FSL0499
- Structure
- InChI=1S/C15H23NO4/c1-8-3-9(2)15(20)11(4-8)12(17)5-10-6-13(18)16-14(19)7-10/h8-12,17H,3-7H2,1-2H3,(H,16,18,19)/t8-,9-,11-,12+/m0/s1
- InChIKey=YPHMISFOHDHNIV-FSZOTQKASA-N
- Synonyms
-
- 66-81-9
- A-67
- Acti-Aid
- Actidione
- Cycloheximide
- Cycloheximide
- D-73-2
- GS-700-II
- Naramycin
- Naramycin-A
- NSC-185
- P-42-A
- Zygomycin-D
- Origin
- Streptomyces griseus
- Biological activities
- Inhibition of eukariotic protein synthesis
- Therapeutic
-
Anticancer
Antifungal
- Target
-
60S ribosomes
- Assay information
-
Inhibitor of protein synthesis in eukaryotes, and works as an antifungal antibiotics
Reduction of the context of total nuclear ribonucleoprotein complexes at non-lethal dose of rat liver (2 mg/kg body weight)
Inhibitor of protein synthesis in rat liver (2-5 mg/kg body weight)
Inducer of apotosis in HL-60 cells, T cell hybridomas, Burkitt’s lymphoma cells, and other cell types
Inhibitor of hFKBP12, peptidyl-prolyl isomerase (PPIase) (Ki = 3.4 μM)
Binding to the tRNA E-site of the 60S subunit