Suberitamides A-C, Aryl Alkaloids from a Pseudosuberites sp. Marine Sponge that Inhibit Cbl-b Ubiquitin Ligase Activity.
Chang-Kwon KimDongdong WangBrice A P WilsonJosep SauríDonna VoellerStanley LipkowitzBarry R O'KeefeKirk R GustafsonPublished in: Marine drugs (2020)
Three new aryl alkaloids named suberitamides A-C (1-3), were isolated from an extract of the marine sponge Pseudosuberites sp. collected along the coast of North Carolina. Their planar structures were established by extensive nuclear magnetic resonance (NMR) and mass spectrometry (MS) analysis. To assign the challenging relative configuration of the saturated five-membered ring in suberitamide A (1), a simple and efficient NMR protocol was applied that is based on the analysis of 2- and 3-bond 1H-13C spin-spin coupling constants using a PIP (pure in-phase) HSQMBC (heteronuclear single quantum multiple bond correlation) IPAP (in-phase and anti-phase) experiment. Suberitamides A (1) and B (2) inhibited Cbl-b, an E3 ubiquitin ligase that is an important modulator of immune cell function, with IC50 values of approximately 11 μM.
Keyphrases
- magnetic resonance
- mass spectrometry
- high resolution
- room temperature
- transition metal
- randomized controlled trial
- density functional theory
- liquid chromatography
- single molecule
- solid state
- oxidative stress
- ms ms
- computed tomography
- molecular dynamics
- high performance liquid chromatography
- ionic liquid
- electron transfer
- quantum dots
- data analysis