A review of results of bioactivity and reactivity examinations of marine sesquiterpene (hydro)quinones is presented. The article is focused mostly on friedo- rearranged drimane structural types, isolated from sponges of the order Dictyoceratida. Examples of structural correlations are outlined. Available results on the mechanism of redox processes and examinations of chemo- and regioselectivity in addition reactions are presented and, where possible, analyzed in relation to established bioactivities. Most of the bioactivity examinations are concerned with antitumor activities and the mechanism thereof, such as DNA damage, arylation of nucleophiles, tubulin assembly inhibition, protein kinase inhibition, inhibition of the arachidonic cascade...
The following thesis presents results from several investigations of marine natural products. It is ...
Abstract: This extensive review covers research published between 2010 and 2012 regarding new compou...
With the aid of circular dichroism, n.m.r. shift reagents, and 13C n.m.r. spectroscopy the absolute ...
A review of results of bioactivity and reactivity examinations of marine sesquiterpene (hydro)quinon...
The 1,4-benzoquinone moiety is a common structural feature in a large number of compounds that have ...
This work extends in vitro screening of antimicrobial activity of the sesquiterpene hydroquinone ava...
This work extends in vitro screening of antimicrobial activity of the sesquiterpene hydroquinone ...
Avarol (I) and the corresponding quinone (avarone) were isolated from D. avara and their structures ...
Nine alkyl(aryl)thio derivatives of the marine sesquiterpene quinone avarone were synthesized by nuc...
The sesquiterpene hydroquinone avarol (1) was isolated from the marine sponge Dysidea avara, whereas...
Within the marine ecosystem, the sessile organisms such as Porifera are considered the most interest...
For more than thirty years, marine natural products chemists have studied sponges, ascidians, and ot...
Investigation of the marine sponge Dysidea avara, family Dysideidae, afforded a new sesquiterpene (-...
Chemical investigation of a southern Australian deep-water marine sponge, Fasciospongia sp., returne...
The oceans are a unique resource that has contributed greatly to the field of natural products chemi...
The following thesis presents results from several investigations of marine natural products. It is ...
Abstract: This extensive review covers research published between 2010 and 2012 regarding new compou...
With the aid of circular dichroism, n.m.r. shift reagents, and 13C n.m.r. spectroscopy the absolute ...
A review of results of bioactivity and reactivity examinations of marine sesquiterpene (hydro)quinon...
The 1,4-benzoquinone moiety is a common structural feature in a large number of compounds that have ...
This work extends in vitro screening of antimicrobial activity of the sesquiterpene hydroquinone ava...
This work extends in vitro screening of antimicrobial activity of the sesquiterpene hydroquinone ...
Avarol (I) and the corresponding quinone (avarone) were isolated from D. avara and their structures ...
Nine alkyl(aryl)thio derivatives of the marine sesquiterpene quinone avarone were synthesized by nuc...
The sesquiterpene hydroquinone avarol (1) was isolated from the marine sponge Dysidea avara, whereas...
Within the marine ecosystem, the sessile organisms such as Porifera are considered the most interest...
For more than thirty years, marine natural products chemists have studied sponges, ascidians, and ot...
Investigation of the marine sponge Dysidea avara, family Dysideidae, afforded a new sesquiterpene (-...
Chemical investigation of a southern Australian deep-water marine sponge, Fasciospongia sp., returne...
The oceans are a unique resource that has contributed greatly to the field of natural products chemi...
The following thesis presents results from several investigations of marine natural products. It is ...
Abstract: This extensive review covers research published between 2010 and 2012 regarding new compou...
With the aid of circular dichroism, n.m.r. shift reagents, and 13C n.m.r. spectroscopy the absolute ...