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FBX-1991

Chemical Structure : FBX-1991

CAS No.:

FBX-1991 (FBX1991)

Catalog No.: PC-24236Not For Human Use, Lab Use Only.

FBX-1991 is a potent, specific small molecule inhibitor of Helicobacter pylori (H. pylori) dehydrogenase/isomerase FabX with IC50 of 0.158 uM, shows potent antibacterial activity against strain BHKS211 with MIC of 16 ug/mL.

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Purity & Documentation Purity: >98% (HPLC)

Biological Activity

FBX-1991 is a potent, specific small molecule inhibitor of Helicobacter pylori (H. pylori) dehydrogenase/isomerase FabX with IC50 of 0.158 uM, shows potent antibacterial activity against strain BHKS211 with MIC of 16 ug/mL.
FabX is essential for H. pylori growth and gastric colonization by retaining UFA synthesis and producing ROS, respectively, and is a species-specific anti-H. pylori drug target.
FBX-1991 does not inhibit the enzymatic activities of the structurally conserved homolog FabK.
FBX-1991 significantly inhibits the growth of H. pylori strain G27 and three clinical drug-resistant isolates with MIC of 16 ug/mL, but does not inhibit the growth of the non-Helicobacter strains at 128 ug/mL.
FBX-1991 partially inhibits UFA and cyclopropane fatty acid synthesis, ROS production and subsequent excretion from H. pylori by specifically targeting FabX in vivo.

Physicochemical Properties

M.Wt 452.31
Formula C19H15Cl2N3O4S
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

methyl 3-((2-((2,4-dichlorophenyl)amino)pyridine)-3-sulfonamido)benzoate

References

1. Zhang L, et al. Adv Sci (Weinh). 2025 Mar 16:e2414844.

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