Suzetrigine
- Product Name
- Suzetrigine
- CAS No.
- 2649467-58-1
- Chemical Name
- Suzetrigine
- Synonyms
- VX-548;suzetrigin;Suzetrigine;Suzetrigine1;FANDACHEM VX-548;SUZETRIGINE/VAX548;VX-548(Suzetrigine);Suzetrigine (VX-548);FANDACHEM Suzetrigine;Suzetrigine,PhEur/USP(DMF)
- CBNumber
- CB412520545
- Molecular Formula
- C21H20F5N3O4
- Formula Weight
- 473.4
- MOL File
- 2649467-58-1.mol
Suzetrigine Property
- Boiling point:
- 591.8±50.0 °C(Predicted)
- Density
- 1.399±0.06 g/cm3(Predicted)
- solubility
- Acetonitrile: Slightly Soluble: 0.1-1 mg/ml
DMSO: Sparingly Soluble: 1-10 mg/ml - form
- Solid
- pka
- 11.74±0.70(Predicted)
- color
- White to light yellow
- InChIKey
- XSQUJFKRXZMOKA-KRZZIQMTNA-N
- SMILES
- C([C@@H]1O[C@@](C)(C(F)(F)F)[C@@H](C)[C@H]1C1C=CC(F)=C(F)C=1OC)(=O)NC1=CC=NC(C(=O)N)=C1 |&1:1,3,9,11,r|
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P332+P313IF SKIN irritation occurs: Get medical advice/attention.
P337+P313IF eye irritation persists: Get medical advice/attention.
P501Dispose of contents/container to..…
Suzetrigine Chemical Properties,Usage,Production
Description
Suzetrigine is an inhibitor of voltage-gated sodium channel 1.8 (Nav1.8; IC50 = 0.7 nM for the human channel).1 It is selective for Nav1.8 over a panel of eight additional voltage-gated sodium channels (IC50s = >10,000 nM for all).WARNING This product is not for human or veterinary use.
Synthesis
The synthesis of Suzetrigine (VX-548) revolves around the highly stereoselective construction of its tetrahydropyran core. A typical synthetic route begins with a chiral starting material (e.g., a chiral epoxide) that undergoes a stereoselective addition reaction with a fluoroaryllithium reagent, introducing a phenyl group and a trifluoromethyl group. Subsequently, a nucleophilic cyclization reaction forms the crucial tetrahydropyran ring, thus determining the correct configuration of the four stereocenters. Subsequent steps involve standard organotransformation reactions, such as cross-coupling reactions (e.g., the Suzuki coupling reaction), to introduce the pyridine moiety, ultimately yielding the final Suzetrigine product via deprotection and salt formation.
References
[1] JIM JONES. Selective Inhibition of NaV1.8 with VX-548 for Acute Pain.[J]. New England Journal of Medicine, 2023, 389 5: 393-405. DOI: 10.1056/nejmoa2209870
Suzetrigine Preparation Products And Raw materials
Raw materials
Preparation Products
Suzetrigine Suppliers
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View Lastest Price from Suzetrigine manufacturers
- Product
- Suzetrigine 2649467-58-1
- Price
- US $0.00/g
- Min. Order
- 1g
- Purity
- 99%
- Supply Ability
- 9999
- Release date
- 2026-03-02
- Product
- SUZETRIGINE 2649467-58-1
- Price
- US $1.00/g
- Min. Order
- 300g
- Purity
- 99.8%
- Supply Ability
- 20 TONS
- Release date
- 2025-11-01
- Product
- Suzetrigine 2649467-58-1
- Price
- US $0.00/g
- Min. Order
- 1g
- Purity
- More Than 99%
- Supply Ability
- 100kg/Month
- Release date
- 2025-09-10