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ml-228

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  • Inhibitors & Agonists
    3
    TargetMol | Inhibitors_Agonists
ML228
T78361357171-62-0In house
ML228 is a potent the Hypoxia Inducible Factor (HIF) pathway activator with EC50 of 1 μM. ML228 potently activates HIF in vitro as well as its downstream target VEGF.
  • $37
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Antibacterial agent 228
T210234
Antibacterial agent 228 (Compound 8) inhibits mycobacterial ribosomes with an IC50 of 2.31 μM against Mycobacterium smegmatis. It demonstrates antibacterial activity with MIC values of 2 and 0.25 μg/mL against both wild-type and Δ1258c mutant strains of M. tuberculosis H37Rv, 8 μg/mL against wild-type and Δ2780c mutant strains of M. abscessus ATCC 19977, and 8 μg/mL against M. smegmatis.
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Pradefovir
Remofovir, MB-6866, MB-06866, ICN-2001-3, ICN-20013
T28449625095-60-5
Pradefovir (Remofovir) is a reverse transcriptase inhibitor potentially for treatment of chronic HBV infection. Pradefovir is also a liver-targeted prodrug of adefovir. After metabolic activation, Pradefovir was converted to PMEA (9-(2-phosphonylmethoxyethyl)adenine) in human liver microsomes with a K(m) of 60 microM, a maximum rate of metabolism of 228 pmol/min/mg protein, and an intrinsic clearance of about 359 ml/min.
  • $238
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