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BMS CCR2 22

BMS CCR2 22
BMS CCR2 22 is a potent and selective antagonist of CCR2 with calcium flux IC50 of 18 nM, chemotaxis IC50 of 1 nM, and binding IC50 of 5.1 nM.
Catalog No. T14688Cas No. 445479-97-0
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BMS CCR2 22

Catalog No. T14688Cas No. 445479-97-0
BMS CCR2 22 is a potent and selective antagonist of CCR2 with calcium flux IC50 of 18 nM, chemotaxis IC50 of 1 nM, and binding IC50 of 5.1 nM.
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Pack SizePriceAvailabilityQuantity
1 mg$53In Stock
5 mg$118In Stock
10 mg$193In Stock
25 mg$387In Stock
50 mg$592In Stock
100 mg$798In Stock
200 mg$1,070In Stock
1 mL x 10 mM (in DMSO)$158In Stock
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Product Introduction

Bioactivity
Description
BMS CCR2 22 is a potent and selective antagonist of CCR2 with calcium flux IC50 of 18 nM, chemotaxis IC50 of 1 nM, and binding IC50 of 5.1 nM.
Targets&IC50
CCR2:5.1 nM
In vitro
BMS CCR2 22 inhibits the internalization of hMCP1_AF647 (IC50 = 2 nM)[2]. HAoECs with BMS CCR2 22 before MCP-1 increases the cell surface levels of VCAM-1 from 72.8 to 160% and PECAM1 from 97.2 and 127%[3].
Chemical Properties
Molecular Weight593.66
FormulaC28H34F3N5O4S
Cas No.445479-97-0
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 225.0 mg/mL (379.0 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.6845 mL8.4223 mL16.8447 mL84.2233 mL
5 mM0.3369 mL1.6845 mL3.3689 mL16.8447 mL
10 mM0.1684 mL0.8422 mL1.6845 mL8.4223 mL
20 mM0.0842 mL0.4211 mL0.8422 mL4.2112 mL
50 mM0.0337 mL0.1684 mL0.3369 mL1.6845 mL
100 mM0.0168 mL0.0842 mL0.1684 mL0.8422 mL

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