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LpxH-IN-AZ1 is a potent inhibitor of the UDP-2,3-diacylglucosamine pyrophosphate hydrolase, LpxH, and sulfonylpiperazine compounds.LpxH-IN-AZ1 exhibits antimicrobial activity and inhibits Klebsiella pneumoniae with an IC50 of 0.36 μM.

| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $50 | In Stock | |
| 5 mg | $122 | In Stock | |
| 10 mg | $193 | In Stock | |
| 25 mg | $455 | In Stock | |
| 50 mg | $669 | In Stock | |
| 100 mg | $953 | In Stock | |
| 500 mg | $1,920 | In Stock |
| Description | LpxH-IN-AZ1 is a potent inhibitor of the UDP-2,3-diacylglucosamine pyrophosphate hydrolase, LpxH, and sulfonylpiperazine compounds.LpxH-IN-AZ1 exhibits antimicrobial activity and inhibits Klebsiella pneumoniae with an IC50 of 0.36 μM. |
| Targets&IC50 | LpxH (Klebsiella pneumoniae):0.36 μM, LpxH (E. coli):0.14 μM |
| In vitro | LpxH-IN-AZ1 (1 μM) inhibits K. pneumoniae LpxH activity by 75% and E. coli LpxH activity by 83% when 100 μM UDPDAGn is present[1]. Additionally, it exhibits IC50 values of 0.36 μM for K. pneumoniae LpxH and 0.14 μM for E. coli LpxH[1]. |
| Molecular Weight | 453.48 |
| Formula | C21H22F3N3O3S |
| Cas No. | 901260-40-0 |
| Smiles | C(C)(=O)N1C=2C(=CC(S(=O)(=O)N3CCN(CC3)C4=CC(C(F)(F)F)=CC=C4)=CC2)CC1 |
| Relative Density. | 1.395 g/cm3 (Predicted) |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||
| Solubility Information | DMSO: 4.53 mg/mL (10 mM), Sonication is recommended. | ||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||
DMSO
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