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Product Name | JNJ-54166060 |
Description | JNJ-54166060 is a novel, potent and selective antagonist of purinergic P2X7 receptors, with IC50 of 4 nM on human receptors. Orally bioavailable, with an ED50 of 2.3 mg/kg and a brain/plasma ratio of close to 3 in rats1. Synthetic. Purity >99% (HPLC). MW: 438.81 |
Size | 10 mg |
Concentration | 10 nM - 1 µM. |
Applications | n/a |
Other Names | n/a |
Gene, Accession, CAS # | n/a |
Catalog # | J-125 |
Price | please inquire |
Order / More Info | JNJ-54166060 from ALOMONE LABS |
Product Specific References | n/a |
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