RESEARCH / DISCOVERY
← Back to the library

Total synthesis and biological evaluation of catenulobactin B as neuroprotective agent.

Total synthesis and biological evaluation of catenulobactin B as neuroprotective agent.

Read the original publication

Where did the research take place?

The study site has not been established. Author addresses may differ from where the research occurred.

Jiangmen, CN · Author affiliation

School of Pharmacy and Food Engineering, Wuyi University, Jiangmen, Guangdong 529020, China.
Location evidence

Explore research worldwide

A plain-language reading has not been prepared for this paper yet.

Original abstract

The first total synthesis of catenulobactin B has been accomplished in longest linear eight steps (34% overall yield). The convergent route featured a molybdenum(VI) oxide-promoted dehydrative cyclization, a key double amide coupling strategy and a set of judicious functional group transformations. Biological evaluation revealed that catenulobactin B markedly inhibited α-synuclein aggregation and attenuated the progression of 6-OHDA-induced dopaminergic neurodegeneration in C. elegans. This neuroprotective effect may be closely associated with the modulation of iron metabolism-related gene expression. These findings identify catenulobactin B as a promising neuroprotective agent targeting iron homeostasis for Parkinson's disease-related neurodegeneration.

Explore another example or bring your own paper

Pasted text and PDF extraction stay on this computer. The local guide explains terms and surfaces passages; rewriting requires a configured local model. Scanned PDFs need OCR first.

RECORD & PROVENANCE