Chemical investigations of the Australian marine sponge Ecionemia geodides resulted in the isolation of two new pyridoacridine alkaloids, ecionines A (1) and B (2), along with the previously isolated marine natural products, biemnadin (3) and meridine (4). Compounds 1 and 2 both contain an imine moiety, which is rare for the pyridoacridine structure class. The chemical structures of 1 and 2 were determined by extensive 1D and 2D NMR, and MS data analyses. All compounds were tested against a panel of human bladder cancer cell lines, the increasingly metastatic TSU-Pr1 series (TSU-Pr1, TSU-Pr1-B1 and TSU-Pr1-B2) and the superficial bladder cancer cell line 5637. Ecionine A (1) displayed cytotoxicity against all cell lines, with IC50 values ra...
Majority of the currently available anticancer drugs are designed to have selective toxicity to rapi...
For more than thirty years, marine natural products chemists have studied sponges, ascidians, and ot...
The structures, origins, biogenesis, synthesis and bioactivity of a selection of N-heterocyclic mari...
Chemical investigations of the Australian marine sponge Ecionemia geodides resulted in the isolation...
Chemical investigation of two marine samples A. geodides and C. stolonifera led to the isolation of ...
AbstractA new pyridoacridine alkaloid named sagitol C (2) together with two known compounds; kuanoni...
A new pyridoacridine alkaloid named sagitol C (2) together with two known compounds; kuanoniamine C ...
Australia's marine environment covers extended areas, from the warm northern tropical, to the sub tr...
Pyridoacridine alkaloids are unique marine nitrogenous compounds that represent a large family of al...
AbstractPyridoacridine alkaloids are unique marine nitrogenous compounds that represent a large fami...
This review focuses on pyridoacridine-related metabolites as one biologically interesting group of a...
Secondary metabolites from marine organisms are a rich source of novel leads for drug development. A...
In continuation of our search for drug leads from Red Sea sponges we have investigated the ethyl ace...
Two new bromotyrosine alkaloids, pseudoceralidinone A (<b>1</b>) and aplysamine 7 (<b>2</b>), along ...
<p>A new alkaloid, 3-dodecyl pyridine containing a terminal cyano group (<b>1</b>), was isolated fro...
Majority of the currently available anticancer drugs are designed to have selective toxicity to rapi...
For more than thirty years, marine natural products chemists have studied sponges, ascidians, and ot...
The structures, origins, biogenesis, synthesis and bioactivity of a selection of N-heterocyclic mari...
Chemical investigations of the Australian marine sponge Ecionemia geodides resulted in the isolation...
Chemical investigation of two marine samples A. geodides and C. stolonifera led to the isolation of ...
AbstractA new pyridoacridine alkaloid named sagitol C (2) together with two known compounds; kuanoni...
A new pyridoacridine alkaloid named sagitol C (2) together with two known compounds; kuanoniamine C ...
Australia's marine environment covers extended areas, from the warm northern tropical, to the sub tr...
Pyridoacridine alkaloids are unique marine nitrogenous compounds that represent a large family of al...
AbstractPyridoacridine alkaloids are unique marine nitrogenous compounds that represent a large fami...
This review focuses on pyridoacridine-related metabolites as one biologically interesting group of a...
Secondary metabolites from marine organisms are a rich source of novel leads for drug development. A...
In continuation of our search for drug leads from Red Sea sponges we have investigated the ethyl ace...
Two new bromotyrosine alkaloids, pseudoceralidinone A (<b>1</b>) and aplysamine 7 (<b>2</b>), along ...
<p>A new alkaloid, 3-dodecyl pyridine containing a terminal cyano group (<b>1</b>), was isolated fro...
Majority of the currently available anticancer drugs are designed to have selective toxicity to rapi...
For more than thirty years, marine natural products chemists have studied sponges, ascidians, and ot...
The structures, origins, biogenesis, synthesis and bioactivity of a selection of N-heterocyclic mari...