Resumen
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.
| Idioma original | English (US) |
|---|---|
| Número de artículo | 70 |
| Publicación | Marine Drugs |
| Volumen | 16 |
| N.º | 2 |
| DOI | |
| Estado | Published - feb 2018 |
| Publicado de forma externa | Sí |
ASJC Scopus subject areas
- Pharmaceutical Science
- Drug Discovery
- Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
Huella
Profundice en los temas de investigación de 'Lactomycins A–C, dephosphorylated phoslactomycin derivatives that inhibit Cathepsin B, from the marine-derived streptomyces sp. ACT232'. En conjunto forman una huella única.Citar esto
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