Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1369659 | Bioorganic & Medicinal Chemistry Letters | 2012 | 5 Pages |
A new cyclic depsipeptide, designated neamphamide B (1), was isolated from a marine sponge of Neamphius sp. collected at Okinawa, Japan in 1993 as an anti-mycobacterial substance against active and dormant bacilli. The planar structure of neamphamide B (1) was determined on the basis of spectroscopic analysis, and stereostructure of amino acid was deduced by chromatographic comparison of the acid hydrolysate of 1 with appropriate amino acid standards after derivatizing with FDAA or GITC. Neamphamide B (1) showed potent anti-mycobacterial activity against Mycobacterium smegmatis under standard aerobic growth conditions as well as dormancy-inducing hypoxic conditions with MIC of 1.56 μg/mL. Neamphamide B (1) was also effective to Mycobacterium bovis BCG with MIC in the ranging of 6.25–12.5 μg/mL.
Graphical abstractA new cyclic depsipeptide, designated neamphamide B, was isolated from marine sponge collected at Okinawa in Japan as an anti-mycobacterial substance with activity against active and dormant bacilli.Figure optionsDownload full-size imageDownload as PowerPoint slide