Four new callipeltin A derivatives (N-Q) have been isolated from the Solomon Island marine sponge Asteropus sp. Their structures were established by spectroscopic techniques followed by acid hydrolysis and derivatisation of the free amino acids, and subsequent LCMS analysis of the derivatives. The compounds were evaluated for their activity against cancer cell lines A2058 (melanoma), HT-29 (colorectal adenocarcinoma) and MCF-7 (breast adenocarcinoma) and non-malignant MRC-5 fibroblast cells. While the acyclic callipeltins P and Q were inactive the cyclic callipeltins N and O showed significant cytotoxicity against all exposed cell lines with IC50 values as low as 0.16 mu M confirming the role of cyclic configuration in biological activity. ...
For more than thirty years, marine natural products chemists have studied sponges, ascidians, and ot...
Continued investigation of the polar extracts of the marine sponge Latrunculia sp. has resulted in t...
Continued investigation of the polar extracts of the marine sponge Latrunculia sp. has resulted in t...
Four new callipeltin A derivatives (N-Q) have been isolated from the Solomon Island marine sponge As...
Following the characterization of callipeltin A (I) two new cytotoxic peptides, callipeltin A (II) a...
Callipeltin A is a cyclic depsidecapeptide from a shallow water sponge of the genus Callipelta (orde...
Two new callipeltin-related acyclic peptides have been isolated, together with callipeltins A-C from...
Two new callipeltin-related acyclic peptides (2 and 3) have been isolated, together with callipeltin...
Bioassay guided fractionation of the EtOAc fraction of the sponge Callyspongia aerizusa yielded seve...
From the ethyl acetate fraction of the Indonesian sponge Callyspongia aerizusa extract, a new cyclic...
Four new antifungal peptides, callipeltins F-1, were isolated from the marine sponge Latrunculia sp....
A number of natural products from marine sponges, such as cyclodepsipeptides, have been identified. ...
Chemical investigation of the Indonesian sponge Callyspongia aerizusa afforded five new cyclic pepti...
Chemical investigation of the Indonesian sponge Callyspongia aerizusa afforded five new cyclic pepti...
For more than thirty years, marine natural products chemists have studied sponges, ascidians, and ot...
Continued investigation of the polar extracts of the marine sponge Latrunculia sp. has resulted in t...
Continued investigation of the polar extracts of the marine sponge Latrunculia sp. has resulted in t...
Four new callipeltin A derivatives (N-Q) have been isolated from the Solomon Island marine sponge As...
Following the characterization of callipeltin A (I) two new cytotoxic peptides, callipeltin A (II) a...
Callipeltin A is a cyclic depsidecapeptide from a shallow water sponge of the genus Callipelta (orde...
Two new callipeltin-related acyclic peptides have been isolated, together with callipeltins A-C from...
Two new callipeltin-related acyclic peptides (2 and 3) have been isolated, together with callipeltin...
Bioassay guided fractionation of the EtOAc fraction of the sponge Callyspongia aerizusa yielded seve...
From the ethyl acetate fraction of the Indonesian sponge Callyspongia aerizusa extract, a new cyclic...
Four new antifungal peptides, callipeltins F-1, were isolated from the marine sponge Latrunculia sp....
A number of natural products from marine sponges, such as cyclodepsipeptides, have been identified. ...
Chemical investigation of the Indonesian sponge Callyspongia aerizusa afforded five new cyclic pepti...
Chemical investigation of the Indonesian sponge Callyspongia aerizusa afforded five new cyclic pepti...
For more than thirty years, marine natural products chemists have studied sponges, ascidians, and ot...
Continued investigation of the polar extracts of the marine sponge Latrunculia sp. has resulted in t...
Continued investigation of the polar extracts of the marine sponge Latrunculia sp. has resulted in t...