PLoS ONE · 2022 · 21 citations · 23 references
MedicineOncologyPharmacologyCancer PharmacologyDrug DesignDrug DiscoveryEnzyme InhibitionOncology PharmacologyAnticancer ActivityAnticancer Natural ProductsAntiproliferative AgentsAntiproliferative Drug ActionBinding Affinity AssessmentCytotoxicity AssaysProtein Interaction AnalysisSelectivity
There is an increasing demand in developing new, effective, and affordable anti-cancer against colon and rectal. In this study, our aim is to identify the potential anthraquinone compounds from the root bark of Morinda citrifolia to be tested in vitro against colorectal cancer cell lines. Eight potential anthraquinone compounds were successfully isolated, purified and tested for both in-silico and in-vitro analyses. Based on the in-silico prediction, two anthraquinones, morindone and rubiadin, exhibit a comparable binding affinity towards multitargets of β-catenin, MDM2-p53 and KRAS. Subsequently, we constructed a 2D interaction analysis based on the above results and it suggests that the predicted anthraquinones from Morinda citrifolia offer an attractive starting point for potential antiproliferative agents against colorectal cancer. In vitro analyses further indicated that morindone and damnacanthal have significant cytotoxicity effect and selectivity activity against colorectal cancer cell lines.
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Selective cytotoxic activities of two novel synthetic drugs on human breast carcinoma MCF-7 cells.
Ramesh Badisa, Selina Darling‐Reed, Patrick Joseph et al. · PubMed · 2009 · 284 citations
Medicine, Pharmacology, Toxicology +15
Physicians' Cancer Chemotherapy Drug Manual 2001
Ellen F. Manzullo, Roger W. Anderson · Annals of Internal Medicine · 2002 · 137 citations
Medicine, Oncology, Pharmacology +9