We report here the enzymatic biosynthesis of FR-900098 analogues and establish an in vivo platform for the biosynthesis of an N-propionyl derivative FR-900098P. FR-900098P is found to be a significantly more potent inhibitor of Plasmodium falciparum 1-deoxy-D-xylulose 5-phosphate reductoisomerase (PfDxr) than the parent compound, and thus a more promising antimalarial drug candidate.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4312176PMC
http://dx.doi.org/10.1039/c4cc09181gDOI Listing

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