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Nav1.7-IN-8
SKU
HY-141547-100mg
Category Reference compound
Tags Cytochrome P450;Sodium Channel, Inflammation/Immunology, Membrane Transporter/Ion Channel;Metabolic Enzyme/Protease
Products Details
Product Description
– Nav1.7-IN-8 is a potent blockage of NaV1.7 with high selectivity for the inhibition of NaV1.7 over the subtypes hNaV1.1 and hNaV1.5. Nav1.7-IN-8 inhibits CYP2C9 and CYP3A4 with an IC50 of 0.17 μM and 0.077 μM, respectively. Nav1.7-IN-8 displays significant analgesic effects in rodent models of acute and inflammatory pain[1].
Web ID
– HY-141547
Shipping
– Room temperature
Applications
– COVID-19-immunoregulation
Molecular Formula
– C21H12ClF2N5O4S2
References
– [1]Focken T, et al. Discovery of Aryl Sulfonamides as Isoform-Selective Inhibitors of NaV1.7 with Efficacy in Rodent Pain Models. ACS Med Chem Lett. 2016;7(3):277-282. Published 2016 Jan 19.
CAS Number
– 1432913-44-4
Molecular Weight
– 535.93
SMILES
– O=S(NC1=NC=NS1)(C2=C(F)C=C(OC3=C(C4=CC=C5ON=C(C5=C4)N)C=C(Cl)C=C3)C(F)=C2)=O
Clinical Information
– No Development Reported
Research Area
– Inflammation/Immunology
Solubility
– 10 mM in DMSO
Target
– Cytochrome P450;Sodium Channel
Isoform
– CYP2;CYP3;Nav1.7
Pathway
– Membrane Transporter/Ion Channel;Metabolic Enzyme/Protease
Product type
– Reference compound
Disclaimer: All products are for Research use only unless clearly stated otherwise on the product datasheet. Datasheets provided on the website are drafts for reference purpose only and you are requested to always refer to the hard copy included in the kit for your experimentation. Agdia Products are available for delivery only in Canada.