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Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
AM-0466 is a sodium channel inhibitor with nanomolar levels of NaV1.7 inhibitory activity. AM-0466 exhibits potent pharmacodynamic activity in a NaV1.7-dependent histamine-induced itch model. AM-0466 also showed significant analgesic effects in capsaicin-induced pain models. After optimizing its pharmacokinetic properties, AM-0466 was advanced into in vivo targeting and efficacy models for testing.
| Canonical Smiles | COC1=C(C=CC(=C1)C2=CC=CC=C2C(F)(F)F)N3C4=C(C=CC3=O)C=C(C=C4)S(=O)(=O)NC5=NC=CC=N5 |
|---|---|
| IUPAC Name | 1-[2-methoxy-4-[2-(trifluoromethyl)phenyl]phenyl]-2-oxo-N-pyrimidin-2-ylquinoline-6-sulfonamide |
| InChIKey | RUFNTHMLMHZGFI-UHFFFAOYSA-N |
| INCHI | 1S/C27H19F3N4O4S/c1-38-24-16-17(20-5-2-3-6-21(20)27(28,29)30)7-10-23(24)34-22-11-9-19(15-18(22)8-12-25(34)35)39(36,37)33-26-31-13-4-14-32-26/h2-16H,1H3,(H,31,32,33) |
| PubChem CID | 129317952 |
| MeSH Entry Terms | 1-(3-methoxy-3'-(trifluoromethyl)-(1,1'-biphenyl)-4-yl)-2-oxo-N-(pyrimidin-2-yl)-1,2-dihydroquinoline-6-sulfonamide;AM-0466 |
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