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Lactomycins A-C, Dephosphorylated Phoslactomycin Derivatives that Inhibit Cathepsin B, from the Marine-derived Streptomyces sp. ACT232.

Authors :
Sun Y
Carandang RR
Harada Y
Okada S
Yoshitake K
Asakawa S
Nogi Y
Matsunaga S
Takada K
Source :
Marine drugs [Mar Drugs] 2018 Feb 21; Vol. 16 (2). Date of Electronic Publication: 2018 Feb 21.
Publication Year :
2018

Abstract

Three new polyketides, lactomycins A (1)-C (3), were isolated from the culture broth of a marine-derived Streptomyces sp. ACT232 as cathepsin B inhibitors. Their structures were determined by a combination of NMR and MS data analyses to be the dephosphorylated derivatives of a phoslactomycin class of metabolites. Lactomycins exhibited cathepsin B inhibitory activity (IC50 0.8 to 4.5 μg/mL). Even though the biosynthetic gene clusters found in the genome of the current strain have high similarity to those of phoslactomycin, neither phoslactomycins nor leustroducsins were detected by LC-MS analyses of the crude extract.<br />Competing Interests: The authors declare no conflict of interest.

Details

Language :
English
ISSN :
1660-3397
Volume :
16
Issue :
2
Database :
MEDLINE
Journal :
Marine drugs
Publication Type :
Academic Journal
Accession number :
29466301
Full Text :
https://doi.org/10.3390/md16020070