NSC-60339 exhibits a wide range of bioactivities, including potent inhibitory effects against multiple biological targets. These targets include MLL CXXC domain-DNA interaction, ALDH1A1, lipid storage modulators in Drosophila S3 cells, Influenza NS1 protein function, DNA Polymerase Beta, N370S glucocerebrosidase, JMJD2A-Tudor Domain, UBC13 Polyubiquitin, T. brucei phosphofructokinase, chronic active B-Cell receptor signaling, the phosphatase activity of Eya2, Histone Lysine Methyltransferase G9a, Rango-Importin beta complex formation, HP1-beta chromodomain interactions with methylated histone tails, Human Flap endonuclease 1 (FEN1), Polymerase Iota, Polymerase Kappa, and human tyrosyl-DNA phosphodiesterase 1 (TDP1). It also affects the growth of Candida albicans, exerts delayed death inhibition on malarial parasite plastids, and interacts with the oncogenic and cytokinetic protein MgcRacGAP, RAD54, SUMO1-mediated protein-protein interactions, WRN Helicase, and the HIV-1 protein Vpr.
NSC-60339 stabilizes DNA duplex hairpin structures and human G-quadruplex F21T by moderately increasing their melting temperatures. The compound also shows potent antimicrobial activity against Escherichia coli, targeting strains with specific mutations or deletions linked to membrane integrity and efflux pump systems. It exhibits varying MIC values from >200000.0 nM to 12500.0 nM and inhibits the AcrA efflux pump, enhancing novobiocin-induced antibacterial activity and impacting bacterial membrane permeability and HT dye uptake.
However, despite its broad biological activity, NSC-60339 exhibits no significant antibacterial, antifungal, or cytotoxic effects in other tested strains or cells, with MIC and cytotoxic concentration (CC50) values exceeding 10000.0 nM in respective assays..
Note: Summary generated by AI. Data source: ChEMBL 