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JMS-17-2

Catalog No.: A19100

CX3CR1 antagonist

JMS-17-2

JMS-17-2 Chemical Structure

CAS NO. 1380392-05-1

JMS-17-2 is a potent and selective CX3CR1 antagonist with an IC50 of 0.32 nM.

Availability: In stock

Package Price Qty
5 mg
$350.00
10 mg
$650.00
50 mg
$2,000.00
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Biological Activity

JMS-17-2 is a potent and selective CX3CR1 antagonist with an IC50 of 0.32 nM.
In vitro DMSO 35 mg/mL (83.34 mM)
Water Insoluble
Ethanol 9 mg/mL (21.43 mM)
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
0.1 mM 23.81 mL 119.06 mL 238.12 mL
0.5 mM 4.76 mL 23.81 mL 47.62 mL
1 mM 2.38 mL 11.91 mL 23.81 mL
5 mM 0.48 mL 2.38 mL 4.76 mL

*The above data is based on the productmolecular weight 419.95. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.

Catalog Num A19100
Actions Antagonist
CAS No. 1380392-05-1
Formula C25H26ClN3O
M. Wt 419.95
Purity >98%
Synonyms JMS17-2, JMS172
SMILES O=C1C2=CC=CN2C3=C(C=CC=C3)N1CCCN4CCC(C5=CC=C(Cl)C=C5)CC4
Storage

Store lyophilized at -20ºC, keep desiccated.
In lyophilized form, the chemical is stable for 36 months.
In solution, store at -20ºC and use within 3 months to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

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