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Suzetrigine

CAT: 0804-HY-148800-01Size: 5 mgDry Ice: NoHazardous: No
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CAT#:0804-HY-148800-01Size:5 mg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Suzetrigine (VX-548) is an orally active and highly selective NaV1.8 inhibitor that acts as an analgesic. Suzetrigine is also a blocker of sodium channel protein type 10 subunit alpha. Suzetrigine is promising for research of acute pain after abdominoplasty and bunionectomy[1][2][3][4][5].
CAS Number
2649467-58-1
Product Name Alternative
VX-548
UNSPSC
12352005
Hazard Statement
H302, H315, H319
Target
Sodium Channel
Type
Reference compound
Related Pathways
Membrane Transporter/Ion Channel
Applications
Neuroscience-Neuromodulation
Field of Research
Neurological Disease
Assay Protocol
https://www.medchemexpress.com/suzetrigine.html
Concentration
10mM
Purity
99.96
Solubility
DMSO : 116.67 mg/mL (ultrasonic)
Smiles
NC(C1=CC(NC([C@H]2[C@H](C3=C(C(F)=C(C=C3)F)OC)[C@@H]([C@@](C)(O2)C(F)(F)F)C)=O)=CC=N1)=O
Molecular Formula
C21H20F5N3O4
Molecular Weight
473.39
Precautions
H302, H315, H319
References & Citations
[1]WHO Drug Information-World Health Organization (WHO) .|[2]Jones J, et al. Selective Inhibition of NaV1.8 with VX-548 for Acute Pain. N Engl J Med. 2023 Aug 3;389 (5) :393-405.|[3]Zhang H, et al. A simple and sensitive ultra-high performance liquid chromatography tandem mass spectrometry method for the quantitative analysis of VX-548 in monkey plasma: Method validation and application to pharmacokinetic study. Biomed Chromatogr. 2024 Jul;38 (7) :e5907. |[4]Yu G, et al. Gender difference in the pharmacokinetics and metabolism of VX-548 in rats. Biopharm Drug Dispos. 2024 Apr;45 (2) :107-114.|[5]Qin H, et al. Discovery of selective NaV1.8 inhibitors based on 5-chloro-2- (4,4-difluoroazepan-1-yl) -6-methyl nicotinamide scaffold for the treatment of pain. Eur J Med Chem. 2023 Jun 5;254:115371.
Shipping Conditions
Blue Ice
Storage Conditions
-20°C, 3 years (Powder)
Scientific Category
Reference compound1
Clinical Information
Launched

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