Chemical Structure : FBX-1991
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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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.
M.Wt | 452.31 | |
Formula | C19H15Cl2N3O4S | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Zhang L, et al. Adv Sci (Weinh). 2025 Mar 16:e2414844.
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