Bistramide D is a member of new class of bioactive molecule isolated from the marine ascidian Lissoclinum bistratum in New Caledonia. Bistramides (A, B, C, D and K) show a broad spectrum of biological activity which includes antiproliferative, immunomodulatory, neurotoxic, cytotoxic and antiparasitic properties; the recent studies also show that bistramides bind to Actin. Bistramide A was reported to be very potent for the P388/dox, B16, HT29, and NSCLC-N6 cell lines. Bistramide D has similar activity in the NSCLC-N6 cell line but is comparatively less toxic in vivo. There has been no total synthesis of bistramide D reported till now to our knowledge. These intriguing biological profiles and challenging molecular architecture of bistram...
The present invention provides bistramide analogs useful for treating various types of cancer
Herein is described in silico repositioning, design, synthesis, biological evaluation and structure-...
Small molecules from natural sources are vital to drug discovery by providing molecular diversity an...
Bistramide D is a member of new class of bioactive molecule isolated from the marine ascidian Lissoc...
The bistramides are a class of natural products isolated from the marine ascidian Lissoclinum bistra...
After the isolation of the bioactive polyether bistramide C from the marine ascidian Lissoclinum bis...
L'étude des molécules issues du milieu naturel a conduit les chercheurs à s'intéresser à la synthèse...
The isolation and structures of two new cyclic hexapeptides and two new macrocyclic ethers from the ...
The enantioselective synthesis of bistramide A has been achieved with a longest linear sequence of 1...
Modern pharmaceuticals originate predominately either from natural products or totally synthetic com...
The convergent total synthesis of the marine natural product (+)-bistramide C confirms the a priori ...
The first chapter describes our preparation of novel analogs of the natural product, palmarumycin CP...
The motuporamines isolated from the sea sponge Xestospongia exigua are of biological interest becaus...
Natural products have long been a source of inspiration for many drugs in human use. The Andersen la...
Herein is described in silico repositioning, design, synthesis, biological evaluation and structure-...
The present invention provides bistramide analogs useful for treating various types of cancer
Herein is described in silico repositioning, design, synthesis, biological evaluation and structure-...
Small molecules from natural sources are vital to drug discovery by providing molecular diversity an...
Bistramide D is a member of new class of bioactive molecule isolated from the marine ascidian Lissoc...
The bistramides are a class of natural products isolated from the marine ascidian Lissoclinum bistra...
After the isolation of the bioactive polyether bistramide C from the marine ascidian Lissoclinum bis...
L'étude des molécules issues du milieu naturel a conduit les chercheurs à s'intéresser à la synthèse...
The isolation and structures of two new cyclic hexapeptides and two new macrocyclic ethers from the ...
The enantioselective synthesis of bistramide A has been achieved with a longest linear sequence of 1...
Modern pharmaceuticals originate predominately either from natural products or totally synthetic com...
The convergent total synthesis of the marine natural product (+)-bistramide C confirms the a priori ...
The first chapter describes our preparation of novel analogs of the natural product, palmarumycin CP...
The motuporamines isolated from the sea sponge Xestospongia exigua are of biological interest becaus...
Natural products have long been a source of inspiration for many drugs in human use. The Andersen la...
Herein is described in silico repositioning, design, synthesis, biological evaluation and structure-...
The present invention provides bistramide analogs useful for treating various types of cancer
Herein is described in silico repositioning, design, synthesis, biological evaluation and structure-...
Small molecules from natural sources are vital to drug discovery by providing molecular diversity an...