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LpxH-IN-AZ1

LpxH-IN-AZ1
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Purity:99.26%
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LpxH-IN-AZ1

Catalog No. T11876Cas No. 901260-40-0
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.
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Pack SizePriceAvailabilityQuantity
1 mg$50In Stock
5 mg$122In Stock
10 mg$193In Stock
25 mg$455In Stock
50 mg$669In Stock
100 mg$953In Stock
500 mg$1,920In Stock
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Product Introduction

Bioactivity
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 (E. coli):0.14 μM, LpxH (Klebsiella pneumoniae):0.36 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].
Chemical Properties
Molecular Weight453.48
FormulaC21H22F3N3O3S
Cas No.901260-40-0
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 4.53 mg/mL (10 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.2052 mL11.0258 mL22.0517 mL110.2584 mL
5 mM0.4410 mL2.2052 mL4.4103 mL22.0517 mL
10 mM0.2205 mL1.1026 mL2.2052 mL11.0258 mL

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Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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