Pyrroloquinoline and guanidine-derived alkaloids present distinct groups of marine secondary metabolites with structural diversity that displayed potentialities in biological research. A considerable number of these molecular architectures had been recorded from marine sponges belonging to different marine genera, including Batzella, Crambe, Monanchora, Clathria, Ptilocaulis and New Caledonian starfishes Fromia monilis and Celerina heffernani. In this review, we aim to comprehensively cover the chemodiversity and the bioactivities landmarks centered around the chemical constituents exclusively isolated from these three marine genera including Batzella, Crambe and Monanchora over the period 1981–2017, paying a special attention to the polycy...
Two novel pentacyclic guanidine alkaloids, celeromycalin 3 and fromiamycalin 4, have been isolated f...
International audienceAmong the outstanding chemical diversity found in marine sponges, cyclic guani...
HPLC-UV-ELSD-MS-guided fractionation of the anti-parasitic extract obtained from the marine sponge M...
Pyrroloquinoline and guanidine-derived alkaloids present distinct groups of marine secondary metabol...
Pyrroloquinoline and guanidine-derived alkaloids present distinct groups of marine secondary metabol...
Sessile marine sponges provide an abundance of unique and diversified scaffolds. In particular, mari...
Over the past seven decades, particularly since the discovery of the first marine-derived nucleoside...
Over the past seven decades, particularly since the discovery of the first marine-derived nucleoside...
For more than thirty years, marine natural products chemists have studied sponges, ascidians, and ot...
For more than thirty years, marine natural products chemists have studied sponges, ascidians, and ot...
Australia's marine environment covers extended areas, from the warm northern tropical, to the sub tr...
Abstract: This extensive review covers research published between 2010 and 2012 regarding new compou...
Two novel pentacyclic guanidine alkaloids, celeromycalin 3 and fromiamycalin 4, have been isolated f...
Two novel pentacyclic guanidine alkaloids, celeromycalin 3 and fromiamycalin 4, have been isolated f...
Two novel pentacyclic guanidine alkaloids, celeromycalin 3 and fromiamycalin 4, have been isolated f...
Two novel pentacyclic guanidine alkaloids, celeromycalin 3 and fromiamycalin 4, have been isolated f...
International audienceAmong the outstanding chemical diversity found in marine sponges, cyclic guani...
HPLC-UV-ELSD-MS-guided fractionation of the anti-parasitic extract obtained from the marine sponge M...
Pyrroloquinoline and guanidine-derived alkaloids present distinct groups of marine secondary metabol...
Pyrroloquinoline and guanidine-derived alkaloids present distinct groups of marine secondary metabol...
Sessile marine sponges provide an abundance of unique and diversified scaffolds. In particular, mari...
Over the past seven decades, particularly since the discovery of the first marine-derived nucleoside...
Over the past seven decades, particularly since the discovery of the first marine-derived nucleoside...
For more than thirty years, marine natural products chemists have studied sponges, ascidians, and ot...
For more than thirty years, marine natural products chemists have studied sponges, ascidians, and ot...
Australia's marine environment covers extended areas, from the warm northern tropical, to the sub tr...
Abstract: This extensive review covers research published between 2010 and 2012 regarding new compou...
Two novel pentacyclic guanidine alkaloids, celeromycalin 3 and fromiamycalin 4, have been isolated f...
Two novel pentacyclic guanidine alkaloids, celeromycalin 3 and fromiamycalin 4, have been isolated f...
Two novel pentacyclic guanidine alkaloids, celeromycalin 3 and fromiamycalin 4, have been isolated f...
Two novel pentacyclic guanidine alkaloids, celeromycalin 3 and fromiamycalin 4, have been isolated f...
International audienceAmong the outstanding chemical diversity found in marine sponges, cyclic guani...
HPLC-UV-ELSD-MS-guided fractionation of the anti-parasitic extract obtained from the marine sponge M...