Mureidomycins (MRDs) E and F were isolated from a culture filtrate of
Streptomyces flavidovirens SANK 60486 which produces MRDs A-D. They po
ssessed the same molecular formulae, C39H48N8O12S and very similar UV,
IR and NMR spectra, but differed clearly from each other in HPLC prof
ile. From the hydrolysates of MRDs E and F, 8-hydroxy-1,2,3,4-tetrahyd
ro-3-isoquinoline carboxylic acid and 6-hydroxy-1,2,3,4-tetrahydro-3-i
soquinoline carboxylic acid were detected, respectively, which were no
t-detected from those of MRDs A-D. They showed strong anti-pseudomonal
activity but less active than MRD A. MRDs E and F were synthesized fr
om MRD A and formaldehyde through Piclet-Spengler reaction.