FSL0578
- Structure
- InChI=1S/C20H40N4O10/c1-6(25)14-11(27)10(26)9(23)18(32-14)33-15-7(21)4-8(22)16(12(15)28)34-19-13(29)17(24-3)20(2,30)5-31-19/h6-19,24-30H,4-5,21-23H2,1-3H3/t6-,7+,8-,9-,10-,11+,12+,13-,14-,15-,16+,17-,18-,19-,20+/m1/s1
- InChIKey=BRZYSWJRSDMWLG-DJWUNRQOSA-N
- Synonyms
-
- Origin
- Micromonospora echinospora
- Biological activities
- Inhibition of protein synthesis
- Therapeutic
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Antibacterial
Antiprotozoal
Coccidiostats
- Target
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80S ribosomes
- Assay information
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Effective inhibition of wheat-germ, cell-free translation programmed with rat-liver polydenylated RNA (Leading to aberrant protein synthesis in both prokaryotic and eukaryotic cells (IC50 of translation inhibition for Eukaryotic system = 2.0 μM ± 0.3 μM, for Prokaryotic system = 8.9 ± 1.5 nM)
Exhibition of antibacterial activity against B. subtilis (MIC Toxicity for HEK-293, human embryonic kidney cell, LC50 = 1.3 ± 0.1 mM
Inhibition of leishmania promastigotes in the low micromolar range: L. major (LC50 = 1.95 ± 0.05 μM), L. donovani (LC50 = 5.8 ± 0.9 μM)
Fungal growth inhibition of Fusarium graminearum and F. culmorum (MIC = 25 μg/mL in PDA for each, 10 days)