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Product Name | MK-5435 |
Description | MK-5435 is a potent and selective allosteric mGluR1 antagonist, inhibiting human and rat mGluR1 with IC50 of 4.3 and 3.6 nM, respectively. It is selective over mGluR5 (IC50 = 1.5 µM), mGluR2 and mGluR8 (IC50 = 10 µM), and has no affinity for the quisqualic binding site (IC50 >10 µM). in vivo, following an oral dose of 1 mg/kg, plasma and brain concentrations in mice were 0.17 µM and 0.45 nmol/g respectively, at 30 min post-dose1. Synthetic. Purity >98%. MW: 368.39 |
Size | 10 mg |
Concentration | 10 nM - 10 µM. |
Applications | n/a |
Other Names | n/a |
Gene, Accession, CAS # | n/a |
Catalog # | M-265 |
Price | please inquire |
Order / More Info | MK-5435 from ALOMONE LABS |
Product Specific References | n/a |
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