Unknown

Dataset Information

0

Synthesis and bioactivity of analogues of the marine antibiotic tropodithietic acid.


ABSTRACT: Tropodithietic acid (TDA) is a structurally unique sulfur-containing antibiotic from the Roseobacter clade bacterium Phaeobacter inhibens DSM 17395 and a few other related species. We have synthesised several structural analogues of TDA and used them in bioactivity tests against Staphylococcus aureus and Vibrio anguillarum for a structure-activity relationship (SAR) study, revealing that the sulfur-free analogue of TDA, tropone-2-carboxylic acid, has an antibiotic activity that is even stronger than the bioactivity of the natural product. The synthesis of this compound and of several analogues is presented and the bioactivity of the synthetic compounds is discussed.

SUBMITTER: Rabe P 

PROVIDER: S-EPMC4142847 | biostudies-literature | 2014

REPOSITORIES: biostudies-literature

altmetric image

Publications

Synthesis and bioactivity of analogues of the marine antibiotic tropodithietic acid.

Rabe Patrick P   Klapschinski Tim A TA   Brock Nelson L NL   Citron Christian A CA   D'Alvise Paul P   Gram Lone L   Dickschat Jeroen S JS  

Beilstein journal of organic chemistry 20140806


Tropodithietic acid (TDA) is a structurally unique sulfur-containing antibiotic from the Roseobacter clade bacterium Phaeobacter inhibens DSM 17395 and a few other related species. We have synthesised several structural analogues of TDA and used them in bioactivity tests against Staphylococcus aureus and Vibrio anguillarum for a structure-activity relationship (SAR) study, revealing that the sulfur-free analogue of TDA, tropone-2-carboxylic acid, has an antibiotic activity that is even stronger  ...[more]

Similar Datasets

| S-EPMC2258615 | biostudies-literature
2016-03-15 | GSE79173 | GEO
| S-EPMC4278212 | biostudies-literature
| S-EPMC2848536 | biostudies-other
| S-EPMC10134463 | biostudies-literature
| S-EPMC3147533 | biostudies-literature
2016-03-15 | E-GEOD-79173 | biostudies-arrayexpress
| S-EPMC5421792 | biostudies-literature
| S-EPMC3253701 | biostudies-literature
| S-EPMC5429656 | biostudies-literature