1235406-03-7
Chemical Structure
PF-05186462
- CAS No.: 1235406-03-7
- Formula:C19H10ClF4N5O3S2
- Molecular Weight:531.89
IUPAC Name: 5-chloro-2-fluoro-4-(2-(pyridazin-4-yl)-4-(trifluoromethyl)phenoxy)-N-(1,3,4-thiadiazol-2-yl)benzenesulfonamide
InChIKey: ZAGGUCLXSCVDCK-UHFFFAOYSA-N
SMILES: O=S(C1=CC(Cl)=C(OC2=CC=C(C(F)(F)F)C=C2C3=CC=NN=C3)C=C1F)(NC4=NN=CS4)=O
Biological Activity: PF-05186462 is a potent and selective inhibitor of human Nav1.7 voltage-dependent sodium channel, with an IC50 of 21 nM. PF-05186462 shows significant selectivity for Nav1.7 versus other sodium channels (Nav 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, and 1.8). PF-05186462 can be used for the research of acute or chronic pain[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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PF-05186462 | 99.69% | PF-05186462 is a potent and selective inhibitor of human Nav1.7 voltage-dependent sodium channel, with an IC50 of 21 nM. PF-05186462 shows significant selectivity for Nav1.7 versus other sodium channels (Nav 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, and 1.8). PF-05186462 can be used for the research of acute or chronic pain. | ||||||||||||||||||||
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Keywords
