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L-NBDNJ is a sugar mimic and an antivirulence agent. It disrupts the expression of proteins that regulate the assembly and organization of the host cell cytoskeleton. In cystic fibrosis (CF) lung disease infection models, L-NBDNJ exhibits both anti-inflammatory and anti-infective properties.
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | L-NBDNJ is a sugar mimic and an antivirulence agent. It disrupts the expression of proteins that regulate the assembly and organization of the host cell cytoskeleton. In cystic fibrosis (CF) lung disease infection models, L-NBDNJ exhibits both anti-inflammatory and anti-infective properties. |
| In vitro | L-NBDNJ is a sugar mimic and an antivirulence agent. It disrupts the expression of proteins that regulate host cell cytoskeletal assembly and organization. L-NBDNJ must interfere with the metabolic pathways involved in host cell cytoskeletal assembly and organization, downregulating key virulence factors of Pseudomonas aeruginosa involved in host response and affecting the adhesion of pathogens to human cells. |
| In vivo | L-NBDNJ (10-100 mg/kg; oral gavage; daily for 6 days) demonstrates anti-inflammatory and anti-infective properties in mice. |
| Formula | C10H21NO4 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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