AbstractPyridoacridine alkaloids are unique marine nitrogenous compounds that represent a large family of alkaloids. They have been reported from different marine organisms like sponges, ascidians, anemones, prosobranch mollusk, and tunicates. Attention to pyridoacridines has risen because of their significant biological activities. The present review emphasizes mainly on pyridoacridines isolated marine organisms over the last years. Thus, the synthetic ones were not discussed. Herein, 95 pyridoacridine alkaloids isolated from marine organisms have been retrieved, in addition to their classification, isolation, sources, structures, molecular weight, physical, and (UV, IR, 1H and 13C NMR) spectral data
The extraction and purification of the bioactive extract of <i>Cystodytes violatinctus</i> (Solomon ...
Chemical investigations of the Australian marine sponge Ecionemia geodides resulted in the isolation...
The structures, origins, biogenesis, synthesis and bioactivity of a selection of N-heterocyclic mari...
Pyridoacridine alkaloids are unique marine nitrogenous compounds that represent a large family of al...
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...
AbstractPyridoacridine alkaloids are unique marine nitrogenous compounds that represent a large fami...
Chemical investigation of two marine samples A. geodides and C. stolonifera led to the isolation of ...
A new hexacyclic pyridoacridine alkaloid, nordehydrocyclodercitin (1), from an ascidian, Aplidium sp...
Nitrogen heterocycles are essential parts of the chemical machinery of life and often reveal intrigu...
The marine organisms, mainly invertebrates such as sponges and ascidians, are a rich source of varie...
Two new pyridoacridine alkaloids, kuanomamines E and F, and a new ring opened pyridoacridine alkaloi...
Chemical investigations of the Australian marine sponge Ecionemia geodides resulted in the isolation...
An intensive research effort during the last 25 years has generated an impressive number of alkaloid...
An intensive research effort during the last 25 years has generated an impressive number of alkaloid...
The extraction and purification of the bioactive extract of <i>Cystodytes violatinctus</i> (Solomon ...
Chemical investigations of the Australian marine sponge Ecionemia geodides resulted in the isolation...
The structures, origins, biogenesis, synthesis and bioactivity of a selection of N-heterocyclic mari...
Pyridoacridine alkaloids are unique marine nitrogenous compounds that represent a large family of al...
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...
AbstractPyridoacridine alkaloids are unique marine nitrogenous compounds that represent a large fami...
Chemical investigation of two marine samples A. geodides and C. stolonifera led to the isolation of ...
A new hexacyclic pyridoacridine alkaloid, nordehydrocyclodercitin (1), from an ascidian, Aplidium sp...
Nitrogen heterocycles are essential parts of the chemical machinery of life and often reveal intrigu...
The marine organisms, mainly invertebrates such as sponges and ascidians, are a rich source of varie...
Two new pyridoacridine alkaloids, kuanomamines E and F, and a new ring opened pyridoacridine alkaloi...
Chemical investigations of the Australian marine sponge Ecionemia geodides resulted in the isolation...
An intensive research effort during the last 25 years has generated an impressive number of alkaloid...
An intensive research effort during the last 25 years has generated an impressive number of alkaloid...
The extraction and purification of the bioactive extract of <i>Cystodytes violatinctus</i> (Solomon ...
Chemical investigations of the Australian marine sponge Ecionemia geodides resulted in the isolation...
The structures, origins, biogenesis, synthesis and bioactivity of a selection of N-heterocyclic mari...