Dysidavarones A–D (<b>1</b>–<b>4</b>), four new sesquiterpene quinones possessing the unprecedented “dysidavarane” carbon skeleton, were isolated from the South China Sea sponge <i>Dysidea avara</i>. The structures were established by spectroscopic methods, and the absolute configurations were determined using quantum mechanical calculation of the electronic circular dichroic (ECD) spectrum and exciton chirality CD method. Their cytotoxic activity against four human cancer cell lines and PTP1B inhibitory activity were also evaluated
A review of results of bioactivity and reactivity examinations of marine sesquiterpene (hydro)quinon...
thesisMarine organisms produce a wide variety of metabolites that display diverse biological activit...
Three new sesquiterpene hydroquinones, avapyran (<b>1</b>), 17-<i>O</i>-acetylavarol (<b>2</b>), and...
Dysideanones A–C (<b>1</b>–<b>3</b>), three unusual sesquiterpene quinones with unprecedented carbon...
Investigation of the marine sponge Dysidea avara, family Dysideidae, afforded a new sesquiterpene (-...
new diterpene with the dolabellane skeleton 1 has been isolated from the sponge of the Indian Ocean,...
The chemical study of two sponges of the genus Dysidea collected in the Gulf of California has led t...
The chemical investigation of the marine sponge Dysidea sp., which was collected from Bohol province...
A GNPS molecular networking approach mapped a library of 960 southern Australian marine sponges and ...
Two new sesquiterpene cyclopentenones, dysidenones A and B (I, II), and a new sesquiterpene aminoqui...
Seven new drimane sesquiterpenoids (1−3, 6−9), along with the known compounds deoxyuvidin B (4), str...
Seven new drimane sesquiterpenoids (1-3, 6-9), along with the known compounds deoxyuvidin B (4), str...
393-395Three new sesquiterpenes (+)-furodysinin lactone 1, (+)-O-methylfurodysinin lactone 2 and sp...
A review of results of bioactivity and reactivity examinations of marine sesquiterpene (hydro)quinon...
Nine new sesquiterpene quinones/hydroquinones (<b>1</b>–<b>7</b>, <b>10</b>, and <b>12</b>), three s...
A review of results of bioactivity and reactivity examinations of marine sesquiterpene (hydro)quinon...
thesisMarine organisms produce a wide variety of metabolites that display diverse biological activit...
Three new sesquiterpene hydroquinones, avapyran (<b>1</b>), 17-<i>O</i>-acetylavarol (<b>2</b>), and...
Dysideanones A–C (<b>1</b>–<b>3</b>), three unusual sesquiterpene quinones with unprecedented carbon...
Investigation of the marine sponge Dysidea avara, family Dysideidae, afforded a new sesquiterpene (-...
new diterpene with the dolabellane skeleton 1 has been isolated from the sponge of the Indian Ocean,...
The chemical study of two sponges of the genus Dysidea collected in the Gulf of California has led t...
The chemical investigation of the marine sponge Dysidea sp., which was collected from Bohol province...
A GNPS molecular networking approach mapped a library of 960 southern Australian marine sponges and ...
Two new sesquiterpene cyclopentenones, dysidenones A and B (I, II), and a new sesquiterpene aminoqui...
Seven new drimane sesquiterpenoids (1−3, 6−9), along with the known compounds deoxyuvidin B (4), str...
Seven new drimane sesquiterpenoids (1-3, 6-9), along with the known compounds deoxyuvidin B (4), str...
393-395Three new sesquiterpenes (+)-furodysinin lactone 1, (+)-O-methylfurodysinin lactone 2 and sp...
A review of results of bioactivity and reactivity examinations of marine sesquiterpene (hydro)quinon...
Nine new sesquiterpene quinones/hydroquinones (<b>1</b>–<b>7</b>, <b>10</b>, and <b>12</b>), three s...
A review of results of bioactivity and reactivity examinations of marine sesquiterpene (hydro)quinon...
thesisMarine organisms produce a wide variety of metabolites that display diverse biological activit...
Three new sesquiterpene hydroquinones, avapyran (<b>1</b>), 17-<i>O</i>-acetylavarol (<b>2</b>), and...