Bromine/Sulfur-Substituted 9 H -Carbazoles Produced by the Marine-Derived Streptomyces sp. OUCMDZ-5511 upon NaBr Exposure.
Pengcheng YanJibin LiuKaixuan LiPeipei LiuNing LiWeiming ZhuPublished in: Journal of natural products (2024)
Ten undocumented carbazole derivatives ( 2 - 11 ) along with the reported analogue ( 1 ) were isolated from the mangrove-derived Streptomyces sp. OUCMDZ-5511, cultured with NaBr-supplemented liquid medium. Compounds 1 - 7 are brominated carbazoles, and 8 , 10 , and 11 feature an additional thiazole or 2,3-dihydro-1,4-oxathiine rings, respectively. Their structures were identified through spectroscopic techniques, computational chemistry, and X-ray crystallography. Notably, compounds 6 and 8 effectively inhibited immune cell migration, indicating anti-inflammatory activity in vivo , potentially via Myd88/Nf-κB pathways, as suggested for compound 6 .
Keyphrases
- cell migration
- molecular docking
- high resolution
- signaling pathway
- machine learning
- endothelial cells
- deep learning
- toll like receptor
- oxidative stress
- lps induced
- ionic liquid
- nuclear factor
- magnetic resonance imaging
- drug discovery
- inflammatory response
- magnetic resonance
- dual energy
- neural network
- structure activity relationship
- contrast enhanced