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DuP-697

DuP-697
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Purity:100%
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DuP-697

Catalog No. T15181Cas No. 88149-94-4
DuP-697 is an irreversible and specific inhibitor of COX-2 with IC50 values of 10 nM and 800 nM for human COX-2 and COX-1. DuP-697 shows antiproliferative activity with an IC50 of 42.8 nM. DuP-697 exhibits antiangiogenic, anti-inflammatory, antipyretic and apoptotic effects.
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Pack SizePriceAvailabilityQuantity
1 mg$89In Stock
5 mg$198In Stock
10 mg$323In Stock
25 mg$553In Stock
50 mg$789In Stock
100 mg$1,070In Stock
500 mg$2,150In Stock
1 mL x 10 mM (in DMSO)$239In Stock
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Product Introduction

Bioactivity
Description
DuP-697 is an irreversible and specific inhibitor of COX-2 with IC50 values of 10 nM and 800 nM for human COX-2 and COX-1. DuP-697 shows antiproliferative activity with an IC50 of 42.8 nM. DuP-697 exhibits antiangiogenic, anti-inflammatory, antipyretic and apoptotic effects.
In vitro
In HT29 cells, DuP-697 (25-100 nM) causes apoptosis in a concentration-dependent manner. DuP-697 in 1, 10, and 100 nM concentrations cause antiangiogenic effects in HT29 colorectal cancer cells with antiangiogenic scores of 0.5, 0.8, and 1.2[1].
In vivo
DuP-697 inhibits bull seminal vesicle prostaglandin synthesis with an IC50 value of 24 μM and rat brain PG synthesis with an IC50 value of 4.5 μM[2].
Chemical Properties
Molecular Weight411.31
FormulaC17H12BrFO2S2
Cas No.88149-94-4
Storage & Solubility Information
Storage Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 45 mg/mL (109.41 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.4313 mL12.1563 mL24.3126 mL121.5628 mL
5 mM0.4863 mL2.4313 mL4.8625 mL24.3126 mL
10 mM0.2431 mL1.2156 mL2.4313 mL12.1563 mL
20 mM0.1216 mL0.6078 mL1.2156 mL6.0781 mL
50 mM0.0486 mL0.2431 mL0.4863 mL2.4313 mL
100 mM0.0243 mL0.1216 mL0.2431 mL1.2156 mL

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