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PB-2.12 (it's an internal name reported in related literature)

Drug details:
Classification: Phenol ethers; Benzenoids; Organic compounds;

Chemical structure:
Depiction based on curated SMILES H 2 N Cl Cl O NH 2 O H 3 C O O

Evidence for compound's anti-virulence activity:

Clostridium
Related VF: theta-toxin/PFO (Perfringolysin O)
Target: PfoA
Drug effect: Blocks Perfringolysin O (PFO)-binding to cholesterol-containing membranes and subsequent pore formation to prevent PFO-mediated cytolysis and cell death during infection.
Max phase: Preclinical (in vitro)
Publication:
Aziz UBA, et al., 2024. Targeted small molecule inhibitors blocking the cytolytic effects of pneumolysin and homologous toxins. Nat Commun 15(1):3537.

Streptococcus
Related VF: Pneumolysin
Target: Ply
Drug effect: Blocks Pneumolysin (PLY)-binding to cholesterol-containing membranes and subsequent pore formation to prevent PLY-mediated cytolysis and cell death during infection.
Max phase: Preclinical (in vitro)
Publication:
Aziz UBA, et al., 2024. Targeted small molecule inhibitors blocking the cytolytic effects of pneumolysin and homologous toxins. Nat Commun 15(1):3537.








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