| Cat. No. | Product Name | Information | 
            
                
            	| PC-23126 | PTB1 BamA inhibitor | Peptide Targeting BamA-1 (PTB1) is a 12-amino acid macrocycle, multi-species BamA inhibitor, binds to purified BamA with SPR Kd of 50 pM, has MIC of 42 ug/mL (25 uM) against wild-type E. coli strain. | 
            
                
            	| PC-22986 | G247 MsbA inhibitor | G247 is a specific MsbA inhibitor, reduces MsbA NBD dimerization efficiency and ATPase activity. | 
            
                
            	| PC-22958 | Virstatin ToxT inhibitor | Virstatin is a small-molecule inhibitor of transcription factor ToxT, inhibits the pili system synthesis and prevents A. baumannii biofilm formation, reduces virulence in vitro. | 
            
                
            	| PC-22943 | Ridinilazole C. difficile inhibitor | Ridinilazole (SMT19969) is a narrow-spectrum, non-absorbable antimicrobial against Clostridium difficile with MIC of 0.125 to 0.5 ug/ml, MIC90 of 0.25 ug/mL,  including ribotype 027 strains. | 
            
                
            	| PC-22942 | Ramoplanin Antibiotic | Ramoplanin (A-16686) is a glycolipodepsipeptide antibiotic with MIC50 of 1.45 ug/mL against methicillin-resistant S. epidermidis (MRSE), shows activity against staphylococci, enterococci and C. difficile. | 
            
                
            	| PC-22941 | OPS-2071 C. difficile inhibitor | OPS-2071 is a novel quinolone antibacterial agent with potent antibacterial activity against 54 clinically isolated C. difficile strains with MIC50 of 0.125 ug/mL, reduces the risk of adverse events typical of fluoroquinolone class antibiotics. | 
            
                
            	| PC-22849 | PBZ1587 GroES/GroEL inhibitor | PBZ1587 is a small-molecule inhibitor of the GroES/GroEL chaperone system with IC50 of 0.44 uM in MDH refolding assay, binds at the GroEL ring–ring interface (RRI). | 
            
                
            	| PC-22848 | PBZ1038 GroES/GroEL inhibitor | PBZ1038 is a small-molecule inhibitor of the GroES/GroEL chaperone system with IC50 of 1.2 uM against E. faecium GroES/GroEL refolding of malate dehydrogenase (MDH), binds at the GroEL ring–ring interface (RRI). | 
            
                
            	| PC-22835 | Cefiderocol Antibiotic | Cefiderocol (CFDC, S-649266) is a siderophore cephalosporin antibiotic, has a potent activity against a broad range of aerobic Gram-negative bacterial species with MIC50 of <2 ug/mL. | 
            
                
            	| PC-22813 | TST1N-224 S. aureus VraRC inhibitor | TST1N-224 is a potent inhibitor targeting the response regulator VraRC of S. aureus, inhibits the formation of the VraRC-DNA complex with IC50 of 60.2 uM, shows strong binding to VraRC (KD=23.4 uM), enhances the susceptibility of vancomycin-intermediate S. aureus (VISA) to both vancomycin and methicillin. | 
            
                
            	| PC-22725 | Kanamycin sulfate Antibiotic | Kanamycin (Kanamycin A) sulfate is an orally active antibacterial (gram-negative/positive bacteria) agent, inhibits translocation and causes misencoding by binding to the 70 S ribosomal subunit. | 
            
                
            	| PC-22724 | Kanamycin Antibiotic | Kanamycin (Kanamycin A) is an orally active antibacterial (gram-negative/positive bacteria) agent, inhibits translocation and causes misencoding by binding to the 70 S ribosomal subunit. |