Biological evaluation of octahydropyrazin [2, 1-a: 5, 4-a′] diisoquinoline derivatives as potent anticancer agents

A Gornowicz, N Pawłowska, A Czajkowska… - Tumor …, 2017 - journals.sagepub.com
In this study, we evaluated the cytotoxic activity and antiproliferative potency of novel
octahydropyrazin [2, 1-a: 5, 4-a′] diisoquinoline derivatives (1–7) in MCF-7 and MDA-MB …

Cytotoxic activity of octahydropyrazin [2, 1-a: 5, 4-a′] diisoquinoline derivatives in human breast cancer cells

M Lepiarczyk, Z Kałuża, A Bielawska… - Archives of Pharmacal …, 2015 - Springer
Abstract Evaluation of the cytotoxicity of novel octahydropyrazin [2, 1-a: 5, 4-a′]
diisoquinoline derivatives (1a–2c) employing a 3-(4, 5-dimethylthiazol-2-yl)-2, 5 …

[HTML][HTML] The molecular mechanism of anticancer action of novel octahydropyrazino [2, 1-a: 5, 4-a′] diisoquinoline derivatives in human gastric cancer cells

N Pawłowska, A Gornowicz, A Bielawska… - Investigational New …, 2018 - Springer
Objective The aim of the current study was to examine the anticancer activity and the
detailed mechanism of novel diisoquinoline derivatives in human gastric cancer cells (AGS) …

Anticancer potential of 3-(arylideneamino)-2-phenylquinazoline-4 (3H)-one derivatives

S Das, N Chatterjee, D Bose, SK Dey… - Cellular Physiology and …, 2012 - karger.com
Different quinazoline derivatives have showed wide spectrum of pharmacological activities.
Some 3-(arylideneamino)-phenylquinazoline-4 (3H)-ones have been reported to possess …

A novel iodomethylene-dimethyl-dihydropyranone induces G2/M arrest and apoptosis in human cancer cells

J Bignon, M Bénéchie, D Herlem, JM Liu… - Anticancer …, 2009 - ar.iiarjournals.org
Background: The putative pharmacophore of a naturally cytotoxic limonoid haperforin B1, E-
5-iodomethylene-6, 6-dimethyl-5, 6-dihydropyran-2-one (IDDP) was synthesized and its …

Modes of cell death induced by tetrahydroisoquinoline-based analogs in MDA-MB-231 breast and A549 lung cancer cell lines

M Nel, AM Joubert, W Dohle, BVL Potter… - Drug Design …, 2018 - Taylor & Francis
Background A and B rings of the steroidal microtubule disruptor, 2-methoxyestradiol, and its
analogs can be mimicked with a tetrahydroisoquinoline (THIQ) core. THIQs are cytotoxic …

Evaluation of the cytotoxic, apoptosis inducing activity and molecular docking of spiroquinazolinone benzamide derivatives in MCF-7 breast cancer cells

M Mahdavi, MM Lavi, R Yekta, MA Moosavi… - Chemico-biological …, 2016 - Elsevier
Previous studies have suggested that quinazolinone derivatives are potent apoptosis-
inducing agents in various cancer cell lines. In the present study, we have investigated …

Cytotoxic activity, apoptosis induction and structure–activity relationship of 8-OR-2-aryl-3, 4-dihydroisoquinolin-2-ium salts as promising anticancer agents

FJ Cao, LF Zhu, Q Kuang, XQ Li, BH Zhou… - Bioorganic & Medicinal …, 2017 - Elsevier
As our continuing research, a series of 2-aryl-8-OR-3, 4-dihydroisoquinolin-2-ium bromides
were evaluated for cytotoxic activity on cancer cells and apoptosis induction in the present …

Synthesis of novel pyrazoline derivatives and the evaluation of death mechanisms involved in their antileukemic activity

NM Stefanes, J Toigo, MF Maioral, AV Jacques… - Bioorganic & Medicinal …, 2019 - Elsevier
Malignant neoplasms are one of the leading causes of death worldwide and hematologic
malignancies, including acute leukemia (AL) is one of the most relevant cancer types …

Synthesis and anticancer activities of 4-(4-substituted piperazin)-5, 6, 7-trialkoxy quinazoline derivatives

Y Zhang, YJ Huang, HM Xiang, PY Wang… - European Journal of …, 2014 - Elsevier
Abstract A series of 4-(4-substituted piperazin)-5, 6, 7-trialkoxy quinazoline was prepared by
conventional heating methods. Among these compounds, the crystal structure of compound …