported in this study. Novel …

Aminoazole-based diversity-oriented synthesis of heterocycles

MV Murlykina, AD Morozova, IM Zviagin… - Frontiers in …, 2018 - frontiersin.org
The comprehensive review contains the analysis of literature data concerning reactions of
heterocyclization of aminoazoles and demonstrates the application of these types of …

Synthesis, cytotoxic activity and docking studies of new 4-aza-podophyllotoxin derivatives

I Hatti, R Sreenivasulu, SS Jadav… - Medicinal Chemistry …, 2015 - Springer
The synthesized nine aza-podophyllotoxin derivatives (8a–f, 10, 12 and 14) have been
evaluated for their cytotoxicity in a panel of tumor cancer cell lines (Zr-75-1, MCF7, KB …

Design and synthesis of resveratrol-based nitrovinylstilbenes as antimitotic agents

MA Reddy, N Jain, D Yada, C Kishore… - Journal of medicinal …, 2011 - ACS Publications
A new series of resveratrol analogues was designed, synthesized, and demonstrated to be
tubulin polymerization inhibitors. Most of these compounds exhibited antiproliferative activity …

In vitro and in silico biological studies of 4-phenyl-2-quinolone (4-PQ) derivatives as anticancer agents

YF Chen, B Lawal, LJ Huang, SC Kuo, MR Sumitra… - Molecules, 2023 - mdpi.com
Our previous study found that 2-phenyl-4-quinolone (2-PQ) derivatives are antimitotic
agents, and we adopted the drug design concept of scaffold hopping to replace the 2 …

BET bromodomain inhibitors with one-step synthesis discovered from virtual screen

AM Ayoub, LML Hawk, RJ Herzig, J Jiang… - Journal of medicinal …, 2017 - ACS Publications
Chemical inhibition of epigenetic regulatory proteins BrdT and Brd4 is emerging as a
promising therapeutic strategy in contraception, cancer, and heart disease. We report an …

Synthesis and cytotoxic evaluation of fluoro and trifluoromethyl substituents containing novel naphthoquinone-fused podophyllotoxins

NH Thanh, HT Phuong, LT Tu Anh… - Natural Product …, 2022 - journals.sagepub.com
A series of novel naphthoquinone-fused podophyllotoxins containing fluoro and
trifluoromethyl substituents were synthesized in a medium with good yields using two …