Caerulomycin D, a novel glycosidic derivative of 3,4-dihydroxy-2,2′-dipyridyl 6-aldoxime from Streptomyces caeruleus

Abstract

Analysis by 1H and 13C NMR spectrometry showed that caerulomycin D, a new metabolite isolated from S. caeruleus, possessed a novel ring system and had the structure (2S,3R,4R,4aS, 10aS)-3,4,4a,10a-tetrahydro-4-hydroxy-3,4a-dimethoxy-2-methyl-9-(2-pyridyl)-2H-pyranol[3'', 2'':5,6]-p-dioxino[2,3-c]pyridine-7-carboxaldehyde (E)-oxime.