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Results for "

23s rrna

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    5
    TargetMol | Activity
  • Natural Products
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  • Recombinant Protein
    1
    TargetMol | natural
S-23
T207891010396-29-8
S-23 ((S)-3-(4-chloro-3-fluorophenoxy)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide) is an oral selective androgen receptor modulator (SARM) with a Ki of 1.7 nM. S-23 increases prostate, seminal vesicle, and levator ani muscle weights in castrated rats.
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(23S,50S)-50-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-23-(tert-butoxycarbonyl)-2,2-dimethyl-4,21,26,35,44-pentaoxo-3,30,33,39,42-pentaoxa-22,27,36,45-tetraazahenpentacontan-51-oic acid
T647671662688-20-1
(23S,50S)-50-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-23-(tert-butoxycarbonyl)-2,2-dimethyl-4,21,26,35,44-pentaoxo-3,30,33,39,42-pentaoxa-22,27,36,45-tetraazahenpentacontan-51-oic acid is a useful organic compound for research related to life sciences and the catalog number is T64767.
    7-10 days
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    3-Methyluridine
    T134992140-69-4
    3-Methyluridine is a modified nucleoside of cellular RNA.
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    Clindamycin hydrochloride monohydrate
    T2229758207-19-5
    Clindamycin hydrochloride monohydrate (Clindamycin alcoholate) is a protein synthesis inhibitor used orally, capable of diminishing virulence factor expression in Staphylococcus aureus at sub-minimum inhibitory concentrations (sub-MICs). It acts by suppressing Panton-Valentine leucocidin (PVL), toxic-shock-staphylococcal toxin (TSST-1), and alpha-haemolysin (Hla) production. Resistance to this compound emerges through enzymatic methylation at the antibiotic's 50S ribosomal subunit binding site (23S rRNA).
    • $53
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    SEQ-9
    T79015
    SEQ-9 is an orally active inhibitor of the Mycobacterium tuberculosis (Mtb) 23S bacterial ribosome, with an inhibitory concentration (IC50) around 170 nM against unmethylated Mtb ribosomes and potent effects on A2296 methylated ribosomes. It is used in research on bacterial infections and drug resistance [1].
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